Viewing Study NCT00050102



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00050102
Status: COMPLETED
Last Update Posted: 2011-01-28
First Post: 2002-11-21

Brief Title: Comparison Study of MDX-010 CTLA-4 Alone and Combined With DTIC in the Treatment of Metastatic Melanoma
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: A Randomized Study Comparing MDX-010 CTLA-4 Alone or in Combination With DTIC in the Treatment of Patients With Chemotherapy Naїve Metastatic Melanoma
Status: COMPLETED
Status Verified Date: 2011-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The objectives of this study are to determine the safety and activity profile of multiple doses of MDX-010 and to determine the whether the addition of cytotoxic chemotherapy decarbazine DTIC can augment the effects of MDX-010 in patients with chemotherapy naïve metastatic melanoma with a tolerable toxicity profile
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
CA184-013 OTHER BMS None