← Eichor
Study identifier: NCT02784392 Synced from ClinicalTrials.gov · July 27, 2026
● Completed

Efficacy, Safety, and Pharmacokinetics (PK) Study of Ulimorelin in Patients With Enteral Feeding Intolerance (EFI): The PROMOTE Trial

Condition: Enteral Feeding Intolerance (EFI)  ·  Sponsor: Lyric Pharmaceuticals

PhasePhase 2
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the effect Ulimorelin in patients with enteral feeding intolerance.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (5)

Study siteNew Orleans, Louisiana, United States
Study siteColumbus, Ohio, United States
Study siteAmsterdam, Netherlands
Study siteBarcelona, Spain
Study siteMadrid, Spain

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT02784392