HER2 Gene Mutation Clinical Trial
Official title:
A Phase II Study to Assess Efficacy of Pan-HER Inhibitor (HM781-36B, Poziotinib) in Stage IV Lung Adenocarcinoma With HER2 Mutation
In this trial, treatment efficacy and safety of Poziotinib will be assessed in patients with stage IV lung adenocarcinoma harboring HER2 mutation.
This study is designed to be multi-center, open-label, single-arm, prospective, phase II
trial of patient with stage IV lung adenocarcinoma with HER2 mutation who have not received
prior EGFR-TKI. Approximately 47 patients will be enrolled into the trial, and expected study
duration is 36 months from IRB and Korea: MFDS approval date.
The study drug(poziotinib) will be administered orally as one 12 mg tablet once a day until
disease progression or manifestation of unacceptable toxicity. The initial dose of the study
drug 12 mg daily can be reduced to 8 mg once daily according to dose reduction criteria in
protocol. A cycle of study treatment is defined as 28 days.
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