The partnership combines Capsigen’s vector engineering with Biogen’s drug pipeline, seeking to develop gene therapies for neuromuscular and central nervous system disorders.
Alfred Sandrock Jr, MD, PhD
Biogen and Capsigen have announced a collaboration to develop novel adeno-associated viral (AAV) capsids to deliver gene therapies to treat various central nervous system (CNS) and neuromuscular disorders.1
Capsids are the protein coat that protect and facilitate delivery of the AAV genetic payload to its target in host cells. The partnership aims to combine Capsigen’s experience in capsid engineering with Biogen’s discovery, development, manufacturing, and commercialization capabilities to accelerate delivery of gene therapies. These novel capsids will be designed to meet highly customized, disease-specific transduction profiles.
“Through this collaboration, we aim to solve key technological challenges in the delivery of gene therapies to target tissues. One of our priorities for technology innovation is the discovery of AAV capsids with improved delivery profiles,” said Alfred Sandrock Jr, MD, PhD, head of research and development, Biogen, in a statement. “We are investing for the long-term by building platform capabilities and advanced manufacturing technologies with the goal of accelerating our efforts in gene therapy.”
Capsigen brings to the partnership its proprietary TRADE™ platform and associated vector engineering technologies to produce dose optimized, fit-for-purpose vectors to use with Biogen’s gene therapy pipeline. As part of the collaboration, Capsigen will receive a $15 million upfront payment and is eligible to receive up to $42 million in potential research milestone payments as well as up to an additional $1.25 billion in development and commercial milestone payments. The company will also receive royalties in future sales that use its capsid technology.
“At Capsigen, we believe the next revolution in gene therapy will be driven by engineered AAV capsids designed to meet disease-specific transduction profiles,” said John Bial, chief executive officer, Capsigen, in a statement. “Biogen is a leader in neuroscience, and we are excited for the opportunity to work with them to potentially bring new treatments to patients. This collaboration is consistent with our strategy to work with world-class companies to develop the next generation of gene therapies.”
In late 2020, Sio Gene Therapies (previously Axovant) entered into a similar partnership with Viralgen to support AAV-based vector manufacturing of material for their phase 1/2 trial (NCT04669535) assessing an investigational agent, AXO-AAV-GM2, in the treatment of GM2 gangliosidosis (GM2-G) also known as Tay-Sachs disease or Sandhoff disease. The first infant patient with GM2-G was dosed in the trial in March 2021. The agent was previously granted an orphan drug and a rare pediatric disease designation by the FDA and is the first GM2-G investigational gene therapy to enter clinical trials.2
At the time, Javiér Garcia, chief executive officer of Viralgen, said that the company was “thrilled to partner with [Sio Gene Therapies]” and that it was excited to offer “support and priority access to our platform as they advance their AAV gene therapies for the rare fatal pediatric diseases GM1 and GM2 gangliosidosis.” He also lauded the company’s production platform as a complement to the development efforts of Sio Gene Therapies on the trials and commercialization fronts.
These efforts likely speak to the rapid expansion of AAV-mediated therapies for neurologic and CNS disorders, with a number of companies in recent weeks announcing positive news for their respective agents. Among them, are Voyager Therapeutics, which in late April announced the lifting of an FDA-driven clinical hold on its investigational new drug (IND) application for VY-HTT01, an AAV1-based gene therapy for patients with Huntington disease. The hold was placed on the application in October 2020, due to chemistry, manufacturing, and controls concerns from the FDA.3 Just a few weeks prior to that, the agency granted a fast-track designation to LEXEO Therapeutics for its AAV-mediated agent LX1001 as a potential treatment for adult patients with APOE4-associated Alzheimer disease.4
Additionally, that news came on the heels of the announcement from REGENXBIO that its AAV9-based single intracisternal injection agent, RGX-121, had been administered to the first patient in a phase 1/2 study for patients up to 5 years old with severe mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome.5
These mark just some of the many efforts to bring gene therapies into the fold for neurologists for the treatment of both rare and more common disorders. These ongoing efforts have spawned, in part, from the success that the oncology field has observed in treating a wide variety of cancers with these approaches. For more information on the latest advances in the pipeline for gene therapies, visit our sister publication, GeneTherapyLive.