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Clinical Trials/NL-OMON22366
NL-OMON22366Not yet recruitingNot Applicable

A randomized, open label balanced two period, two-treatment, two-sequence crossover study to evaluate the effect of food on the pharmacokinetics of buspirone after a single oral administration of Lybridos in healthy female subjects

EB FSD0 sites18 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
18

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • 1. Provision of informed consent
  • 2. Females between 18 and 55 years of age (both inclusive)

Exclusion Criteria

  • Cardiovascular conditions
  • 1. Systolic blood pressure ≥ 140 mmHg and/or diastolic blood pressure ≥ 90 mmHg.

Investigators

Sponsor
EB FSD

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