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

2019-05-30 22:08:16 | BioPortfolio

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.

Study Design

Conditions

Healthy

Intervention

RDN-929 oral capsule, Placebo oral capsule

Location

QPS Netherlands B.V.
Leeuwarden
Netherlands

Status

Recruiting

Source

Rodin Therapeutics

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-05-30T22:08:16-0400

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