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  • Weekly HIV Pill Moves Closer to Reality as Gilead and Merck Report Positive Phase 3 Results

    In a major advancement for HIV treatment, Gilead Sciences and Merck have announced positive topline results from two pivotal Phase 3 clinical trials evaluating an investigational once-weekly oral HIV therapy that combines islatravir and lenacapavir. The promising findings bring the healthcare industry one step closer to introducing what could become the world's first long-acting oral HIV treatment taken just once a week.

  • Takeda Faces Financial Hit as Amitiza Antitrust Case Impacts Earnings
    Takeda Faces Financial Hit as Amitiza Antitrust Case Impacts Earnings
    Takeda Pharmaceutical has revised its financial results for fiscal year 2025 following a significant legal development in the United States involving its constipation drug, Amitiza, lubiprostone
  • Bayer’s Finerenone Shows Strong Protection Against Kidney and Heart Complications in CKD Patients
    Bayer’s Finerenone Shows Strong Protection Against Kidney and Heart Complications in CKD Patients

    Bayer has announced promising new findings showing that finerenone, its non-steroidal mineralocorticoid receptor antagonist, significantly lowers the risk of chronic kidney disease (CKD) progression and major cardiovascular complications across a broad range of patients living with CKD. The latest results were presented during the 63rd European Renal Association (ERA) Congress.

  • Granules Pharmaceuticals, Inc. Receives USFDA EIR for Chantilly Facility
    Granules Pharmaceuticals, Inc. Receives USFDA EIR for Chantilly Facility
    Granules India Limited today announced that its wholly-owned subsidiary, Granules Pharmaceuticals, Inc. (GPI), located in Chantilly, Virginia, US, has received the Establishment Inspection Report (EIR) from the US Food and Drug Administration (FDA), with a Voluntary Action Indicated (VAI) classification.
  • Glenmark Expands U.S. Injectable Portfolio with Launch of Generic Lacosamide Injection
    Glenmark Expands U.S. Injectable Portfolio with Launch of Generic Lacosamide Injection

    Glenmark Pharmaceuticals Ltd. has announced that its U.S.-based subsidiary, Glenmark Pharmaceuticals Inc., USA, has launched Lacosamide Injection USP 200 mg/20 mL (10 mg/mL) Single-Dose Vials in the United States market. The product is the generic equivalent of Vimpat Injection marketed by UCB Inc. and is indicated for the treatment of seizures associated with epilepsy.

  • Alkem Expands Semaglutide Portfolio with India’s First Single-Shot Pre-Filled Syringe, Starting at ₹350
    Alkem Expands Semaglutide Portfolio with India’s First Single-Shot Pre-Filled Syringe, Starting at ₹350

    In a move aimed at improving access to diabetes and obesity treatment, Alkem Laboratories has launched India's first semaglutide single-shot pre-filled syringes, with prices starting at just ₹350.

    The launch marks another milestone in the rapidly evolving obesity and diabetes care market, as Alkem continues to expand its semaglutide portfolio following the introduction of pre-filled disposable and reusable injection pens earlier this year.

  • Gilead’s Livdelzi Achieves Key Phase 3 Success in Liver Disease Trial, Strengthening Treatment Outlook for PBC Patients
    Gilead’s Livdelzi Achieves Key Phase 3 Success in Liver Disease Trial, Strengthening Treatment Outlook for PBC Patients

    Gilead Sciences has announced positive results from its Phase 3 IDEAL trial evaluating Livdelzi (seladelpar)in adults with primary biliary cholangitis (PBC), a rare chronic autoimmune liver disease. The study met its primary endpoint, demonstrating statistically significant improvement in a composite measure of alkaline phosphatase (ALP) normalization compared with placebo.

  • Serum Institute to Manufacture Oxford’s Experimental Ebola Vaccine After CEPI Commits 8.6 Million USD Funding
    Serum Institute to Manufacture Oxford’s Experimental Ebola Vaccine After CEPI Commits 8.6 Million USD Funding

    The Serum Institute of India (SII) has joined hands with the University of Oxford and the Coalition for Epidemic Preparedness Innovations (CEPI) to accelerate the development of an experimental vaccine targeting the Bundibugyo strain of Ebola virus, a deadly pathogen currently driving outbreaks in the Democratic Republic of Congo (DRC) and Uganda. CEPI has committed up to 8.6 million USD to support the vaccine's advancement toward clinical testing.

  • Indoco Remedies Shares Jump Over 4% After EU GMP Certification for Baddi Plant
    Indoco Remedies Shares Jump Over 4% After EU GMP Certification for Baddi Plant

    Shares of Indoco Remedies gained 4.12% on Friday after the company announced that its Oral Solid Dosage (OSD) manufacturing facility at Baddi, Himachal Pradesh, has received European Union Good Manufacturing Practice (EU GMP) certification from the German Health Authority, Berlin. The regulatory approval is expected to strengthen the company's position in regulated European markets and has been welcomed positively by investors.

  • Regeneron Chooses Hyderabad for Its First Global Capability Centre Outside the US
    Regeneron Chooses Hyderabad for Its First Global Capability Centre Outside the US

    Global biotechnology company Regeneron Pharmaceuticals has announced plans to establish its first Global Capability Centre (GCC) outside the United States in Hyderabad, further strengthening Telangana's position as a leading destination for global life sciences and technology investments.

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