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Bioequivalence Study of Ciprofloxacin in Healthy Adult Subjects Under Fasting Condition

NCT05532267 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2022-09-08

No results posted yet for this study

Summary

To evaluate and compare the relative plasma bioavailability and therefore the bioequivalence of two different immediate release products each containing Ciprofloxacin 750 mg, after administering a single oral dose, to healthy adult subjects under fasting conditions.

Conditions

  • Healthy Subjects

Interventions

DRUG

Ciprofloxacin 750 mg

an immediate release film-coated tablet containing 750 mg Ciprofloxacin

DRUG

Ciproxin 750 mg

an immediate release film-coated tablet containing 750 mg Ciprofloxacin

Sponsors & Collaborators

  • Future University in Egypt

    lead OTHER

Principal Investigators

  • Hala Masoud, PhD · Future Research Center (FRC)

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2020-11-04
Primary Completion
2020-11-13
Completion
2020-11-13

Countries

  • Egypt

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 NCT05532267 on ClinicalTrials.gov