MM summer98 - fda 2025

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Most FDA-approved human drugs and therapeutic biological products are listed in Drugs @ FDA, a searchable database. The database allows you to search by drug name, active ingredient, or application (NDA, ANDA, or BLA) number.
The FDA has granted breakthrough therapy designation (BTD) to lysergide (LSD) d-tartrate (MM-120; Mind Medicine [MindMed]) for the treatment of generalized anxiety disorder (GAD).
TEMBEXA is a U.S. Food and Drug Administration (FDA) approved oral (tablets and suspension) small molecule antiviral to treat human smallpox disease caused by variola virus in adults and children, including neonatal populations.
Setmelanotide (Imcivree, Rhythm Pharmaceuticals) is a melanocortin-4 receptor agonist that the FDA previously approved for chronic weight management in people with Bardet-Biedl syndrome in 2022 and those with pro-opiomelanocortin (POMC) deficiency, proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency or
On September 20, 2024, the Food and Drug Administration approved isatuximab-irfc (Sarclisa, Sanofi-Aventis U.S. LLC) with bortezomib, lenalidomide, and dexamethasone for adults with newly diagnosed multiple myeloma who are not eligible for autologous stem cell transplant (ASCT).
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In August 2023, elranatamab received its first approval in the USA for the treatment of adult patients with relapsed or refractory multiple myeloma (RRMM) who have received at least four prior lines of therapy including a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody.
ELREXFIO may cause side effects that are serious, life-threatening, or can lead to death, including cytokine release syndrome (CRS) and neurologic problems.
FDA Approves Elranatamab for Resistant Multiple Myeloma.

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