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NCT06767891

Real-world Study of Acalabrutinib

ENROLLING BY INVITATION Last updated 10 January 2025
What this trial tests

trial in MCL in 200 participants. Enrolling by invitation.

Timeline
2 July 2024
Primary endpoint
30 July 2026
30 January 2028

Quick facts

Lead sponsorRuijin Hospital
StatusENROLLING BY INVITATION
Study typeOBSERVATIONAL
Enrollment200
Start date2 July 2024
Primary completion30 July 2026
Estimated completion30 January 2028
Sites1 location across China

Conditions studied

Sponsor

Ruijin Hospital

Who can join

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

Sponsor's own description

The primary purpose of this study was to describe acotinib treatment patterns among Chinese patients with CLL and MCL who received acotinib according to the label. Secondary objectives include: 1) To evaluate the safety of acotinib in Chinese patients with CLL and MCL who received acotinib according to the label. 2) Evaluate the dose of acotinib in Chinese patients with CLL and MCL who receive acotinib according to the label. 3) Describe the baseline clinical and demographic characteristics of patients with CLL and MCL who received acotinib according to the label. The exploratory objectives of the study include: 1) To describe the real-world overall survival (rwOS) of Chinese CLL and MCL patients treated with acotinib according to the label. 2) Describe the real-world clinical progression-free survival (rwPFS) of Chinese CLL and MCL patients who received acotinib according to the label. 3) Describe the real-world response rate (rwRR) in Chinese CLL and MCL patients who received acotinib according to the label.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for MCL

Currently open trials in the same condition.

Other Ruijin Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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