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  • Venus Remedies Secures First-Ever Global Approval for Plerixafor in Saudi Arabia

    Venus Remedies has achieved a major milestone after receiving Marketing Authorization from the Saudi Food and Drug Authority for its specialty oncology therapy Plerixafor. The approval marks the company’s first-ever global authorization for the drug and strengthens its growing focus on complex injectable therapies in regulated international markets.

  • PCI Makes AEBAS Mandatory for Pharmacy Colleges; Institutions Told to Complete Compliance
    The Pharmacy Council of India has intensified the implementation of the Aadhaar Enabled Biometric Attendance System (AEBAS) across all PCI-approved pharmacy institutions in India.
  • Dr. Reddy’s Launches Oral semaglutide in India, Expands GLP-1 Diabetes Portfolio

    Dr. Reddy’s Laboratories has announced the launch of Obeda® tablets, an oral semaglutide therapy for patients with diabetes in India. The launch marks another major step in the company’s expansion of its GLP-1 portfolio after recently introducing semaglutide injections in India and Canada.

  • Eli Lilly’s Retatrutide Helps Patients Lose Up to 28.3% Body Weight

    Eli Lilly has announced encouraging results from its late-stage Phase 3 clinical trial of retatrutide, an investigational next-generation obesity treatment that delivered dramatic weight reduction in adults living with obesity or overweight conditions.

  • Injectable Cosmetics Not Allowed in India, Clarifies CDSCO

    The Central Drugs Standard Control Organisation (CDSCO) has issued a public notice clarifying that cosmetic products cannot be used through injections and are not permitted for treatment purposes under Indian law.

    The notice, released by the Directorate General of Health Services under the Ministry of Health and Family Welfare, comes amid rising use of aesthetic and beauty procedures in clinics and salons across the country.

  • Targeted Therapy Helps Children With Rare Bone Disease Regain Mobility

    A promising targeted therapy may offer new hope to children and adults living with fibrous dysplasia, a rare bone disorder that weakens bones and severely affects mobility. Researchers have reported that the drug burosumab significantly improved phosphate balance and physical function in patients suffering from the debilitating condition.

  • India Rejects AbbVie’s Hepatitis C Patent Bid Amid Growing Push for Affordable Medicines

    India has once again delivered a setback to global pharmaceutical major AbbVie after the company lost its attempt to secure patent protection for its Hepatitis C therapy in the country, a move that could strengthen access to affordable generic medicines.

  • Takeda Faces Major Legal Setback as US Jury Rules in Amitiza Antitrust Case

    Japanese drugmaker Takeda Pharmaceutical Company is facing a major financial and legal challenge after a U.S. federal jury found the company liable in a high-profile antitrust lawsuit involving its constipation drug Amitiza (lubiprostone).

  • Roche and MPP Partner to Expand Access to Influenza Drug in 129 Countries

    In a major step toward improving global pandemic preparedness, Swiss pharmaceutical giant Roche and the Medicines Patent Pool (MPP) have signed a voluntary licensing agreement to expand access to the influenza antiviral drug Xofluza (baloxavir marboxil) across 129 low and middle-income countries (LMICs).

  • Merck’s Experimental Cancer Drug Shows Survival Benefit in Landmark Endometrial Cancer Trial

    Merck has announced encouraging Phase 3 results for its investigational cancer therapy sacituzumab tirumotecan (sac-TMT), offering new hope for patients with advanced or recurrent endometrial cancer who have limited treatment options after standard therapies fail.

    The company revealed that the global TroFuse-005 clinical trial successfully achieved its two primary goals, improving overall survival (OS) and progression-free survival (PFS), when compared with conventional chemotherapy in previously treated patients.

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