
Mavatar has announced the initiation of a non-clinical research collaboration with Sobi, using Mavatarโs technology to generate data insights into …

STADA and Bio-Theraโs Gotenfia (golimumab), a biosimilar of Janssenโs Simponi, has received a positive opinion from the European Medicines Agency …

Celltrionโs Remsima IV, the first-ever liquid formulation of infliximab for autoimmune diseases, has been approved by the European Commission (EC). …

The European Commission (EC) has granted marketing authorisation for Gobivaz, Alvotechโs first-in-market biosimilar of Simponi (golimumab), which is used for …

The current forms of immunotherapy, how T cell therapy works and what the future holds

Swedish biotech, Neogap Therapeutics, has appointed Jonas Mattson, an authority in cell therapy, to its board of directors. His appointment …

The National Institute for Health and Care Excellence (NICE) has recommended AstraZenecaโs benralizumab (Fasenra) as an add-on treatment for adult …

Novartis has reported positive results from two phase 3 clinical trials โ NEPTUNUS-1 and NEPTUNUS-2 โ evaluating ianalumab in adults …

Swedish immunotherapy company, CuraCell, has received approval from the Paul-Ehrlich-Institut in Germany to begin a phase 1/2a clinical trial of …

By Holly Thomas, Associate Vice-President Specialty Care at Lilly UK and Ireland Immunology care in the UK is at a …

ViroCell Biologics has announced a new manufacturing collaboration with AvenCell Therapeutics to produce a high-yield retroviral vector supporting the clinical …

Amarna Therapeutics and NorthX Biologics have finalised an agreement to accelerate the development of Nimvec AM510, a gene therapy targeting …

Hansa Biopharma has announced that Richard Philipson has been appointed chief medical officer, effective 14 July. Philipson will join the …

The US Food and Drug Administration (FDA) has approved Gamifant (emapalumab-lzsg) for the treatment of macrophage activation syndrome (MAS) in …

Sanofi has announced that the US Food and Drug Administration (FDA) has granted orphan drug designation (ODD) to riliprubart for …