Study identifier:D7409C00001
ClinicalTrials.gov identifier:NCT07509151
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase III, Randomised, Open-label, Multicentre, Study of Surovatamig as Consolidation Therapy versus Observation after First-line Induction Therapy in Participants with Chronic Lymphocytic Leukaemia or Small Lymphocytic Lymphoma with Unmutated IGHV (SOUNDTRACK-C1)
Chronic Lymphocytic Leukaemia or Small Lymphocytic Lymphoma with unmutated IGHV
Phase 3
No
Surovatamig
All
420
Interventional
18 Years - 18 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Sequential Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Mar 2026 by AstraZeneca
AstraZeneca
PAREXEL
No locations available
| Arms | Assigned Interventions |
|---|---|
| Experimental: Dose Optimisation and Safety run-in (DOSRI)- Surovatamig Dose 1 Participants will receive Surovatamig Dose 1 subcutaneously (SC) for 6 cycles (each cycle is 28 days in length). | Drug: Surovatamig Surovatamig will be administered as a subcutaneous injection. Other Name: TNB-486 Other Name: AZD0486 |
| Experimental: DOSRI-Surovatamig Dose 2 Participants will receive Surovatamig Dose 2 SC for 6 cycles (each cycle is 28 days in length). | Drug: Surovatamig Surovatamig will be administered as a subcutaneous injection. Other Name: TNB-486 Other Name: AZD0486 |
| Experimental: Phase III-Arm A: Surovatamig SC Participants will receive Surovatamig at RP3D subcutaneously for 6 cycles (each cycle is 28 days in length). | Drug: Surovatamig Surovatamig will be administered as a subcutaneous injection. Other Name: TNB-486 Other Name: AZD0486 |
| No Intervention: Phase III-Arm B: Observation Participants will undergo observation for 24 weeks. | - |