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  • Sanofi to acquire Kymab

    Sanofi and Kymab, a clinical-stage biopharmaceutical company developing fully human monoclonal antibodies with a focus on immune-mediated diseases and immuno-oncology therapeutics, have entered into an agreement under which Sanofi will acquire Kymab for an upfront payment of approximately USD 1.1 billion and up to 350 million upon achievement of certain milestones.

  • Novel coronavirus found in air samples : CCMB study

    Airborne transmission of the novel coronavirus is possible under certain conditions, cautions a study undertaken by the Centre for Cellular and Molecular Biology (CCMB). The research was conducted to determine the transmission pattern of the virus in various enclosures in hospitals to assess the risks posed to healthcare workers. Air samples were collected from hospitals in Hyderabad and Mohali for the study.

  • New Class of Antibiotics Active Against a Wide Range of Bacteria : Reports

    Wistar Institute scientists have discovered a new class of compounds that uniquely combine direct antibiotic killing of pan drug-resistant bacterial pathogens with a simultaneous rapid immune response for combatting antimicrobial resistance (AMR).

  • Scientists reach new milestone in vaccine development for leishmaniasis

    Researchers have taken an important step forward in developing a controlled human infection model to test leishmaniasis vaccines.

    The University of York-led study identified and characterised a new strain of Leishmania parasite that will form the basis of a new controlled human infection model for the disease which is transmitted by the bite of sand flies. The team then produced the parasite to the standards required for use in human clinical studies.

  • Recruitment for Scientists at NIAB - Government of India Job

  • Joint Efforts on Drug Development with Industry for Covid 19 is Important for Positioning AYUSH Globally

    The webinar was graced with the presence of Shri Vaidya Rajesh Kotecha, Secretary, Ministry of AYUSH, Govt. of India, Padma Bhushan Vd. Devendera Triguna, President of AMAM, All India Ayurvedic Congress and Ayurveda Mahasammelan, Shri Pramod Kumar Pathak, Additional Secretary, Ministry of AYUSH, Govt. of India, Dr. Manoj Nesari, Advisor (Ay.) Ministry of AYUSH, Govt. of India, Dr. D.C. Katoch, Advisor(Ay.) Ministry of AYUSH, Govt. of India, Dr.

  • Babysteps to be taken for harmonizing the international regulatory standards for medical devices

    India has come a long way by showing its capabilities & its manufactures have come a long way by showing their capacity, the capability to sustain all the odds & deliver the services. The government support through PLI Schemes has been a boom and indication that what government wants, deliberated Dr.

  • WuXi Biologics to Acquire Drug Substance Facility in Wuppertal, Germany from Bayer

    WuXi Biologics a global company with leading open-access biologics technology platforms, and Bayer, announced an acquisition deal, under which WuXi Biologics will take over and operate the Drug Substance (DS) facility at Bayer’s Wuppertal site. The companies also plan to enter into a long-term sublease agreement and a transition service contract. The volume of the transaction, including the sublease agreement, amounts to approximately 150 million euros. 

  • SOURCE Phase III trial for tezepelumab in patients with severe, oral corticosteroid-dependent asthma

    AstraZeneca and Amgen announced high-level results from the SOURCE Phase III trial which assessed the efficacy and safety of the potential new medicine tezepelumab compared to placebo in 150 severe asthma patients who required maintenance use of oral corticosteroids (OCS) on top of standard of care (SoC).

  • Pfizer and BioNTech Receive Authorization in the European Union for COVID-19 Vaccine

    Pfizer and BioNTech SE announced that the European Commission (EC) has granted a conditional marketing authorization (CMA) to Pfizer and BioNTech for COMIRNATY® (also known as BNT162b2), for active immunization to prevent COVID-19 caused by SARS-CoV-2 virus, in individuals 16 years of age and older. This follows the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) positive opinion to authorize the vaccine earlier today.

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