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OpenTrials
Completed

NCT Number: NCT01986660

Open-Label, Maximum-Dose Pharmacokinetic Study of 7.5% Ibuprofen Cream (SST-0225) in Healthy Adults

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.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

SST Investigational Site

New York, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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
  • Tobacco use/caffeine use within 48 hours of Day 1

Treatment and study plan

Ibuprofen Cream (SST-0225)

Drug

Primary outcomes

  1. Cmax, Tmax, Trough Concentrations Days 2 to 8, AUC 0-24, Steady State, T1/2

    Time frame: 9 days

Secondary outcomes

  1. Clinical laboratory change from baseline

    Time frame: 14 days

  2. Modified Berger Bowman Skin Assessment

    Time frame: 14 days

  3. Vital Signs

    Time frame: 14 days

  4. Adverse Events

    Time frame: 14 days

Sponsors and collaborators

Lead sponsor

Strategic Science & Technologies, LLC

Industry

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Nov 18, 2013
Registry last updated
Jan 27, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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