Fractyl Announces Closing of $100 Million Series F Financing to Expand Clinical Development Programs in Type 2 Diabetes

Fractyl Announces Closing of $100 Million Series F Financing to Expand Clinical Development Programs in Type 2 Diabetes




Fractyl Announces Closing of $100 Million Series F Financing to Expand Clinical Development Programs in Type 2 Diabetes

– Financing will support multiple late-stage clinical studies of potential of Revita® DMR to reduce insulin dependence in type 2 diabetes –

– Company renamed Fractyl Health to better reflect mission to restore health for patients struggling with metabolic diseases –

– Marc Elia, founder of M28 Capital, and Clive Meanwell, executive chairman and founder of Population Health Partners, join Board of Directors –

LEXINGTON, Mass.–(BUSINESS WIRE)–Fractyl Health, a life sciences company dedicated to developing novel therapeutic interventions aimed at reversing the metabolic disease epidemic, today announced the closing of a $100 million Series F financing. The financing was led by new investors Maverick Capital, M28 Capital, and Population Health Partners, with participation by other new and existing investors. As part of this financing, Marc Elia, founder of M28 Capital, and Clive Meanwell, M.D., Ph.D., executive chairman and founder of Population Health Partners, have joined Fractyl’s Board of Directors.

“We’re immensely proud of the leadership role Fractyl has established in creating innovative treatments to address the root cause of metabolic disease, with an initial focus on type 2 diabetes. The closing of this Series F financing, the significant experience of our new board members and our company’s renaming as Fractyl Health reflect the momentum we have built and the vast potential that lies ahead for our approach,” said Harith Rajagopalan, M.D., Ph.D., co-founder and CEO of Fractyl. “By controlling the body’s central metabolic control organ, the duodenum, we believe we’ve discovered a novel way to treat metabolic disease at its source. This financing will enable the expansion and acceleration of our clinical development efforts with the goal of reducing insulin dependence for patients with type 2 diabetes on a global scale.”

Fractyl recently obtained FDA Breakthrough Device Designation for Revita DMR in patients with type 2 diabetes (T2D) who are currently treated with insulin. Proceeds from the financing will support initiation of multiple late-stage clinical studies to assess the potential for RevitaDMR to treat and halt the progression of metabolic disease. These upcoming clinical studies, alongside the ongoing REVITA-T2Di clinical study, aim to establish RevitaDMR as a cornerstone therapy in T2D, while eliminating burdensome, expensive, and outmoded therapies.

“Fractyl is developing technology that stands apart from the rest of the landscape in metabolic therapeutic innovation. Patients with diabetes — and our broader society — desperately need a therapy that offers disease modification as well as relief from the clinical, practical, and financial burden inherent in the current metabolic standard of care,” said Marc Elia, founder of M28 Capital. “Eliminating the need for insulin therapy from type 2 diabetes would be a landmark achievement for patients and society. I look forward to helping Fractyl as it works toward its mission.”

“Type 2 diabetes is one of the most urgent health problems of our time, but there has been a lack of investment in truly innovative approaches to take on the challenge of this population-level crisis,” said Clive Meanwell, M.D., Ph.D., executive chairman and founder of Population Health Partners, vice chairman of BB Biotech, and previously founder and CEO of The Medicines Company. “Revita DMR is the first novel therapeutic approach in type 2 diabetes in many years to offer the promise of treating the root cause of the disease. We are enthusiastically committed to supporting Fractyl as it drives forward its development and commercial programs to realize the full range of Revita’s potential in type 2 diabetes.”

About the Revita® DMR Treatment

Revita DMR is based on Fractyl’s groundbreaking insights surrounding the role of the gut in metabolic diseases. An outpatient endoscopic procedure, Revita DMR resurfaces the lining of the upper intestine (duodenal mucosa). Revita DMR has been studied in clinical trials involving close to 300 patients. Revita DMR has received FDA Breakthrough Device Designation and a European Union CE mark. In the United States, the device has not yet been authorized for marketing, but is the subject of an FDA-approved Investigational Device Exemption study. The Revita DMR System may be available for investigational use in other regions.

About Fractyl Health

Fractyl is pioneering treatments for metabolic diseases based on revolutionary scientific insights into the root causes of metabolic dysfunction. Fractyl’s lead program is Revita DMR, an outpatient endoscopic procedural therapy designed to treat insulin resistance in T2D. The company’s groundbreaking discoveries offer the potential to address other metabolic diseases in the future, including nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH), in an effort to reduce the global economic and healthcare burden of metabolic disease. Fractyl is a private biotechnology company based in Lexington, Mass. For more information, visit www.fractyl.com or www.twitter.com/FractylHealth

Contacts

Corporate Contact:
Lisa Davidson, Chief Financial Officer

Lisa@fractyl.com, 781.902.8800

Media Contact:
Lisa Raffensperger, Ten Bridge Communications

lisa@tenbridgecommunications.com, 617.903.8783