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NCT03884205

GDPE/CEOPE Compared With CEOPE for Newly Diagnosed Patients With PTCL

Status unknown Last updated 21 March 2019
What this trial tests

trial in PTCL in 120 participants. Status unknown.

Timeline
1 April 2019
Primary endpoint
31 March 2020
30 September 2020

Quick facts

Lead sponsorShandong Provincial Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment120
Start date1 April 2019
Primary completion31 March 2020
Estimated completion30 September 2020
Sites1 location across China

Conditions studied

Sponsor

Shandong Provincial Hospital

Who can join

Adults 16 to 75, any sex, with PTCL or Gemcitabine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Peripheral T-cell Lymphoma (PTCL) is a heterogenic malignancy with poor outcome. There is no standardized treatment protocol for this kind of lymphoma. So, clinical trials are encouraged by National Comprehensive Cancer Network (NCCN) for those patients. Former studies confirmed that GDP (Gemcitabine, Dexamethasone, and Cis-platinum) is superior with CHOP (Cyclophosphamide, Adriamycin, Vincristine, and Prednisone). Combination with etoposide can improve the outcome of some patients with high risk factors. The aim of our study is to compare the response and survival rate of GDPE/CEOPE (gemcitabine, cis-platinum, etoposide, and dexamethasone/cyclophosphamide, vincristine, pharmorubicin, etoposide, and prednisone) with those of CEOPE regimen, looking forward to its superiority in efficacy and safety for the newly diagnosed adult patients with PTCL.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for PTCL

Currently open trials in the same condition.

Other Shandong Provincial Hospital trials

Trials by the same sponsor.

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Data sources for this page

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