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OncoMatch/Clinical Trials/NCT07179679

A Clinical Study Assessing the Subcutaneous Formulation of TQB2934 for Injection in Subjects With Malignant Plasma Cell Tumors

Is NCT07179679 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies TQB2934 for multiple myeloma.

Phase 1RecruitingChia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.NCT07179679Data as of May 2026

Treatment: TQB2934TQB2934 is an anti-Cluster of Differentiation 3 (CD3) (Early T Cell Marker)×B cell maturation antigen (BCMA) double-specific antibody,and the isoform is IgG1(Native Immunoglobulin G1), which at one end binds to the CD3 receptor on the surface of T cells ,and the other end binds to BCMA(B cell maturation antigen) to recruit T cells around BCMA-positive cells, which can activate T cells .Active T cells release granzyme and perforin to kill BCMA-positive target cells. TQB2934 for injection (subcutaneous injection) is intended for the treatment of patients with multiple myeloma.

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 1 prior line

Must have received: proteasome inhibitor

at least one proteasome inhibitor (PI)...are refractory

Must have received: immunomodulator

at least one...immunomodulator (IMiD)...are refractory

Must have received: CD38 monoclonal antibody

at least one...Cluster of Differentiation 38 (CD38) monoclonal antibody are refractory

Cannot have received: allogeneic hematopoietic stem cell transplantation

Exception: within 1 year before the first medication

Have received allogeneic hematopoietic stem cell transplantation within 1 year before the first medication

Cannot have received: autologous hematopoietic stem cell transplantation

Exception: within 12 weeks before the first medication

have received autologous hematopoietic stem cell transplantation (ASCT) within 12 weeks before the first medication

Cannot have received: CD3×BCMA dual antibody therapy

Have received CD3×BCMA dual anti-anti-treatment in the past

Cannot have received: glucocorticoid (dexamethasone)

Exception: cumulative dose >160 mg or equivalent within 4 weeks before the first medication

Cumulative treatment of dexamethasone >160 mg or equivalent dose of other glucocorticoids within 4 weeks before the first medication

Cannot have received: targeted therapy

Exception: within 3 weeks before the first medication

received targeted therapy, cytotoxic drugs or any antibody therapy within 3 weeks before the first medication

Cannot have received: cytotoxic chemotherapy

Exception: within 3 weeks before the first medication

received targeted therapy, cytotoxic drugs or any antibody therapy within 3 weeks before the first medication

Cannot have received: antibody therapy

Exception: within 3 weeks before the first medication

received targeted therapy, cytotoxic drugs or any antibody therapy within 3 weeks before the first medication

Cannot have received: proteasome inhibitor

Exception: within 2 weeks before the first medication

received proteasome inhibitor therapy or radiotherapy within 2 weeks before the first medication

Cannot have received: radiation therapy

Exception: within 2 weeks before the first medication

received proteasome inhibitor therapy or radiotherapy within 2 weeks before the first medication

Cannot have received: immunomodulator

Exception: within 1 week before the first medication

received immunomodulatory therapy within 1 week before the first medication

Cannot have received: Chinese patent medicine with anti-tumor indications

Exception: within 2 weeks before the first medication

received Chinese patent medicine treatments within 2 weeks before the first medication have received National Medical Products Administration (NMPA) -approved drug instructions that clearly have anti-tumor indications

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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