Compare Pharmacokinetic (PK) Profiles of Naproxen Sodium, Diphenhydramine Hydrochloride, and Naproxen Sodium and Diphenhydramine Hydrochloride Combination

NCT ID: NCT01666678

Last Updated: 2014-08-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 32 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-01-31
• Study Completion Date: 2012-03-31

Brief Summary

The purpose of the current trial is to evaluate the bioavailability of a single oral dose of naproxen sodium 440 mg and DPH HCL 50 mg under fasting and fed conditions and currently marketed single ingredient products containing naproxen sodium (2 x Aleve® 220 mg tablets) or DPH HCL (2 Allergy Relief x 25 mg tablets) under fasting conditions.

Conditions

Therapeutic Equivalence

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: NONE

Study Groups

Arm 1

Group Type: EXPERIMENTAL

BAY98-7111

Intervention Type: DRUG

2 x Naproxen Sodium 220 mg / Diphenhydramine HCl 25 mg combination under fasting conditions

Arm 2

Group Type: ACTIVE_COMPARATOR

Naproxen Sodium (Aleve, BAYH6689)

Intervention Type: DRUG

2 x Naproxen Sodium 220 mg under fasting conditions

Arm 3

Group Type: ACTIVE_COMPARATOR

Diphenhydramine HCl

Intervention Type: DRUG

2 x Diphenhydramine HCl 25 mg under fasting conditions

Arm 4

Group Type: EXPERIMENTAL

BAY98-7111

Intervention Type: DRUG

2 x Naproxen Sodium 220 mg / Diphenhydramine HCl 25 mg combination under fed conditions

Interventions

BAY98-7111

2 x Naproxen Sodium 220 mg / Diphenhydramine HCl 25 mg combination under fasting conditions

Intervention Type: DRUG

Naproxen Sodium (Aleve, BAYH6689)

2 x Naproxen Sodium 220 mg under fasting conditions

Intervention Type: DRUG

Diphenhydramine HCl

2 x Diphenhydramine HCl 25 mg under fasting conditions

Intervention Type: DRUG

BAY98-7111

2 x Naproxen Sodium 220 mg / Diphenhydramine HCl 25 mg combination under fed conditions

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Health, ambulatory male and female subjects between 18 to 55 years of age inclusive
• Body Mass Index (BMI) of approximately 18 to 30 kg/m2; and a total body weight >50 kg (110 lbs)
• Results of screening and clinical laboratory tests are within normal range or considered not clinically significant by the Principal Investigator or Sponsor
• Female subjects of childbearing potential must be using a medically acceptable form of birth control for at least 1 month prior to screening (3 months on oral contraceptives), e.g., oral or patch contraceptives, intrauterine device, Depo-Provera, or a double barrier and have a negative pregnancy test at Screening and Day 0 for each Dosing Period. Female subjects of non childbearing potential must be amenorrheic for at least 2 years or had a hysterectomy and/or bilateral oophorectomy

Exclusion Criteria

• History of hypersensitivity to aspirin (ASA), naproxen sodium, NSAIDs, acetaminophen, DPH HCL, and similar pharmacological agents or components of the products
• History of hypersensitivity to any of the food products in the standardized breakfast or cannot consume all food/beverage items contained in the standardized breakfast
• Have taken ASA, ASA-containing products, acetaminophen or any other NSAID (OTC or prescription) 7 days prior to dosing or during the Dosing Periods, other than trial treatment
• Use of any over-the-counter or prescription medications (except acceptable forms of birth control) within 10 days prior to dosing or throughout the trial, unless in the opinion of the Investigator, the medication will not interfere with the trial procedures, data integrity, or compromise the safety of the subject
• Recently had (past 30 days) or plan to have surgery, an invasive procedure, tattoos or piercings during the trial or 1-2 weeks after treatment
• Loss of blood in excess of 500 ml within 56 days of the first dose of trial treatment (e.g., donation, plasmapheresis or injury)
• History of gastrointestinal bleeding or perforation, related to previous NSAID therapy or active or history of recurrent peptic ulcer/hemorrhage (two or more distinct episodes of proven ulceration or bleeding)
• Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic diseases or malignancies
• Smokers or currently consuming any type of tobacco product(s) including any smoking cessation nicotine-containing product (e.g., nicotine patch, nicotine gum)
• Have taken any vitamin or herbal supplement within 7 days prior to dosing or refuse to refrain from use during the trial

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bayer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bayer Study Director

Role: STUDY_DIRECTOR

Bayer

Locations

Hackensack, New Jersey, United States

Countries

United States

Other Identifiers

16135

Identifier Type: -

Identifier Source: org_study_id