Status:
COMPLETED
ARQ 197 in Subjects With Metastatic Solid Tumors
Lead Sponsor:
ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
Conditions:
Cancer
Tumor
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
To determine the safety, tolerability and recommended Phase 2 dose (RP2D) of ARQ 197.
Detailed Description
To determine the safety, tolerability and recommended Phase 2 dose (RP2D) of ARQ 197 given orally. This is an open label, dose escalation study of ARQ 197 administered orally at a starting dose of 10 ...
Eligibility Criteria
Inclusion
- Signed written informed consent must be obtained and documented according to ICH GCP, the local regulatory requirements, and permission to use private health information in accordance with HIPPA prior to study-specific screening procedures
- A histologically or cytologically confirmed RCC or other c-Met expression tumors that is metastatic
- Patient must have available archival tumor tissue or accessible tumor that is safely amenable to tumor biopsy
- ≥ 18 years of age
- Measurable disease as defined by Response Evaluation Criteria in Solid Tumors
- Karnofsky performance status ≥ 70%
- Male or female patients of child-producing potential must agree to use contraception or avoidance of pregnancy measures during the study and for 30 days after the last ARQ 197 dose
- Females of childbearing potential must have a negative serum pregnancy test
- Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 × upper limit of normal (ULN) or ≤ 5.0 × ULN with metastatic liver disease.
- Hemoglobin (Hgb) ≥ 10 g/dl
- Total bilirubin ≤ 1.5 × ULN
- Creatinine ≤ 1.5 x ULN
- Absolute neutrophil count ≥ 1.5 x 10\^9/L
- Platelets ≥ 100 x 10\^9/L
Exclusion
- Anti-cancer chemotherapy, radiotherapy, immunotherapy, or investigational agents within four weeks of first dose
- Surgery within 4 weeks prior to first dose
- Known brain metastases
- Pregnant or breastfeeding
- Significant gastrointestinal disorder(s), in the opinion of the Principal Investigator, (e.g., Crohn's disease, ulcerative colitis, extensive gastric resection)
- Unable or unwilling to swallow ARQ 197 capsules twice daily
- Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, clinically significant non-healing or healing wounds, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, significant pulmonary disease (shortness of breath at rest or mild exertion), uncontrolled infection or psychiatric illness/social situations that would limit compliance with study requirements
- Bradycardia at baseline or known history of arrhythmia
Key Trial Info
Start Date :
January 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
Estimated Enrollment :
78 Patients enrolled
Trial Details
Trial ID
NCT00302172
Start Date
January 1 2006
Last Update
August 26 2009
Active Locations (3)
Enter a location and click search to find clinical trials sorted by distance.
1
Premiere Oncology
Santa Monica, California, United States, 90404
2
The Cleveland Clinic
Cleveland, Ohio, United States, 44195
3
Mary Crowley Medical Research Center
Dallas, Texas, United States, 75246