CompletedInterventionalPhase 1Updated May 27, 2015
Open-Label, Maximum-Dose Pharmacokinetic Study of 7.5% Ibuprofen Cream (SST-0225) in Healthy Adults | NCT01986660 | Trialant
CompletedInterventionalPhase 1Updated Jan 27, 2014
Open-Label, Maximum-Dose Pharmacokinetic Study of 7.5% Ibuprofen Cream (SST-0225) in Healthy Adults
ClinicalTrials.gov ID
NCT01986660
Lead Sponsor
Strategic Science & Technologies, LLCINDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Phase 1
Enrollment
14Actual
Last Update Posted
Jan 27, 2014Estimated
Start Date
Oct 2013
Primary Completion Date
Oct 2013Actual
Completion Date
Oct 2013Actual
Brief Summary
The purpose of this study is to evaluate how Ibuprofen Cream (SST-0225) is absorbed and eliminated by the body under defined maximum dosing conditions and to evaluate the safety under these conditions.
Healthy
Ibuprofen Cream (SST-0225)
Ages Eligible for Study
Adult (18-64)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
Yes
Eligibility Criteria
Inclusion Criteria:
Signed consent form
Men, women, 18 to 55 years
Females must not be pregnant or plan to become pregnant
BMI 18 to 30 kg/m2
Past or non-smoker
High probability of compliance with completion of study
Healthy as determined by investigator based on medical history, physical exam, clinical laboratory tests, vital sign measurements, ECGs
Exclusion Criteria:
Presence or history of disorder that could interfere with completion of study
Unstable medical condition
Surgical or medical condition that may interfere with absorption, distribution, metabolism or excretion of test drug
Positive Hep B, Hep C and/or HIV test
Positive urine drug screen
Any history of skin disorders, including psoriasis, eczema, tattoos, significant scarring, healing wounds, skin lesions on knees or elbows
Significant disease
Any clinically important deviation from normal limits in physical exam, vital sign measurements, 12 lead ECG, clinical laboratory test
History of drug abuse with 1 year
History of alcoholism with 1 year
Use of prescription medications or ibuprofen within 30 days of Day 1, use of OTC drugs, herbal supplements and vitamins within 14 days of Day 1.
Use of investigational drug within 30 day of Day 1
Acute disease state within 7 days of Day 1
Consumption of grapefruit or grapefruit containing products within 72 hours of Day 1