Bioequivalence Study for Mejoral 500 Product

NCT ID: NCT02504775

Last Updated: 2018-07-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-08-01
• Study Completion Date: 2015-08-19

Brief Summary

This will be a monocentric, single blinded, randomized, single-dose, two-periods, two-sequence, crossover bioequivalence study of two oral formulations in healthy participants under fasting conditions.

Conditions

Pain

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

Tylenol® Caplets, then Mejoral® 500 Tablets

Participants will first receive one tablet \[500 milligram (mg) of paracetamol\] of Tylenol® Caplets, orally with 250 mL of water at room temperature, in a single dose, under minimum 10 h fasting. After a washout period of 72 h, they then will receive one tablet (500 mg of paracetamol) of Mejoral® 500 tablets, orally with 250 mL of water at room temperature, in a single dose, under minimum 10 h fasting.

Group Type: EXPERIMENTAL

Mejoral® 500 Tablets

Intervention Type: DRUG

500 mg tablet of paracetamol

Tylenol® Caplets

Intervention Type: DRUG

500 mg tablet of paracetamol

Mejoral® 500 Tablets, then Tylenol® Caplets

Participants will first receive one tablet (500 mg of paracetamol) of Mejoral® 500 tablets, orally with 250 mL of water at room temperature, in a single dose, under minimum 10 h fasting. After a washout period of 72 h, they then will receive one tablet (500 mg of paracetamol) of Tylenol® Caplets, orally with 250 mL of water at room temperature, in a single dose, under minimum 10 h fasting.

Group Type: EXPERIMENTAL

Mejoral® 500 Tablets

Intervention Type: DRUG

500 mg tablet of paracetamol

Tylenol® Caplets

Intervention Type: DRUG

500 mg tablet of paracetamol

Interventions

Mejoral® 500 Tablets

500 mg tablet of paracetamol

Intervention Type: DRUG

Tylenol® Caplets

500 mg tablet of paracetamol

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Understanding of the study procedures, restrictions and willingness to participate as evidenced by voluntary written informed consent
• Men and women between 18 to 55 years of age, with good state of health
• Participants' body mass index must be between 18.0 and 27.0
• Blood pressure (seated) up to 139 milliliters of mercury (mm/Hg) systolic and up to 89 mm/Hg diastolic, heart rate between 60 and 100 beats per minute and respiratory frequency between 14 and 20 breaths per minute
• The laboratory tests: Complete blood count with differential count, Chemical blood of 27 elements, Urinalysis, Non-Reactive Anti-hepatitis B virus (HBV) hepatitis B and Anti-hepatitis C antibodies (HCV) hepatitis C, Non-Reactive Human immunodeficiency virus (HIV) test, Negative Venereal Disease Research Laboratory (VDRL) test with maximum 3 months validity and allowed variation of +/-10% of the normal range
• Electrocardiogram (ECG) with no more than three months validity and with no clinically significant findings
• Pregnancy test, drug abuse test and alcohol test with negative results at selection visit and approximately 12 h before drug product administration in both study periods

• Participants with a history of suffering cardiovascular, renal, hepatic, muscle, metabolic, gastrointestinal, neurological problems, endocrine, hematopoietic or any type of anemia, asthma, mental illness or other organic abnormalities. Participants who have had a muscle injury within the 21 days prior to the study
• Clinically significant abnormalities in the ECG, dyspepsia, gastritis, esophagitis, gastric or duodenal ulcer; participants who require any drug product other than test product during the course of study
• Exposed to inductors or liver enzyme inhibitors or drugs capable of altering urinary pH or any potentially toxic drugs, vitamins, herbal remedies within the 30 days prior to the beginning of the study
• Participant hospitalized for any problem during the seven months prior to the study start; received investigational product within 90 days prior to the study
• Allergic to any drug product, food or substance, require special diet; positive drug abuse, alcohol, pregnancy test, breast feeding women
• Donated or lost 450 milliliter (mL) or more blood within the 60 days prior to the beginning of the study
• Participants who have not been recorded in the the Federal Commission for the Protection against Sanitary Risks (COFEPRIS) page
• Ingested alcohol, carbonated beverage, products containing xanthines, charcoal grilled nourishment, grapefruit or orange or who have smoked 24 h prior to the beginning of both study periods
• Subordination relationship between participants and investigators, an employee of the sponsor or the study site or members of their immediate family

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

Sponsors

GlaxoSmithKline

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

GSK Investigational Site

Mexico City, , Mexico

Countries

Mexico

Other Identifiers

204779

Identifier Type: -

Identifier Source: org_study_id