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A Retrospective Clinical Study on the First-line Maintenance Treatment of PTCL With Chidamide.

A Retrospective (Non-interventional) Clinical Study on the First-line Maintenance Treatment of Peripheral T-cell Lymphoma (PTCL) With Chidamide.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05967949
Enrollment
200
Registered
2023-08-01
Start date
2023-04-01
Completion date
2028-04-01
Last updated
2023-08-01

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

Conditions

PTCL

Keywords

chidamide, maintenance treatment

Brief summary

The efficacy and safety of chidamide in first-line maintenance therapy for PTCL will be assessed through a retrospective case analysis.

Detailed description

The study design belongs to a retrospective study, collecting information on patients with PTCL who were diagnosed and treated with chidamide as maintenance therapy at our center. The collected data includes age, gender, previous treatment regimens, results of auxiliary examinations (such as blood routine, biochemistry, bone marrow cytology, pathology, flow cytometry, NGS, etc.), as well as PET-CT images. The safety and efficacy of Chidemide as first-line maintenance therapy in PTCL will be analyzed.

Interventions

DRUGchidamide

This subset of patients received chidamide as first-line maintenance therapy.

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* (1) Age: 18 years and older; (2) Gender: Male/Female; (3) Diagnosed with PTCL; (4) Received chidamide as maintenance therapy after first-line treatment.

Exclusion criteria

* (1) Patients with other types of lymphomas; (2) Pregnant women.

Design outcomes

Primary

MeasureTime frameDescription
PFS2 yearsprogression free survival

Secondary

MeasureTime frameDescription
OS2 yearsoverall survival
CR2 yearscomplete remission
DOR2 yearsduration of remission

Countries

China

Contacts

Primary Contactwei xu
xuwei10000@hotmail.com+862568302182

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026