drugset / Trial / NCT00473083

Systemic and Topical Treatments for Rash Secondary to Erlotinib in Lung Cancer

NCT00473083

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this trial is to determine if rash caused by erlotinib can be successfully treated and if so to determine the optimal treatment approach. Hypothesis: Hypothesis 1: If the incidence of rash is 50% while on erlotinib, prophylactic monotherapy with minocycline can prevent occurrence in 50% of these patients. Hypothesis 2: Treatment of rash is successful in improving rash by at least one Grade in 80% of patients. Hypothesis 3: In patients with untreated rash, the rash will be self-limiting in 25% of patients, and 65% will be grade 1, 2A, and 2b. Ten percent will be grade 3 requiring treatment with monotherapy intervention.

Timeline

Start
2009-01
Primary completion
2012-12
Completion
2013-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Clindamycin Unknown 2 % Topical
Subject Hydrocortisone Other / unclassified 1 % Topical
Subject Minocycline Small molecule 100 mg Oral
Subject Triamcinolone Acetonide Other / unclassified 0.1 % Topical
Background Erlotinib Small molecule 100 mg Oral
Background Erlotinib Small molecule 150 mg Oral

Indications