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908259_13_item7_p27_s1
908259_12_item7_p28_s6
The agreement may be terminated by us at any time, at our sole discretion, without any cost or penalty.
The LPC Purchase Agreement may be terminated by us at any time, at our sole discretion, without any cost or penalty.
2
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[]
[ "LPC", "Purchase", "Agreement" ]
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908259_13_item7_p29_s5
908259_12_item7_p29_s0
In December 2011, we established a partnership agreement with Azanta Danmark A/S, or Azanta, to provide access to ZYBRESTAT for the treatment of patients in a specified territory with ATC on a compassionate use basis.
In December 2011, we established a distribution agreement with Azanta, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
2
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[]
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908259_13_item7_p30_s7
908259_12_item7_p30_s11
If we are unable to access additional funds when needed, we may not be able to continue the development of our product candidates or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
If we are unable to raise additional funds when needed, we will not be able to continue development of our product candidates or we will be required to delay, scale back or eliminate some or all of our development programs or cease operations.
2
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908259_13_item7_p31_s0
908259_12_item7_p30_s13
If we access funds through collaborative or licensing arrangements, we may be required to relinquish rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize on our own, on terms that are not favorable to us.
If we raise funds through collaborative or licensing arrangements, we may be required to relinquish, on terms that are not favorable to us, rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize.
2
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908259_13_item7_p30_s1
908259_12_item7_p30_s7
However, this level of cash utilization does not provide for the initiation of any significant projects to further the development of our most advanced product candidates, primarily ZYBRESTAT in ATC.
However, this level of cash utilization does not allow for the initiation of any significant projects, including clinical trials, to further the development of our most advanced product candidates, primarily ZYBRESTAT.
2
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908259_13_item7_p5_s12
908259_12_item7_p30_s7
However, this level of cash utilization does not provide for the initiation of any significant projects to further the development of our most advanced product candidates, primarily ZYBRESTAT in ATC.
However, this level of cash utilization does not allow us to initiate any significant projects, including clinical trials, to further the development of our most advanced product candidates, primarily ZYBRESTAT.
2
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908259_13_item7_p6_s3
908259_12_item7_p33_s0
The preparation of financial statements in conformity with U.S. generally accepted accounting principles requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the re...
The preparation of these financial statements requires us to make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosure of contingent assets and liabilities at the date of the financial statements, as well as the reported revenues and expenses during the reporting perio...
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[ "us", "well", "revenues", "periods" ]
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908259_13_item7_p29_s5
908259_12_item7_p58_s0
In December 2011, we established a partnership agreement with Azanta Danmark A/S, or Azanta, to provide access to ZYBRESTAT for the treatment of patients in a specified territory with ATC on a compassionate use basis.
In December 2011, we established a distribution agreement with Azanta, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
2
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[]
[ "distribution", "expanded", "August", "2012", "certain", "territories" ]
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908259_13_item7_p20_s0
908259_12_item7_p80_s0
The Other income amounts are generally derived from net gains on foreign currency exchange.
The Other income (expense) amounts are generally derived from net gains and losses on foreign currency exchange.
2
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[]
[ "expense", "losses" ]
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908259_13_item7_p21_s0
908259_12_item7_p81_s0
The table below summarizes the components of the change in fair value of warrants for the twelve month periods ended December 31, 2011 and December 31, 2010, in thousands.
The table below summarizes the components of the change in fair value of warrants for the periods indicated, in thousands:
2
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[]
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908259_13_item7_p28_s0
908259_12_item7_p98_s0
On July 21, 2010, we entered into an at the market (ATM) equity offering sales agreement with McNicoll, Lewis Vlak LLC, (MLV), pursuant to which we may issue and sell shares of our common stock from time to time through MLV acting as our sales agent and underwriter.
On July 21, 2010, we entered into an at the market equity offering sales agreement, or ATM Agreement, with MLV Co. LLC, or MLV, pursuant to which we may issue and sell shares of our common stock from time to time through MLV who will act as our sales agent and underwriter.
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908259_13_item7_p5_s7
908259_12_item7_p98_s0
On July 21, 2010, we entered into an at the market (ATM) equity offering sales agreement with McNicoll, Lewis Vlak LLC, (MLV), pursuant to which we may issue and sell shares of our common stock from time to time through MLV acting as our sales agent and underwriter.
We also have entered into an at the market equity offering sales agreement, or the ATM Agreement, with MLV Co. LLC, or MLV, pursuant to which we may issue and sell shares of common stock from time to time through MLV acting as our sales agent and underwriter.
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908259_14_item7_p12_s0
908259_13_item7_p12_s0
In December 2011, we established a distribution agreement with Azanta Danmark A/S, or Azanta, to provide access to ZYBRESTAT for the treatment of patients with ATC on a compassionate use basis in certain specified territories.
In December 2011, we established a distribution agreement to provide access to ZYBRESTAT for the treatment of patients with ATC in certain specified territories on a compassionate use basis.
2
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[ "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "patients", "with", "ATC", "in", "certain", "specified", "territories", "on", "a", "compassionate...
[]
[]
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908259_14_item7_p41_s0
908259_13_item7_p12_s0
In December 2011, we established a distribution agreement with Azanta Danmark A/S, or Azanta, to provide access to ZYBRESTAT for the treatment of patients with ATC on a compassionate use basis in certain specified territories.
In December 2011, we established a distribution agreement with a Danish company, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
2
[ "<tag1>", "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "with", "Azanta", "Danmark", "A", "/", "S", ",", "or", "Azanta", ",", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "patients", ...
[ "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "with", "Azanta", "Danmark", "A", "/", "S", ",", "or", "Azanta", ",", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "patients", "with", "...
[ "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "with", "a", "Danish", "company", ",", "which", "was", "expanded", "in", "August", "2012", ",", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of...
[]
[ "Danish", "company", "expanded", "August", "2012" ]
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908259_14_item7_p41_s1
908259_13_item7_p13_s0
healthcare professionals in the specified territories to prescribe ZYBRESTAT to individual ATC patients while it is still in development.
Our Named Patient Program, managed by the Danish company, provides a regulatory mechanism to allow healthcare professionals in the specified territories to prescribe ZYBRESTAT to individual ATC patients while it is still in development.
2
[ "<tag1>", "healthcare", "professionals", "in", "the", "specified", "territories", "to", "prescribe", "ZYBRESTAT", "to", "individual", "ATC", "patients", "while", "it", "is", "still", "in", "development", ".", "<tag2>", "Our", "Named", "Patient", "Program", ",", ...
[ "healthcare", "professionals", "in", "the", "specified", "territories", "to", "prescribe", "ZYBRESTAT", "to", "individual", "ATC", "patients", "while", "it", "is", "still", "in", "development", "." ]
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[]
[ "Named", "Patient", "Program", "managed", "Danish", "company", "provides", "regulatory", "mechanism", "allow" ]
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908259_14_item7_p13_s1
908259_13_item7_p13_s1
Our agreement with Azanta provides that upon the receipt of ZYBRESTAT by Azanta for distribution and sale to compassionate use patients, Azanta has 30 days to inspect the product for defects and to ensure that the product conforms to the warranties made by us.
Our agreement provides that upon the receipt of ZYBRESTAT by the distributor for distribution and sale to compassionate use patients, the distributor has 30 days to inspect the product for defects and to ensure that the product conforms to the warranties made by us.
2
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[]
[ "distributor", "distributor" ]
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908259_14_item7_p16_s3
908259_13_item7_p13_s10
We recognized approximately $148,000 of product revenues in 2012, after delivery of our drug for compassionate use to Azanta and the 30 day inspection period had expired at which point the drug was deemed accepted.
In both years, we recognized product revenues after delivery of ZYBRESTAT for compassionate use to the distributor and the 30 day inspection period had expired at which point the drug was deemed accepted.
2
[ "<tag1>", "We", "recognized", "approximately", "$", "148,000", "of", "product", "revenues", "in", "2012", ",", "after", "delivery", "of", "our", "drug", "for", "compassionate", "use", "to", "Azanta", "and", "the", "30", "day", "inspection", "period", "had", ...
[ "We", "recognized", "approximately", "$", "148,000", "of", "product", "revenues", "in", "2012", ",", "after", "delivery", "of", "our", "drug", "for", "compassionate", "use", "to", "Azanta", "and", "the", "30", "day", "inspection", "period", "had", "expired", ...
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[]
[ "years", "ZYBRESTAT", "distributor" ]
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908259_14_item7_p16_s4
908259_13_item7_p13_s11
Additionally, we recognized approximately $8,000 as payment for 20% of Azanta s gross margin, as defined in the agreement, on its sales in the preceding quarter, in 2012, after Azanta notified us of the amount.
Additionally, in 2012, we recognized approximately $8,000 as revenue for 20% of the distributor s gross margin, as defined in the agreement, on its sales in the preceding quarter, after the distributor notified us of the amount.
2
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[ "Additionally", ",", "we", "recognized", "approximately", "$", "8,000", "as", "payment", "for", "20", "%", "of", "Azanta", "s", "gross", "margin", ",", "as", "defined", "in", "the", "agreement", ",", "on", "its", "sales", "in", "the", "preceding", "quarter...
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[]
[ "revenue", "distributor", "distributor" ]
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908259_14_item7_p16_s5
908259_13_item7_p13_s12
In 2013, we expect approximately the same levels of revenue as 2012, although there can be no assurance of this and at this time, we have no future firm orders from Azanta.
In 2014, we expect approximately the same range of revenue as 2013 and 2012, although there can be no assurance of this and at this time, we have no future firm orders from the distributor.
2
[ "<tag1>", "In", "2013", ",", "we", "expect", "approximately", "the", "same", "levels", "of", "revenue", "as", "2012", ",", "although", "there", "can", "be", "no", "assurance", "of", "this", "and", "at", "this", "time", ",", "we", "have", "no", "future", ...
[ "In", "2013", ",", "we", "expect", "approximately", "the", "same", "levels", "of", "revenue", "as", "2012", ",", "although", "there", "can", "be", "no", "assurance", "of", "this", "and", "at", "this", "time", ",", "we", "have", "no", "future", "firm", ...
[ "In", "2014", ",", "we", "expect", "approximately", "the", "same", "range", "of", "revenue", "as", "2013", "and", "2012", ",", "although", "there", "can", "be", "no", "assurance", "of", "this", "and", "at", "this", "time", ",", "we", "have", "no", "fut...
[]
[ "range", "distributor" ]
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908259_14_item7_p17_s0
908259_13_item7_p13_s13
Our drug was expensed in the period it was manufactured, since it is in the development stage and does not have an alternative future use.
ZYBRESTAT is expensed in the period it is manufactured because it is in the development stage and does not have an alternative future use.
2
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[ "Our", "drug", "was", "expensed", "in", "the", "period", "it", "was", "manufactured", ",", "since", "it", "is", "in", "the", "development", "stage", "and", "does", "not", "have", "an", "alternative", "future", "use", "." ]
[ "ZYBRESTAT", "is", "expensed", "in", "the", "period", "it", "is", "manufactured", "because", "it", "is", "in", "the", "development", "stage", "and", "does", "not", "have", "an", "alternative", "future", "use", "." ]
[]
[ "ZYBRESTAT" ]
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908259_14_item7_p17_s1
908259_13_item7_p13_s14
As a result, the product provided to Azanta had a zero cost basis, and therefore there is no cost-of-goods sold.
As a result, the product provided to the distributor had a zero cost basis, and therefore there is no cost-of-goods sold.
2
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[ "As", "a", "result", ",", "the", "product", "provided", "to", "Azanta", "had", "a", "zero", "cost", "basis", ",", "and", "therefore", "there", "is", "no", "cost", "-", "of", "-", "goods", "sold", "." ]
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[]
[ "distributor" ]
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908259_14_item7_p13_s2
908259_13_item7_p13_s2
If Azanta does not notify us of any defective product within the 30-day period it will be deemed to have accepted the product.
If the distributor does not notify us of any defective product within the 30-day period it will be deemed to have accepted the product.
2
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[ "If", "Azanta", "does", "not", "notify", "us", "of", "any", "defective", "product", "within", "the", "30", "-", "day", "period", "it", "will", "be", "deemed", "to", "have", "accepted", "the", "product", "." ]
[ "If", "the", "distributor", "does", "not", "notify", "us", "of", "any", "defective", "product", "within", "the", "30", "-", "day", "period", "it", "will", "be", "deemed", "to", "have", "accepted", "the", "product", "." ]
[]
[ "distributor" ]
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908259_14_item7_p13_s5
908259_13_item7_p13_s5
This revenue will be recognized upon notification from Azanta of the gross margin earned.
This revenue will be recognized upon notification from the distributor of the gross margin earned.
2
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[ "This", "revenue", "will", "be", "recognized", "upon", "notification", "from", "Azanta", "of", "the", "gross", "margin", "earned", "." ]
[ "This", "revenue", "will", "be", "recognized", "upon", "notification", "from", "the", "distributor", "of", "the", "gross", "margin", "earned", "." ]
[]
[ "distributor" ]
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908259_14_item7_p13_s7
908259_13_item7_p13_s7
As a result, the product provided to the Azanta has a zero cost basis, and therefore there is no cost-of-goods sold.
As a result, the product provided to the distributor has a zero cost basis, and therefore no cost-of-goods sold has been recorded.
2
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[]
[ "distributor", "recorded" ]
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908259_14_item7_p17_s1
908259_13_item7_p13_s7
As a result, the product provided to the Azanta has a zero cost basis, and therefore there is no cost-of-goods sold.
As a result, the product provided to the distributor had a zero cost basis, and therefore there is no cost-of-goods sold.
2
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[]
[ "distributor" ]
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908259_14_item7_p21_s2
908259_13_item7_p16_s1
The reduction in employee compensation and related expenses for the two years ended December 31, 2012 and 2011 is primarily due to the reduction of research and development programs as noted above and associated restructuring and reduction of staff for the decreased level of activity.
The reduction for the year ended December 31, 2012, as compared to the year ended December 31, 2011, was primarily due to the reduction of research and development programs as noted above and associated restructuring and reduction of staff for the decreased level of activity.
2
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[]
[ "year", "compared", "year" ]
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908259_14_item7_p22_s11
908259_13_item7_p16_s8
As a result, research and development expenses in the future could vary significantly from those incurred in the 2012 fiscal year.
As a result, general and administrative expenses in the future could vary significantly from those incurred in the 2013 fiscal year.
2
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[]
[ "general", "administrative" ]
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908259_14_item7_p22_s10
908259_13_item7_p18_s8
If we receive funding, as discussed above, we may begin new clinical trials in which case general and administrative expenses could increase in support of research and development activities.
As discussed above, we expect to begin new clinical trials and may incur increased manufacturing costs in the 2014 fiscal year, in which case general and administrative expenses could increase in support of research and development activities.
2
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[ "If", "we", "receive", "funding", ",", "as", "discussed", "above", ",", "we", "may", "begin", "new", "clinical", "trials", "in", "which", "case", "general", "and", "administrative", "expenses", "could", "increase", "in", "support", "of", "research", "and", "...
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[]
[ "expect", "incur", "increased", "manufacturing", "costs", "2014", "fiscal", "year" ]
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908259_14_item7_p0_s6
908259_13_item7_p1_s5
Accordingly, our resources have been focused primarily on supporting our ovarian Phase 2 clinical trial which is being conducted by the Gynecological Oncology Group, or GOG, our acute myeloid leukemia, or AML Phase 1 clinical trial being conducted by the University of Florida, our distribution agreement with Azanta, pr...
Accordingly, during 2013 our resources were focused on supporting our ovarian Phase 2 clinical trial which is being conducted by the Gynecologic Oncology Group, or GOG, our Phase 1 clinical trial in acute myeloid leukemia, or AML, being conducted by the University of Florida, our distribution agreement for the compassi...
2
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[ "Accordingly", ",", "our", "resources", "have", "been", "focused", "primarily", "on", "supporting", "our", "ovarian", "Phase", "2", "clinical", "trial", "which", "is", "being", "conducted", "by", "the", "Gynecological", "Oncology", "Group", ",", "or", "GOG", "...
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[]
[ "2013", "Gynecologic", "compassionate", "use", "ZYBRESTAT", "anaplastic", "thyroid", "cancer", "ATC" ]
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908259_14_item7_p0_s7
908259_13_item7_p1_s6
We have also spent resources completing our ATC trial (FACT trial) and designing a Phase 3 registrational study in anaplastic thyroid cancer, or ATC (FACT 2 trial), and while we were successful in receiving a SPA with the FDA for the FACT 2 trial, we have subsequently determined that this trial is not financially feasi...
In 2012 and earlier years, we also spent resources completing our ATC trial (FACT trial) and designing a Phase 3 registrational study in ATC (FACT 2 trial), and while we were successful in receiving a SPA with the FDA for the FACT 2 trial, we have subsequently determined that this trial is not financially feasible.
2
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[]
[ "2012", "earlier", "years" ]
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908259_14_item7_p30_s1
908259_13_item7_p24_s1
The net cash used in both periods was primarily attributable to the net losses, adjusted to exclude certain non-cash items, primarily in the 2011 period from a change in the fair value of warrants and other financial instruments of $2,222,000.
The net cash used in both periods was primarily attributable to the net losses, adjusted to exclude certain non-cash items, primarily stock based compensation.
2
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[]
[ "stock", "based", "compensation" ]
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908259_14_item7_p41_s5
908259_13_item7_p29_s10
OXiGENE and Azanta will cooperate on regulatory activities relating to ZYBRESTAT for the treatment of ATC within the territory.
OXiGENE and the Danish company will cooperate on regulatory activities relating to ZYBRESTAT for the treatment of ATC within the specified territories.
2
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[ "OXiGENE", "and", "Azanta", "will", "cooperate", "on", "regulatory", "activities", "relating", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "ATC", "within", "the", "territory", "." ]
[ "OXiGENE", "and", "the", "Danish", "company", "will", "cooperate", "on", "regulatory", "activities", "relating", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "ATC", "within", "the", "specified", "territories", "." ]
[]
[ "Danish", "company", "specified", "territories" ]
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908259_14_item7_p41_s6
908259_13_item7_p29_s11
There will be no transfer of ownership of intellectual property rights for ZYBRESTAT to Azanta under the terms of the agreement.
There will be no transfer of ownership of intellectual property rights for ZYBRESTAT to the Danish company under the terms of the agreement.
2
[ "<tag1>", "There", "will", "be", "no", "transfer", "of", "ownership", "of", "intellectual", "property", "rights", "for", "ZYBRESTAT", "to", "Azanta", "under", "the", "terms", "of", "the", "agreement", ".", "<tag2>", "There", "will", "be", "no", "transfer", "...
[ "There", "will", "be", "no", "transfer", "of", "ownership", "of", "intellectual", "property", "rights", "for", "ZYBRESTAT", "to", "Azanta", "under", "the", "terms", "of", "the", "agreement", "." ]
[ "There", "will", "be", "no", "transfer", "of", "ownership", "of", "intellectual", "property", "rights", "for", "ZYBRESTAT", "to", "the", "Danish", "company", "under", "the", "terms", "of", "the", "agreement", "." ]
[]
[ "Danish", "company" ]
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908259_14_item7_p41_s7
908259_13_item7_p29_s12
We do not expect to receive significant income from Azanta under this arrangement.
We do not expect to receive significant income from the Danish company under this arrangement.
2
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[ "We", "do", "not", "expect", "to", "receive", "significant", "income", "from", "Azanta", "under", "this", "arrangement", "." ]
[ "We", "do", "not", "expect", "to", "receive", "significant", "income", "from", "the", "Danish", "company", "under", "this", "arrangement", "." ]
[]
[ "Danish", "company" ]
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908259_14_item7_p12_s0
908259_13_item7_p29_s5
In December 2011, we established a distribution agreement with Azanta, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
In December 2011, we established a distribution agreement to provide access to ZYBRESTAT for the treatment of patients with ATC in certain specified territories on a compassionate use basis.
2
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[ "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "with", "Azanta", ",", "which", "was", "expanded", "in", "August", "2012", ",", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "patients", "...
[ "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "patients", "with", "ATC", "in", "certain", "specified", "territories", "on", "a", "compassionate...
[]
[]
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908259_14_item7_p41_s0
908259_13_item7_p29_s5
In December 2011, we established a distribution agreement with Azanta, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
In December 2011, we established a distribution agreement with a Danish company, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
2
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[ "In", "December", "2011", ",", "we", "established", "a", "distribution", "agreement", "with", "Azanta", ",", "which", "was", "expanded", "in", "August", "2012", ",", "to", "provide", "access", "to", "ZYBRESTAT", "for", "the", "treatment", "of", "patients", "...
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[]
[ "Danish", "company" ]
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908259_14_item7_p13_s0
908259_13_item7_p29_s6
The Named Patient Program, to be managed by Azanta, provides a regulatory mechanism to allow healthcare professionals in the specified territories to prescribe ZYBRESTAT to individual ATC patients while it is still in development.
provides a regulatory mechanism to allow healthcare professionals in the specified territories to prescribe ZYBRESTAT to individual ATC patients while it is still in development.
2
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[]
[]
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908259_14_item7_p41_s1
908259_13_item7_p29_s6
The Named Patient Program, to be managed by Azanta, provides a regulatory mechanism to allow healthcare professionals in the specified territories to prescribe ZYBRESTAT to individual ATC patients while it is still in development.
Our Named Patient Program, managed by the Danish company, provides a regulatory mechanism to allow healthcare professionals in the specified territories to prescribe ZYBRESTAT to individual ATC patients while it is still in development.
2
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[]
[ "Danish", "company" ]
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908259_14_item7_p41_s2
908259_13_item7_p29_s7
Under the terms of the agreement, we will provide ZYBRESTAT to Azanta.
Under the terms of the agreement, we provide ZYBRESTAT to the Danish company.
2
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[]
[ "Danish", "company" ]
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908259_14_item7_p41_s3
908259_13_item7_p29_s8
Azanta will serve as exclusive distributor for ZYBRESTAT in the specified territories for this purpose and will provide ZYBRESTAT to physicians solely to treat ATC on a compassionate use basis in the specified territories until such time as ZYBRESTAT may obtain marketing approval in that territory.
The Danish company serves as exclusive distributor for ZYBRESTAT in the specified territories for this purpose and provides ZYBRESTAT to physicians solely to treat ATC on a compassionate use basis in the specified territories until such time as ZYBRESTAT may obtain marketing approval in that territory.
2
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[]
[ "Danish", "company", "serves", "provides" ]
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908259_14_item7_p5_s9
908259_13_item7_p30_s2
Any significant further development of ZYBRESTAT or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to our existing financing arrangements.
Any significant further development of ZYBRESTAT such as conducting pivotal Phase 3 studies in ovarian cancer or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to our existing financing arrangements, as to which we can give you no assurance.
2
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[]
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908259_14_item7_p42_s4
908259_13_item7_p30_s6
While we believe we have addressed these findings, we have no assurance that the FDA may not require more information or more changes in the future, which may be significant See Item 1A Risk Factors above regarding regulatory compliance and approvals; the progress of our research and development programs; the time and ...
Our ongoing capital requirements will depend on numerous factors, including: the progress and results of preclinical testing and clinical trials of our product candidates under development, including ZYBRESTAT and OXi4503; the costs of complying with FDA and other regulatory agency requirements; the progress of our res...
2
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[]
[ "ongoing", "capital", "requirements", "depend", "numerous", "factors", "results", "preclinical", "testing", "trials", "candidates", "ZYBRESTAT", "OXi4503", "complying", "agency", "requirements" ]
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908259_14_item7_p6_s2
908259_13_item7_p31_s0
If we raise funds through collaborative or licensing arrangements, we may be required to relinquish, on terms that are not favorable to us, rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize.
If we access funds through collaborative or licensing arrangements, we may be required to relinquish rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize on our own, on terms that are not favorable to us.
2
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[]
[ "access" ]
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908259_14_item7_p4_s1
908259_13_item7_p5_s1
We expect to incur significant additional operating losses over at least the next several years, principally as a result of our continuing clinical trials and anticipated research and development expenditures.
We expect to incur significant additional operating losses over at least the next several years, principally as a result of our plans to develop and commercialize ZYBRESTAT for the treatment of ovarian cancer, neuroendocrine tumors and potentially ATC in Europe, continuing and new clinical trials and anticipated resear...
2
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[]
[ "plans", "develop", "commercialize", "ZYBRESTAT", "treatment", "ovarian", "cancer", "neuroendocrine", "tumors", "potentially", "ATC", "Europe", "new" ]
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908259_14_item7_p5_s9
908259_13_item7_p5_s13
Any significant further development of ZYBRESTAT or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to our existing financing arrangements, as to which we can give you no assurance.
Any significant further development of ZYBRESTAT such as conducting pivotal Phase 3 studies in ovarian cancer or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to our existing financing arrangements, as to which we can give you no assurance.
2
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[ "Any", "significant", "further", "development", "of", "ZYBRESTAT", "or", "other", "capital", "intensive", "activities", "will", "be", "contingent", "upon", "our", "ability", "to", "raise", "additional", "capital", "in", "addition", "to", "our", "existing", "financ...
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[]
[ "conducting", "pivotal", "Phase", "3", "studies", "ovarian", "cancer" ]
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908259_14_item7_p42_s5
908259_13_item7_p5_s16
If we are unable to access additional funds when needed, we may not be able to continue the development of our product candidates or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
If we are unable to raise additional funds when needed, we will not be able to continue development of our product candidates or we will be required to delay, scale back or eliminate some or all of our development programs or cease operations.
2
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[]
[ "raise", "cease" ]
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908259_14_item7_p6_s0
908259_13_item7_p5_s16
If we are unable to access additional funds when needed, we may not be able to continue the development of our product candidates or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
2
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[]
[]
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908259_14_item7_p43_s0
908259_13_item7_p6_s0
If we access funds through collaborative or licensing arrangements, we may be required to relinquish rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize on our own, on terms that are not favorable to us.
If we raise funds through collaborative or licensing arrangements, we may be required to relinquish, on terms that are not favorable to us, rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize.
2
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[]
[ "raise" ]
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908259_15_item7_p13_s0
908259_14_item7_p12_s0
In December 2011, we established a distribution agreement to provide access to ZYBRESTAT for the treatment of patients with ATC in certain specified territories on a compassionate use basis.
In December 2011, we established a distribution agreement to provide access to fosbretabulin for the treatment of patients with ATC in certain specified territories on a compassionate use basis.
2
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[]
[ "fosbretabulin" ]
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908259_15_item7_p14_s0
908259_14_item7_p13_s1
Our agreement provides that upon the receipt of ZYBRESTAT by the distributor for distribution and sale to compassionate use patients, the distributor has 30 days to inspect the product for defects and to ensure that the product conforms to the warranties made by us.
Our agreement provided that upon the receipt of fosbretabulin by the distributor for distribution and sale to compassionate use patients, the distributor had 30 days to inspect the product for defects and to ensure that the product conforms to the warranties made by us.
2
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908259_15_item7_p14_s3
908259_14_item7_p13_s4
Also, the distributor will pay to us, on a quarterly basis, an amount equal to 20% of the distributor s gross margin, as defined in the agreement, on its sales of ZYBRESTAT in the preceding quarter, less the cost of introductory drug provided at no cost.
Also, the distributor paid to us, on a quarterly basis, an amount equal to 20% of the distributor s gross margin, as defined in the agreement, on its sales of fosbretabulin in the preceding quarter, less the cost of introductory drug provided at no cost.
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908259_15_item7_p16_s6
908259_14_item7_p15_s0
The Series A Preferred Stock was valued using Level 2 inputs by reference to the market value of our common stock into which the Series A Preferred Stock was convertible.
The fair value of the Series B Preferred Stock was valued using Level 2 inputs by reference to the market value of the Company s common stock into which the Series B Preferred Stock is convertible.
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908259_15_item7_p16_s7
908259_14_item7_p15_s1
The Series A Warrants and Series B Warrants granted were valued using the Black-Scholes valuation model and the following Level 3 input assumptions:
The fair values for the Warrants granted were valued using the Black-Scholes valuation model and the following Level 3 input assumptions:
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908259_15_item7_p16_s0
908259_14_item7_p15_s6
The fair value of the Series B Preferred Stock was valued using Level 2 inputs by reference to the market value of the Company s common stock into which the Series B Preferred Stock is convertible.
The Series A Preferred Stock was valued using Level 2 inputs by reference to the market value of our common stock into which the Series A Preferred Stock was convertible.
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908259_15_item7_p16_s1
908259_14_item7_p15_s7
The fair values for the Warrants granted were valued using the Black-Scholes valuation model and the following Level 3 input assumptions:
The Series A Warrants and Series B Warrants granted were valued using the Black-Scholes valuation model and the following Level 3 input assumptions:
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908259_15_item7_p18_s2
908259_14_item7_p18_s1
In 2013, the increase as compared to 2012 is primarily due to external services costs for the manufacturing of drug product for clinical use and potentially for the filing of a European Marketing Authorization application for ZYBRESTAT in ATC.
In 2013, the increase as compared to 2012 is primarily due to external services costs for the manufacturing of drug product for clinical use and potentially to support any regulatory filings.
2
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908259_15_item7_p18_s4
908259_14_item7_p20_s1
Such drug is expensed as manufactured and the associated cost can be impacted by the timing of when we need drug product for research and clinical trials and supplying drug for the EMA filing.
The cost of drug product is expensed as manufactured and the associated cost can be impacted by the timing of when we need drug product for research and clinical trials and supplying drug for potential regulatory filings.
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908259_15_item7_p39_s3
908259_14_item7_p21_s16
Any significant further development of ZYBRESTAT or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to our existing financing arrangements.
Any significant further development of fosbretabulin or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to the capital available to us under our existing financing arrangements.
2
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[ "fosbretabulin", "available", "us" ]
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908259_15_item7_p24_s4
908259_14_item7_p27_s0
LIQUIDITY AND CAPITAL RESOURCES To date, we have financed our operations principally through net proceeds received from private and public equity financings and through a strategic development arrangement with Symphony Capital Partners, L.P., which concluded in 2009.
LIQUIDITY AND CAPITAL RESOURCES To date, we have financed our operations principally through net proceeds received from private and public equity financings and through a strategic development arrangement which concluded in 2009.
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908259_15_item7_p25_s1
908259_14_item7_p30_s5
The net cash used in both periods was primarily attributable to the net losses, adjusted to exclude certain non-cash items, primarily in the year 2011 from a change in the fair value of warrants and other financial instruments of $2,222,000.
The net cash used in both periods was primarily attributable to the net losses, adjusted to exclude certain non-cash items, primarily stock based compensation.
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908259_15_item7_p25_s4
908259_14_item7_p30_s5
The net cash used in both periods was primarily attributable to the net losses, adjusted to exclude certain non-cash items, primarily in the year 2011 from a change in the fair value of warrants and other financial instruments of $2,222,000.
The net cash used in both periods was primarily attributable to the net losses, adjusted to exclude certain non-cash items, primarily stock based compensation.
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908259_15_item7_p32_s1
908259_14_item7_p32_s1
The Series A Preferred Stock was not redeemable or contingently redeemable, did not have a dividend right, nor did it have any preferences over our common stock, including liquidation rights.
The Series B Preferred Stock was not redeemable or contingently redeemable, did not have a dividend right, nor did it have any preferences over the common stock, including liquidation rights.
2
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[]
[ "B" ]
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908259_15_item7_p30_s1
908259_14_item7_p34_s1
The Series B Preferred Stock was not redeemable or contingently redeemable, did not have a dividend right, nor did it have any preferences over the common stock, including liquidation rights.
The Series A Preferred Stock was not redeemable or contingently redeemable, did not have a dividend right, nor did it have any preferences over our common stock, including liquidation rights.
2
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[]
[]
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908259_15_item7_p28_s1
908259_14_item7_p36_s6
Each unit consisted of one share of common stock and 0.5 of a warrant to purchase a share of our common stock.
Investors purchased units, at a price per unit of $2.05, which consisted of one share of common stock and 0.5 of a warrant to purchase a share of our common stock.
2
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[ "Investors", "purchased", "units", "price", "per", "2.05" ]
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908259_15_item7_p34_s1
908259_14_item7_p38_s3
Subject to these restrictions, the Company may be able to sell more shares over the next twelve months under this agreement depending on several factors, including the Company s stock price, the number of shares of our common stock outstanding and the timing of the occurrence of the sales.
Subject to these restrictions, we may be able to sell more shares under this agreement depending on several factors, including the Company s stock price, the number of shares of our common stock outstanding and the timing of the occurrence of the sales.
2
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[]
[]
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908259_15_item7_p7_s7
908259_14_item7_p38_s3
Subject to these restrictions, the Company may be able to sell more shares over the next twelve months under this agreement depending on several factors, including the Company s stock price, the number of shares of our common stock outstanding and the timing of the occurrence of the sales.
We may be able to sell more shares under this agreement depending on several factors including our stock price, the number of shares of our common stock outstanding as well as the timing of the occurrence of the sales.
2
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[]
[ "well" ]
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908259_15_item7_p13_s0
908259_14_item7_p41_s0
In December 2011, we established a distribution agreement with a Danish company, which was expanded in August 2012, to provide access to ZYBRESTAT for the treatment of patients in certain specified territories with ATC on a compassionate use basis.
In December 2011, we established a distribution agreement to provide access to fosbretabulin for the treatment of patients with ATC in certain specified territories on a compassionate use basis.
2
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[]
[ "fosbretabulin" ]
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908259_15_item7_p39_s3
908259_14_item7_p42_s2
Any significant further development of ZYBRESTAT or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to our existing financing arrangements.
Any significant further development of fosbretabulin or other capital intensive activities will be contingent upon our ability to raise additional capital in addition to the capital available to us under our existing financing arrangements.
2
[ "<tag1>", "Any", "significant", "further", "development", "of", "ZYBRESTAT", "or", "other", "capital", "intensive", "activities", "will", "be", "contingent", "upon", "our", "ability", "to", "raise", "additional", "capital", "in", "addition", "to", "our", "existing...
[ "Any", "significant", "further", "development", "of", "ZYBRESTAT", "or", "other", "capital", "intensive", "activities", "will", "be", "contingent", "upon", "our", "ability", "to", "raise", "additional", "capital", "in", "addition", "to", "our", "existing", "financ...
[ "Any", "significant", "further", "development", "of", "fosbretabulin", "or", "other", "capital", "intensive", "activities", "will", "be", "contingent", "upon", "our", "ability", "to", "raise", "additional", "capital", "in", "addition", "to", "the", "capital", "ava...
[]
[ "fosbretabulin", "available", "us" ]
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908259_15_item7_p8_s3
908259_14_item7_p42_s5
If we are unable to raise additional funds when needed, we will not be able to continue development of our product candidates or we will be required to delay, scale back or eliminate some or all of our development programs or cease operations.
If we are unable to access additional funds when needed, we may not be able to continue the development of our product candidates or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
2
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[]
[ "access", "may", "could" ]
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908259_15_item7_p8_s5
908259_14_item7_p43_s0
If we raise funds through collaborative or licensing arrangements, we may be required to relinquish, on terms that are not favorable to us, rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize.
If we access funds through collaborative or licensing arrangements, we may be required to relinquish rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize on our own, on terms that are not favorable to us.
2
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[]
[ "access" ]
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908259_15_item7_p44_s2
908259_14_item7_p46_s5
Under the license agreement, BMS is entitled to low-single-digit royalty payments for all commercial sales plus any remuneration OXiGENE receives for sale of ZYBRESTAT under named patient or compassionate use programs.
Under the license agreement, BMS is entitled to low-single-digit royalty payments for all commercial sales plus any remuneration OXiGENE receives for sale of fosbretabulin under named patient or compassionate use programs.
2
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[]
[ "fosbretabulin" ]
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908259_15_item7_p6_s1
908259_14_item7_p4_s1
We expect to incur significant additional operating losses over at least the next several years, principally as a result of our plans to develop and commercialize ZYBRESTAT for the treatment of ovarian cancer, neuroendocrine tumors and potentially ATC in Europe, continuing and new clinical trials and anticipated resear...
We expect to incur significant additional operating losses over the next several years, principally as a result of our plans to develop and commercialize fosbretabulin for the treatment of ovarian cancer and neuroendocrine tumors, and OXi4503 for the treatment of AML, continuing and new clinical trials and anticipated ...
2
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[]
[ "fosbretabulin", "OXi4503", "AML" ]
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908259_15_item7_p7_s1
908259_14_item7_p4_s3
We currently have no recurring material amount of licensing or other income.
We currently have no recurring material amount of income.
2
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[ "We", "currently", "have", "no", "recurring", "material", "amount", "of", "licensing", "or", "other", "income", "." ]
[ "We", "currently", "have", "no", "recurring", "material", "amount", "of", "income", "." ]
[]
[]
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908259_15_item7_p34_s1
908259_14_item7_p5_s4
We may be able to sell more shares under this agreement over the next twelve months depending on several factors including our stock price, the number of shares of our common stock outstanding as well as the timing of the occurrence of the sales.
Subject to these restrictions, we may be able to sell more shares under this agreement depending on several factors, including the Company s stock price, the number of shares of our common stock outstanding and the timing of the occurrence of the sales.
2
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[ "Subject", "restrictions", "Company" ]
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908259_15_item7_p8_s3
908259_14_item7_p6_s0
or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
If we are unable to access additional funds when needed, we may not be able to continue the development of our product candidates or we could be required to delay, scale back or eliminate some or all of our development programs and other operations.
2
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908259_15_item7_p41_s0
908259_14_item7_p6_s2
If we access funds through collaborative or licensing arrangements, we may be required to relinquish rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize on our own, on terms that are not favorable to us.
If we raise funds through collaborative or licensing arrangements, we may be required to relinquish, on terms that are not favorable to us, rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize.
2
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908259_16_item7_p0_s2
908259_15_item7_p0_s2
Important factors that we believe may cause such differences are discussed in the Risk Factors section of this Annual Report and in the cautionary statements accompanying the forward- looking statements in this Annual Report.
Important factors that we believe may cause such differences are discussed in the Risk Factors section of this Annual Report and in the Safe Harbor for Forward-Looking Statements Under the Private Securities Litigation Reform Act of 1995 section of this Annual Report.
2
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908259_16_item7_p7_s0
908259_15_item7_p10_s0
The valuation of employee stock options is an inherently subjective process, since market values are generally not available for long-term, non-transferable employee stock options.
The valuation of stock options is an inherently subjective process, since market values are not available for long-term, non-transferable stock options in our equity securities.
2
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[]
[ "equity", "securities" ]
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908259_16_item7_p15_s10
908259_15_item7_p40_s4
If we are unable to raise additional funds when needed, we will not be able to continue development of our product candidates or we will be required to delay, scale back or eliminate some or all of our development programs or cease operations.
If we are unable to access additional funds when needed, we may not be able to continue the development of our product candidates or we could be required to delay, scale back or eliminate some or all of our development programs and operations.
2
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[]
[ "access", "may", "could" ]
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908259_16_item7_p16_s0
908259_15_item7_p41_s0
If we raise funds through collaborative or licensing arrangements, we may be required to relinquish, on terms that are not favorable to us, rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize.
If we are able to access funds through collaborative or licensing arrangements, we may be required to relinquish rights to some of our technologies or product candidates that we would otherwise seek to develop or commercialize on our own, on terms that are not favorable to us.
2
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[]
[ "able", "access" ]
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908259_16_item7_p18_s3
908259_15_item7_p43_s3
From the inception of the agreement through December 31, 2013, we have paid a total of $2,600,000 in connection with this license.
From the inception of the ASU license agreement through December 31, 2015, we have paid a total of $2,700,000 in connection with this license.
2
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[]
[ "ASU", "2,700,000" ]
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908259_16_item7_p18_s4
908259_15_item7_p43_s4
The agreement provides for additional payments in connection with the license arrangement upon the initiation of certain clinical trials or the completion of certain regulatory approvals, which payments could be accelerated upon the achievement of certain financial milestones, as defined in the agreement.
The ASU license agreement provides for additional payments in connection with the license arrangement upon the initiation of certain clinical trials or the completion of certain regulatory approvals.
2
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[]
[ "ASU" ]
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908259_16_item7_p18_s5
908259_15_item7_p43_s5
The license agreement also provides for additional payments upon our election to develop certain additional compounds, as defined in the agreement.
The ASU license agreement also provides for additional payments upon our election to develop certain additional compounds, as defined in the ASU license agreement.
2
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[]
[ "ASU", "ASU" ]
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908259_16_item7_p19_s0
908259_15_item7_p44_s0
We also have an exclusive, world-wide, royalty-bearing license from Bristol-Myers Squibb, or BMS, for the commercial development, use and sale of products or services covered by certain patent rights to particular combretastatins, including among others, fosbretabulin.
We also have an exclusive, world-wide, royalty-bearing license from Bristol-Myers Squibb, or BMS, for the commercial development, use and sale of products or services covered by certain patent rights to particular combretastatins, including CA4P. BMS granted this license to us in February of 2002 in connection with the...
2
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[]
[ "CA4P.", "granted", "us", "February", "2002", "connection", "termination", "prior", "research", "collaboration", "agreement", "us" ]
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908259_16_item7_p18_s7
908259_15_item7_p45_s1
Either party may terminate the license upon material default of the other party.
Either party may terminate the ASU license agreement upon material default or bankruptcy of the other party.
2
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[]
[ "ASU", "agreement", "bankruptcy" ]
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908259_16_item7_p20_s1
908259_15_item7_p45_s1
Either party may terminate the license upon material default of the other party.
Either party may terminate the BMS license upon material default of the other party.
2
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[]
[ "BMS" ]
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908259_17_item7_p11_s2
908259_16_item7_p12_s0
Timing of drug manufacturing costs is variable and is impacted by the timing of when drug product is needed for clinical trials, product expiration or re-test requirements, potential regulatory filings and scheduling of production batches based on the drug manufacturer s generally long lead time requirements.
In addition, during 2015 we incurred a higher level of consulting costs as we sought additional outside expertise as we evaluated various development strategies for CA4P. Timing of drug manufacturing costs is variable and is impacted by the timing of when drug product is needed for clinical trials, product expiration o...
2
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[]
[ "addition", "2015", "incurred", "higher", "level", "consulting", "sought", "additional", "outside", "expertise", "evaluated", "various", "development", "strategies", "CA4P." ]
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908259_17_item7_p9_s4
908259_16_item7_p12_s6
General and administrative expenses The table below summarizes the most significant components of our general and administrative expenses for the periods indicated and the amount and percentage change in these components (in thousands):
RESULTS OF OPERATIONS Years ended December 31, 2016 and 2015 Research and Development expenses The table below summarizes the most significant components of our research and development expenses for the periods indicated and provides the amount and percentage change in these components (in thousands):
2
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908259_17_item7_p13_s4
908259_16_item7_p14_s2
Although general and administrative expenses decreased in 2015 compared to 2014, we expect general and administrative expenses to increase in 2016 to support our planned increase in research and development, as well as for additional business development and investor relations efforts.
We expect general and administrative expenses to increase in 2017 to support our planned increase in clinical development activities, as well as for additional business development and investor relations efforts.
2
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[]
[ "clinical", "activities" ]
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908259_17_item7_p13_s5
908259_16_item7_p15_s0
LIQUIDITY AND CAPITAL RESOURCES We are developing two investigational drugs, both VDAs, for the treatment of cancer and currently have no sources of revenue.
We are developing two investigational drugs, both VDAs, for the treatment of cancer and currently have no sources of revenue.
2
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[ "We", "are", "developing", "two", "investigational", "drugs", ",", "both", "VDAs", ",", "for", "the", "treatment", "of", "cancer", "and", "currently", "have", "no", "sources", "of", "revenue", "." ]
[]
[]
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908259_17_item7_p2_s1
908259_16_item7_p2_s1
Bevacizumab and other currently approved AA drugs work by preventing the growth of new blood vessels which can supply nutrients to tumor cells.
Bevacizumab (marketed under the brand name Avastin by Roche/Genentech) and other currently-approved AA drugs work by preventing the growth of new blood vessels which can supply nutrients to tumor cells.
2
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[ "Bevacizumab", "and", "other", "currently", "approved", "AA", "drugs", "work", "by", "preventing", "the", "growth", "of", "new", "blood", "vessels", "which", "can", "supply", "nutrients", "to", "tumor", "cells", "." ]
[ "Bevacizumab", "(", "marketed", "under", "the", "brand", "name", "Avastin", "by", "Roche", "/", "Genentech", ")", "and", "other", "currently", "-", "approved", "AA", "drugs", "work", "by", "preventing", "the", "growth", "of", "new", "blood", "vessels", "whic...
[]
[ "marketed", "brand", "name", "Avastin", "Roche", "Genentech" ]
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908259_17_item7_p6_s0
908259_16_item7_p5_s7
These estimates are based on actual time and expenses incurred by the CRO and the clinical investigators.
on actual time and expenses incurred by the CRO and the clinical investigators.
2
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[]
[]
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908259_17_item7_p11_s7
908259_16_item7_p9_s4
RESULTS OF OPERATIONS Years ended December 31, 2015 and 2014 Research and Development expenses The table below summarizes the most significant components of our research and development expenses for the periods indicated and provides the amount and percentage change in these components (in thousands):
General and administrative expenses The table below summarizes the most significant components of our general and administrative expenses for the periods indicated and the amount and percentage change in these components (in thousands):
2
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[]
[ "General", "administrative", "general", "administrative" ]
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908259_18_item7_p10_s4
908259_17_item7_p11_s7
General and administrative expenses The table below summarizes the most significant components of our general and administrative expenses for the periods indicated and the amount and percentage change in these components (in thousands):
RESULTS OF OPERATIONS Years ended December 31, 2017 and 2016 Research and Development expenses The table below summarizes the most significant components of our research and development expenses for the periods indicated and provides the amount and percentage change in these components (in thousands):
2
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[]
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908259_18_item7_p14_s6
908259_17_item7_p13_s16
Additional funding may not be available to us on acceptable terms, or at all.
We will require additional capital before we can complete the development of OXi4503 and CA4P. Additional funding may not be available to us on acceptable terms, or at all.
2
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[]
[ "require", "additional", "capital", "complete", "development", "OXi4503", "CA4P." ]
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908259_18_item7_p14_s0
908259_17_item7_p13_s6
We measure liquidity by the cash and other capital we have available to fund our operations, which are primarily focused on the advancement of our VDAs.
LIQUIDITY AND CAPITAL RESOURCES We measure liquidity by the cash and other capital we have available to fund our operations, which are primarily focused on the development of our drug candidates.
2
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[]
[ "LIQUIDITY", "CAPITAL", "RESOURCES", "development", "drug", "candidates" ]
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908259_18_item7_p15_s3
908259_17_item7_p15_s1
If our current drug candidates are approved, we will be required to pay low to mid-single-digit royalties on future net sales of products associated with the ASU patent rights until these patent rights expire.
If CA4P is approved, we will be required to pay low-single-digit royalties on future net sales of products associated with the BMS patent rights until these patent rights expire.
2
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[ "If", "CA4P", "is", "approved", ",", "we", "will", "be", "required", "to", "pay", "low", "-", "single", "-", "digit", "royalties", "on", "future", "net", "sales", "of", "products", "associated", "with", "the", "BMS", "patent", "rights", "until", "these", ...
[]
[ "CA4P", "BMS" ]
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908259_18_item7_p15_s1
908259_17_item7_p15_s3
If CA4P is approved, we will be required to pay low-single-digit royalties on future net sales of products associated with the BMS patent rights until these patent rights expire.
If our current drug candidates are approved, we will be required to pay low to mid-single-digit royalties on future net sales of products associated with the ASU patent rights until these patent rights expire.
2
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[]
[ "current", "drug", "candidates", "mid", "ASU" ]
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908259_18_item7_p6_s7
908259_17_item7_p6_s0
on actual time and expenses incurred by the CRO and the clinical investigators.
These estimates are based on actual time and expenses incurred by the CRO and the clinical investigators.
2
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908259_18_item7_p12_s0
908259_17_item7_p9_s4
RESULTS OF OPERATIONS Years ended December 31, 2016 and 2015 Research and Development expenses The table below summarizes the most significant components of our research and development expenses for the periods indicated and provides the amount and percentage change in these components (in thousands):
General and administrative expenses The table below summarizes the most significant components of our general and administrative expenses for the periods indicated and the amount and percentage change in these components (in thousands):
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