MedMira Secures Health Canada Approval for Reveal G4 Rapid HIV Test

MedMira Inc. (MedMira) announced that it has secured approval from Health Canada for its Reveal Rapid G4 HIV-1/2 Test (Reveal HIV test) intended for Point-of-Care (POC) applications. The Reveal HIV rapid test boasts a sensitivity of 99.64% and a...

Alembic Pharma Secures USFDA Nod for Generic Brexpiprazole Tablets

Alembic Pharmaceuticals Ltd announced that it has secured final approval from the US health regulator for its generic variant of Brexpiprazole tablets, which are used in treating major depressive disorder. The company announced that the US Food &...

AstraZeneca, Daiichi Sankyo's Dato-DXd Earns Priority Review for EGFR NSCLC

The Biologics License Application (BLA) for datopotamab deruxtecan (Dato-DXd) from AstraZeneca and Daiichi Sankyo has been accepted and awarded Priority Review status in the US for treating adult patients with locally advanced or metastatic...

Roche Secures US FDA Approval for its Ultra-Sensitive ISH test

Roche announced that it has obtained 510(k) approval from the United States Food and Drug Administration (FDA) for its ultra-sensitive in-situ hybridisation (ISH) assay, the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail. The assessment...

Cycle Pharma Acquires Banner Life Sciences

Cycle Pharmaceuticals, Inc. (Cycle) has announced the successful acquisition of Banner Life Sciences, LLC (Banner), which encompasses its BAFIERTAM® (monomethyl fumarate) product for treating relapsing forms of multiple sclerosis (MS) in adults...

FOPE Calls for Extended Deadline for Schedule M Compliance

Pharma lobby group Federation of Pharma Entrepreneurs (FOPE) has urged the government to extend the deadline for compliance with the revised Schedule M by two years. This comes as the government is nearing finalisation of a draft notification...

US FDA Nods Mineraly's Phase 2 Trial for Lorundrostat in Hypertension

Mineralys Therapeutics, Inc., a biopharmaceutical company in clinical development concentrating on creating therapies for hypertension, chronic kidney disease (CKD), and other ailments linked to dysregulated aldosterone, revealed that the US Food...

WHO Prequalifies First G6PD Test to Boost Safe Treatment of P. vivax Malaria

The World Health Organization (WHO) has prequalified the initial diagnostic test for glucose-6-phosphate dehydrogenase (G6PD) deficiency, which can assist in the safe administration of WHO-approved treatments to prevent recurrence of Plasmodium...

Roche's Digital Pathology System Gains US FDA 510 Clearance

Roche announced that its complete slide imaging system, Roche Digital Pathology Dx, has obtained an additional 510(k) clearance from the U.S. Food and Drug Administration (FDA). This approval alters the one Roche obtained on June 14, 2024, for Ro...

US FDA Grants Priority Review to Dizal's Sunvozertinib NDA

Dizal, a biopharmaceutical firm dedicated to creating innovative therapies for cancer and immunological disorders, revealed that the U.S. Food and Drug Administration (FDA) has accepted and assigned priority review to the company's New Drug...

© 2025 India Pharma Outlook. All Rights Reserved.

Safety Monitoring