Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BEBT-109 is an oral, small molecule pan-mutant-selective inhibitor of the epidermal growth factor receptor (EGFR). It is designed to target a broad spectrum of EGFR mutations, including T790M and exon 20 insertion mutations that are commonly associated with resistance to earlier-generation EGFR inhibitors in non-small cell lung cancer (NSCLC). Preclinical and early clinical studies have demonstrated promising antitumor activity and an acceptable safety profile. The drug has shown efficacy in patients with advanced or refractory NSCLC harboring EGFR T790M or exon 20 insertion mutations, with objective response rates around 44% and median progression-free survival of approximately 8 months. Common adverse events include diarrhea, rash, and anemia. BEBT-109 is being developed by BeBetter Med as a new molecular entity for the treatment of NSCLC[1][3][5][9].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on BEBT-109.