Logo

Roche Collaborated with Avista to Develop AAV Gene Therapy Vectors for the Treatment of Ocular Diseases

Share this

Roche Collaborated with Avista to Develop AAV Gene Therapy Vectors for the Treatment of Ocular Diseases

Shots:

  • Avista to receive $7.5M up front & will be eligible to receive an additional fee in the research phase, clinical and sales milestones along with royalties with a total deal value of ~$1B
  • Roche gets the right to license novel capsids & will be responsible to conduct preclinical, clinical, and commercialization activities for gene therapy programs using novel capsids
  • The collaboration will use Avista’s scAAVengr platform technology to develop IVT AAV capsids for retinal diseases with reduced immunogenicity. The technology uses a high-throughput technique & built-in quantitative validation of novel cell-specific AAVs, facilitating the quick development of gene therapies for clinical use 

Ref: Bussinesswire | Image: Roche

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions