A Phase 1b, Open-Label, Multicenter Study to Evaluate the Safety and Efficacy of TAK-007, an Allogeneic Anti-CD19 Chimeric Antigen Receptor Natural Killer Cell (CD19 CAR-NK) Therapy, in Adult Subjects With Refractory Lupus Nephritis
Latest Information Update: 09 Apr 2025
At a glance
- Drugs TAK 007 (Primary)
- Indications Lupus nephritis; Systemic scleroderma
- Focus Adverse reactions
- Sponsors Takeda
Most Recent Events
- 06 Apr 2025 The protocol has been amended to addition in to addition of SSc subjects and addition in treatment arms with change in Interventional Study Model as Sequential Assignment.
- 06 Apr 2025 Planned End Date changed from 23 Apr 2029 to 2 Sep 2030.
- 06 Apr 2025 Planned primary completion date changed from 23 Apr 2029 to 2 Sep 2030.