Erlotinib (Tarceva (Trademark), OSI-774) in Treating Patients With Advanced Non-Small Cell Lung Cancer

Part of paid clinical trials in San Antonio, Texas.

Sponsor
OSI Pharmaceuticals
Study ID
NCT00072631
Phase
PHASE2
Status
Completed

Conditions

  • Advanced Non Small Cell Lung Cancer
  • Failed Prior Chemotherapy

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

Study Details

The purpose of this study is to determine if erlotinib will improve disease at doses that produce its characteristic rash in patients with advanced Non-Small Cell Lung Cancer.

Key Dates

First listed
Nov 7, 2003
Start date
Nov 5, 2003
Status verified
Jun 2015
Primary completion
Mar 14, 2007
Completion
Mar 14, 2007

Study Design

Enrollment
43 participants (actual)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: 1 erlotinib

Primary Outcome Measure

Feasibility of intrapatient dose escalation of erlotinib HCI to introduce a characteristic, target rash, and evaluate the effect on objective response rate [ Time Frame: 3 years ]

Locations (1)

FacilityCityStateZIPSite coordinators
Institute for Drug Development Cancer Therapy and Research CenterSan AntonioTexas78229-

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