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Travere Therapeutics and CSL Vifor Announce European Commission Approves FILSPARI® (sparsentan) for the treatment of IgA Nephropathy - Vimarsana News

Travere Therapeutics and CSL Vifor Announce European Commission Approves FILSPARI® (sparsentan) for the treatment of IgA Nephropathy

First non-immunosuppressive therapy for the treatment of IgA nephropathy approved in Europe Conditional marketing authorization is based on statistically significant and clinically meaningful...

Potential for Astellas' new prostate cancer drug with EC approval - Vimarsana News

Potential for Astellas' new prostate cancer drug with EC approval

Today (April 24), Astellas Pharma Inc. revealed that XTANDITM (enzalutamide) has received a label extension from the European Commission, marking it as the inaugural and only novel hormone therapy endorsed for high-risk biochemical recurrent non-metastatic hormone-sensitive prostate cancer (nmHSPC) treatment in the European Union (EU).

Enzalutamide Receives Go Ahead From European Commission in nmHSPC - Vimarsana News

Enzalutamide Receives Go Ahead From European Commission in nmHSPC

The European Commission has approved enzalutamide as monotherapy and in combination with ADT in BCR nonmetastatic hormone-sensitive prostate cancer.

AstraZeneca: Voydeya approved in the EU as a treatment for HPN - Vimarsana News

AstraZeneca: Voydeya approved in the EU as a treatment for HPN

AstraZeneca announces that Voydeya has been approved in the European Union as an adjunct to ravulizumab or eculizumab for the treatment of adult patients with paroxysmal nocturnal hemoglobinuria ...

Tislelizumab Receives EU Approval in 3 Indications for First- and Second-Line NSCLC - Vimarsana News

Tislelizumab Receives EU Approval in 3 Indications for First- and Second-Line NSCLC

Tislelizumab has been approved in Europe across 3 indications in the first and second line for select patients with non–small cell lung cancer.