BBOT Announces Multiple Presentations at the American Association for Cancer Research (AACR) Annual Meeting 2026

On March 18, 2026 BridgeBio Oncology Therapeutics, Inc. ("BBOT") (Nasdaq: BBOT), a clinical-stage biopharmaceutical company focused on RAS-pathway malignancies, reported multiple presentations at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2026 being held on April 17-22, 2026, in San Diego, California. The abstracts released today can be found on the AACR (Free AACR Whitepaper) website here.

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Details on the presentations are as follows:

Title: The RAS: PI3Kα breaker BBO-10203 inhibits PI3Kα/AKT activity in HER2+ models through non-canonical RAS signaling blockade
Session Category: Experimental and Molecular Therapeutics
Session Title: Targeted Protein Degradation and Non-cannonical Oncogenic Signaling
Session Type: Oral Presentation
Session Date/Time: Tuesday, April 21, 2:30 p.m. – 4:30 p.m. PT
Location: Upper Level Ballroom 6DE
Abstract Number: 6780
Presenter: James Stice, PhD, Director, BBOT

Title: BBO-11818: an orally bioavailable, highly potent and selective non-covalent pan-KRAS (ON) and (OFF) inhibitor with robust anti-tumor activity in KRAS-mutant preclinical models
Session Category: Experimental and Molecular Therapeutics
Session Title: Novel Antitumor Agents 3
Session Type: Poster Presentation
Session Date/Time: Wednesday, April 22, 9:00 a.m. – 12:00 p.m. PT
Location: Poster Section 13
Poster Board Number: 24
Poster Number: 7104
Presenter: Carlos Stahlhut, PhD, Associate Director, BBOT

About BBO-11818
BBO-11818 is a selective, orally bioavailable non-covalent inhibitor that targets KRAS in both the ON and OFF states, has high selectivity over HRAS and NRAS, and displays strong activity in KRAS-mutant preclinical models, including KRASG12D and KRASG12V. BBO-11818 potently suppresses MAPK signaling and inhibits cell proliferation in KRAS-mutant cell lines and mouse models. BBO-11818 is currently being evaluated in the Phase 1 KONQUER-101 trial in subjects with locally advanced unresectable or metastatic KRAS-mutant solid tumors.

About BBO-10203
BBO-10203 is a first-in-class small molecule which breaks the protein-protein interaction between RAS and PI3Kα and inhibits RAS-mediated activation of the PI3Kα pathway. It selectively disrupts oncogenic RAS-PI3Kα signaling while sparing insulin-mediated glucose uptake, potentially maintaining efficacy with reduced risk of hyperglycemia or hyperinsulinemia. BBO-10203 is currently being evaluated in the Phase 1 BREAKER-101 trial for patients with locally advanced or metastatic HER2+ breast cancer, HR+/HER2- breast cancer, KRAS-mutant colorectal cancer, and KRAS-mutant non-small cell lung cancer.

(Press release, BridgeBio Oncology Therapeutics, MAR 18, 2026, View Source [SID1234663727])