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TrialNCT06641609

A Phase I Study of CFT8919 in Patients With Advanced NSCLC

Status
RECRUITING
Phase
PHASE1
Last update posted
09/04/2026
Start
11/04/2024
Sponsor
Betta Pharmaceuticals Co., Ltd.
Specialties
oncology

Conditions: Non-Small Cell Lung Cancer With EGFR Mutation

Brief summary

The goal of this clinical trial is to evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of CFT8919 capsules in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) carrying EGFR mutations. The main questions it aims to answer are: * What is the maximum tolerated dose (MTD) of CFT8919? * Does CFT8919 demonstrate antitumor activity in these patients? Participants will: * Take CFT8919 capsules at different doses. * Undergo regular assessments for safety, pharmacokinetics, and tumor response. Researchers will compare different dose levels to determine the best balance between safety and efficacy.

Protocol documents and results are not hosted here. Verify every detail on ClinicalTrials.gov.

Clinical Evidence