Bayer’s new treatment Kerendia (finerenone) approved in EU for adult patients with chronic kidney disease associated with type 2 diabetes

21 February 2022 - Kerendia is the first non-steroidal, selective mineralocorticoid receptor antagonist to demonstrate positive kidney and cardiovascular outcomes in ...

Read more →

BioNTech plans to make vaccines in shipping containers

19 February 2022 - These standardised factories could be quickly scaled up to expand capacity worldwide. ...

Read more →

Regulatory decisions diverge over aducanumab for Alzheimer’s disease

19 February 2022 - The EMA refused marketing authorisation for aducanumab (Aduhelm), a monoclonal antibody targeted at amyloid β, in December ...

Read more →

Sandoz launches generic lenalidomide in 19 countries across Europe, expanding access to essential oncology medicine

18 February 2022 - Cost savings from Lenalidomide Sandoz can expand treatment options for patients with haemato-oncology conditions. ...

Read more →

European Commission approves Tepmetko (tepotinib) for patients with advanced NSCLC with METex14 skipping alterations

18 February 2022 - Approval is based on Phase II results from VISION, the largest interventional study to date of patients ...

Read more →

Nirsevimab EMA regulatory submission accepted under accelerated assessment for RSV protection in all infants

17 February 2022 - Nirsevimab is the first investigational long-acting antibody designed to protect all infants for the respiratory syncytial ...

Read more →

European Commission approves Oxbryta (voxelotor) for the treatment of haemolytic anaemia in patients with sickle cell disease age 12 years and older

16 February 2022 - The first sickle haemoglobin polymerisation inhibitor approved in Europe, Oxbryta increases haemoglobin levels and reduces sickling ...

Read more →

Merck struggles to win European approval for Covid antiviral pill

16 February 2022 - EMA said to be unlikely to grant marketing authorisation to molnupiravir this month after ‘problematic’ data. ...

Read more →

Pfizer and OPKO’s once weekly Ngenla (somatrogon) injection receives marketing authorisation in European Union for treatment of paediatric growth hormone deficiency

15 February 2022 - Pfizer and OPKO Health announced today that the European Commission has granted marketing authorisation for the next ...

Read more →

Saphnelo approved in the EU for the treatment of moderate to severe systemic lupus erythematosus

16 February 2022 - Saphnelo is a first in class type I interferon receptor antibody and the only new medicine ...

Read more →

European Medicines Agency approves Pfizer’s 20 valent pneumococcal conjugate vaccine against invasive pneumococcal disease and pneumonia in adults

15 February 2022 - Apexxnar [pneumococcal polysaccharide conjugate vaccine (20 valent, adsorbed)] is the first pneumococcal conjugate vaccine to help protect ...

Read more →

GE Healthcare's stress agent Rapiscan approved for use in stress cardiac magnetic resonance imaging

14 February 2022 - Already used in single photon emission computed tomography (SPECT) myocardial perfusion imaging for adult patients, Rapiscan is ...

Read more →

Human medicines: highlights of 2021

15 February 2022 - In 2021, EMA recommended 92 medicines for marketing authorisation. Of these, 53 had a new active substance ...

Read more →

EMA starts safety review of Janus kinase inhibitors for inflammatory disorders

11 February 2022 - EMA’s safety committee, PRAC, has started a review of the safety of Janus kinase (JAK) inhibitors ...

Read more →

Novavax underdelivers on COVID vaccine promises

9 February 2022 - Novavax has delivered just a small fraction of the 2 billion COVID-19 shots it plans to ...

Read more →