New Drug Application for K-911 Targeting Patients with Glaucoma and Ocular Hypertension Accepted for Filing in the U.S., Food and Drug Administration
Published on 08/27/2026 at 16:05 | dgap, AD HOC NEWS| Kowa Company Ltd. / Key word(s): Miscellaneous/Miscellaneous 27.08.2026 / 16:05 CET/CEST The issuer is solely responsible for the content of this announcement. NAGOYA, Japan, Aug. 27, 2026 /PRNewswire/ -- Kowa Company, Ltd. (hereafter referred to as "Kowa") is developing K-911 for the indication of reducing intraocular pressure (IOP) in patients with glaucoma or ocular hypertension through its affiliated company engaged in pharmaceutical development in the United States, Kowa Research Institute, Inc. (headquartered in North Carolina, USA). Kowa today announced that the New Drug Application (NDA) submitted to the U.S. Food and Drug Administration (FDA) on June 30, 2026 has been accepted for filing. The FDA will conduct its review of the NDA with a target action date of April 30, 2027, under the Prescription Drug User Fee Act (PDUFA). ![]() 27.08.2026 CET/CEST Dissemination of a Corporate News, transmitted by EQS News - a service of EQS Group. The issuer is solely responsible for the content of this announcement. The EQS Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases. View original content: EQS News |
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