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NCT04293172: HESTIA5

Study to Evaluate the Effect of Ticagrelor Versus Placebo in Reducing Vaso-Occlusive Crises Rate in Pediatric Patients With Sickle Cell Disease.

Withdrawn Phase 3 Last updated 15 July 2020
What this trial tests

Phase 3 trial testing Brilinta in Sickle Cell Disease. Withdrawn.

Timeline
30 June 2020
Primary endpoint
10 October 2022
10 October 2022

Quick facts

Lead sponsorAstraZeneca
PhasePhase 3
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Start date30 June 2020
Primary completion10 October 2022
Estimated completion10 October 2022

Drugs / interventions tested

Conditions studied

Sponsor

AstraZeneca — full company profile →

Who can join

Under 17, any sex, with Sickle Cell Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to compare the effect of ticagrelor vs placebo for the reduction of Vaso-Occlusive crises in paediatric patients with Sickle Cell Disease

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Sickle Cell Disease

Currently open trials in the same condition.

Other AstraZeneca trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04293172.

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