Last reviewed · How we verify

NCT01905202

Phase 1 Safety and Tolerability of Secretrol in Patients With Barrett's Esophagus

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

Phase 1 trial testing Secretrol in Barrett's Esophagus in 13 participants. Status unknown.

Timeline
1 April 2013
Primary endpoint
1 April 2015

Quick facts

Lead sponsorEffexus Pharmaceutical
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment13
Start date1 April 2013
Primary completion1 April 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 Barrett's Esophagus. 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

Secretrol administered over a 6 month period to patients with Barrett's Esophagus will be safe and well tolerated. Further, pH control will be evaluated in the distal esophageal mucosa and just below the squamocolumnar junction.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Barrett's Esophagus

Currently open trials in the same condition.

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/NCT01905202.

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