Unity Biotechnology’s investigational eye treatment failed to match Eylea at 20 weeks—part of the mid-stage trial’s primary ...
A team of scientists at the National Institutes of Health (NIH) has developed an eye drop that successfully slowed vision ...
The investigators retrospectively evaluated 126 consecutive treatment-naïve nAMD patients (126 eyes) who received a loading ...
Alvotech's 427% revenue surge in 2024—fueled by its biosimilar portfolio and global expansion—highlights the booming ...
8d
Clinical Trials Arena on MSNOpthia could owe $1bn to investors amid sozinibercept trial failureThe Australian biotech could potentially be on the hook for more than $1bn after its Wet AMD therapy failed to show impact ...
Opthea's Phase 3 COAST trial for wet AMD did not meet its primary endpoint, raising financial concerns as the company faces ...
Australian-US biotech Opthea Ltd has reported disappointing phase 3 results with its lead drug for vision-robbing disease wet age-related macular degeneration (AMD), throwing its future into doubt.
"Regeneron has invested many years of effort into its design and development of EYLEA® (aflibercept) Injection 2 mg. This work has resulted in numerous patents, reflecting our important research ...
7d
Zacks Investment Research on MSNUBX Stock Down 29% on Mixed Results From Phase II Eye Disease StudyShares of UNITY Biotechnology UBX crashed 28.8% yesterday, following mixed results from a mid-stage non-inferiority study of ...
The Phase 2b ASPIRE clinical trial of intravitreal UBX1325 involed patients with diabetic macular edema (DME) who had poor ...
intravitreal UBX1325 compared with Regeneron’s REGN Eylea (aflibercept) in diabetic macular edema (“DME”) patients. The primary efficacy endpoint of the phase IIb ASPIRE study is ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results