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Clinical study for chidamide combined with bortezomib, dexamethasone and doxorubicin hydrochloride liposome injection in the treatment of relapse/refractory multiple myeloma

Clinical study for chidamide combined with bortezomib, dexamethasone and doxorubicin hydrochloride liposome injection in the treatment of relapse/refractory multiple myeloma

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027562
Enrollment
Unknown
Registered
2019-11-18
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Multiple myeloma

Interventions

Case series:Refractory/relapsed multiple myeloma patient group

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosis of active multiple myeloma patients, refractory recurrence; 2. Secretory multiple myeloma with measurable indicators; 3. Age 18 or older, gender is not limited; 4. The general condition of the body is scored ECOG0-2, and the expected survival period is more than 3 months; 5. Serum liver enzyme value =0.5x10^9/L, platelet count >=70x 10^9/L, glomerular filtration rate (eGFR) >=50 mL/min; 6. Left ventricular ejection fraction is normal, no obvious heart, lung and other dysfunction (<=1 degree); 7. Can accept adverse reactions and therapeutic effects according to the test requirements; 8. Patients must have the ability to understand and voluntarily sign an informed consent form, and the informed consent form must be signed prior to any testing process.

Exclusion criteria

Exclusion criteria: 1. Initially diagnosed multiple myeloma patients; 2. There are more than grade 3 peripheral neuropathy when enrolled; 3. Those who are receiving other effective treatments; 4. Patients with severe lung and heart dysfunction (including history of prolonged QTc interval, ventricular tachycardia, ventricular fibrillation, myocardial infarction) or other serious medical problems; 5. Pregnant and lactating patients; 6. Allergies, such as those who have a history of allergies to two or more drugs or foods; or those who are known to be allergic to the components of the drug; 7. People with mental disorders that are difficult to control; 8. People with active infections; 9. Patients who had previous grade 4 thrombocytopenia (PLT <=25x10^9/L) with bortezomib.

Design outcomes

Primary

MeasureTime frame
Blood routine;Biochemistry;Electrocardiogram;

Secondary

MeasureTime frame
Proteasome activity;Cardiac ultrasound (angiography);M protein of blood;M protein of urine;

Countries

China

Contacts

Public ContactJin Lu

Peking University People's Hospital

Jin1lu@sina.com+86 13311491805

Outcome results

None listed

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