Bioequivalence Study of Ciprofloxacin in Healthy Adult Subjects Under Fasting Condition

NCT ID: NCT05532267

Last Updated: 2022-09-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-11-04
• Study Completion Date: 2020-11-13

Brief 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.

Detailed Description

Enrolled subjects were randomized in a two-phase, two-sequence, cross-over design to receive a single dose of the test product (T) or the reference product (R) at each phase, under fasting conditions, with a wash-out period of 7 days.

Ciprofloxacin plasma concentrations were determined using a validated LC-MS-MS method, followed by Pharmacokinetics, and statistical analysis using Phoenix WinNonlin® software to determine the average bioequivalence.

Conditions

Healthy Subjects

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: HEALTH_SERVICES_RESEARCH
• Blinding Strategy: NONE

Study Groups

Test Product (T)

subjects were administered a single film-coated tablet of 750 mg Ciprofloxacin with approximately 240 ml water after an overnight fast of 10 hours

Group Type: EXPERIMENTAL

Ciprofloxacin 750 mg

Intervention Type: DRUG

an immediate release film-coated tablet containing 750 mg Ciprofloxacin

Reference Product (R)

subjects were administered a single film-coated tablet of 750 mg Ciprofloxacin with approximately 240 ml water after an overnight fast of 10 hours

Group Type: ACTIVE_COMPARATOR

Ciproxin 750 mg

Intervention Type: DRUG

an immediate release film-coated tablet containing 750 mg Ciprofloxacin

Interventions

Ciprofloxacin 750 mg

an immediate release film-coated tablet containing 750 mg Ciprofloxacin

Intervention Type: DRUG

Ciproxin 750 mg

an immediate release film-coated tablet containing 750 mg Ciprofloxacin

Intervention Type: DRUG

Other Intervention Names

Test product (T); Reference product (R)

Eligibility Criteria

Inclusion Criteria

• Written informed consent is obtained for study.
• Age 18 - 55 years,
• Body mass index between 18.5 and 30 kg/m2
• Have no clinically significant diseases captured in the medical history or evidence of clinically significant findings on physical examination.
• Vital signs without significant deviations.
• All laboratory screening results are within the normal range or clinically non-significant

Exclusion Criteria

• History or presence of any disorder or condition that would render the subject unsuitable for the study, place the subject at undue risk or interfere with the ability of the subject to complete the study in the opinion of the investigator.
• History of any significant cardiovascular, hepatic, renal, respiratory, gastrointestinal, endocrine, immunologic, allergic, dermatologic, hematologic, neurologic, or psychiatric disease, or cancer.
• Any confirmed significant allergic reactions against any drug or multiple allergies.
• Clinically significant illness 28 days before study phase I.
• Alcohol or any solvent intake.
• Regular use of medication.
• Positive urine screening of drugs of abuse.
• Use of any systemic medications (prescription medications, OTC products, supplements, or herbal preparations) for 14 days prior to dosing and during the study.
• History or presence of significant smoking (more than one pack per day of cigarettes) or refusal to abstain from smoking for 48 hours before dosing until checkout.
• Blood donation within the past 60 days.
• Participation in another bioequivalence study within 60 days prior to the start of phase I of the study

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Future University in Egypt

OTHER

Sponsor Role: lead

Responsible Party

Hala Masoud

FRC Technical Director & CEO

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hala Masoud, PhD

Role: PRINCIPAL_INVESTIGATOR

Future Research Center (FRC)

Locations

Future Research Center (FRC)

Cairo, New Cairo, Egypt

Countries

Egypt

Other Identifiers

CIP-B-20-030

Identifier Type: -

Identifier Source: org_study_id