Drug: |
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Trial Name: |
A Pilot Study of CS-1008, A Humanized Monoclonal Antibody Targeting Death Receptor 5, Alone or In Combination with Imatinib Mesylate or Sunitinib Malate In Subjects with Advanced Gastrointestinal Stromal Tumors |
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NCT#: |
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Conditions: |
Gastrointestinal Stromal Tumor |
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Status: |
Withdrawn |
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Phase: |
1 |
Start Date |
Age of Trial (yrs) |
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Treatment Phase: |
Gleevec-resistant |
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Drug Category: |
KIT/PDGFRA inhibitor + Death receptor activator
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Strategy: |
Activate death receptors + Block KIT |
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Trial Type: |
Specifically GIST and only GIST |
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Other Protocol IDs: |
RRC0708 |
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Sponsor: |
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Patient Contact: |
Monica Davey |
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Contact email: |
M_Davey@fccc.edu |
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Contact Phone: |
215-728-5534 |
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Randomized: |
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IV or Oral: |
Oral |
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Trial Notes: |
According to Melissa Spence at U. of Minn. the pharma has halted this study and is not going ahead. This is a phase I trial with CS-1008, a monoclonal anitbody targeting death receptor 5. CS-1008 will be given either alone or in combination with imatinib (Gleevec) or sunitinib (Sutent). The goal of any phase I trial is to determine if the drug or drug combination can safety be given to humans and to determine the maximum tolerated dose of the drug or drug combination and a drug schedule. CS-1008 is designed to increase the number of tumor cells killed by activating a "cell death" pathway, the death receptor 5 (DR5) pathway. Giving this drug will imatinib or sunitinib might increase the effectiveness of these drugs. |
Trial Links |
Trial Results |
Drug Information |
CS-1008 - NCI definition |
ASCO phase I results for CS-1008 |
Daiichi-Sankyo pipeline page (CS-1008) |
Name |
Address |
City |
State |
Zip |
Country |
333 Cottman Ave |
Philadelphia |
PA |
19111 |
USA |
|
2450 Riverside Ave. |
Minneapolis |
MN |
55454 |
USA |