Skip to content

Prospective intervention study of entinostat + azacitidine +CHOP in the treatment of nodal follicular helper T cell lymphoma

Prospective intervention study of entinostat + azacitidine +CHOP in the treatment of nodal follicular helper T cell lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108694
Enrollment
Unknown
Registered
2025-09-03
Start date
2025-09-05
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

nodal follicular helper T cell lymphoma

Interventions

Therapeutic Group:Entinostat + azacitidine +CHOP for nodal follicular helper T-cell lymphoma

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients with confirmed nTFHL; 2. no previous chemotherapy, radiotherapy, or other treatments; 3. Aged from 18 to 80 years; 4.ECOG score 0-2; 5. Predicted survival >=3 months; 6. Normal major organ function with laboratory findings meeting the following criteria: (1) alanine aminotransferase (ALT)<=3.0× upper limit of normal value (ULN), aspartate aminotransferase (AST)<=3.0×ULN; (2) Serum total bilirubin <=1.5×ULN; (3) Serum creatinine <=1.5×ULN; 7. Voluntarily participate in the clinical trial, understand the study procedures, and be able to sign in-person informed consent;

Exclusion criteria

Exclusion criteria: 1.Failure to meet the inclusion criteria; 2.women who are pregnant or breastfeeding; 3.Allergy to study drugs and associated metabolites; 4.Active infections difficult to control; 5.Concomitant diseases that, in the judgment of the investigator, seriously endanger patient safety or prevent patients from completing the study; 6.Other conditions judged by the investigator to be unsuitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
progression free survival;

Secondary

MeasureTime frame
complete remission;overall response rate;overall survival;duration of response;disease-free survival;event-free survival;

Countries

China

Contacts

Public ContactXin Wang

The First Affiliated Hospital of Chongqing Medical University

925170788@qq.com+86 186 9660 9008

Outcome results

None listed

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