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  2. Lifileucel - Wikipedia

    en.wikipedia.org/wiki/Lifileucel

    Lifileucel is the first tumor-derived T cell immunotherapy approved by the US Food and Drug Administration (FDA). [3] It was approved for medical use in the United States in February 2024. [ 2 ] [ 4 ]

  3. Mavorixafor - Wikipedia

    en.wikipedia.org/wiki/Mavorixafor

    Mavorixafor improved absolute neutrophil counts and absolute lymphocyte counts, assessed over a 24-hour period four times throughout the study. [2] Absolute neutrophil counts below 500 cells/μL and absolute lymphocyte counts below 1000 cells/μL are associated with an increased risk of infections. [ 2 ]

  4. Tisagenlecleucel - Wikipedia

    en.wikipedia.org/wiki/Tisagenlecleucel

    Tisagenlecleucel is indicated for the treatment of those under 25 years of age with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse; or adults with relapsed or refractory (r/r) large B-cell lymphoma after two or more lines of systemic therapy including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, high grade B-cell lymphoma ...

  5. A cancer treatment that one expert called the 'most exciting ...

    www.aol.com/article/news/2017/08/30/a-cancer...

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  6. Iovance Biotherapeutics - Wikipedia

    en.wikipedia.org/wiki/Iovance_Biotherapeutics

    In 2024 the US FDA gave accelerated approval to Lifileucel, the company's tumor-infiltrating lymphocyte drug for the treatment of unresectable or metastatic melanoma. [4]

  7. Afamitresgene autoleucel - Wikipedia

    en.wikipedia.org/wiki/Afamitresgene_autoleucel

    Afamitresgene autoleucel is a melanoma-associated antigen A4 (MAGE-A4)-directed genetically modified autologous T cell immunotherapy indicated for the treatment of adults with unresectable or metastatic synovial sarcoma who have received prior chemotherapy, are HLA-A*02:01P, -A*02:02P, -A*02:03P, or -A*02:06P positive and whose tumor expresses the MAGE-A4 antigen as determined by FDA-approved ...

  8. Merck Nabs Expanded Keytruda Label For Hodgkin Lymphoma - AOL

    www.aol.com/news/merck-nabs-expanded-keytruda...

    Merck (MRK) has announced that the U.S. Food and Drug Administration (FDA) has approved an expanded label for Keytruda, Merck’s anti-PD-1 therapy, as monotherapy for the treatment of adult ...

  9. Teplizumab - Wikipedia

    en.wikipedia.org/wiki/Teplizumab

    Teplizumab, sold under the brand name Tzield, is a humanized anti-CD3 monoclonal antibody that is the first approved treatment indicated to delay the onset of stage 3 type 1 diabetes (T1D) in people with stage 2 T1D. [3] [4] [5] The Fc region of this antibody has been engineered to have Fc receptor non-binding (FNB) properties. [6]