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A prospective, single-arm, exploratory clinical study on the treatment of refractory and relapsed multiple myeloma (MM) patients with Chidamide combined with Thalidomide, Cyclophosphamide and Dexamethasone (TC2D)

A prospective, single-arm, exploratory clinical study on the treatment of refractory and relapsed multiple myeloma (MM) patients with Chidamide combined with Thalidomide, Cyclophosphamide and Dexamethasone (TC2D)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035100
Enrollment
Unknown
Registered
2020-07-31
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-08-03

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:Chidamide combined with Thalidomide, Cyclophosphamide and Dexamethasone

Sponsors

The First Affiliated Hospital of Medical College of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Understand and voluntarily sign informed consent form of patients; 2. Patients with age >= 18-75 years old; 3. According to the IMWG diagnostic criteria for multiple myeloma in 2014, the patients who were diagnosed as refractory and relapsed and needed immediate rescue treatment; 4. Patients who have been treated with bortezomib and lenalidomide in the past and assessed as disease progression after the final course of treatment.

Exclusion criteria

Exclusion criteria: 1. Patients with any serious illness that can lead to an unbearable risk when participating in this study; 2. Patients with diseases that need continuous active treatment, such as unstable heart disease, stroke, rheumatoid arthritis, lupus, etc.; 3. Pregnant or lactating women; 4. Patients with a history of malignant tumor other than mm, unless the patient has no disease and survived for more than 3 years; 5. Patients who were vaccinated with live vaccine and live attenuated vaccine within 4 weeks before randomization.

Design outcomes

Primary

MeasureTime frame
Overall response rate;safety;

Secondary

MeasureTime frame
Progression free survival;Overall survival;

Countries

China

Contacts

Public ContactZhen Cai

The First Affiliated Hospital of Medical College of Zhejiang University

caiz@zju.edu.cn+86 13657190311

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026