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ReForm Biologics, MilliporeSigma Enter Excipient Agreement

Deal covers excipient development and commercialization

By: Tiffany Coppolino

ReForm Biologics, a pharmaceutical technology company developing innovative platforms to improve biologic formulations, and MilliporeSigma have entered a global license agreement and collaboration to commercialize proprietary ReForm excipients used in biotherapeutic formulations.
 
MilliporeSigma and ReForm Biologics will conduct research, development and qualification of ReForm Biologics’ excipients for pharmaceutical use. MilliporeSigma will fund the research and development and be responsible for global commercialization, GMP manufacturing, and sale of ReForm Biologics’ excipients to MilliporeSigma’s customers for use in biologic formulations. ReForm Biologics will receive revenues from MilliporeSigma for sublicensing ReForm Biologics’ technology to MilliporeSigma’s customers in biologic formulations.
 
“MilliporeSigma is a global leader in providing pharmaceutical excipients for biologic formulation. This agreement will make ReForm Biologics’ excipients available through their GMP manufacturing and distribution network, accelerate our research and development activities, and greatly expand our presence in biological drug development,” said John Sorvillo, chief executive officer, ReForm Biologics. “As more biologics are being developed to treat a broad range of diseases ranging from cancer to orphan indications, we believe there will be a growing demand for new excipients that can enhance the patient experience, improve patient outcomes, and potentially extend the patent life of a therapeutic.”

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