Clinical Study of TQB2934 Injection in Relapsed/Refractory Multiple Myeloma

Starting soon · Phase 3

Conditions studied: Multiple Myeloma

In brief

This study is a randomized, open-label, multicenter Phase III clinical trial involving patients with relapsed/refractory multiple myeloma. The estimated total sample size is 260 cases, who will be randomly assigned in a 1:1 ratio to the test group and the control group. The primary objective of the study is to demonstrate the efficacy of TQB2934 for injection compared to the investigator-selected regimen in subjects with relapsed or refractory multiple myeloma (RRMM) by evaluating progression-free survival (PFS).

Key facts

Study ID

NCT07569757

Run by

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

People needed

260

Starts

2026-06-01

Expected to finish

2030-12-01

Last updated by the study team

2026-05-08

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Voluntarily join this study, sign the Informed Consent Form (ICF), and demonstrate good compliance.
• Aged 18 to 75 years old (as of the date of signing the ICF); gender not limited; Eastern Cooperative Oncology Group Performance Status (ECOG) of 0-2.
• Expected survival greater than 3 months.
• Patients with relapsed or refractory multiple myeloma.
• During or after the most recent treatment, there is evidence of disease progression or failure to achieve remission after the last line of treatment。
• Measurable disease at screening.
• Adequate organ function as indicated by laboratory tests meeting the criteria.
• Women of childbearing potential must agree to use effective contraception during the study and for 12 months after the last dose of study treatment, and agree not to donate eggs for reproduction during this period. Must not be breastfeeding and must have a negative serum or urine pregnancy test within 7 days prior to enrollment. Men who have not had a vasectomy and their female partners of childbearing potential should also agree to use effective contraception during the study and for 12 months after the last dose of study treatment, and agree not to donate sperm during this period.

You may not qualify if…

• History of other malignancies within 5 years prior to informed consent or concurrent presence of other malignancies. The following exceptions are allowed: other malignancies cured by surgery alone with a disease-free survival (DFS) ≥5 years; cured carcinoma in situ of the cervix, non-melanoma skin cancer, and superficial bladder tumors [Ta (non-invasive tumor), Tis (carcinoma in situ), and T1 (tumor invading the basement membrane)].
• Diagnosis of plasma cell leukemia (defined as circulating plasma cells ≥5% in peripheral blood according to standard classification), Waldenström macroglobulinemia, primary light-chain (AL) amyloidosis, POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein [M protein], and skin changes), or solitary plasmacytoma.
• History of prior anticancer treatment, including but not limited to:
• Receipt of chimeric antigen receptor T-cell (CAR-T), Chimeric Antigen Receptor T-Cell Immunotherapy(CAR-T), Chimeric Antigen Receptor Natural Killer Cells (CAR-NK), or other cellular therapies within 3 months prior to randomization;
• Receipt of autologous stem cell transplantation within 3 months prior to randomization;
• Receipt of allogeneic stem cell transplantation within 6 months prior to randomization; subjects must have discontinued all immunosuppressive therapy for ≥6 weeks and have no signs or symptoms of graft-versus-host disease (GVHD);
• Receipt of molecular targeted therapy, investigational drugs, or invasive investigational medical devices within 3 weeks or 5 drug half-lives (whichever is shorter) prior to randomization;
• Receipt of monoclonal antibodies, bispecific antibodies, chemotherapy, etc., within 3 weeks prior to randomization;
• Receipt of proteasome inhibitors (PI), immunomodulatory drugs (IMiDs), localized radiotherapy, palliative radiotherapy, or Chinese patent medicines with antitumor indications approved by the National Medical Products Administration (NMPA) within 2 weeks prior to randomization.
• Previously refractory to control group drugs, or with contraindications, life-threatening allergic reactions, or intolerance to previous treatments.
• Receipt of systemic corticosteroids at a cumulative dose ≥140 mg prednisone (or equivalent) within 2 weeks prior to randomization. Topical, ophthalmic, intra-articular, intranasal, and inhaled corticosteroids are excluded from the cumulative dose calculation (see Appendix for dose conversion).
• Toxicities from prior antitumor therapy have not recovered to baseline or ≤ Grade 1, except for Grade 2 alopecia, non-clinically significant and asymptomatic laboratory abnormalities, and hypothyroidism stabilized by hormone replacement therapy, as judged by the investigator to pose no safety risk.
• History of Grade ≥3 cytokine release syndrome (CRS) associated with any T-cell redirecting therapy (e.g., CD3-redirecting therapies or CAR-T cell therapy).
• Presence of conditions affecting intravenous infusion or blood collection, dysphagia, chronic diarrhea, intestinal obstruction, or other active gastrointestinal dysfunction that may interfere with drug administration or absorption.
• Known central nervous system (CNS) involvement of multiple myeloma (MM), or clinical signs/symptoms suggestive of leptomeningeal involvement. If either is suspected, both brain MRI and lumbar puncture cytology must be negative.
• Major surgery, significant traumatic injury, or planned major surgery during the study treatment period within 4 weeks prior to randomization, or presence of non-healed wounds or fractures (major surgery defined as Grade ≥3 according to the 2022 national surgical classification catalogue).
• Any severe (≥ CTCAE Grade 3) bleeding or hemorrhagic event within 6 months prior to randomization.
• Arterial or venous thrombotic events within 6 months prior to randomization, including cerebrovascular events (including transient ischemic attack), deep vein thrombosis, pulmonary embolism, or any other serious thromboembolism (implantable venous port- or catheter-related thrombosis and superficial thrombosis are not considered "serious").
• Active hepatitis or decompensated cirrhosis (Child-Pugh Class B or C)
• Significant cardiovascular disease.
• Neurological or psychiatric disorders.
• Pulmonary diseases, including any of the following:
• Current or prior non-infectious pneumonitis requiring corticosteroid treatment (including but not limited to acute respiratory distress syndrome, acute hypersensitivity pneumonitis, drug-related pneumonitis, bronchospasm, acute interstitial pneumonitis, idiopathic pulmonary fibrosis, etc.);
• Known or suspected chronic obstructive pulmonary disease (COPD) with forced expiratory volume in 1 second (FEV1) <60% of predicted.
• Active or uncontrolled infections (≥ CTCAE Grade 2), including bacterial, fungal, or viral infections, such as active pneumonia/pulmonary infection, syphilis, tuberculosis, or Corona Virus Disease 2019 (COVID-19). Subjects with positive Cytomegalovirus (CMV) DNA or Epstein-Barr virus (EBV) plasma DNA during screening are not eligible.

Where it is running

• The First Affiliated Hospital of Bengbu Medical University — Bengbu, Anhui, China
• The First Affiliated Hospital of Anhui Medical University — Hefei, Anhui, China
• Beijing Chao-Yang Hospital,Capital Medical University — Beijing, Beijing Municipality, China
• Beijing Jishuitan Hospital,Capital Medical University — Beijing, Beijing Municipality, China
• The First Affiliated Hospital of Chongqing Medical University — Chongqing, Chongqing Municipality, China
• The Southwest Hospital of Amu — Chongqing, Chongqing Municipality, China
• Gansu Provincial Maternal and Child Health Hospital (Gansu Provincial Central Hospital) — Lanzhou, Gansu, China
• Lanzhou University Second Hospital — Lanzhou, Gansu, China
• Sun Yat-sen Memorial Hospital, Sun Yat-sen University — Guangzhou, Guangdong, China
• Sun Yat-Sen University Cancer Center — Guangzhou, Guangdong, China
• Zhujiang Hospital of Southern Medical University — Guangzhou, Guangdong, China
• Affiliated Hospital of Guangdong Medical University — Zhanjiang, Guangdong, China
• The First Affiliated Hospital of Guangxi Medical University — Nanning, Guangxi, China
• The Affiliated Hospital of Guizhou Medical University — Guiyang, Guizhou, China
• Cangzhou People'S Hospital — Cangzhou, Hebei, China
• Affiliated Hospital of Chengde Medical University — Chengde, Hebei, China
• The Second Hospital of Hebeimedical University — Shijiazhuang, Hebei, China
• The Second Affiliated Hospital of Harbin Medical University — Harbin, Heilongjiang, China
• Luoyang Central Hospital — Luoyang, Henan, China
• Henan Cancer Hospital — Zhengzhou, Henan, China
• Henan Provincial People'S Hospital — Zhengzhou, Henan, China
• The First Affiliated Hospital Of Zhengzhou University — Zhengzhou, Henan, China
• The Third Xiangya Hospital of Central South University — Changsha, Hunan, China
• Zhuzhou Central Hospital — Zhuzhou, Hunan, China
• Zhongda Hospital Southeast University — Nanjing, Jiangsu, China

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.