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NCT05491044

A Study of Orelabrutinib in CLL/SLL Patients Who Are Slowly Responding to Ibrutinib

Status unknown Phase 2 Last updated 26 October 2023
What this trial tests

Phase 2 trial testing orelabrutinib in CLL/SLL in 30 participants. Status unknown.

Timeline
1 January 2022
Primary endpoint
28 August 2024
30 August 2024

Quick facts

Lead sponsorPeking University People's Hospital
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date1 January 2022
Primary completion28 August 2024
Estimated completion30 August 2024
Sites2 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University People's Hospital

Who can join

18 and older, any sex, with CLL/SLL. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a single arm, multi-center study to evaluate the efficacy and safety of orelabrutinib for Chronic lymphocytic lymphoma(CLL)/small lymphocytic lymphoma (SLL) patients who are slowly responding to Ibrutinib switched to Orelabrutinib.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of orelabrutinib

Trials testing the same drug.

Other recruiting trials for CLL/SLL

Currently open trials in the same condition.

Other Peking University People's Hospital 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/NCT05491044.

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