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NCT02210494

Phase 1 Study of Safety of Secretrol® in the Short-term Management of Patients Undergoing Endoscopic Mucosal Resection (EMR)

Status unknown Phase 1 Last updated 4 August 2014
What this trial tests

Phase 1 trial testing Secretrol in EMR Ulcer in 5 participants. Status unknown.

Timeline
1 April 2013
Primary endpoint
1 August 2015

Quick facts

Lead sponsorEffexus Pharmaceutical
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment5
Start date1 April 2013
Primary completion1 August 2015
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Effexus Pharmaceutical — full company profile →

Who can join

18 and older, any sex, with EMR Ulcer. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

Evaluate the safety of Secretrol® in patients undergoing endoscopic mucosal resection for early adenocarcinoma of the esophagus.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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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/NCT02210494.

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