Calquence CLL rr Japan PMS_Japan Post-Marketing Surveillance (PMS) Study - All Patient Investigation

  • STATUS
    Not Recruiting
  • End date
    Sep 30, 2024
  • participants needed
    84
  • sponsor
    AstraZeneca
Updated on 27 June 2022
Investigator
AstraZeneca Clinical Study Information Center
Primary Contact
Research Site (8.3 mi away) Contact
+11 other location

Summary

To understand the incidence of ADRs of Calquence 100 mg capsules (acalabrutinib) used in patients with relapsed or refractory chronic lymphocytic leukaemia (including small lymphocytic lymphoma) in a real-world post-marketing setting

Description

To understand the incidence of ADRs of Calquence 100 mg capsules (acalabrutinib) used in patients with relapsed or refractory chronic lymphocytic leukaemia (including small lymphocytic lymphoma) in a real-world post-marketing setting.

This investigation will be conducted for application for re-examination specified in Article 14-4 of the Pharmaceutical Affairs Law. In addition, after launch, the data for a certain number of all cases are collected and the survey is required to be conducted for all cases as conditions of approval.

Details
Condition Relapsed or Refractory Chronic Lymphocytic Leukemia (Including Small Lymphocytic Lymphoma)
Clinical Study IdentifierNCT04872621
SponsorAstraZeneca
Last Modified on27 June 2022

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