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Efficacy and Safety of CDOP vs CHOP for Newly Diagnosed Peripheral T-cell Lymphoma - Trial NCT03952572

Access comprehensive clinical trial information for NCT03952572 through Pure Global AI's free database. This Phase 3 trial is sponsored by Peking University and is currently Recruiting. The study focuses on Peripheral T-cell Lymphoma. Target enrollment is 244 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.

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NCT03952572
Phase 3
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT03952572
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Efficacy and Safety of CDOP vs CHOP for Newly Diagnosed Peripheral T-cell Lymphoma
Open-label Multi-center Randomized Non-inferiority Study to Compare Efficacy and Safety of Pegylated Liposomal Doxorubicin Versus Doxorubicin for Newly Diagnosed Peripheral T-cell Lymphoma

Study Focus

Cyclophosphamide

Interventional

drug

Sponsor & Location

Peking University

Beijing, China

Timeline & Enrollment

Phase 3

May 10, 2019

Apr 30, 2023

244 participants

Primary Outcome

Response rate

Summary

Primary objective of the study is to compare the efficacy and safety of CDOP versus CHOP for
 newly diagnosed peripheral T-cell lymphoma (PTCL).

ICD-10 Classifications

Peripheral T-cell lymphoma, not elsewhere classified
Cutaneous T-cell lymphoma, unspecified
Mature T/NK-cell lymphomas
Angioimmunoblastic T-cell lymphoma
Other mature T/NK-cell lymphomas

Data Source

ClinicalTrials.gov

NCT03952572

Non-Device Trial