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NCT00481273: AVIDA

AVIDA The Vidaza® (Azacitidine) Patient Registry

Completed Last updated 3 May 2018
What this trial tests

trial testing Azacitidine in Myelodysplastic Syndromes in 479 participants. Completed in 31 August 2010.

Timeline
31 October 2006
Primary endpoint
31 August 2010
31 August 2010

Quick facts

Lead sponsorCelgene
StatusCompleted
Study typeOBSERVATIONAL
Enrollment479
Start date31 October 2006
Primary completion31 August 2010
Estimated completion31 August 2010
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Celgene — full company profile →

Who can join

Eligibility, any sex, with Myelodysplastic Syndromes. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This registry is a prospective, multi-center, observational study compiling data on the natural history and management of patients receiving Vidaza, and will provide unique insights into the management of myelodysplastic syndromes (MDS) and other hematological disorders and the impact of these disorders on patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Azacitidine

Trials testing the same drug.

Other recruiting trials for Myelodysplastic Syndromes

Currently open trials in the same condition.

Other Celgene 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/NCT00481273.

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