drugset / Trial / NCT03569007

Study to Evaluate the Efficacy and Safety of Larazotide Acetate for the Relief of CeD Symptoms

NCT03569007 ↗

Phase 3 Terminated 307 enrolled 9 Meters Biopharma, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

To assess the efficacy and safety of larazotide acetate versus placebo for the relief of persistent symptoms in adult celiac disease patients.

Timeline

Start
2019-05-29
Primary completion
2022-07-21
Completion
2022-07-21

Outcome

Outcome not reported

Stopped: “Trial terminated by Sponsor”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Larazotide Peptide 0.25 mg —
Comparator Larazotide Peptide 0.5 mg —

Indications