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ODM-108 Part III

Orion Corporation, Orion Pharma · discontinued Small molecule

ODM-108 mechanism of action is not publicly disclosed; Phase 1 evaluation focused on safety and pharmacokinetics in healthy volunteers.

ODM-108 is a small-molecule investigational drug developed by Orion Corporation (Orion Pharma) that was discontinued during early clinical development. The compound, with a molecular weight of 529.67 Da, was evaluated in Phase 1 trials for safety, tolerability, and pharmacokinetic/pharmacodynamic effects in healthy volunteers, but the program did not advance to later-stage development. No FDA approval was obtained, and the drug never reached marketed status. The discontinuation suggests either unfavorable safety/tolerability findings, lack of differentiation versus existing therapies, or strategic portfolio reprioritization by Orion. Without published clinical data or regulatory filings, ODM-108 remains a failed early-stage asset with no commercial significance or ongoing development.

At a glance

Generic nameODM-108 Part III
SponsorOrion Corporation, Orion Pharma
Drug classUnknown — investigational small molecule
TargetNot publicly disclosed
ModalitySmall molecule
Therapeutic areaMetabolic
Phasediscontinued

Mechanism of action

ODM-108 was an investigational small-molecule compound developed by Orion Corporation that entered Phase 1 clinical testing to assess basic safety, tolerability, and how the body processes the drug (pharmacokinetics) and how the drug affects the body (pharmacodynamics). The trial enrolled 85 healthy male volunteers but was terminated before completion, suggesting either safety concerns, lack of efficacy signals, or strategic discontinuation. Without published data or regulatory filings, the specific molecular target, binding mechanism, and intended therapeutic indication remain undisclosed in the public domain.

Approved indications

No approved indications tracked.

Pipeline indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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