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Pharmaceutical Technology on MSNSanofi’s Sarclisa gains EC approval for multiple myeloma treatmentThe European Commission (EC) has granted approval to Sanofi's Sarclisa in combination with a regimen of bortezomib, ...
Sanofi’s Sarclisa approved in the EU for the treatment of transplant-eligible newly diagnosed multiple myeloma Approval based on GMMG-HD7 phase 3 study demonstrating that Sarclisa with VRd induction ...
Sanofi’s Sarclisa receives European approval to treat transplant-eligible newly diagnosed multiple myeloma: Paris Saturday, July 26, 2025, 09:00 Hrs [IST] Following the positive ...
Following the positive opinion by the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) on ...
Sarclisa Phase 3 IKEMA pivotal trial results supporting approval The FDA approval is based on data from the Phase 3 IKEMA study, a randomized, multi-center, open label clinical trial that enrolled ...
Sanofi’s Sarclisa scored a recommendation from Europe’s Committee for Medicinal Products for Human Use back in March in combo with Bristol Myers Squibb's Pomalyst and dexamethasone (pom-dex ...
Sarclisa approved in the EU as the first anti-CD38 therapy in combination with standard-of-care VRd to treat transplant-ineligible newly diagnosed multiple myeloma Approval is based on positive ...
PARIS – June 2, 2020 – Sarclisa ® (isatuximab) added to carfilzomib and dexamethasone (Sarclisa combination therapy) reduced the risk of disease progression or death by 47% (hazard ratio 0. ...
Paris: Sanofi has announced that the European Commission has approved Sarclisa in combination with bortezomib, lenalidomide, ...
PARIS, March 31, 2021 /PRNewswire/ -- The U.S. Food and Drug Administration (FDA) has approved Sarclisa ® (isatuximab-irfc) in combination with carfilzomib and dexamethasone (Kd), for the ...
Sanofi’s Sarclisa approved in the EU for the treatment of transplant-eligible newly diagnosed multiple myeloma Approval based on GMMG-HD7 phase 3 study demonstrating that Sarclisa with VRd induction ...
Sarclisa regimen reduced risk of disease progression or death by 45% compared to standard of care in patients who had relapsed after one to three prior therapies While the median progression free ...
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