Skip to content

A prospective, single-arm, multicenter, exploratory clinical study of Selinexor combined with bortezomib, thalidomide, and dexamethasone (SPTD) in patients with relapsed and refractory multiple myeloma

A prospective, single-arm, multicenter, exploratory clinical study of Selinexor combined with bortezomib, thalidomide, and dexamethasone (SPTD) in patients with relapsed and refractory multiple myeloma

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055486
Enrollment
Unknown
Registered
2022-01-10
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

multiple myeloma

Interventions

therapy group:selinexor combined with bortezomib, thalidomide and dexamethasone

Sponsors

First Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Understand and voluntarily sign the informed consent; 2. Aged between 18 (inclusive) and 75 (inclusive); 3. Patients with multiple myeloma who have received previous treatment (induction, autologous transplantation and maintenance of the same line of treatment), and who have obtained at least partial remission in the induction treatment stage, but patients with disease progression, the criteria for disease progression must meet the IMWG 2016 diagnostic and efficacy evaluation criteria; 4. Have measurable multiple myeloma; 5. No severe liver and kidney insufficiency; 6. Expected survival greater than 6 months.

Exclusion criteria

Exclusion criteria: 1. Intolerance to thalidomide and or bortezomib; 2. Patients with unstable or active cardiovascular system diseases; 3. Peripheral neuropathy of grade >=3 and painful neuropathy of grade >=2 within 3 weeks before administration; 4. Selective nuclear export inhibitors have been used.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Minimal residual disease;Progression-free survival;Overall survival;Safety;

Countries

China

Contacts

Public ContactCai Zhen
caiz@zju.edu.cn+86 13657190311

Outcome results

None listed

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