BioLight announces that the first patient has been enrolled in the U.S. into a FDA Phase 1/2a clinical trial with Eye-D®, the company’s controlled-release latanoprost insert for the treatment of glaucoma.
Link to NewsroomBioLight announces that the first patient has been enrolled in the U.S. into a FDA Phase 1/2a clinical trial with Eye-D®, the company’s controlled-release latanoprost insert for the treatment of glaucoma.
Link to Newsroom