Viewing Study NCT00135408



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Last Modification Date: 2024-10-26 @ 9:13 AM
Study NCT ID: NCT00135408
Status: COMPLETED
Last Update Posted: 2016-09-28
First Post: 2005-08-25

Brief Title: A Study of MDX-010 BMS-734016 Administered With or Without Prophylactic Oral Budesonide
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: Randomized Double-Blind Placebo-Controlled Phase II Study Comparing the Safety of MDX-010 BMS-734016 Administered With or Without Prophylactic Oral Budesonide Entocort EC in Patients With Previously Treated Unresectable Stage III or IV Malignant Melanoma
Status: COMPLETED
Status Verified Date: 2016-09
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 purpose of the study is to determine Efficacy Safety and Tolerability of MDX-010 BMS-734016 administered with or without Prophylactic Oral Budesonide
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