Early this year, the Boston-based company received a $1 million grant from the Muscular Dystrophy Association (MDA)’s Venture Philanthropy Fund to start producing its gene therapy candidate, expected to be tested in a Phase 2 clinical trial in the near future.
AavantiBio’s funding was a result of series A financing featuring the biotech company Sarepta Therapeutics (which provided a $15 million equity investment), hedge fund sponsor Perceptive Advisors, and investment managers RA Capital Management and Bain Capital Life Sciences.
“AavantiBio has a unique opportunity to change the lives of those living with FA and other rare diseases,” Alexander “Bo” Cumbo, AavantiBio’s CEO and president, and former chief commercial officer and executive vice president at Sarepta, said in a press release.
“Central to our mission is building on the advancements in gene transfer therapies and harnessing these revolutionary technologies to realize their potential as life-altering medicines,” Cumbo said.
The investor group noted its investment “represents a truly unique opportunity to thoughtfully advance a differentiated pipeline of innovative gene transfer therapies in areas of high unmet medical need.”
“We are excited to collaborate with Bo Cumbo, an accomplished executive leader, and to provide the necessary resources to enable the company to build a best-in-class gene therapy platform that brings transformative products to patients and families impacted by these devastating diseases,” the group stated.
Since frataxin is essential for the normal functioning of mitochondria (the cell’s powerhouses), its deficiency leads to mitochondrial malfunction, impaired energy production, and progressive neuromuscular and cardiac damage.
Contrary to current symptom-managing treatments for Friedreich’s ataxia, the company’s gene therapy candidate is meant to target the underlying cause of the disease. It does so by delivering a healthy copy of the FXN gene to cells through a modified and harmless adeno-associated virus (AAV).
Experimental gene therapies for Friedreich’s ataxia have shown promising results in animal models of the disease.
AavantiBio has said it intends to test the therapy in both pediatric and adult patients in clinical trials.
The company’s research expands on foundational gene therapy studies conducted by its co-founders, University of Florida (UF) researchers Barry Byrne, MD, PhD, and Manuela Corti, PhD. Byrne is an associate chair of pediatrics and the director of UF’s Powell Gene Therapy Center; Corti is an assistant professor of pediatrics at UF.
Since 2015, Corti has received several awards to advance the development of a gene therapy for Friedreich’s ataxia and assess which is its best route of administration in mouse models of the disease. She also is working on the best combination of immunosuppressive medications to prevent immune reactions against the virus.
AavantiBio will benefit from strategic partnerships with the Powell Gene Therapy Center and the MDA Care Center at UF Health, where the two renowned gene therapy researchers maintain their research and clinical practices.
Doug Ingram, Sarepta’s president and CEO, said its equity participation in AavantiBio serves the strategy to build a “gene therapy engine through targeted investment in potentially life-enhancing therapies as well as partnering with renowned genetic medicine pioneers such as Drs. Byrne and Corti.”
“We look forward to continuing to work with Bo as he builds a strong AavantiBio team and advances therapies to treat FA and other rare diseases,” Ingram added.
“I’m excited to build a company focused on deep science, innovation, and collaboration, and grateful for the partnership with three of the biotechnology industry’s most respected investors,” Cumbo said, adding that he is “thrilled to continue to collaborate with the talented team at Sarepta.”
Cumbo, Byrne, and Corti will be part of AavantiBio’s board of directors, alongside two independent directors and representatives of the investor group. Louise Rodino-Klapac, PhD, senior vice president of Sarepta’s gene therapy, will serve as a board observer.
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