Civamide Patch Safety, Tolerability and PK Study

Completed · Phase 1 · Has a placebo group

Conditions studied: Healthy Volunteers

In brief

To evaluate the tolerability of two different strengths of a Civamide Patch (0.0075% and 0.0150%) compared to the placebo patch and each other in healthy adult volunteers. To assess the pharmacokinetics of civamide and to determine if there is systemic absorption of the drug from civamide patch in a subset of study subjects.

Key facts

Study ID

NCT00758433

Run by

Winston Laboratories

People needed

39

Starts

2008-09-01

Expected to finish

2009-04-01

Last updated by the study team

2011-06-10

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Inclusion Criteria
• Subject voluntarily agrees to participate in this study and signs an IRB- approved informed consent prior to performing any of the screening procedures.
• Subject is healthy, determined by pre-study medical evaluation medical history, physical examination of the treatment area, and vital signs).
• Males or females between 18 to 60 years of age, inclusive.
• Non-pregnant, non-lactating females of childbearing potential who agree to use medically acceptable forms of birth control (abstinence, hormonal contraceptives, diaphragm with spermicide, condom with spermicide, or intrauterine device) from Screening to Day 10 follow-up or females of nonchildbearing potential (surgically sterile [hysterectomy or bilateral tubal ligation] or post-menopausal ≥ 1 year).
• Subject has a blood pressure reading lower than or equal to 144/92 mmHg.
• Subject has an oral temperature reading lower than 99.6F.
• Subjects must have an area of the skin on the abdomen that is without active skin disease, infection, severe erythema, or other compromise in the integrity of the skin at or near the intended treatment area.
• The subject has no visual or motor impairments that will make it difficult to complete the VAS scales or apply the patch.
• Non-smoker as determined by history over the past year.
• Subject has a body mass index (BMI) between 18.5 and 30.5 kg/m2, in pk subset only.
• Subject is willing and able to cooperate to the extent required by the protocol.

You may not qualify if…

• Subject has known allergy or hypersensitivity to
• a) Civamide, capsicum, or capsaicin-containing products,
• b) any other ingredient of the patch or
• c) adhesives.
• Presence of any cutaneous abnormality or condition that may adversely impact the application of the test patches.
• History of frequent headache or other painful conditions within the past 30 days that has required or is expected to require the chronic use of prescription or over the counter pain relief medications, such as non- steroidal anti-inflammatory agents, including COX-2 inhibitors, systemic opiates or derivatives, or acetaminophen, prior to Day 1 or within 48 hours prior to Day 1.
• Use of alcohol or alcohol-containing foods, medications or beverages within 24 hours prior to Day 1 until after the completion of the Study on Day 10.
• Topical use of any moisturizer or medicated products on or near the treatment area within 48 hours of Day 1 until after the completion of the Study on Day 10.
• Topical use of any capsaicin-containing product for 60 days prior to Day 1 until completion of the Study on Day 10.
• Subject has a history of alcohol and/or drug abuse within two years of study entry.
• Female subjects who are breastfeeding.
• Unwilling to maintain usual consumption of caffeine containing beverages within 24 hours prior to Day -1 until completion of Day 8.
• Subject is unwilling to abstain from vigorous exercise for 48 hours prior to Day 1 until completion of the Study on Day 10.
• Subject is unwilling to abstain from swimming, baths and prolonged with direct stream of water when showering from Day 1 until Day 8
• Use of an investigational drug within 30 days prior to Day 1.
• Donation of blood (> 250 ml) or blood products within 2 months (56 days) prior to Day 1.
• Ingestion of any capsaicin-containing foods for 24 hours before Day 1 and during the study.
• If for any other reason the subject is not deemed to be healthy by the investigator.

Where it is running

• International Research Services, Inc. — Port Chester, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.