The FDA granted orphan drug designation to OpCT-001 for the treatment of retinitis pigmentosa, according to a press release from BlueRock Therapeutics.The investigational induced pluripotent stem cell-derived cell therapy is currently being evaluated i…
Novaliq Receives FDA IND Clearance to Advance NOV05 in a Phase II Clinical Trial in Non-infectious Anterior Uveitis
HEIDELBERG, Germany & CAMBRIDGE, Mass.–(BUSINESS WIRE)– #FDA–Novaliq, a biopharmaceutical company focusing on first- and best-in-class ocular therapeutics based on its unique water-free EyeSol® drug category, today announced that the U.S. Food and D…
Urcosimod 0.05% granted single-patient use for neuropathic corneal pain
The FDA has authorized urcosimod 0.05% for single-patient expanded access, or compassionate use, in a patient with neuropathic corneal pain, according to a press release from Okyo.The terms of the Investigational New Drug (IND) application stipulate th…
Patient assistance programs yield vision gains
WAIKOLOA, Hawaii — Patients with retinal diseases who were treated with anti-VEGF therapies through manufacturer patient assistance programs showed sustained vision gains and central subfield thickness reduction.During a presentation at Retina 2026, Mu…
Now that split is final, what if US wants to rejoin WHO?
On Thursday, HHS announced that the United States has completed its withdrawal from WHO.The process began a year ago when President Donald J. Trump, on the night of his inauguration, announced plans to leave WHO, complaining that the agency demanded to…
Listen to patients, determine their needs to choose right IOL
WAIKOLOA, Hawaii — In this Healio Video Perspective from Hawaiian Eye 2026, Audrey Talley Rostov, MD, of Bellevue Precision Vision, discusses how to choose the right IOL.Rostov said surgeons have a lot of factors to consider, such as the ocular surface…