
Microbial Resource Management (MRM) Health has announced that its lead programme, MH002, has received Investigational New Drug (IND) clearance from …

Polpharma Biologics has signed a global licensing agreement with Fresenius Kabi for the commercialisation of PB016, a proposed biosimilar to …
1 October 2024 โ Saint-Prex, Switzerland โ Ferring Pharmaceuticals today announces results from the OPTIMISE study showing the first real-world …

The National Institute for Health and Care Excellence (NICE) have recommended adult patients in England or Wales with moderately or …

AbbVie has announced that the European Medicines Agencyโs (EMA) Committee for Medicinal Products for Human Use (CHMP) has granted a …

Johnson & Johnson (J&J) has announced the first data from its phase 3 QUASAR maintenance study which assessed Tremfya (guselkumab) …

Pfizer has announced that the European Commission (EC) has granted marketing authorisation for Velsipity (etrasimod) in the European Union (EU). …

Landos Biopharma has announced that it has shared safety, tolerability, pharmacokinetics and clinical efficacy results for the NX-13 phase 1b …

Eli Lilly has announced that the US Food and Drug Administration (FDA) has approved Omvoh (mirikizumab-mrkz) infusion (300mg/15mL)/injection (100mg/mL) for …

Sanofi and Teva Pharmaceuticals have announced that they will collaborate for the co-development and co-commercialisation of TEVโ574, a treatment for …

Frenchย biotech company OSE Immunotherapeutics has announced that its Ulcerative Colitis (UC) trialโs Independent Drug Safety Monitoring Board (DSMB) has provided …

A new drug, being investigated by Amsterdam UMC along with colleagues at various universities, has been shown to be effective …

Eli Lillyโs mirikizumab treatment for ulcerative colitis (UC) patients has met the primary endpoints and all key secondary endpoints in …

Roche has voiced its disappointment after its investigational therapy etrolizumab showed โmixed resultsโ as a treatment for moderately to severely …

The European Commission has awarded marketing approval to Takedaโs subcutaneous formulation of its gut-selective biologic therapy Entyvio (vedolizumab) as a …