The path ahead for UNITY Biotechnology, Inc.’s UBX1325 in patients with wet age-related macular degeneration (AMD) has become less straightforward as the company announced that its Phase II study did not show non-inferiority to Regeneron Pharmaceuticals, Inc.’s Eylea (aflibercept). Consequently, there is greater hope among analysts for Unity’s diabetic macular edema (DME) program, particularly the Phase II BEHOLD clinical trial of UBX1325, a program that has shown stronger data to date.
Unity announced results from Part A of the Phase II ENVISION trial in AMD on 27 March, saying that UBX1325 administered as a monotherapy did not achieve non-inferiority compared with Eylea through 24 weeks due, in part, to an unexpected 3.5-letter gain in the control arm
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?