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NCT03597516

Evaluation of the Efficacy, Durability, Safety, and Tolerability of RP-G28 in Patients With Lactose Intolerance

Completed Phase 3 Last updated 8 July 2019
What this trial tests

Phase 3 trial testing RP-G28 in Lactose Intolerance in 557 participants. Completed in 2 July 2019.

Timeline
26 June 2018
Primary endpoint
2 July 2019
2 July 2019

Quick facts

Lead sponsorRitter Pharmaceuticals, Inc.
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment557
Start date26 June 2018
Primary completion2 July 2019
Estimated completion2 July 2019
Sites35 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Ritter Pharmaceuticals, Inc. — full company profile →

Who can join

Adults 18 to 75, any sex, with Lactose Intolerance. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group study conducted in the United States (US) to assess the efficacy of RP-G28 compared to placebo on symptom reduction related to lactose intolerance.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of RP-G28

Trials testing the same drug.

Other Ritter Pharmaceuticals, Inc. trials

Trials by the same sponsor.

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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/NCT03597516.

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