Viewing Study NCT00612703


Ignite Creation Date: 2025-12-24 @ 7:18 PM
Ignite Modification Date: 2026-01-04 @ 6:07 PM
Study NCT ID: NCT00612703
Status: COMPLETED
Last Update Posted: 2012-07-23
First Post: 2008-01-30
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: A Phase 1 Study of ARQ 197 in Adult Patients With Advanced Solid Tumors
Sponsor: ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
Organization:

Study Overview

Official Title: A Phase 1 Dose Escalation Study of ARQ 197 Administered in Combination With Erlotinib in Adult Patients With Advanced Solid Tumors
Status: COMPLETED
Status Verified Date: 2012-07
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: To determine the safety, tolerability and recommended Phase 2 dose of ARQ 197 when administered in combination with erlotinib to patients with advanced solid tumors
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: