Clinical Trial Information of This SBP |
EUCTR2008-006561-89-FR
|
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Indication |
Metastatic Colorectal Cancer |
Phase |
Phase II |
Title |
A Randomized, Double-Blind, Phase II Trial of CT-322 (BMS-844203) plus Irinotecan, 5-FU and Leucovorin (FOLFIRI) versus Bevacizumab plus FOLFIRI as Second-Line Treatment for Metastatic Colorectal Cancer |
Status |
Not Recruiting |
Sponsor |
Bristol Myers Squibb International Corporation |
EUCTR2008-006561-89-IT
|
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Indication |
Metastatic Colorectal Cancer |
Phase |
Phase II |
Title |
A Randomized, Double-Blind, Phase II Trial of CT-322 (BMS-844203) plus Irinotecan, 5-FU and Leucovorin (FOLFIRI) versus Bevacizumab plus FOLFIRI as Second-Line Treatment for Metastatic Colorectal Cancer.-ND |
Status |
Not Recruiting |
Sponsor |
Bristol Myers Squibb International Corporation |
EUCTR2008-007768-41-GB
|
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Indication |
Recurrent or Advanced Non-Small Cell Lung Cancer With Non-Squamous Histology (NSCLC) |
Phase |
Phase II |
Title |
A Randomized Double-Blinded Phase II Study of Carboplatin/Paclitaxel/CT-322 versus Carboplatin/Paclitaxel/Bevacizumab as First-Line Treatment for Recurrent or Advanced Non-Small Cell Lung Cancer with Non-Squamous Histology Revised Protocol Number 04, incorporating Amendment 05 + Pharmacogenetics Blood Sample Amendment Number 01-Site Specific (version 2.0, dated 07-Jan-09) |
Status |
Not Recruiting |
Sponsor |
. |
EUCTR2008-007768-41-IT
|
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Indication |
Recurrent or Advanced Non-Small Cell Lung Cancer With Non-Squamous Histology (NSCLC) |
Phase |
Phase II |
Title |
A Randomized Double-Blinded Phase II Study of Carboplatin/Paclitaxel/CT-322 versus Carboplatin/Paclitaxel/Bevacizumab as First-Line Treatment for Recurrent or Advanced Non-Small Cell Lung Cancer with Non-Squamous Histology. Revised Protocol Number 01, incorporating Amendment 02.-ND |
Status |
Not Recruiting |
Sponsor |
Bristol-Myers Squibb International Corporation |
NCT00374179
|
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Indication |
Advanced Solid Tumor; Non-Hodgkin's Lymphoma (NHL) |
Phase |
Phase I |
Title |
A Phase I, Escalating Dose Study of?CT-322, a VEGFR-2 Antagonist, as Monotherapy in Patients With Advanced Solid Tumors and Non-Hodgkin's Lymphoma |
Status |
Completed |
Sponsor |
Adnexus, A Bristol-Myers Squibb R&D Company |
NCT00562419
|
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Indication |
Recurrent Glioblastoma Multiforme |
Phase |
Phase II |
Title |
Phase II, 2-Part, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, and Efficacy of CT-322 Monotherapy and Combination Therapy With Irinotecan in Patients With Recurrent Glioblastoma Multiforme |
Status |
Unknown |
Sponsor |
Adnexus, A Bristol-Myers Squibb R&D Company |
NCT00768911
|
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Indication |
Glioblastoma Multiforme |
Phase |
Phase I |
Title |
Phase I, Open Label, Multi-Center Study To Evaluate The Safety And Tolerability of?CT-322?Administered In Combination With Focal Brain Radiotherapy And Temozolomide To Subjects With Newly Diagnosed Glioblastoma Multiforme |
Status |
Unknown |
Sponsor |
Adnexus, A Bristol-Myers Squibb R&D Company |
NCT00850577
|
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Indication |
Recurrent or Advanced Non-Small Cell Lung Cancer With Non-Squamous Histology (NSCLC) |
Phase |
Phase II |
Title |
A Randomized Double-Blinded Phase II Study of Carboplatin/Paclitaxel/CT-322 Versus Carboplatin/Paclitaxel/Bevacizumab as First-Line Treatment for Recurrent or Advanced Non-Small Cell Lung Cancer With Non-Squamous Histology |
Status |
Terminated |
Sponsor |
Bristol-Myers Squibb |
NCT00851045
|
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Indication |
Metastatic Colorectal Cancer |
Phase |
Phase II |
Title |
A Randomized, Double-Blind, Phase II Trial of?CT-322?(BMS-844203) Plus Irinotecan, 5-FU and Leucovorin (FOLFIRI) Versus Bevacizumab Plus FOLFIRI as Second-Line Treatment for Metastatic Colorectal Cancer |
Status |
Completed |
Sponsor |
Bristol-Myers Squibb |
NCT01146171
|
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Indication |
Solid Tumor |
Phase |
Phase I |
Title |
A Phase I Multiple Ascending Dose Study of BMS-844203 (CT-322) Monotherapy in Japanese Patients With Solid Tumors |
Status |
Withdrawn |
Sponsor |
Bristol-Myers Squibb |
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