Aprea Therapeutics Inc. reported additional preliminary data from its ongoing Phase 1 ACESOT-1051 trial evaluating the investigational WEE1 kinase inhibitor APR-1051 in advanced solid tumors. The company said a patient with advanced endometrial cancer treated at the 220 mg dose level achieved an unconfirmed partial response at the first on-treatment scan, with a 50% reduction in target lesions and a CA-125 decrease from 362 U/mL to 47 U/mL; the tumor harbored a PPP2R1A mutation and the patient experienced Grade 1 adverse events. Aprea also summarized that 22 patients have been treated across 10–220 mg, with two unconfirmed partial responses (both PPP2R1A-mutated endometrial cancer) and five cases of stable disease reported to date. The company said a further trial update is expected in the second quarter of 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Aprea Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9656458-en) on February 18, 2026, and is solely responsible for the information contained therein.
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