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NCT05557903

Phase Ⅰ Clinical Study of Anti-CD52 Monoclonal Antibody in NHL and T-PLL

Status unknown Phase 1 Last updated 28 September 2022
What this trial tests

Phase 1 trial testing Recombinant Humanized Anti-CD52 Monoclonal Antibody Injection in Lymphoma, Non-Hodgkin in 71 participants. Status unknown.

Timeline
20 December 2021
Primary endpoint
30 December 2022
30 June 2023

Quick facts

Lead sponsorLanzhou Institute of Biological Products Co., Ltd
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment71
Start date20 December 2021
Primary completion30 December 2022
Estimated completion30 June 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Lanzhou Institute of Biological Products Co., Ltd — full company profile →

Who can join

Adults 18 to 70, any sex, with Lymphoma, Non-Hodgkin or Lymphoma, T-Cell. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Phase I clinical study of multicenter, single-arm, open, non-randomized evaluation of recombinant humanized anti-CD52 monoclonal antibody in the NHL and T-PLL

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Lymphoma, Non-Hodgkin

Currently open trials in the same condition.

Other Lanzhou Institute of Biological Products Co., Ltd trials

Trials by the same sponsor.

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/NCT05557903.

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