Less than a week after Allergan and Duke University dropped their allegation that Novartis' Sandoz willfully infringed Duke’s patent for eyelash growth serum Latisse (bimatoprost), a federal jury in Colorado has still sided with the plaintiffs, ordering Sandoz to pay $39 million.
Sandoz is on the hook for $39 million to Allergan and Duke University for infringing on their patent for an eyelash-growth drug, Latisse (bimatoprost ophthalmic solution), a Colorado federal jury decided Friday.
Eugia's Generic Bimatoprost Receives Approval in the U.S.
NORTH CHICAGO, Ill., Feb. 24, 2022 /PRNewswire/ -- Allergan, an AbbVie (NYSE: ABBV) company, today announced new data to be presented from Allergan's leading portfolio of eye care treatments at the 2022 American Glaucoma Society (AGS) Annual Meeting being held in Nashville, TN and virtually from March 3-6. Presentations will include updated analyses that help further scientific understanding of DURYSTA® (bimatoprost intracameral implant), as well as new data on the XEN® Gel Stent. The DURYSTA data presentations coincide with the two-year anniversary of the U.S. Food and Drug Administration (FDA) approval of this first-of-its-kind eye pressure lowering treatment for glaucoma patients in March 2020.
Micro Labs`s Generic Bimatoprost Receives Approval In US
09/02/2021 PRESS ANNOUNCEMENT Medicom Healthcare Limited (Medicom) and Famar Health Care Services Madrid (Famar) are pleased to announce...
Micro Labs's Generic Bimatoprost Receives Approval In US
DURYSTA™ lowered intraocular pressure in patients with open-angle glaucoma or ocular hypertension by approximately 30 percent from baseline in two Phase 3 studies
The active ingredient in Allergan’s eyelash-growing solution Latisse has found a new form with the FDA’s approval of the glaucoma drug bimatoprost developed as a long-term, biodegradable eye implant.
Allergan plc, (NYSE: AGN), a leading global pharmaceutical company with a more than 70-year heritage in ophthalmology, will present new data from investigational Bimatoprost Sustained-Release (SR) at the Annual Meeting of the American Glaucoma Society (AGS) to be held in Washington, D.C. Data from the Phase 3 ARTEMIS studies will be presented during an oral session and will provide visual field (VF) outcomes and effects of Bimatoprost SR on disease progression in patients with open-angle glaucoma (OAG). A New Drug Application (NDA) for Bimatoprost SR is currently under review with the U.S. Food and Drug Administration, and if approved, has the potential to be the first and only biodegradable, intracameral implant indicated to reduce intraocular pressure in patients with open-angle glaucoma or ocular hypertension via a sustained-release drug delivery system.