Erlotinib Hydrochloride in Treating Patients With Advanced Esophageal Cancer or Stomach Cancer
Part of paid clinical trials in New York, New York.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT00045526
- Phase
- PHASE2
- Status
- Completed
Conditions
- Adenocarcinoma of the Esophagus
- Adenocarcinoma of the Gastroesophageal Junction
- Recurrent Esophageal Cancer
- Squamous Cell Carcinoma of the Esophagus
- Stage III Esophageal Cancer
- Stage IV Esophageal Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- erlotinib hydrochloride — DRUGGiven PO
- laboratory biomarker analysis — OTHERCorrelative studies
Study Details
This phase II trial is studying erlotinib hydrochloride to see how well it works in treating patients with advanced esophageal cancer or stomach cancer. Erlotinib hydrochloride may stop the growth of cancer by blocking the enzymes necessary for tumor cell growth.
Key Dates
- First listed
- Jan 27, 2003
- Start date
- Jun 30, 2002
- Status verified
- Jun 2013
- Primary completion
- Feb 28, 2007
Study Design
- Enrollment
- 48 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (erlotinib hydrochloride)Patients receive erlotinib hydrochloride PO QD. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Major response rate (complete and partial response) [ Time Frame: Up to 5 years ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Memorial Sloan-Kettering Cancer Center | New York | New York | 10065 | - |
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