Author: admin

  • What Holds the Future of Pharma in the Middle East?

    What Holds the Future of Pharma in the Middle East?

    At the Economic Times Healthcare Leaders Summit Middle East 2025, pharmaceutical experts examined the shifting dynamics of the region’s drug market, discussing emerging trends, regulatory developments, and challenges that will shape the sector’s next phase of growth.

  • Co-creating the digital front door to the NHS

    The NHS App enables millions of people to access essential healthcare services, but some struggle to use it. Tanja Galloway, Lisa Collins and Simon Davis explore the challenges and share practical insights for making user research inclusive and accessible so no one is left behind.

    The NHS App enables millions of people to access essential healthcare services. As part of the government’s 10 Year Health Plan, by 2028 the NHS App will become a full digital front door to the NHS. Yet for many, this digital future feels out of reach. 

    Some risk being left behind due to barriers that prevent them from accessing, or confidently using, the NHS App. 

  • Dr. Kyle Walsh Selected to Lead the National Institute of Environmental Health Sciences

    Dr. Kyle Walsh Selected to Lead the National Institute of Environmental Health Sciences

    Kyle Walsh, Ph.D., was selected as the director of the National Institute of Environmental Health Sciences (NIEHS), which is part of the National Institutes of Health (NIH), by Health and Human Services Secretary Robert F. Kennedy, Jr. As part of his responsibilities, Dr. Walsh will also direct the National Toxicology Program, which is headquartered administratively at NIEHS. 

    Dr. Walsh is a leading neuro-epidemiologist whose work on glial senescence and gliomagenesis has shed light on how genetic, epigenetic, and environmental factors can interact to influence the development of human disease. Before joining NIEHS on Oct.10, he led a pioneering, interdisciplinary research program at Duke University, Durham, North Carolina, where he studied how the interplay of both heritable and modifiable risk factors can affect brain health, cancer outcomes, and aging. 

    “Today marks an exciting new era for NIEHS,” said Secretary Kennedy. “Dr. Walsh’s scientific expertise and leadership will drive the institute toward even greater breakthroughs in our understanding of how the environment can affect biological systems and human disease.” 

    “Dr. Walsh is laser-focused on advancing rigorous research that leads to real-world insight and improves the health of all Americans,” said NIH Director Jay Bhattacharya, M.D., Ph.D. “I look forward to seeing NIEHS innovate under his leadership.” 

    “I am deeply honored to serve as the director of NIEHS, which is the world’s leading research organization focused on how the environment affects human health,” said Dr. Walsh. 

    “Our institute is well positioned to merge population-level scientific approaches with laboratory research on how environmental factors can affect key biological mechanisms, all while integrating insights from genomics, metabolomics, and other ‘omics’ frameworks,” added Dr. Walsh. “We will foster an interdisciplinary, collaborative research approach that builds on the expertise of NIEHS scientists and grant recipients as well as other NIH institutes and centers. In doing so, we will continue to advance critical scientific knowledge that helps to promote health across the lifespan and prevent chronic illnesses such as cancer, cardiovascular diseases, and dementia, among other conditions.” 

    At Duke University, Dr. Walsh served as associate professor of neurosurgery, pathology, population health sciences, and pediatrics. He also directed the Division of Neuro-epidemiology. He was a Senior Fellow in the Duke Center for the Study of Aging and Human Development and a member of the Duke Cancer Institute, where he co-led the Neuro-Oncology Research Program. In addition, Dr. Walsh helped to guide research efforts following the 2023 train derailment in East Palestine, Ohio, providing scientific leadership to U.S. Senators in the state and opening the door for important collaborations across multiple federal agencies. 

    Dr. Walsh holds bachelor’s degrees in molecular genetics and anthropology from The Ohio State University, Columbus. He earned his Ph.D. in chronic disease epidemiology from the Yale School of Public Health, New Haven, Connecticut, and completed postdoctoral training at the University of California, San Francisco. At NIEHS, Dr. Walsh succeeds the institute’s previous director, Rick Woychik, Ph.D., who took a new position in the NIH Office of the Director to help advance Make America Healthy Again initiatives.


    See all News Releases

  • What’s powering Mounjaro’s rise to the top of Indian drug market

    What’s powering Mounjaro’s rise to the top of Indian drug market

    Top officials and industry insiders attribute this ascent to a flurry of reasons – from the US drug maker’s shrewd marketing strategy and smart brand positioning as a weight-loss drug first to superior patient experience with faster and higher weight-loss efficacy and precise timing.

  • Lilly partners with Nvidia on AI supercomputer to speed up drug development

    Lilly partners with Nvidia on AI supercomputer to speed up drug development

    Using the supercomputer, scientists at Lilly will be able to train AI models on millions of experiments to test potential medicines, expanding the scope of drug discovery efforts, the company said.

  • Trump administration plans new probe into global drug pricing

    Trump administration plans new probe into global drug pricing

    • Updated On Oct 22, 2025 at 03:12 PM IST
    • Read by 100 Professionals

    Bengaluru: President Donald Trump’s administration is preparing a new probe into drug pricing practices among U.S. trading partners, a move that would lay the ground for fresh tariffs, the Financial Times reported on Wednesday, citing sources familiar with the matter.

    Reuters could not immediately verify the report.

    The imminent investigation would consider whether U.S. trading partners are underpaying for drugs, the report said, adding that the investigation would come under Section 301 of the Trade Act of 1974.

    The White House did not immediately respond to a Reuters’ request for comment.

    U.S. patients currently pay by far the most for prescription medicines, often nearly three times more than in other developed nations.

    In late September, Trump said the U.S. would impose a 100% tariff on imports of branded or patented pharmaceutical products, unless a pharmaceutical company is building a manufacturing plant in the United States.

    Trump has not followed through on the threat as he presses pharmaceutical companies to lower U.S. drug prices.

    Earlier this year, Trump sent letters to the leaders of 17 major pharmaceutical companies outlining how they should slash U.S. prescription drug prices to match those paid abroad.

    (Reporting by Ananya Palyekar in Bengaluru; Editing by Jacqueline Wong)

    • Published On Oct 22, 2025 at 03:02 PM IST

    Join the community of 2M+ industry professionals.

    Subscribe to Newsletter to get latest insights & analysis in your inbox.

    All about ETHealthworld industry right on your smartphone!

  • HC bins Roche's injunction plea, allows generic version of only drug for SMA

    HC bins Roche's injunction plea, allows generic version of only drug for SMA

    • Published On Oct 11, 2025 at 12:32 PM IST
    • Read by 100 Professionals

    Times News Network

    A division bench of Delhi high court Thursday rejected the appeal of pharma giant, Roche, seeking an injunction against Indian pharma company Natco Pharma launching a generic version of Risdiplam, the only available drug to treat a rare genetic disorder, spinal muscular atrophy (SMA). This comes as a major relief for Indian SMA patients.

    Govt’s one-time aid of Rs 50 lakh for patients of rare diseases was not enough to cover even a year’s treatment using Roche’s patented version of Risdiplam, but at Natco’s price for the generic version of the drug, treatment cost could be covered for 10-16 years.

    In March this year, a single-judge bench of Delhi HC rejected Roche’s injunction plea against Hyderabad-based Natco Pharma in a patent infringement dispute related to Risdiplam. Roche’s patent expires only in March 2035. However, Natco applied for a patent for an improved process for the preparation of Risdiplam and intermediates in Sept 2022. The court had ruled Natco had prima facie raised credible challenges to the validity of Roche’s patent and ruled in favour of Natco.

    Several public health groups had opposed Roche seeking a permanent injunction against Natco, arguing that Roche’s patent infringement lawsuit against Natco prioritised profits over patients’ access to affordable treatment, potentially violating India’s National Rare Disease Policy.

    Roche’s patented medicine costs roughly Rs 6 lakh a bottle. An individual with a body weight of over 20kg needs roughly 2.5-3 bottles per month, or 30-36 bottles per year. Roche gives two bottles for free if you buy one, and so the patient would have to pay about Rs 60-72 lakh per year for treatment, unaffordable for most patients in India. Drug costing experts peg the cost of producing the drug at roughly Rs 3,000 for a year’s supply.

    In April, Natco revealed in a “legal update regarding Risdiplam launch in India” that the “company has decided to price the product (Risdiplam) at Rs 15,900” per 60mg bottle, reducing the price by as much as 97%. This would bring down the cost to less than Rs 5 lakh per year. Bulk buying by govt could bring down the price to Rs 10,000 per bottle, which could bring the cost down to Rs 3.1 lakh per year, said health activists. The financial assistance for patients with rare diseases was increased to Rs 50 lakh in Sept 2024. At Natco’s price, those living with SMA would be able to afford treatment for up to 16 years.

    The Working Group on Access to Medicines and Treatment welcomed HC’s decision and said it highlighted harmful effects of patent evergreening, which could delay access to affordable medicines and lead to unnecessary litigation. It reaffirmed that access to lifesaving drugs should not depend on one’s ability to pay.

    • Published On Oct 11, 2025 at 12:32 PM IST

    Join the community of 2M+ industry professionals.

    Subscribe to Newsletter to get latest insights & analysis in your inbox.

    All about ETHealthworld industry right on your smartphone!

  • CDSCO to inspect cough syrup manufacturing units

    CDSCO to inspect cough syrup manufacturing units

    Teena Thacker

    New Delhi: The central drug regulator is set to launch nationwide inspections and auditing of cough syrup manufacturing units even as the World Health Organization sought clarification from India on recent child deaths allegedly after consuming toxic syrup.

    The Central Drugs Standard Control Organisation (CDSCO) has asked all states and union territories to provide a list of cough syrup manufacturers in their jurisdiction for audit and surveillance as part of a drive to ensure stricter quality control, people aware of the development said.

    At least 15 children aged below six have died in Madhya Pradesh and Rajasthan, allegedly due to toxic cough syrups. Government officials, however, said the deaths reported in Rajasthan are not linked to cough syrups.

    The WHO has, meanwhile, expressed concern regarding the regulatory gap in diethylene glycol and ethylene glycol screening for domestically marketed medicines in India.

    DEG has been detected in at least three oral syrup medicines tested so far, the CDSCO has informed the international health agency. The WHO said it is monitoring media reports regarding clusters of paediatric illnesses and deaths in Madhya Pradesh and Rajasthan.

    “These reports…describe symptoms consistent with acute renal failure and acute encephalitis syndrome, with suspected links to the use of oral syrup medicines. WHO is deeply saddened by the reported fatalities and extends its sincere condolences to the affected families and communities,” it said.

    “WHO communicated that it stood ready to support national authorities in investigating and responding to these tragic events,” one of the persons cited above said.

    The WHO had on October 1 contacted the CDSCO for clarification regarding potential links to contaminated medicines and whether the products were exported to other countries.

    Join the community of 2M+ industry professionals.

    Subscribe to Newsletter to get latest insights & analysis in your inbox.

    All about ETHealthworld industry right on your smartphone!

  • US FDA approves first treatment for rare, life-threatening disease in males

    US FDA approves first treatment for rare, life-threatening disease in males

    • Published On Sep 20, 2025 at 06:49 AM IST
    • Read by 100 Professionals

    Bengaluru: The U.S. Food and Drug Administration said on Friday it had approved Stealth Biotherapeutics‘ once-daily injection for a rare, genetic disease that primarily affects males, making it the first treatment to be greenlit for the condition.

    Stealth’s Forzinity was granted accelerated approval for treating Barth syndrome, in patients weighing at least 30 kg.

    Barth syndrome is a rare, serious and life-threatening disease of the mitochondria, the energy-producing parts of cells.

    It typically starts with severe heart failure in infancy, and causes premature death. Patients who survive into adolescence and adulthood often have fatigue, poor stamina and exercise intolerance, according to the FDA.

    According to a study on the National Institutes of Health’s website, as of 2020, an estimated 230 to 250 males were identified with Barth syndrome worldwide.

    The under-the-skin or subcutaneous injection works by binding to the inner part of the mitochondria, improving its structure and function.

    The accelerated approval is based on improved strength of the muscle used to straighten the leg at the knee. The FDA said it considers this improvement reasonably likely to predict patient benefit, such as an ability to stand more easily or walk farther.

    Under the FDA’s accelerated approval pathway that allows earlier approval of medications that treat serious conditions and fill an unmet medical need, it mandates additional post-market trials that verify the drug’s benefits.

    Privately held Stealth will conduct a trial to confirm the changes seen on knee muscle strength translate into patient benefit.

    If data from the trial do not show the drug’s effectiveness, the regulator can ask the company to withdraw it from the market.

    (Reporting by Puyaan Singh in Bengaluru; Editing by Krishna Chandra Eluri)

    • Published On Sep 20, 2025 at 06:49 AM IST

    Join the community of 2M+ industry professionals.

    Subscribe to Newsletter to get latest insights & analysis in your inbox.

    All about ETHealthworld industry right on your smartphone!

  • 4 dead in gas leak at pharma firm

    4 dead in gas leak at pharma firm

    • Published On Aug 23, 2025 at 11:44 AM IST
    • Read by 100 Professionals

    Mumbai: Four workers were killed and two others hospitalised after inhalation of nitrogen gas that leaked at a pharmaceutical company in Tarapur MIDC of Maharashtra’s Palghar district on Thursday, officials said.

    The incident occurred in the afternoon at Medley Pharma located in the industrial area of Boisar, around 130 km from here, they said.

    Chief of Palghar district disaster management cell, Vivekanand Kadam, said that between 2.30 pm and 3 pm, gas leaked from the nitrogen reaction tank at the pharma company, seriously affecting six persons working there.

    “The six workers were rushed to a hospital, where four of them died around 6.15 pm,” he said.

    Two others are currently undergoing treatment in the intensive care unit (ICU) at the hospital, he added. The deceased were identified as Kalpesh Raut, Bangali Thakur, Dheeraj Prajapati and Kamlesh Yadav, while Rohan Shinde and Nilesh Hadal are undergoing treatment, officials said.

    • Published On Aug 23, 2025 at 11:44 AM IST

    Join the community of 2M+ industry professionals.

    Subscribe to Newsletter to get latest insights & analysis in your inbox.

    All about ETHealthworld industry right on your smartphone!