Dr. Reddy’s to introduce Sanofi’s novel RSV drug in India

Dr. Reddy’s Laboratories will expand its partnership with Sanofi Healthcare India (SHIPL) by launching the latter’s novel drug Beyfortus (nirsevimab) in India.

Containing monoclonal antibody nirsevimab in a prefilled injection, Beyfortus is used for prevention of respiratory syncytial virus (RSV) lower respiratory tract disease (LRTD) in newborns and infants born during or entering their first RSV season.

Dr. Reddy’s will get exclusive rights from SHIPL to promote and distribute Beyfortus. The announcement follows an exclusive distribution partnership it had forged for Sanofi portfolio of vaccines in India last year. Beyfortus is expected to be launched in the second quarter of the current fiscal year, the Hyderabad-based pharma major said.

RSV is a highly contagious virus that can lead to serious respiratory illness for infants. In addition to being the most common cause of LRTD such as bronchiolitis and pneumonia in infants, it is also a leading cause of hospitalisation in infants worldwide, with most hospitalisations occurring in healthy infants born at term. In 2019, there were approximately 33 million cases of acute lower respiratory infections globally, leading to more than 3 million hospitalisations, and it was estimated that there were 26,300 in-hospital deaths of children younger than 5 years, Dr.Reddy’s said in a release.

Launch of Beyfortus will help strengthen its immunisation portfolio in India, CEO-Branded Markets (India and Emerging Markets) M.V. Ramana said.

Beyfortus, which has been approved for use in the EU, the U.S., China, Japan and many other countries, received marketing authorisation approval in India from the Central Drugs Standard Control Organization (CDSCO) in June.

“In India, where the disease burden is significant and early protection is critical, this collaboration with Dr. Reddy’s enables us to reach parents and healthcare providers with an innovative solution,” Head of Sanofi Vaccines (India) Nitya Padmanabhan said.

  • Related Posts

    WHO launches new primary health care course to strengthen health systems globally

    Health is a human right – yet not everyone can access the health services they need, when and where they need them, without financial hardship. Primary health care (PHC) provides…

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Bengaluru: The Central Council for Research in Ayurvedic Sciences (CCRAS) has called for stronger scientific evidence, safety monitoring and translation of research into market-ready technologies to improve the credibility and…

    Leave a Reply

    Your email address will not be published. Required fields are marked *

    You Missed

    WHO launches new primary health care course to strengthen health systems globally

    WHO launches new primary health care course to strengthen health systems globally

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Yashoda Medicity Successfully Performs High-Risk Kidney Transplant in 28-Year- Old Woman

    Yashoda Medicity Successfully Performs High-Risk Kidney Transplant in 28-Year- Old Woman

    Avacta delivers two clinical stage peptide-drug conjugates to target delivery of toxic payloads into the tumour microenvironment

    Avacta delivers two clinical stage peptide-drug conjugates to target delivery of toxic payloads into the tumour microenvironment

    US FDA approves first gene therapy for paediatric patients with Sanfilippo syndrome type A

    US FDA approves first gene therapy for paediatric patients with Sanfilippo syndrome type A

    Technology and accessibility are key to growth of advanced treatment of heart diseases, says expert

    Technology and accessibility are key to growth of advanced treatment of heart diseases, says expert