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A Clinical Study on the Efficacy and Safety of Continuous Ixazomib and Pomalidomide Therapy after BCMA CAR-T Treatment in High-Risk Multiple Myeloma

A Clinical Study on the Efficacy and Safety of Continuous Ixazomib and Pomalidomide Therapy after BCMA CAR-T Treatment in High-Risk Multiple Myeloma

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126595
Enrollment
Unknown
Registered
2026-06-11
Start date
2026-07-15
Completion date
Unknown
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

high-risk multiple myeloma

Interventions

Observation Group:None

Sponsors

Beijing Chao-Yang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with high-risk myeloma who have received CAR-T therapy; 2.Age >= 18 years; 3.Expected survival >= 12 months; 4.Voluntarily sign the informed consent form approved by the ethics committee;

Exclusion criteria

Exclusion criteria: 1.Patients with active hepatitis B (HBV), hepatitis C (HCV), and other acquired or congenital immunodeficiency diseases. 2.Presence of severe thrombotic events before treatment. 3.Patients with uncontrolled or severe cardiovascular diseases, including myocardial infarction within 6 months before enrollment, heart failure of NYHA class ? - ?, uncontrolled angina pectoris, clinically significant pericardial diseases or cardiac amyloidosis. 4.Patients with epilepsy, dementia and other mental disorders requiring drug treatment who cannot understand or comply with the research protocol. 5.According to the protocol or the judgment of the researcher, patients with severe physical or mental diseases that may interfere with their participation in this clinical study. 6.Drug abuse, medical, psychological or social conditions that may interfere with the subject's participation in the study or the evaluation of the study results. 7.Patients who are currently receiving treatment with other investigational drugs. 8.Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival(PFS);Overall Response Rate(ORR);

Secondary

MeasureTime frame
MRD negativity rate(MRD);Overall survival(OS);Complete Response Rate(CRR);Progression-free Survival(PFS);

Countries

China

Contacts

Public ContactAijun Liu

Beijing Chao-Yang Hospital, Capital Medical University

laj0628@163.com+86 10 85231473

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026