NCT04880746

Efficacy and Safety of Cladribine Combined With BEAC Pretreatment Regimen in the Treatment of Peripheral T-cell Lymphoma: a Multicenter Clinical Study

Efficacy and Safety of Cladribine Combined With BEAC ( Semustine, Etoposide, Cytarabine, Cyclophosphamide) Pretreatment Regimen in the Treatment of Peripheral T-cell Lymphoma: a Multicenter Clinical Study
Ruijin Hospital·Phase 3·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
BEAC
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Ruijin Hospital
Location
Shanghai, China
Timeline & enrollment
Phase
Phase 3
Start date
Oct 17, 2020
End date
Oct 17, 2025
Enrollment
266 participants
Primary outcome

Progression free survival

Summary

This multi-center clinical study will evaluate the efficacy and safety of Cladribine Combined
 With BEAC Pretreatment Regimen in the Treatment of Peripheral T-cell Lymphoma.

ICD-10 classifications
Peripheral T-cell lymphoma, not elsewhere classifiedCutaneous T-cell lymphoma, unspecifiedMature T/NK-cell lymphomasAngioimmunoblastic T-cell lymphomaOther mature T/NK-cell lymphomas
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT04880746
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT04880746 through Pure Global AI's free database. This Phase 3 trial is sponsored by Ruijin Hospital and is currently Recruiting. The study focuses on Peripheral T-cell Lymphoma. Target enrollment is 266 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.