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NCT00664066: DELFT

DELFT (Dynepo Evaluation of Long-Term Follow-Up Treatment)

Terminated Results posted Last updated 25 June 2021
What this trial tests

trial testing DYNEPO (epoetin delta) in Anemia in 3 participants. Terminated before completion.

Timeline
25 April 2008
Primary endpoint
30 July 2008
30 July 2008

Quick facts

Lead sponsorShire
StatusTerminated
Study typeOBSERVATIONAL
Enrollment3
Start date25 April 2008
Primary completion30 July 2008
Estimated completion30 July 2008
Sites2 locations across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Shire — full company profile →

Who can join

Eligibility, any sex, with Anemia or Kidney Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a post-authorisation safety study to assess the incidence and severity of all pre-defined cardiovascular events in patients treated with DYNEPO, as well as to detect \& describe less common adverse drug reactions, and to summarise DYNEPO drug utilisation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Anemia

Currently open trials in the same condition.

Other Shire 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/NCT00664066.

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