A Randomized Phase 2 Study of Erlotinib + ARQ 197 Versus Erlotinib + Placebo in Previously Treated Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)

Completed · Phase 2 · Has a placebo group

Conditions studied: Non Small Cell Lung Cancer

In brief

This is a randomized, placebo-controlled, double blind phase 2 study designed to compare treatment with ARQ 197 plus erlotinib to erlotinib plus placebo in patients with non-small cell lung cancer. The study will enroll patients who have had one prior chemotherapy regimen (other than erlotinib) for NSCLC.

Key facts

Study ID

NCT00777309

Run by

ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)

People needed

167

Starts

2008-09-01

Expected to finish

2011-08-01

Last updated by the study team

2013-02-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provide signed and dated informed consent prior to study-specific screening procedures
• ≥ 18 years old
• Histologically or cytologically confirmed inoperable locally advanced or metastatic (stage IIIB/IV) NSCLC
• ≥ one prior chemotherapy regimen (including adjuvant chemotherapy)(not to have included erlotinib or other EGFR inhibiting agent)
• Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST)
• Eastern Cooperative Oncology Group (ECOG) performance status 0 to 1
• Male or female patients of child-producing potential must agree to use double barrier contraception, oral contraceptives or avoidance of pregnancy measures during the study and for 90 days after the last day of treatment
• Females of childbearing potential must have a negative serum pregnancy test
• Good organ function
• Confirmed availability of archival pathology samples (10 unstained paraffin-embedded slides) or tissue block suitable for subsequent analysis of KRAS, EGFR, and c-Met

You may not qualify if…

• Previous receipt of erlotinib or other EGFR inhibiting therapy
• Receipt of any anti-tumor treatment for NSCLC within 4 weeks (2 weeks for radiotherapy) prior to the start of designated treatment
• Documented major surgical procedure within 4 weeks prior to randomization.
• Symptomatic central nervous system metastases either considered in the opinion of investigator to be clinically unstable or which require steroids, anti-epileptics, or other symptom-relieving medications
• Pregnant, breast-feeding, or refusing double barrier contraception, oral contraceptives or avoidance of pregnancy measures
• Significant gastrointestinal disorder that, in opinion of Investigator, could interfere with the absorption of ARQ 197 and/or erlotinib (e.g. Crohn's disease, small or large bowel resection, malabsorbtion syndrome)
• Unable or unwilling to swallow the complete dose of erlotinib or ARQ 197
• Any known contraindication to treatment with ARQ 197 or erlotinib
• Any known hypersensitivity to any of component of ARQ 197 or erlotinib
• Other malignancy within 5 years of randomization, with the exception of adequately treated intraepithelial carcinoma of the cervix uteri, prostate carcinoma with a PSA value < 0.2 ng/ml or basal or squamous cell carcinoma of the skin
• Previously diagnosed grade 3 or 4 (CTCAE) bradycardia or other heart arrhythmia
• Any other significant co-mormid condition that, in opinion of the Investigator, would impair study participation or cooperation
• Known human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV) infection

Where it is running

• Study site — Burbank, California, United States
• Study site — Santa Monica, California, United States
• Study site — Torrington, Connecticut, United States
• Study site — Jacksonville, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Batesville, Indiana, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Louisville, Kentucky, United States
• Study site — Boston, Massachusetts, United States
• Study site — Worcester, Massachusetts, United States
• Study site — Charlotte, North Carolina, United States
• Study site — Canton, Ohio, United States
• Study site — Corpus Christi, Texas, United States
• Study site — Dallas, Texas, United States
• Study site — Dallas, Texas, United States
• Study site — Houston, Texas, United States
• Study site — Salt Lake City, Utah, United States
• Study site — Gauting, Germany
• Study site — Großhansdorf, Germany
• Study site — Hamburg, Germany
• Study site — Mainz, Germany
• Study site — Mannheim, Germany
• Study site — Villingen-Schwenningen, Germany
• Study site — Daugavpils, Latvia

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.