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  • Johnson & Johnson Reports Strong Q2 2026 Results, Raises Full-Year Outlook

    Johnson & Johnson has reported strong financial results for the second quarter of 2026, driven by continued growth across its Innovative Medicine and MedTech businesses.
  • FDA Issues Form 483 to Catalent Indiana Over Sterile Drug Manufacturing Concerns
    FDA Issues Form 483 to Catalent Indiana Over Sterile Drug Manufacturing Concerns
    The U.S. Food and Drug Administration, FDA has issued a Form FDA 483 to Catalent Indiana LLC. The inspection identified multiple observations related to quality systems, contamination control, investigations, and sterile manufacturing practices at the facility.
  • European Commission Approves Novo Nordisk's Oral Wegovy, Marking New Era in Obesity Treatment
    European Commission Approves Novo Nordisk's Oral Wegovy, Marking New Era in Obesity Treatment

    Novo Nordisk has announced that the European Commission (EC) has approved Wegovy® (semaglutide) tablets for chronic weight management, making it the first oral GLP-1 receptor agonist authorized in the European Union for the treatment of obesity and overweight. The approval also includes a single, ready-to-use 7.2 mg Wegovy injection pen, providing healthcare professionals and patients with additional treatment options.

  • Sanofi Files Patent Lawsuit Against Moderna Over mRNA Vaccine Technology
    Sanofi Files Patent Lawsuit Against Moderna Over mRNA Vaccine Technology

    Sanofi has filed a patent infringement lawsuit against Moderna in the U.S. District Court for the District of New Jersey, alleging that Moderna's mRNA vaccine technologies infringe a portfolio of patents originally developed by Translate Bio, a biotechnology company acquired by Sanofi in 2021. The complaint names Translate Bio, Translate Bio MA, Sanofi Vaccines US, and VaxServe as plaintiffs, while Moderna, ModernaTX, and Moderna US are listed as defendants.

  • Emcure Takes Full Control of Gennova, Bets Big on Biologics and Biosimilars Under New Leadership
    Emcure Takes Full Control of Gennova, Bets Big on Biologics and Biosimilars Under New Leadership

    Emcure Pharmaceuticals Limited has announced a major strategic restructuring of its biopharmaceutical business by acquiring the remaining 12.05% minority stake in Gennova Biopharmaceuticals Limited, making it a wholly owned subsidiary. The company also announced a leadership transition, appointing Samit Mehta to lead Gennova as it sharpens its focus on biologics, biosimilars, and next-generation therapeutic platforms.

  • Evonik invests USD 100 million to upgrade drug substance manufacturing site in Lafayette, Indiana
    Evonik invests USD 100 million to upgrade drug substance manufacturing site in Lafayette, Indiana

    Evonik, one of the world's leading specialty chemicals companies, is making a significant investment to strengthen manufacturing capabilities at its Tippecanoe Labs site in Lafayette, Indiana. The site is home to one of the world's largest facilities for the production of active pharmaceutical ingredients (APIs), the industry's biggest high-potency API operation, and a major employer in the Greater Lafayette region.

  • CDSCO Rejects Trial Waiver for Roche’s Glofitamab, Seeks Phase III Study Before India Approval
    CDSCO Rejects Trial Waiver for Roche’s Glofitamab, Seeks Phase III Study Before India Approval

    The Subject Expert Committee (SEC) on Oncology has declined Roche Products (India) Private Limited's request for a waiver of local Phase III and Phase IV clinical trials for Glofitamab and has instead recommended that the company conduct Phase III clinical trials in India before the drug can be considered for marketing approval.

  • AstraZeneca’s Wainua Falls Short in Late-Stage Heart Disease Trial, Misses Primary Goal
    AstraZeneca’s Wainua Falls Short in Late-Stage Heart Disease Trial, Misses Primary Goal

    AstraZeneca and its partner Ionis Pharmaceuticals have announced that the Phase III CARDIO-TTRansform trial evaluating Wainua (eplontersen) for adults with transthyretin-mediated amyloid cardiomyopathy (ATTR-CM) did not meet its primary efficacy endpoint, marking a significant setback for the investigational indication.

  • FDA Pulls Up Lundbeck Over Allegedly Misleading Vyepti Migraine Promotion
    FDA Pulls Up Lundbeck Over Allegedly Misleading Vyepti Migraine Promotion

    The U.S. Food and Drug Administration (FDA) has issued a Letter to Lundbeck Seattle Biopharmaceuticals, alleging that promotional materials for its migraine treatment Vyepti (eptinezumab-jjmr) contained false or misleading claims that overstated the drug's benefits.

  • Marksans Pharma to acquire Germany-Based ABCnow GmbH to Strengthen European Market Presence
    Marksans Pharma to acquire Germany-Based ABCnow GmbH to Strengthen European Market Presence

    Marksans Pharma Ltd. has announced the acquisition of 100% share capital of ABCnow GmbH, a Germany-based pharmaceutical wholesale and distribution company, in a strategic move to strengthen its presence across regulated European markets. The company has entered into a definitive agreement to acquire the business as part of its forward integration strategy.

    The acquisition will be completed through a cash consideration of €892,384, with the transaction expected to close by July 31, 2026. Marksans stated that no government or regulatory approvals are required for the acquisition.

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