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NCT01084408: PEPCAD-DEBonly

Efficacy of the SeQuent®Please in the Treatment of De-novo Stenoses Versus Taxus™Liberté™

Terminated Phase 3 Last updated 25 March 2021
What this trial tests

Phase 3 trial testing SeQuent®Please (Paclitaxel coated balloon) in Coronary De-novo Stenoses in 90 participants. Terminated before completion.

Timeline
1 March 2010
Primary endpoint
1 March 2012
1 March 2013

Quick facts

Lead sponsorUniversity Hospital, Saarland
PhasePhase 3
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment90
Start date1 March 2010
Primary completion1 March 2012
Estimated completion1 March 2013
Sites2 locations across Germany

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Saarland

Who can join

19 and older, any sex, with Coronary De-novo Stenoses. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the trial is to assess the efficacy of the Paclitaxel-coated SeQuent®Please angioplasty balloon in the treatment of stenoses in native coronary arteries compared to a drug eluting stent.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other University Hospital, Saarland 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/NCT01084408.

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