Table 3.
Clinical Trial | Phase | Drugs | Comments | Mechanism of action | Primary Endpoints | Key Secondary Endpoints | Estimated Enrollment |
---|---|---|---|---|---|---|---|
NCT05424822 | I | JNJ-80948543 | B-NHL and CLL | CD3 x CD20 x CD79b | DLT, AEs | Pharmacokinetics, ORR, CR, TTR, DOR | 180 |
NCT04594642 | I | TNB-486 | R/R B-NHL | CD19 x CD3 | DLT | ORR, PFS, DOR | 116 |
NCR04077723 | I/II | RO7227166 | R/R B-NHL | 41BBL + CD20 X CD3 | DLT, AEs, ORR, DCR, DOR, PFS, OS, CR | Pharmacokinetics, AEs, ADA, TFR, Quality of life | 498 |
NCT05397496 | I | PIT565 | R/R- B-NHL | CD19 x CD3 x CD2 | DLT | Pharmacokinetics, ORR, CR, OS,PFS, EFS, | 140 |
NCT05219513 | I | RO7443904 | R/R- B-NHL | CD19 x CD28 + CD20 X CD3 | DLT, AEs | Pharmacokinetics | 53 |
DLT = Drug limiting toxicities; AEs = adverse effects; ORR = overall response rate; CR = complete metabolic response; TTR = time to response; DOR = duration of response; PFS = progression-free survival; OS = overall survival; DOCR = duration of complete response; ADA = anti-drug antibodies; EFS = event-free survival; DCR = Disease control rate; TFR = time to response.