Iclusig® (Ponatinib) in Clinical Practice for the Treatment of Chronic Myeloid Leukemia or Ph+ Acute Lymphoblastic Leukemia in Belgium

NCT03678454 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2022-04-12

No results posted yet for this study

Summary

This prospective registry is initiated to follow up on the use of Iclusig® in patients with CML or Ph+ ALL in routine practice in Belgium.

Conditions

  • Chronic Myeloid Leukemia
  • CML
  • Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia
  • Ph+ ALL

Sponsors & Collaborators

  • Incyte Biosciences Benelux

    lead INDUSTRY

Principal Investigators

  • Michael Beck, PhD · Incyte Biosciences Benelux

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-03
Primary Completion
2022-03-31
Completion
2022-03-31

Countries

  • Belgium

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03678454 on ClinicalTrials.gov