4D Molecular Therapeutics, Inc. ((FDMT)) announced an update on their ongoing clinical study.
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4D Molecular Therapeutics, Inc. is conducting a Phase 3 clinical trial titled ‘A Phase 3, Randomized, Double-Masked, Active-Controlled Trial of a Single Intravitreal Injection of 4D-150 in Adults With Macular Neovascularization Secondary to Age-Related Macular Degeneration.’ The study aims to evaluate the efficacy and safety of the 4D-150 treatment for patients suffering from macular neovascularization due to age-related macular degeneration, a significant cause of vision loss in older adults.
The intervention being tested is a biological treatment known as 4D-150, administered as a single intravitreal injection. It is designed to offer a new therapeutic option for managing macular neovascularization. The study compares this treatment to EYLEA® (aflibercept), a currently available treatment.
This interventional study is randomized and follows a parallel assignment model with quadruple masking, meaning that the participant, care provider, investigator, and outcomes assessor are unaware of the treatment allocations. The primary purpose of the study is treatment-focused.
The study began on March 3, 2025, and is currently recruiting participants. The last update was submitted on July 15, 2025. These dates are crucial as they mark the progression and current status of the trial, which is essential for stakeholders tracking the development of this potential treatment.
The outcome of this study could significantly impact 4D Molecular Therapeutics’ market position, potentially boosting its stock performance if results are favorable. It may also influence investor sentiment positively, especially in comparison to competitors in the ophthalmology sector.
The study is ongoing, and further details can be accessed on the ClinicalTrials portal.