Glenmark Pharma submits Company’s First New Drug Application for Ryaltris™ for Patients with Seasonal Allergic Rhinitis

GlenmarkLogo

Glenmark Pharmaceuticals, announced that the company has submitted a New Drug Application (NDA) to the U.S. Food & Drug Administration (FDA) for its leading respiratory pipeline candidate Ryaltris™ , an investigational fixed-dose combination nasal spray of an antihistamine and a steroid, as a treatment for seasonal allergic rhinitis (SAR) in patients 12 years of age and older. Ryaltris (olopatadine hydrochloride (665 mcg) and mometasone furoate (25 mcg)), formerly GSP 301 Nasal Spray, has been conditionally accepted by the FDA as the brand name.

Glenmark said it expects the USFDA will determine whether the new drug application is complete for filing within 60 days. “If the new drug application is accepted, the Prescription Drug User Fee Act (PDUFA) target action date will be assigned at that time