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NCT02455024: OMNI

An Observational Registry to Evaluate the Incidence of and Risk Factors for Vascular Occlusive Events Associated With ICLUSIG®

Terminated Last updated 4 April 2024
What this trial tests

trial in Myeloid Leukemia, Chronic-Phase, Accelerated-Phase, Blast-Phase, Ph+ALL in 3 participants. Terminated before completion.

Timeline
2 March 2018
Primary endpoint
19 February 2019
19 February 2019

Quick facts

Lead sponsorAriad Pharmaceuticals
StatusTerminated
Study typeOBSERVATIONAL
Enrollment3
Start date2 March 2018
Primary completion19 February 2019
Estimated completion19 February 2019
Sites2 locations across United States

Conditions studied

Sponsor

Ariad Pharmaceuticals — full company profile →

Who can join

18 and older, any sex, with Myeloid Leukemia, Chronic-Phase, Accelerated-Phase, Blast-Phase, Ph+ALL. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an observational registry to further characterize the safety profile of patients with chronic myeloid leukemia in the chronic phase (CP-CML), accelerated phase (AP-CML), blast phase (BP-CML), or Ph+ALL treated with Iclusig (ponatinib) in routine clinical practice in the US. The registry is focused on analysis of vascular occlusive events.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Ponatinib: a novel multi-tyrosine kinase inhibitor against human malignancies.
    Tan FH, Putoczki TL, Stylli SS, Luwor RB. · · 2019 · cited 142× · PMID 30705592 · DOI 10.2147/ott.s189391

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Other Ariad Pharmaceuticals trials

Trials by the same sponsor.

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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/NCT02455024.

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