Drugs / Mezagitamab

Trials 12

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 14 trials
Phase 1 NCT05174221 Aug 2022 → Dec 2025 glomerulonephritis Takeda Completed No outcome recorded
Phase 1 NCT03984097 Jul 2019 → Mar 2026 plasma cell myeloma Takeda Completed No outcome recorded
Phase 1 NCT03724916 Nov 2018 → Nov 2021 systemic lupus erythematosus Millennium Pharmaceuticals, Inc. Completed No outcome recorded
Phase 1 NCT02219256 Aug 2014 → Apr 2016 autoimmune disease Takeda Completed No outcome recorded
Phase 1/22 trials
Phase 1/2 NCT04776018 Apr 2021 → Aug 2023 refractory plasma cell neoplasm Takeda Terminated No outcome recorded Stop: Business
Phase 1/2 NCT03439280 Apr 2018 → Jan 2022 plasma cell myeloma Millennium Pharmaceuticals, Inc. Completed No outcome recorded
Phase 23 trials
Phase 2 NCT07613359 Oct 2026 → Jan 2029 expected transplant rejection Takeda Not yet recruiting No outcome recorded
Phase 2 NCT04278924 Nov 2020 → Apr 2024 autoimmune thrombocytopenia Takeda Completed No outcome recorded
Phase 2 NCT04159805 Jan 2020 → Jul 2022 generalized myasthenia gravis Takeda Completed No outcome recorded
Phase 33 trials
Phase 3 NCT06948318 Aug 2025 → Jul 2029 expected autoimmune thrombocytopenic purpura Takeda Recruiting No outcome recorded
Phase 3 NCT06963827 Jul 2025 → Sep 2028 expected kidney disorder Takeda Recruiting No outcome recorded
Phase 3 NCT06722235 Feb 2025 → Mar 2028 expected autoimmune thrombocytopenic purpura Takeda Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 4

DateIssuerRelease
2025-11-07 Takeda Results Takeda Presents New Data Showing Mezagitamab (TAK-079) Sustained Effect on Kidney Function 18 Months After Treatment in Primary IgA Nephropathy takeda.com ↗
Data from the study showed that kidney function (eGFR) remained stable in patients with IgA nephropathy through Week 96 – up to 18 months after the last mezagitamab dose.
2024-06-24 Takeda Results Takeda Presents Late-Breaking Data from Phase 2b Study of Mezagitamab, Demonstrating Potential to Transform Treatment of Primary Immune Thrombocytopenia takeda.com ↗
Takeda ( TSE:4502/NYSE:TAK ) today presented positive results from its Phase 2b, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability and efficacy of mezagitamab (TAK-079) in patients with persistent or chronic primary immune thrombocytopenia (ITP), a rare immune-mediated bleeding disorder.
2024-03-13 Takeda Results Takeda Announces Positive Topline Results from Phase 2 Study Evaluating Mezagitamab (TAK-079), a Potential Best-in-Class Anti-CD38 Monoclonal Antibody, for Primary Immune Thrombocytopenia takeda.com ↗
Takeda ( TSE:4502/NYSE:TAK ) today announced positive topline results from a Phase 2, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability and efficacy of mezagitamab (TAK-079) in patients with persistent or chronic primary immune thrombocytopenia (ITP).
2020-11-05 Takeda Results Takeda Oncology Demonstrates Leadership in Hematologic Cancers at 62nd American Society of Hematology (ASH) Annual Meeting takeda.com ↗
Mezagitamab Induces Immunomodulatory Effect in Patients with Relapsed/Refractory Multiple Myeloma (RRMM).

All press releases naming this drug 9 releases

DateIssuerRelease

Evidence & citations 7 cited values

Every value below carries the sentence it was read from. 15 sources stand behind the page.

FieldValueCited text
Known as mezagitamab “Mezagitamab is an anti-CD38 antibody that targets plasma cells, plasmablasts, and natural killer cells.” PMID 41950473 ↗ Apr 2026
7

NCT06963827 ↗

NCT04776018 ↗

NCT03439280 ↗

NCT06948318 ↗

NCT06722235 ↗

NCT05174221 ↗

NCT07613359 ↗

Known as TAK-079 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04159805 ↗
4

NCT02219256 ↗

NCT03984097 ↗

NCT04278924 ↗

NCT03724916 ↗

Action Deplete “coincided with reduction in CD38-expressing cells” PMID 32045493 ↗ Feb 2020
Modality Monoclonal antibody “a subcutaneously administered anti-CD38 monoclonal antibody” PMID 40552138 ↗ Sep 2024
Route Intravenous “single intravenous (IV) infusion or subcutaneous (SC) administration” NCT02219256 ↗
Route Subcutaneous “single intravenous (IV) infusion or subcutaneous (SC) administration” NCT02219256 ↗
Target CD38 “anti-CD38 cytolytic antibody TAK-079” PMID 32045493 ↗ Feb 2020