17 stories found
A significant step has been taken in the fight against Lyme disease as the European Medicines Agency (EMA) begins evaluating the application for a vaccine candidate developed by Pfizer and Valneva, which could become the first human vaccine against the disease in Europe if approved.
Regeneron (REGN) has announced that the European Medicines Agency (EMA) has accepted its application for Otarmeni for review.
The European Medicines Agency (EMA) has approved updated transport conditions for Novo Nordisk's injectable GLP-1 therapy used for weight management.
The 'VetMedSafety Day' information campaign, designed by the European Medicines Agency (EMA) and the Federation of European Veterinarians (FVE), is actively raising awareness about the safe and correct use of veterinary drugs for both animals and humans, with the participation of the National Organization for Medicines.
Researchers at the Universitat Autònoma de Barcelona (UAB) have created a new drug aimed at treating spinal cord injuries, which has received orphan drug designation from the European Medicines Agency (EMA). The team is now proceeding with regulatory preclinical studies to confirm the product's safety.
The European Medicines Agency (EMA) has recommended the authorization of Moderna's combination vaccine targeting both COVID-19 and influenza.
Zai Lab Limited (ZLAB) has received Orphan Drug Designation from the European Medicines Agency (EMA) for its DLL3-targeting cancer therapy.
The European Medicines Agency (EMA) has recommended that the next season's Covid-19 vaccines should be designed to target the XFG variant.
The European Medicines Agency (EMA) has approved updated conditions for injectable semaglutide, used for obesity treatment, allowing it to be stored for up to 48 hours at temperatures up to 30°C during the final stage of delivery to patients.
Europe’s medicines regulator, the European Medicines Agency (EMA), has recommended approval for several new treatments, including three cancer therapies targeting aggressive forms of the disease, alongside other innovative medicines for serious conditions.
The European Medicines Agency (EMA) and national drug agencies are on increased alert for potential medicine shortages, as geopolitical tensions in the Middle East could impact the pharmaceutical supply chain in the European Union.
Moldova is considering withdrawing antiparasitic drugs containing levamisole from sale after the European Medicines Agency (EMA) concluded that the substance can cause a rare but serious brain condition called leukoencephalopathy.
A new combination therapy for acute Hepatitis C infection in adults and children aged 3 and above has received a positive opinion from the European Medicines Agency (EMA).
The European Medicines Agency (EMA) has recommended the approval of Wegovy in pill form, a significant step for the weight-loss medication.
The European Medicines Agency (EMA) has recommended marketing authorization for Imdylltra (tarlatamab) in the European Union. This new drug is intended for adult patients with advanced small cell lung cancer that has relapsed.
The European Medicines Agency (EMA) has accepted the application from Nuvation Bio and Eisai for taletrectinib, a drug intended for the treatment of non-small cell lung cancer (NSCLC).
The European Medicines Agency (EMA) panel has recommended the approval of Dupixent for the treatment of urticaria (hives) in children.