US FDA grants breakthrough therapy designation to Innate Pharma’s lacutamab for relapsed or refractory Sézary syndrome: Marseille, France Tuesday, February 18, 2025, 12:00 Hrs ...
Innate Pharma has secured US Food and Drug Administration (FDA) breakthrough therapy designation for lacutamab to treat ...
Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) ("Innate" or the "Company") today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD) to ...
Researchers sought to determine whether the CAR-T therapy volamcabtagene durzigedleucel (CTX130) would be effective in patients with T-cell lymphoma.
The cause of mycosis fungoides is unknown and, with the possible exception of very early stage disease, no cure is available. Fortunately, patients with MF have a number of therapeutic options and ...
The first step in this bilateral agreement will be to deliver funding to the province to provide access to five drugs under the National Strategy for Rare Diseases: Poteligeo, for the treatment of ...
TORONTO – The Ontario government is connecting more people to the care they need by ensuring Ontarians, of all ages, living with rare diseases have faster and easier access to new and emerging ...
The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression ...
Tulmimetostat is under development for the treatment of the solid tumors including metastatic castration-resistant prostate cancer, mycosis fungoides, Sezary syndrome, peripheral T-cell lymphoma (PTCL ...
Tulmimetostat is under development for the treatment of the solid tumors including metastatic castration-resistant prostate cancer, mycosis fungoides, Sezary syndrome, peripheral T-cell lymphoma (PTCL ...
including the most common subtypes mycosis fungoides and Sézary syndrome, were given DD-cxdl for five consecutive days every 21 days. Roughly 36% of patients responded to the treatment ...
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