Collaboration boosts AAV vectors for gene therapy

Article

Avalanche Biotechnologies Inc. and Lonza have announced a manufacturing collaboration focused on process development and scale-up efforts for the manufacturing of adeno-associated viral (AAV) vectors for gene therapy.

San Francisco and Basel, Switzerland-Avalanche Biotechnologies Inc. and Lonza have announced a manufacturing collaboration focused on process development and scale-up efforts for the manufacturing of adeno-associated viral (AAV) vectors for gene therapy.

Terms of the agreement were not disclosed.

AAV vectors are becoming a promising gene delivery vehicle for the treatment of various diseases, including inherited retinal disorders and age-related macular degeneration.

As part of the agreement, Avalanche and Lonza will make the technology available to third parties and share in the revenue. The Avalanche/Lonza manufacturing collaboration will focus on the development and high-yield production of AAV vectors based on technology that uses stable baculovirus. This technology was licensed by Avalanche from Virovek, which also will play a key role in the collaboration.

“We are delighted to have such a skilled and reputable manufacturing partner in Lonza to help us advance our robust research and development programs using AAV to treat macular degeneration and other blinding diseases,” said Thomas W. Chalberg, PhD, chief executive officer, Avalanche Biotechnologies. “By making our combined technology available to third parties, we hope to allow the entire AAV field to benefit from this best-in-class production process.”

Avalanche Biotechnologies is a privately held biotechnology company that develops technologies and products for sustained delivery of therapeutic proteins to the eye. Lonza is a supplier to the pharmaceutical, healthcare, and life science industries.

For more articles in this issue of Ophthalmology Times eReport, click here.

Newsletter

Stay at the forefront of cutting-edge science with CGT—your direct line to expert insights, breakthrough data, and real-time coverage of the latest advancements in cell and gene therapy.

Recent Videos
Nathan Yozwiak, PhD, the head of research at the GCTI
Derek Jackson, BS, MA, the vice president of cell & gene therapy product development at Pacira, and Kilian Guse, PhD, the vice president of genetic medicine platforms at Pacira
Derek Jackson, BS, MA, the vice president of cell & gene therapy product development at Pacira
Jeffrey Chamberlain, PhD
Tami John, MD
Tami John, MD
Tami John, MD
Matthew Ku, MBBS, FRACP, RACP, FRCPA/RCPA, PhD, an associate professor and the lymphoma stream lead at St Vincent’s Hospital
Saurabh Dahiya, MD, FACP, an associate professor of medicine at Stanford University School of Medicine; as well as clinical director of Cancer Cell Therapy in the Division of Blood and Marrow Transplantation and Cell Therapy at Stanford Medicine
Shahzad Raza, MD, a hematologist/oncologist at the Cleveland Clinic
Related Content
© 2025 MJH Life Sciences

All rights reserved.