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Efficacy and safety of teniposide, cyclophosphamide and dexamethasone combination in transplant-ineligible patients with relapsed/refractory multiple myeloma: a phase 2, single center, single arm study

Efficacy and safety of teniposide, cyclophosphamide and dexamethasone combination in transplant-ineligible patients with relapsed/refractory multiple myeloma: a phase 2, single center, single arm study

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-15007636
Enrollment
Unknown
Registered
2015-12-17
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Multiple Myeloma

Interventions

Treatment Group:VM26+CTX+DXM regimen

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Men and women, aged above 18 years; 2. Subjects have diagnosed multiple myeloma, and previously treated; 3. ECOG performance status (PS) score 0-2; 4. AST and ALT <=3 times the institutional ULN; Total bilirubin <=2.0 times the institutional ULN Serum creatinine<2.0 times the institutional ULN; 5. Women or men must take effective contraceptive measures, in women Serum or urine pregnancy tests must be negative in the screening and study periods; 6. Patients understand the disease and voluntarily received the study regimen and follow-up.

Exclusion criteria

Exclusion criteria: 1. Frail to receive chemotherapy; 2. Uncontrolled DM; 3. Subjects suffered from the AIDSactivity hepatitis B or C virus; 4. Dementia or altered mental status that would prohibit the understanding or rendering of informed consent;

Design outcomes

Primary

MeasureTime frame
Complete response rate;Overall response rate;

Secondary

MeasureTime frame
Progression free survival;Overall survival;

Countries

China

Contacts

Public ContactYue Lv
lvyue@sysucc.org.cn+86 13925084058

Outcome results

None listed

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