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Clinical trial of Venetoclax in combination with DA-EPOCH-R regimen for double/triple-hit high-grade B-cell lymphoma

Clinical trial of Venetoclax in combination with DA-EPOCH-R regimen for double/triple-hit high-grade B-cell lymphoma

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048811
Enrollment
Unknown
Registered
2021-07-16
Start date
2021-07-07
Completion date
Unknown
Last updated
2022-03-28

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

Conditions

Double-/Triple-Hit high-grade B-cell Lymphoma

Interventions

experimental group:Venetoclax combined with DA-EPOCH-R

Sponsors

The First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed DH/TH HGBL by pathology; 2. Aged from 18 to 75 years; 3. ECOG 0-3; 4. Obtain the informed consent signed by the patient or his family.

Exclusion criteria

Exclusion criteria: 1. Received systemic or local treatment including chemotherapy in the first three weeks; 2. Blood bilirubin >2mg/dl(35µmol/L), AST/ALT was more than 2 times of the upper limit of normal, serum creatinine was more than 177µmol/L, the creatinine clearance rate was less than 60ml/min; 3. Normal heart function: EF <=50%; 4. The expected survival time was less than 3 months; 5. Chronic or current active infectious diseases requiring systemic antibiotics, antifungal agents or antiviral therapy; 6. Other concurrent and uncontrollable factors are considered by the researchers to affect the medical status of patients participating in the study, psychiatric patients or other patients who are known or suspected to be unable to fully comply with the study protocol; 7. People living with HIV; 8. Pregnant or lactating women,women/men with planned parenthood during the study period or within 3 months after treatment.

Design outcomes

Primary

MeasureTime frame
Complete response rate;

Secondary

MeasureTime frame
Overall survival;Objective response rate;Progression free survival;Safety;

Countries

China

Contacts

Public ContactJin Jie/Yu Wenjuan

The First Affiliated Hospital, Zhejiang University School of Medicine

zhuynzzz@126.com+86 571 87236898

Outcome results

None listed

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