A Study of Laropiprant (MK-0524) in Participants With Moderate to Severe Erythematotelangiectatic Rosacea (MK-0524-155)
Primary Purpose
Rosacea
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Laropiprant
Placebo for Laropiprant
Sponsored by
About this trial
This is an interventional treatment trial for Rosacea
Eligibility Criteria
Inclusion Criteria:
- Moderate to severe erythematotelangiectatic rosacea with moderate to severe erythema of facial lesion
- Generally healthy excluding rosacea
- Presence of telangiectasia
- Five or less facial inflammatory lesions
- Able to restrict diet in order to avoid foods/drinks (including alcohol) that are known to exacerbate the signs/symptoms of rosacea
- Females of childbearing potential must have negative serum pregnancy test and agree to use one form of contraception
Exclusion Criteria:
- Diagnosis of skin disorders, including psoriasis, acne vulgaris, perioral dermatitis or atopic dermatitis that would interfere with the clinical evaluations of rosacea
- Using and unable to discontinue use of phosphodiesterase (PDE) 4 inhibitors, theophylline, niacin greater than 500 mg/day
- Known or suspected excessive alcohol intake
- Sensitivity to tetracyclines
- Ocular rosacea and/or blepharitis/meibomianitis
- Pregnant or breastfeeding
- Perimenopausal and has symptoms that cause flushing that may affect rosacea
- Initiated hormonal method of birth contraception within 4 months of baseline, discontinues use during the course of the study, or changes hormonal method within 4 months
- Active mycobacterial infection of any species within 3 years
- History of mycobacterium tuberculosis infection
- History of recurrent bacterial infection
- Congenital or acquired immunodeficiency common variable immunodeficiency (CVID), Hepatitis B surface antigen positive or Hepatitis B core antibody positive
- Human immunodeficiency virus (HIV) infection
- Positive for hepatitis C antibodies
- Malignancy or has had a history of malignancy greater than 3 years prior
- Will continue to use any of the following treatments during the study: Systemic retinoids, therapeutic vitamin A supplements of greater than 10,000 units/day, systemic steroids, systemic antibiotics known to have an impact on the severity of facial rosacea, systemic treatment for acne, topical steroids, topical retinoids, topical acne treatments including prescription and over-the-counter (OTC) preparations, topical anti-inflammatory agents, topical antibiotics, topical imidazole antimycotics, cryodestruction or chemodestruction, dermabrasion, photodynamic therapy, acne surgery, intralesional steroids, X-ray therapy, pulse-dye laser, intense pulse light, astringents, abrasives, benzoyl peroxide products, sulfur containing washes, eye washes, Beta blockers, vasodilators, vasoconstrictors and/or chronic use (>14 days) of topical or systemic anti-inflammatory agents
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Laropiprant
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Change in Clinician's Erythema Assessment (CEA) Scale Score from Baseline
Secondary Outcome Measures
Change in Patient Self Assessment (PSA) Score from Baseline
Full Information
NCT ID
NCT01451619
First Posted
October 11, 2011
Last Updated
March 24, 2015
Sponsor
Merck Sharp & Dohme LLC
1. Study Identification
Unique Protocol Identification Number
NCT01451619
Brief Title
A Study of Laropiprant (MK-0524) in Participants With Moderate to Severe Erythematotelangiectatic Rosacea (MK-0524-155)
Official Title
A Randomized, Double-blind, Placebo-controlled, Multi-center, Parallel Group Study to Assess the Pharmacodynamics of MK-0524 in Subjects With Moderate to Severe Erythematotelangiectatic Rosacea. (Protocol No. 155)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Merck Sharp & Dohme LLC
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will assess the effect of MK-0524 relative to placebo, on signs and symptoms of rosacea and to determine the safety and tolerability profile of MK-0524 in participants with rosacea.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rosacea
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Laropiprant
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Laropiprant
Other Intervention Name(s)
MK-0524
Intervention Description
One 100-mg tablet orally once daily for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo for Laropiprant
Intervention Description
One tablet orally once daily for 4 weeks
Primary Outcome Measure Information:
Title
Change in Clinician's Erythema Assessment (CEA) Scale Score from Baseline
Time Frame
Baseline and Week 4
Secondary Outcome Measure Information:
Title
Change in Patient Self Assessment (PSA) Score from Baseline
Time Frame
Baseline and Week 4
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Moderate to severe erythematotelangiectatic rosacea with moderate to severe erythema of facial lesion
Generally healthy excluding rosacea
Presence of telangiectasia
Five or less facial inflammatory lesions
Able to restrict diet in order to avoid foods/drinks (including alcohol) that are known to exacerbate the signs/symptoms of rosacea
Females of childbearing potential must have negative serum pregnancy test and agree to use one form of contraception
Exclusion Criteria:
Diagnosis of skin disorders, including psoriasis, acne vulgaris, perioral dermatitis or atopic dermatitis that would interfere with the clinical evaluations of rosacea
Using and unable to discontinue use of phosphodiesterase (PDE) 4 inhibitors, theophylline, niacin greater than 500 mg/day
Known or suspected excessive alcohol intake
Sensitivity to tetracyclines
Ocular rosacea and/or blepharitis/meibomianitis
Pregnant or breastfeeding
Perimenopausal and has symptoms that cause flushing that may affect rosacea
Initiated hormonal method of birth contraception within 4 months of baseline, discontinues use during the course of the study, or changes hormonal method within 4 months
Active mycobacterial infection of any species within 3 years
History of mycobacterium tuberculosis infection
History of recurrent bacterial infection
Congenital or acquired immunodeficiency common variable immunodeficiency (CVID), Hepatitis B surface antigen positive or Hepatitis B core antibody positive
Human immunodeficiency virus (HIV) infection
Positive for hepatitis C antibodies
Malignancy or has had a history of malignancy greater than 3 years prior
Will continue to use any of the following treatments during the study: Systemic retinoids, therapeutic vitamin A supplements of greater than 10,000 units/day, systemic steroids, systemic antibiotics known to have an impact on the severity of facial rosacea, systemic treatment for acne, topical steroids, topical retinoids, topical acne treatments including prescription and over-the-counter (OTC) preparations, topical anti-inflammatory agents, topical antibiotics, topical imidazole antimycotics, cryodestruction or chemodestruction, dermabrasion, photodynamic therapy, acne surgery, intralesional steroids, X-ray therapy, pulse-dye laser, intense pulse light, astringents, abrasives, benzoyl peroxide products, sulfur containing washes, eye washes, Beta blockers, vasodilators, vasoconstrictors and/or chronic use (>14 days) of topical or systemic anti-inflammatory agents
12. IPD Sharing Statement
Citations:
PubMed Identifier
25142778
Citation
Krishna R, Guo Y, Schulz V, Cord-Cruz E, Smith S, Hair S, Nahm WK, Draelos ZD. Non-obligatory role of prostaglandin D2 receptor subtype 1 in rosacea: laropiprant in comparison to a placebo did not alleviate the symptoms of erythematoelangiectaic rosacea. J Clin Pharmacol. 2015 Feb;55(2):137-43. doi: 10.1002/jcph.383. Epub 2014 Sep 4.
Results Reference
result
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A Study of Laropiprant (MK-0524) in Participants With Moderate to Severe Erythematotelangiectatic Rosacea (MK-0524-155)
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