drugset / Trial / NCT03963973

A 28 Day Parallel Group Study to Assess the Effects of RDN-929

NCT03963973 ↗

Phase 1 Terminated 7 enrolled Alkermes, Inc.
RandomizedParallel-groupQuadruple-blindOther

Summary

Eligibility will be assessed during a screening period of up to 4 weeks. Subjects will take study medication once daily up to and including Day 28. Safety, tolerability and PK will be measured at each visit.

Timeline

Start
2019-05-16
Primary completion
2020-01-22
Completion
2020-01-22

Outcome

Outcome not reported

Stopped: “Participants no longer receiving intervention”

Drugs

EvaluationDrugModalityDoseRoute
Subject RDN-929 Unknown — Oral

Indications

No indication recorded.