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  • BiologyWorks k(now) COVID-19 Clinical Trial matches 99.1 percent accuracy to RT-PCR Tests

    The independent clinical trial, conducted by Locus Medicus in Athens, Greece, prospectively tested 330 patients with symptomatic and asymptomatic cases of COVID-19. For the study, staff at the clinical laboratory collected two bilateral anterior nasal swabs from each patient. Immediately after collection, one swab was tested in the lab’s standard of care CE-Mark RT-PCR test and the other swab was tested by BiologyWorks k(now). Results from the BiologyWorks k(now) molecular test were 99.1% in overall percent agreement with the results of the RT-PCR lab tests.

  • Nuclei-free Cells Prove Utility in Delivering Therapeutics to Diseased Tissues

    Researchers at University of California San Diego School of Medicine and Moores Cancer Center at UC San Diego Health report successfully removing the nucleus out of a type of ubiquitous cell, known as enucleation, then using the genetically engineered cell as a unique cargo-carrier to deliver therapeutics precisely to diseased tissues.

  • Nanotherapy offers new hope for the treatment of Type 1 diabetes

    Individuals living with Type 1 diabetes must carefully follow prescribed insulin regimens every day, receiving injections of the hormone via syringe, insulin pump or some other device. And without viable long-term treatments, this course of treatment is a lifelong sentence.

  • Glenmark Pharmaceuticals receives ANDA tentative approval for Regadenoson Injection

    Glenmark Pharmaceuticals Inc., USA (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Regadenoson Injection, 0.4 mg/5 mL (0.08 mg/mL) Single-Dose Pre-Filled Syringe, the generic version of Lexiscan®1 Injection, 0.4 mg/5 mL (0.08 mg/mL), of Astellas US, Inc.

    According to IQVIATM sales data for the 12 month period ending November 2021, the Lexiscan® Injection, 0.4 mg/5 mL (0.08 mg/mL) market2 achieved annual sales of approximately $659.9 million*.

  • IIHMR University, Jaipur selected globally for second phase of TDR Postgraduate Training Scheme to train the next generation of public health leaders

    IIHMR University, Jaipur has been selected from India to implement the second phase of TDR’s Postgraduate Training Scheme (2022-2026). TDR’s Postgraduate Training Scheme will provide a full academic scholarship though IIHMR University for selected students from Low- and Middle-Income Countries (LMICs). Students will obtain master’s degrees focused on implementation research on malaria, TB and neglected tropical diseases.

  • CuraTeQ and Orion expand licensing deal for biosimilars distribution in select European markets

    Aurobindo Pharma Limited announced that its subsidiary CuraTeQ Biologics Pvt Ltd. has expanded the scope of its marketing and distribution agreement with Orion Corporation (Orion) to commercialize its biosimilars pipeline to include the Baltic states in Europe. Earlier in 2020, CuraTeQ and Orion had entered into a licensing agreement, granting marketing and distribution rights for CuraTeQ’s biosimilar products under development in the Nordic states, Austria, Hungary and Slovenia.

  • New Method to Increase Effectiveness of Nanomedicines

    Researchers at Penn Medicine have discovered a new, more effective method of preventing the body’s own proteins from treating nanomedicines like foreign invaders, by covering the nanoparticles with a coating to suppress the immune response that dampens the therapy’s effectiveness.

  • Macrophages are fighting against plaque formation in the artery, suggests study

    A new study reveals the existence of a powerful ally in the fight against cardiovascular disease, a protective subset of vascular macrophages expressing the C-type lectin receptor CLEC4A2, a molecule which fosters "good" macrophage behaviour within the vessel wall.

  • Webinar on Meeting Indias Target of Eradication of TB by 2025 by Testing and Treating the Missing Millions with Tuberculosis

    IIHMR University a premier Health Care Research institution with a prime focus on delivering skill-based knowledge and about the future of healthcare organised a Webinar – Meeting India’s Target of Eradication of TB by 2025 by Testing and Treating the Missing Millions with Tuberculosis.

  • EU approves Lumykras on conditional basis for lung cancer

    Amgen announced that the European Commission has granted conditional marketing authorization for LUMYKRAS® (sotorasib), a first-in-class KRASG12C inhibitor, for the treatment of adults with advanced non-small cell lung cancer (NSCLC) with KRAS G12C mutation and who have progressed after at least one prior line of systemic therapy. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

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