drugset / Trial / NCT03768024

A Clinical Study in Healthy Adults Who Sometimes Take Drugs for Pleasure Which Aims to Evaluate Whether GRT0151Y is Likely to be Abused

NCT03768024

Phase 1 Completed 76 enrolled Grünenthal GmbH
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The purpose of this clinical study was to evaluate whether healthy adults, who sometimes take drugs for pleasure, are likely to abuse GRT0151Y. This abuse potential is assessed at three different doses of GRT0151Y. During a Qualification Phase, a single dose of hydromorphone IR 8 mg and a single dose of placebo were separately administered orally over 4 days in a randomized, double-blinded manner. During the Treatment Phase, single doses of GRT0151Y free base (100 mg, 200 mg and 400 mg), hydromorphone Immediate-release (IR) (4 mg, 8 mg, and 16 mg), and placebo were administered orally over 7 Treatment Periods. Participants received the treatments according to a 7-sequence, 7-period balanced design.

Timeline

Start
2007-06-21
Primary completion
2007-10-25
Completion
2007-10-25

Drugs

EvaluationDrugModalityDoseRoute
Subject GRT0151Y Unknown 100 mg Oral
Subject GRT0151Y Unknown 200 mg Oral
Subject GRT0151Y Unknown 400 mg Oral
Subject Hydromorphone Other / unclassified 4 mg Oral
Subject Hydromorphone Other / unclassified 8 mg Oral
Subject Hydromorphone Other / unclassified 16 mg Oral

Indications

No indication recorded.