This is a randomized, double-blind, placebo-controlled study that will compare the effect of 2 different dosage regimens of PCS12852 on gastric emptying time to placebo in both idiopathic gastroparesis (IG) and diabetic gastroparesis (DG) patients.
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in Gastric Emptying Rate From Baseline as Determined by the Area Under the Curve (AUC) of the Gastric Emptying Rate
Timeframe: ~28 days
Change in Gastric Emptying Rate From Baseline Using t50 Metric for Gastric Emptying Rate
Timeframe: ~28 days
Concentrations of PCS12852 in Plasma - Cmax
Timeframe: Day 1
Concentrations of PCS12852 in Plasma - AUC0-last
Timeframe: Day 1
Concentrations of PCS12852 in Plasma - AUC0-last
Timeframe: Day 28
Concentrations of PCS12852 in Plasma - Cmax
Timeframe: Day 28