Glenmark Pharmaceuticals Ltd - 532296 - Announcement under Regulation 30 (LODR)-Analyst / Investor Meet - Intimation
Glenmark Pharmaceuticals has scheduled an earnings call on August 3, 2026, from 8:30 AM to 9:30 AM IST. The call will discuss the company's unaudited financial results for the first quarter of FY27 (ended June 30, 2026).
Jul 21 2026 15:20:12
Glenmark Pharmaceuticals Ltd - 532296 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
Glenmark Specialty S.A. (Glenmark) received U.S. FDA approval for expanded use of RYALTRIS® Nasal Spray for treating seasonal allergic rhinitis in pediatric patients aged 6 to under 12 years. This approval strengthens Glenmark's US respiratory portfolio.
Jul 21 2026 08:43:01
Glenmark Pharmaceuticals Ltd - 532296 - Board Meeting Intimation for Considering And Approving Unaudited Financial Results Of Glenmark Pharmaceuticals Limited For The Quarter Ended June 30, 2026
Glenmark Pharma announced a board meeting on July 31, 2026, to consider and approve the unaudited financial results for the quarter ended June 30, 2026. The meeting will review both standalone and consolidated financials.
Jul 15 2026 15:30:11
Glenmark Pharmaceuticals Ltd - 532296 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
Glenmark Pharmaceuticals Inc., USA launched Olanzapine for Injection, 10 mg/vial. This new product is bioequivalent and therapeutically equivalent to Zyprexa®, targeting a market with annual sales of approximately $25.4 million. This launch expands Glenmark's injectables portfolio and institutional channel presence.
Jul 06 2026 08:36:45
Glenmark Pharmaceuticals Ltd - 532296 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
Glenmark Pharmaceuticals announced the advancement of its multi-country Phase 3 clinical trial for Trastuzumab rezetecan (SHR-A1811) in platinum-resistant ovarian cancer. India will be the first market to initiate patient enrollment following DCGI approval.
Jul 02 2026 08:36:14
Glenmark Pharmaceuticals Ltd - 532296 - Disclosure Under Regulation 30 Of SEBI (Listing Obligations And Disclosure Requirements) Regulations, 2015
Glenmark Pharmaceuticals' manufacturing facility in Goa received a Form 483 with six procedural observations from the US FDA after a recent inspection. The company stated that these observations are not related to data integrity, are not repeat observations, and anticipates no impact on commercial product supply.
Jun 30 2026 22:01:19
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