Skip to main content

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.

  • Seizures more common after venous stroke

    Epileptic seizures are frequent among patients with cerebral venous thrombosis - a blood clot affecting the venous system of the brain. A thesis from University of Gothenburg suggests that some of these patients should be diagnosed with epilepsy and offered medication to prevent further seizures.

  • Lupin Receives Approval from USFDA for Darunavir Tablets
    Lupin Receives Approval from USFDA for Darunavir Tablets

    Lupin is an innovation-led transnational pharmaceutical company headquartered in Mumbai, India. The Company develops and commercializes a wide range of branded and generic formulations, biotechnology products, and APIs in over 100 markets in the U.S., India, South Africa, and across the Asia Pacific (APAC), Latin America (LATAM), Europe, and Middle East regions.

  • Zydus receives tentative approval from the USFDA for Amantadine Extended-Release Capsules
    Zydus receives tentative approval from the USFDA for Amantadine Extended-Release Capsules

    Zydus Lifesciences Limited U.S. subsidiary Zydus Pharmaceuticals (USA) Inc. has received tentative approval from the United States Food and Drug Administration (USFDA) to market Amantadine Extended-Release Capsules USP 68.5 mg and 137 mg (USRLD: Gocovri).

  • Nanoparticles can improve stroke recovery by enhancing brain stimulation : study
    Nanoparticles can improve stroke recovery by enhancing brain stimulation : study

    In a recent study, researchers from Xi’an Jiaotong-Liverpool University and other universities in China have reported that brain stimulation combined with a nose spray containing nanoparticles can improve recovery after ischemic stroke in an animal model.

  • SEC recommends to grant permission to Biocon to conduct phase 2 trial for Itolizumab
    SEC recommends to grant permission to Biocon to conduct phase 2 trial for Itolizumab

    Subject Expert Committee of CDSCO recommends to grant permission to Biocon to conduct phase 2 clinical trial for Itolizumab for Injection (r-DNA origin) 100 mg per vial.

  • Amylyx Pharmaceuticals announces FDA approval of RELYVRIO for the Treatment of ALS
    Amylyx Pharmaceuticals announces FDA approval of RELYVRIO for the Treatment of ALS

    Amylyx Pharmaceuticals, Inc announced that the U.S. Food and Drug Administration (FDA) has approved RELYVRIO (sodium phenylbutyrate and taurursodiol) for the treatment of adults with amyotrophic lateral sclerosis (ALS). RELYVRIO (previously known as AMX0035 in the U.S.) significantly slowed the loss of physical function in people living with ALS in a randomized, placebo-controlled clinical trial. RELYVRIO can be taken as a monotherapy or with existing approved treatments.

  • Living donor transplantation offers a safe alternative for liver transplant patients
    Living donor transplantation offers a safe alternative for liver transplant patients

    Demand for donor livers for transplant patients outstrips supply with over 15% of waitlist patients dying after a year. A new international study offers support for increasing the use of living donor liver transplantation (LDLT) in Western countries and reducing the imbalance between organ supply and demand. This study is reported in the Journal of Hepatology, the official journal of the European Association for the Study of the Liver, published by Elsevier.

  • Fasting-Mimicking Diet Reduces Signs of Dementia in Mice
    Fasting-Mimicking Diet Reduces Signs of Dementia in Mice

    Short cycles of a low-calorie diet that replicates fasting appeared to reduce inflammation and delay cognitive decline in mouse models of Alzheimer’s disease; initial data indicates diet’s safety in Alzheimer’s patients.

  • New Zika Vaccine Shows Promise in Animal Models
    New Zika Vaccine Shows Promise in Animal Models

    Researchers from the University of California, Los Angeles (UCLA) have developed a Zika vaccine technology that is highly effective and safe in preclinical mouse models. In a pregnant mouse model, the vaccine prevented both the pregnant mothers and the developing fetuses from developing systemic infection. The research is published in Microbiology Spectrum, a journal of the American Society for Microbiology.

  • Mercks Keytruda gets Japanese approval
    Mercks Keytruda gets Japanese approval

    Merck known as MSD outside of the United States and Canada, announced that KEYTRUDA, Merck’s anti-PD-1 therapy, received four new approvals from Japan’s Ministry of Health, Labor and Welfare (MHLW)

Subscribe to Pharma News