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CD38: Sarclisa approved in the US as the first anti-CD38 therapy in combination with standard-of-care treatment for adult patients with newly diagnosed multiple myeloma not eligible for transplant
吉满生物
2024-09-23

June 3, 2024. Sanofi issued a press release stating that its CD38 monoclonal antibody Sarclisa has been approved in the United States as the first anti-CD38 therapy.

Sarclisa is the first anti-CD38 drug to significantly improve progression-free survival in combination with VRd for the treatment of newly diagnosed transplant-eligible multiple myeloma.

Approval based on positive results from the IMROZ phase 3 study demonstrating Sarclisa in combination with bortezomib, lenalidomide, and dexamethasone (VRd) significantly improved progression-free survival (PFS), compared to standard-of-care in newly diagnosed adult patients not eligible for autologous stem cell transplant (ASCT).

Third indication for Sarclisa, evaluated under FDA Priority Review, underscores Sanofi’s commitment to helping close a critical care gap in multiple myeloma (MM).

Genomeditech launches stable high-expression cell lines and antibody products to help CD38 drug development! Click here to learn more about our CD38 catalog

Current position:News > News > Insights
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CD38: Sarclisa approved in the US as the first anti-CD38 therapy in combination with standard-of-care treatment for adult patients with newly diagnosed multiple myeloma not eligible for transplant
吉满生物
2024-09-23

June 3, 2024. Sanofi issued a press release stating that its CD38 monoclonal antibody Sarclisa has been approved in the United States as the first anti-CD38 therapy.

Sarclisa is the first anti-CD38 drug to significantly improve progression-free survival in combination with VRd for the treatment of newly diagnosed transplant-eligible multiple myeloma.

Approval based on positive results from the IMROZ phase 3 study demonstrating Sarclisa in combination with bortezomib, lenalidomide, and dexamethasone (VRd) significantly improved progression-free survival (PFS), compared to standard-of-care in newly diagnosed adult patients not eligible for autologous stem cell transplant (ASCT).

Third indication for Sarclisa, evaluated under FDA Priority Review, underscores Sanofi’s commitment to helping close a critical care gap in multiple myeloma (MM).

Genomeditech launches stable high-expression cell lines and antibody products to help CD38 drug development! Click here to learn more about our CD38 catalog

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