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Pharmacokinetic Study of Single Doses of ORM-12741

NCT02319057 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2015-05-06

No results posted yet for this study

Summary

The purpose of this study is to evaluate ORM-12741 concentrations in the blood after different study drug formulations

Conditions

  • Healthy

Interventions

DRUG

ORM-12741 MR A

Modified release formulation of ORM-12741

DRUG

ORM-12741 IR

Immediate release formulation of ORM-12741

DRUG

ORM-12741 MR B

Modified release formulation of ORM-12741

Sponsors & Collaborators

  • Orion Corporation, Orion Pharma

    lead INDUSTRY

Principal Investigators

  • Mika Scheinin, MD · Clinical Research Services Turku, CRST

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2015-02-28
Completion
2015-02-28

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02319057 on ClinicalTrials.gov