Skip to main content

Pharma News

Get the latest news from world and India’s leading pharmaceutical companies Pharma Industry, pharmaceutical marketing, generic drugs, and Complete news for Pharmacy and Life Sciences professionals.

  • AbbVie Submits Regulatory Applications to FDA and EMA for Upadacitinib (RINVOQ®)

    The regulatory submissions to the FDA and EMA are supported by previously announced results from the Viti-Up studies evaluating the safety and efficacy of upadacitinib in patients with NSV.
  • Alembic Pharma Wins USFDA Nod for Parkinson Combination Therapy Tablets
    Alembic Pharmaceuticals Limited has strengthened its US generics portfolio with the final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) covering Carbidopa, Levodopa and Entacapone Tablets.
  • Zydus Desidustat Secures USFDA Orphan Drug Status for Sickle Cell Therapy

    Zydus Lifesciences has achieved a significant regulatory milestone as the U.S. Food and Drug Administration (USFDA) granted Orphan Drug Designation (ODD) to its novel molecule Desidustat for the treatment of Sickle Cell Disease (SCD). The designation highlights the growing recognition of the urgent need for new and effective therapies in this rare and challenging condition.

  • Blocking pain at the source : Hormone therapy rewires nerve signals in aging spines

    Low back pain (LBP) is one of the most common health problems worldwide, affecting people of all ages and placing a heavy burden on healthcare systems. Many patients experience persistent discomfort that interferes with work, sleep, and daily activities. Yet in most cases, doctors cannot identify a clear structural cause, making long-term treatment difficult.

  • Emcure Pharmaceuticals Posts Strong Q3 FY26 Performance; profit Surges 48%

    Emcure Pharmaceuticals Ltd. announced robust financial results for the third quarter of the 2025-26 fiscal year, marking significant growth across both domestic and international businesses. The company reported a notable rise in profitability and topline performance, underpinned by diversified portfolio strength and strategic initiatives.

  • World NTD Day 2026 Highlights Progress, Warns of Sharp Decline in Global Funding

    As the world observes World Neglected Tropical Diseases (NTD) Day 2026, global health leaders are celebrating major gains against neglected diseases while raising serious concern over declining financial support. The World Health Organization (WHO) has warned that a 41% decline in NTD aid between 2018 and 2023 threatens to stall or reverse years of progress.

  • Novo Nordisk’s CagriSema Signals a New Benchmark in Diabetes Care, Shows Edge Over Existing Therapies

    Novo Nordisk has reported encouraging Phase 3 results for CagriSema, its investigational once-weekly treatment for adults with type 2 diabetes, positioning the therapy as a strong next-generation option in an increasingly competitive metabolic disease market. The findings come from the REIMAGINE-2 trial, where the combination therapy delivered superior glycaemic control and weight reduction compared to semaglutide alone.

  • Breakthrough in HIV Vaccine Research : Single-Shot Candidate Shows Neutralizing Success in Primates
    Scientists at The Wistar Institute have reported a major step forward in HIV vaccine development with a novel vaccine candidate that can induce neutralizing antibodies after a single immunization in nonhuman primates, an achievement never before demonstrated in the field.
  • Piramal Pharma Solutions Expands Advanced Oral Drug Delivery with Tablet-in-Capsule Technology
    Piramal Pharma Solutions (PPS), a global Contract Development and Manufacturing Organization (CDMO) and a part of Piramal Pharma Ltd., has strengthened its advanced dosage form portfolio with the successful development and commercialization of tablet-in-capsule drug delivery technology at its integrated drug product facilities in Pithampur and Ahmedabad, India.
  • IPC Urges Medical Device Companies to Strengthen Adverse Event Reporting Under MvPI
    The Indian Pharmacopoeia Commission (IPC), under the Ministry of Health and Family Welfare, has urged all Medical Device Marketing Authorisation Holders (MAHs) to ensure strict compliance with adverse event reporting under the Materiovigilance Programme of India (MvPI), stressing that timely reporting is critical to patient safety and effective regulatory oversight.
Subscribe to Pharma News