Viewing Study NCT00441337



Ignite Creation Date: 2024-05-05 @ 5:24 PM
Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00441337
Status: COMPLETED
Last Update Posted: 2015-02-20
First Post: 2007-02-27

Brief Title: A Study of MDX-1106 in Patients With Selected Refractory or Relapsed Malignancies
Sponsor: Bristol-Myers Squibb
Organization: Bristol-Myers Squibb

Study Overview

Official Title: A Phase 1 Open Label Dose-escalation Safety and Pharmacokinetic Study of MDX-1106 in Patients With Selected or Relapsed Malignancies
Status: COMPLETED
Status Verified Date: 2015-02
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: MDX1106-01
Brief Summary: To evaluate the safety tolerability efficacy and pharmacokinetics of MDX-1106 when administered to patients with advanced non-small cell lung cancer colorectal cancer malignant melanoma clear cell renal cell cancer or hormone refractory prostate cancer
Detailed Description: Six patients enrolled at each dose level of 03 10 30 and 10mgkg the remaining 10 to 15 patients may subsequently be enrolled at a dose at or below the maximum tolerated dose MTD during the dose-escalation portion of the study Patients who respond may receive additional doses of drug

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
MDX1106-01 OTHER BMS None