Consumer Preference Study of Two Formulations of Phenylephrine Hydrochloride (Study CL2008-15)(P07530)(COMPLETED)

NCT00976209 | Completed Phase 3 Results

• 3 other identifiers: 18122CL2008-15P07530
• Study Type: interventional
• Target: 331
• Locations: 0 countries
• Sites: N/A

Brief Summary

This is a randomized, two-way crossover, multicenter study evaluating the consumer preference of Phenylephrine Extended Release Tablets, 30 mg to be taken as one tablet every 12 hours, or Phenylephrine Immediate Release Tablets, 10 mg to be taken as one tablet every 4 hours in subjects with at least mild allergic rhinitis and nasal congestion. Approximately 250 participants will complete a questionnaire after taking one test product for 3 days followed by a 3 day (± 1 day) washout period; and then taking the alternate test product for 3 days. Analysis of which product the consumer preferred, if any, and which product was more convenient, if any, will be evaluated.

Conditions

Vasomotor Rhinitis; Seasonal Allergic Rhinitis

Outcome Measures

Primary Outcomes (1)

• Percentage of Participants That Preferred Phenylephrine HCl 30 mg Extended Release Tablets, as Compared to Phenylephrine HCl 10 mg Immediate Release Tablets for the Relief of Nasal Congestion

  Preference was calculated based on total participants that completed the study. Responses to the following questions in the consumer preference questionnaire were the basis for the preference endpoints: Which product, if any, did you prefer for the relief of nasal congestion? The possible answers were: * I preferred the relief of Treatment A (the every 12 hours white tablet; Phenylephrine HCl 30 mg Extended Release Tablet) * I preferred the relief of Treatment B (the every 4 hours red tablet; Phenylephrine HCl 10 mg Immediate Release tablet) or • I did not have a preference

  Visit 6 (Period 2, Day 4)

Secondary Outcomes (1)

• Percentage of Participants That Preferred the Convenience of Phenylephrine HCl 30 mg Extended Release Tablets, as Compared to Phenylephrine HCl 10 mg Immediate Release Tablets

  Visit 6 (Period 2, Day 4)

Study Arms (2)

Phenylephrine Hydrochloride Extended Release Tablets, 30 mg

EXPERIMENTAL

Drug: Phenylephrine Hydrochloride (HCl) Extended Release (ER) Tablets 30 mg

Phenylephrine Hydrochloride Immediate Release Tablets, 10 mg

ACTIVE COMPARATOR

Drug: Phenylephrine Hydrochloride (HCl) Immediate Release (IR) tablets, 10 mg

Interventions

Phenylephrine Hydrochloride (HCl) Extended Release (ER) Tablets 30 mg DRUG

Phenylephrine HCl ER tablets 30 mg taken every 12 hours, twice daily, for 3 days.

Phenylephrine Hydrochloride Extended Release Tablets, 30 mg

Phenylephrine Hydrochloride (HCl) Immediate Release (IR) tablets, 10 mg DRUG

Phenylephrine HCl IR tablets 10 mg taken every four hours (no more than 6 times daily) for 3 days.

Also known as: Sudafed PE®

Phenylephrine Hydrochloride Immediate Release Tablets, 10 mg

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Healthy male or female volunteers must be 18 years or older.
• Participants must be willing to stop use of current decongestant and allergy medications during the study, and at the start of the run-in period (Visit 2).
• Participants must have a documented history of allergic rhinitis caused by ragweed allergen for at least the prior two years.
• Participants must have a documented skin testing (prick with wheal \>= 3 mm larger than the diluent or intradermal with wheal \>=7 mm larger than the diluent control) or a positive in vitro test for specific IgE to the ragweed allergen within the last four years.
• Participants must have signs by clinical evaluation and symptoms of nasal congestion of at least mild severity (sign/symptom clearly present, but minimal awareness; easily tolerated) at Visit 3 following the run-in period and at visit 5 following the washout period.
• Clinical laboratory tests (complete hematology, blood chemistries, urinalysis) must be within normal limits or clinically acceptable to the Investigator/Sponsor. Sponsor will not grant waivers.
• Participants must have a seated (after 5 minutes of rest) systolic/diastolic blood pressure ≤ 138/88 mmHg.
• Participants must have normal or clinically acceptable physical exam and electrocardiogram (ECG) on 12-lead ECG (recorded at 25 mm/s).
• Participants must be free of any clinically significant disease that requires a physician's care and/or would interfere with study evaluations, procedures or participation.
• Participants must agree not to take monoamine oxidase inhibitor (MAOI) for 14 days before study participation and 14 days after the end of the study.
• Participants must be willing to give written informed consent (prior to any study related procedures being performed) and able to adhere to restrictions and examination schedules.
• Female participants of childbearing potential (a non-menopausal female who has not had a hysterectomy, bilateral oophorectomy, or medically documented ovarian failure, including a young woman who has not yet started menstruating) must be using medically acceptable (documented failure rate of less than 1%) birth control measures. Examples of medically acceptable contraception include hormonal contraceptives, intrauterine device (IUD), double-barrier method (any combination of male or female condom, diaphragm, spermicidal gel, sponge) or sterilization.
• Participants must be able to read and write English, and must understand the dosing schedule.

You may not qualify if:

• Participants must not have any significant medical condition which, in the judgment of the investigator, is a contraindication to the use of phenylephrine HCl, might interfere with the study or requires treatment expected to affect the blood pressure. These may include thyroid disease (e.g. hyperthyroidism, hypothyroidism), uncontrolled diabetes mellitus, coronary heart disease, ischemic heart disease, elevated intraocular pressure, prostatic hypertrophy, etc.
• Participants that have received allergen immunotherapy or Xolair (omalizumab) therapy within the past two years.
• Participants who have a history of any clinically significant local or systemic infectious disease within four weeks prior to initial treatment administration.
• Participants who have participated in a clinical trial of an investigational treatment within 30 days prior to the start of the study (Run-in Period Day 1).
• Participants who are, appear to be, or are known to be, current or former addicts or alcoholics.
• Participants who have a known allergy or intolerance to phenylephrine HCl, any other decongestant, loratadine, desloratadine or any other antihistamine.
• Females who are pregnant, nursing or unwilling to use/practice medically acceptable contraception (documented failure rate of less than 1%).
• Participants with a history of asthma, rhinitis medicamentosa, or acute or chronic sinusitis.
• Participants that have used use of inhaled, oral, rectal, topical, intramuscular, and/or intravenous potent chronic or intermittent corticosteroids (up to 1% topical hydrocortisone is permitted).
• Participants who work at the study site and/or for the Investigator or are family members of study staff and/or the Investigator.

Sponsors & Collaborators

• Bayer: lead

MeSH Terms

Conditions

Rhinitis, Vasomotor; Rhinitis, Allergic, Seasonal

Interventions

Phenylephrine; Tablets; Oxymetazoline

Condition Hierarchy (Ancestors)

Rhinitis; Nose Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Rhinitis, Allergic; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Intervention Hierarchy (Ancestors)

Ethanolamines; Amino Alcohols; Alcohols; Organic Chemicals; Amines; Dosage Forms; Pharmaceutical Preparations; Imidazoles; Azoles; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds

Results Point of Contact

• Title: Senior Vice President, Global Clinical Development
• Organization: Merck Sharp & Dohme Corp.

ClinicalTrialsDisclosure@merck.com

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 11, 2009
• First Posted: September 14, 2009
• Study Start: August 1, 2009
• Primary Completion: November 1, 2009
• Study Completion: November 1, 2009
• Last Updated: March 11, 2015
• Results First Posted: March 25, 2011

Record last verified: 2015-02