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Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

A phase II clinical study evaluating the efficacy and safety of HL-085 capsules in combination with vemurafenib for the treatment of patients with BRAF V600E-mutant locally advanced or metastatic non-small cell lung cancer.

Excerpt:
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Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

1378P - Efficacy and safety of tunlametinib (HL-085) combined with vemurafenib in patients with advanced BRAF V600-mutated solid tumors: A multicenter, phase I study

Published date:
10/16/2023
Excerpt:
33 pts with non-small cell lung cancer (NSCLC) have been evaluated for response. The objective response rate (ORR) was 60.6% (95%CI: 42.1%, 77.1%), a median duration of response (DoR) was 11.3 months (95% CI: 3.9, NE), and a median progression free survival (PFS) was 11.7 months (95% CI: 5.6, NE)....Tunlametinib in combination with vemurafenib showed promising antitumor activity and manageable safety profile in pts with BRAF V600-mutated solid tumors.
Trial ID: