Lilly ends partnership with Foghorn after lead cancer drug fails efficacy tests
Lilly announced it is ending its collaboration with Foghorn Therapeutics after the biotech's lead cancer candidate, FHD-909, did not meet efficacy benchmarks in testing. The decision halts the joint synthetic lethality program and a second experimental medicine targeting the SMARCA2 gene.
Foghorn said it will cut about 40% of its workforce as it discontinues the failed programs and severs the partnership that began in 2021. The move follows earlier setbacks for the company, including a 2022 hold on a leukemia trial after patient deaths.
Analysts noted the termination is a disappointment because FHD-909 was Foghorn's most advanced and valuable asset. The company's shares have already fallen dramatically since its 2020 IPO, reflecting the cumulative impact of these challenges.
This writeup was produced by pharmadog from original reporting by BioPharma Dive.
Original headline: “Lilly, Foghorn part ways; Wave’s FDA-approved plans”
read at BioPharma Dive ↗
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