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Lonza to Partner with Capricor Therapeutics for the Development of Duchenne Muscular Dystrophy Cell Therapy

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Lonza and Capricor Therapeutics, a US-based clinical-stage biotechnology company, announced on Jan. 12, 2020 that they are entering into an agreement for the development of CAP-1002, Capricor’s clinical cell therapy that uses allogeneic cardiosphere-derived cells technology for the treatment of Duchenne Muscular Dystrophy. The therapy is also in a clinical trial to treat complications arising from COVID-19.

Under the terms of the agreement, operations will be initiated at Lonzaโ€™s Houston, TX Center of Excellence where Lonza will handle process development activities for late-clinical and commercial-scale GMP manufacturing of the cell therapy, Lonza said in a company press release. Additionally, the collaboration will work to expand Capricorโ€™s manufacturing capacity for possible late-stage clinical trials and commercialization.

As we continue to expand our manufacturing efforts for CAP-1002, our lead cell therapy product candidate, this collaboration with Lonza provides us with a partner which has world-class expertise in technology transfer and an established track record of commercializing biologics,โ€ said Linda Marbรกn, CEO, Capricor Therapeutics, in the press release. โ€œWe are excited because this is an important step in our ability to potentially bring CAP-1002 closer to commercialization and allows us to bring this important therapy to patients with Duchenne Muscular Dystrophy as quickly as possible, if approved.โ€

โ€œCapricorโ€™s lead candidate CAP-1002 is demonstrating efficacy in late-stage clinical studies to significantly benefit patients,โ€ added Alberto Santagostino, senior vice president, head of Cell and Gene Technologies, Lonza, in the press release. โ€œWe will leverage our process development expertise and industrial manufacturing capabilities to enable Capricor to scale this therapy and make it available to patients globally, once approved for commercialization.โ€

Capricor also received FDA acceptance of an investigational new drug application for a phase II clinical trial of CAP-1002 in patients with COVID-19, in August 2020.

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