Aldeyra Therapeutics, Inc. announced enrollment of the first patient in the Phase III TRANQUILITY Trial of 0.25% reproxalap ophthalmic solution for the treatment of dry eye disease.
Aldeyra Therapeutics, Inc. announced the achievement of the primary endpoint in the Phase III TRANQUILITY-2 clinical trial (TRANQUILITY-2) of reproxalap, an investigational new drug candidate, for the treatment of dry eye disease.
Aldeyra Therapeutics, Inc. announced top-line results from the Phase III TRANQUILITY Trial of 0.25% reproxalap ophthalmic solution (reproxalap), an investigational product candidate for the treatment of dry eye disease.
Novaliq announced that results from the second pivotal Phase III ESSENCE-2 trial for CyclASol (cyclosporine 0.05 in SFA) have been published in Journal of the American Medical Association (JAMA) Ophthalmology
Novaliq announced that the FDA has accepted the New Drug Application (NDA) for CyclASol (cyclosporine ophthalmic solution), a first-of-its-kind anti-inflammatory product for the treatment for the signs and symptoms of dry eye disease (DED)
Aldeyra Therapeutics, Inc. announced the resubmission of a New Drug Application (NDA) to the FDA for topical ocular reproxalap, an investigational new drug candidate, for the treatment of signs and symptoms of dry eye disease
Novaliq GmbH, a biopharmaceutical company focusing on first- and best-in-class ocular therapeutics, announced that the FDA has approved Vevye (cyclosporine ophthalmic solution) 0.1% for the treatment of the signs and symptoms of dry eye disease
Purpose: To define unmet needs in ophthalmology that can realistically be addressed in the next 5 years (2019-2025) and describe potential avenues for research to address these challenges.
Aldeyra Therapeutics, Inc. announced the achievement of the primary endpoints in a sequence-randomized, double-masked, vehicle-controlled crossover clinical trial of 0.25% reproxalap ophthalmic solution, an investigational new drug candidate, for the treatment of dry eye disease.