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Real-World Research: The application of selinexor in the total therapy of newly diagnosed high-risk multiple myeloma

Real-World Research:The application of selinexor in the total therapy of newly diagnosed high-risk multiple myeloma

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096268
Enrollment
Unknown
Registered
2025-01-21
Start date
2025-02-06
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Multiple Myeloma

Interventions

The treatment group with Selinexor:None
The treatment group without Selinexor:None

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age> = 18 years, gender is not limited; 2. Confirmed diagnosis of MM according to IMWG criteria, and at least one of the following high-risk factors: t(4,14), t(14,16), t(14,20), del(17/17p), del(13), 1q amplification, R-ISS stage III, plasma cell leukemia, central involvement, combined with extramedullary clonal plasma cells, etc.; 3. Have not received any anti-MM treatment regimen in the past or have received anti-MM therapy regimen without recurrence or refractory.

Exclusion criteria

Exclusion criteria: 1.The patient has previously received SINE (including selinexor), or has a suspected allergy to SINE or similar drugs. 2.The patient has participated in the use of investigational drugs in other anti - tumor clinical trials within 3 weeks. 3.There are mental illnesses/social situations that limit compliance with the study requirements. 4.The patient is unable to swallow oral medications, or is unable or unwilling to abide by the drug administration requirements. 5.Pregnant women, lactating women, or women of childbearing age who are planning to conceive.

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival, PFS;

Secondary

MeasureTime frame
Overall Response Rate, ORR;Duration of Response, DOR;

Countries

China

Contacts

Public ContactZhang Li

West China Hospital of Sichuan University

drzhangli2014@sina.com+86 189 8060 6690

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026