drugset / Trial / NCT02993055

A Study to Assess Ulimorelin in Healthy Subjects

NCT02993055 ↗

Phase 1 Completed 39 enrolled Lyric Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

A Phase I dose escalation study involving healthy subjects.

Timeline

Start
2015-01
Primary completion
2015-11
Completion
2015-11

Outcome

Mixed primary results

paper Ulimorelin 150-600 µg kg-1 every 8 hours resulted in statistically significant improvements (∆t50 = 23% to 46% (P < .05)) in gastric emptying from baseline PMID 32017341 ↗

paper However, no effects on GC24 were observed. PMID 32017341 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ulimorelin Small molecule 80 ug/kg —
Subject Ulimorelin Small molecule 600 ug/kg —
Subject Ulimorelin Small molecule 1200 ug/kg —

Indications

No indication recorded.