This is a Single Ascending Dose Tolerance Study

NCT01133574 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2011-08-29

No results posted yet for this study

Summary

This is a single rising dose tolerance (Part A) followed by a functional magnetic resonance imaging (Part B)

Conditions

  • Cognition Disorders

Interventions

DRUG

SLV354 capsules

20 mg

DRUG

SLV354 capsules

60 mg

DRUG

SLV354 capsules

120 mg

DRUG

SLV354 capsules

250 mg

DRUG

SLV354 capsules

500 mg

DRUG

SLV354 capsules

750 mg

DRUG

SLV354 capsules

1000 mg

DRUG

SLV354 capsules

1250 mg

DRUG

Placebo capsules

placebo

DRUG

SLV354 capsules

low dose group 1

DRUG

SLV354 capsules

high dose group 1

DRUG

SLV354 capsules

low dose group 2

DRUG

SLV354 capsules

high dose group 2

DRUG

Placebo capsules

placebo

Sponsors & Collaborators

  • Quintiles, Inc.

    collaborator INDUSTRY
  • Abbott

    lead INDUSTRY

Principal Investigators

  • Beatrice Rendenbach-Mueller, PhD · Abbott

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2010-07-31
Completion
2010-07-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Companies

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 NCT01133574 on ClinicalTrials.gov