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NCT04620655

RD13-01 for Patients With r/r CD7+ T-ALL/T-LBL

Status unknown NA Last updated 9 November 2020
What this trial tests

NA trial testing RD13-01 cell infusion in T Acute Lymphoblastic Leukemia in 24 participants. Status unknown.

Timeline
15 November 2020
Primary endpoint
15 November 2021
15 November 2022

Quick facts

Lead sponsorMin Xiang
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment24
Start date15 November 2020
Primary completion15 November 2021
Estimated completion15 November 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Min Xiang

Who can join

Adults 3 to 70, any sex, with T Acute Lymphoblastic Leukemia or T-lymphoblastic Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is designed to explore the safety of RD13-01 for patients with CD7+ relapsed and/or refractory T cell acute lymphoblastic leukemia or lymphoblastic lymphoma. And to evaluate the efficacy and pharmacokinetics of RD13-01 in patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of RD13-01 cell infusion

Trials testing the same drug.

Other recruiting trials for T Acute Lymphoblastic Leukemia

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04620655.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing