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Find Clinical Drug Pipeline Developments & Deals by Finch Therapeutics
Under the clinical trial agreement, Brigham and Women’s Hospital will conduct an investigator-sponsored trial that is designed to compare two doses of CP101, a Complete Consortia microbiome therapeutic, in ulcerative colitis.
CP101 is an investigational, orally administered microbiome therapeutic designed to prevent recurrent C. diff and enable early intervention in the management of C. diff.
CP101 is an investigational microbiome therapeutic designed to deliver a diverse microbial community in a one-time oral administration, without the need for bowel preparation.
FIN-524 and FIN-525 are investigational, orally administered targeted consortia product candidates composed of both spore-forming and non-spore-forming bacterial strains selected for the treatment of ulcerative colitis and Crohn’s disease, respectively.
CP101 is the Company’s investigational orally administered microbiome therapeutic which is in late-stage clinical development for the prevention of recurrent C. difficile infection (CDI).
Finch was able to continue dosing patients in its then-ongoing PRISM-EXT Phase 2 open-label trial of CP101 in recurrent CDI as all of the CP101 lots used for PRISM-EXT were manufactured from material donated prior to December 1, 2019.
Two New U.S. Patents Granted for FIN-211, the first patent covers key technologies involved in addressing ASD and GI symptoms and, the second patent covers encapsulated compositions and methods of manufacturing such compositions.
CP101 demonstrated efficacy through week 24, with 73.5% of participants in the CP101 arm (n=102) experiencing a sustained clinical cure (defined as absence of CDI recurrence) through week 24 versus 59.4% in the placebo arm (n=96) (p=0.0347).
Takeda will assume primary development responsibility for the program, now known as TAK-524. The transition will enable Takeda to leverage its expertise in inflammatory bowel disease (IBD) throughout the clinical development of FIN-524/TAK-524.
Late-breaker oral presentations expand on previously announced positive topline data showing that CP101 met the primary efficacy endpoint with statistically significant improvement in the prevention of recurrent C. difficile infection compared to placebo.
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