Drug: |
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Trial Name: |
Safety and Pharmacology of SNX-5422 Mesylate in Subjects With Refractory Solid Tumor Malignancies |
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NCT#: |
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Conditions: |
Solid Tumors |
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Status: |
Completed |
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Phase: |
1 |
Start Date 06/15/2007 |
Age of Trial (yrs) 17.4 |
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Treatment Phase: |
Gleevec-resistant |
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Drug Category: |
HSP90 inhibitor |
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Strategy: |
Destroy KIT |
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Trial Type: |
GIST not specified. GIST patient enrollment unknown. |
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Other Protocol IDs: |
SNX-5422-CLN1-001 |
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Sponsor: |
Pfizer
Serenex, Inc. |
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Patient Contact: |
Pfizer Oncology Clinical Trial Information
1-877-369-9753
PfizerCancerTrials@emergingmed.com
Pfizer CT.gov Call Center
1-800-718-1021 |
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Contact email: |
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Contact Phone: |
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Randomized: |
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IV or Oral: |
Oral |
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Trial Notes: |
Note: The development of SNX-5422 has been discontinued because of ocular toxicity seen in animal models and in a phase I study. Clin Cancer Res; 17(21); 1–9. ©2011 AACR. Hsp90 is a chemical in the body that is involved in promotion of cancer. SNX-5422 is an experimental drug that blocks Hsp90. It is being evaluated for safety and efficacy in patients with cancer. Study Type: Interventional Study Design: Treatment, Open Label, Uncontrolled, Single Group Assignment, Safety Study Number of arms in study: 1 Primary Outcome Measures: * adverse events and other safety assessments [Time Frame: continuous] Secondary Outcome Measures: * tumor response measured by X-rays or scans [Time Frame: after every 2 cycles] |
Trial Links |
Trial Results |
Drug Information |
Name |
Address |
City |
State |
Zip |
Country |
10460 N. 92nd Street, Suite 206 |
Scottsdale |
AZ |
85248 |
USA |
|
3322 West End Avenue |
Nashville |
TN |
37203 |
USA |