Bioequivalence of Two Tablet Forms of MK0974 (0974-045) | NCT00965887

Studies
Bioequivalence of Two Tablet Forms of MK0974 (0974-045)

NCT00965887

Sponsor

Merck Sharp & Dohme LLC

Status

Completed

Last Update Posted

Jul 7, 2015Estimated

Enrollment

36Actual

Phase

Phase 1

Conditions

Migraine

Interventions

MK0974 Ethanolate formulation
Comparator: MK0974 Hydrate formulation

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Jul 2015

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Mar 2008

Primary Completion Date

May 2008Actual

Completion Date

May 2008Actual

First Submitted Date

Aug 24, 2009

First Submission Date that Met QC Criteria

Aug 24, 2009

First Posted Date

Aug 26, 2009Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Jul 3, 2015

Last Update Posted Date

Jul 7, 2015Estimated

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Phase 1

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

36Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
1	Active Comparator	MK0974 Ethanolate	Drug: MK0974 Ethanolate formulation
2	Active Comparator	MK0974 Hydrate	Drug: Comparator: MK0974 Hydrate formulation

Interventions

Name	Type	Description	Arm Group Labels	Other Names
MK0974 Ethanolate formulation	Drug	Single dose MK0974 280 mg tablet in one of two treatment periods	1

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Area under the curve (AUC(0 to infinity) following single dose administration of MK0974 ethanolate or hydrate formulations		Through 48 hours postdose
Peak plasma concentration (Cmax) following single dose administration of MK0974 ethanolate or hydrate formulations		Through 48 Hours Post Dose

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Subject is in good health
Subject is a non-smoker
Subject is willing to comply with the study restrictions

Exclusion Criteria:

Subject has a history of stroke, chronic seizures, or major neurological disorder
Subject has a history of cancer
Subject is a nursing mother
Subject has or has a history of any disease or condition that might make participation in the study unsafe or that might confound the results of the study

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

55 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Name	Affiliation	Role
Medical Monitor	Merck Sharp & Dohme LLC	Study Director

Condition Browse Module

MeSH Terms

ID	Term
D008881	Migraine Disorders

Ancestor Terms

ID	Term
D051270	Headache Disorders, Primary
D020773	Headache Disorders
D001927	Brain Diseases
D002493	Central Nervous System Diseases

Browse Leaves

Not provided

Browse Branches

Not provided

ID	Type	Description	Link
MK0974-045
2009_650