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Spots Global Cancer Trial Database for Safety Study of Two Oral Formulations of MGCD265 Administered in Healthy Subjects in the Fasting State

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Trial Identification

Brief Title: Safety Study of Two Oral Formulations of MGCD265 Administered in Healthy Subjects in the Fasting State

Official Title: Phase 1 Single Dose 2-Way Crossover Comparative Bioavailability Study Of Two Oral Formulations Of MGCD265 In Healthy Male And Female Subjects - Fasting State

Study ID: NCT01930006

Interventions

MGCD265

Study Description

Brief Summary: In this study two MGCD265 oral formulations at dose level of 100 mg are administered to healthy male and female subjects under fasting conditions.

Detailed Description: The objective of this study is to compare the rate and extent of absorption of two MGCD265 oral formulations at a dose level of 100 mg administered to healthy male and female subjects under fasting conditions.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Vince & Associates Clinical Research, Inc., Overland Park, Kansas, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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