The Real World Study of Zanubrutinib in the Treatment of Chronic Lymphocytic Leukemia in China

NCT ID: NCT06489184

Last Updated: 2024-07-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

490 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-08-01

Study Completion Date

2025-12-30

Brief Summary

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This is a Multicenter, Retrospective Real-world Study of Zanubrutinib in the Treatment of Chronic Lymphocytic Leukemia in China

Detailed Description

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Conditions

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CLL

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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Zanubrutinib

patients with treatment naive or R/R CLL who treatment with Zanubrutinib

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* 1\. Patients aged ≥18 years old
* 2\. Must have a confirmed diagnosis of Chronic Lymphocytic Leukemia (CLL) requiring treatment (iwCLL \[International Workshop on Chronic Lymphocytic Leukemia\] criteria);
* 3\. Treatment-naïve OR Refractory Recurrence CLL patients who were initiated on Zanubrutinib;
* 4.Prior or current use of Zanubrutinib for ≥3 months
* 5.At least one follow-up was recorded during Zanubrutinib treatment

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking University People's Hospital

OTHER

Sponsor Role lead

Responsible Party

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Xiao-Jun Huang

Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Peking University People's Hospital

Beijing, Beijing Municipality, China

Site Status

Countries

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China

Central Contacts

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Shenmiao Yang

Role: CONTACT

Other Identifiers

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2024Zanu-RW-01

Identifier Type: -

Identifier Source: org_study_id

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