Effects of ICA-105665 Using the Intradermal Capsaicin and Ultraviolet B (UV-B) Models in Healthy Male Subjects

• Status: Completed
• Trial end date: 2009-12-01
• Target enrollment: 0
• Participant gender: Male

Summary

The purpose of this study is; to determine the pharmacodynamic (PD) effects of ICA-105665 using the intradermal (ID) capsaicin model in healthy male subjects, and to investigate the effect of ICA-105665 on inflammatory hyperalgesia using the ultraviolet B (UV-B) model in healthy male subjects.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Pfizer
• Treatments: Capsaicin; Ibuprofen

Criteria

Inclusion Criteria:

• Healthy males aged 18 to 55 years (inclusive).

• Body mass index (BMI) of 18 to 30 kg/m2.

• Non-smokers and smokers of up to 5 cigarettes or equivalent per day.

• Must be able to abstain from smoking during residential periods.

• Demonstration of positive hyperalgesia as defined by an area of hyperalgesia = 15 cm2 15 minutes after ID administration of 100 µg capsaicin.

• Demonstration of negative hyperalgesia as defined by an area of hyperalgesia < 5 cm2 15 minutes after ID administration of capsaicin vehicle.

• Subject with a skin type compatible with the measures, and without significant skin allergies, pigmentary disorders, or any active dermatological conditions that might interfere with the conduct of the study.

Exclusion Criteria:

• Subject has had a clinically significant illness in the 4 weeks before screening.

• Use of prescribed medications and herbal supplements in the 7 days prior to dosing or over the counter preparations, including multivitamins and paracetamol, in the 48 h before dosing.

• Subject has a significant history of drug/solvent abuse (within 2 years prior to Day 1), or a positive drugs of abuse test at screening.

• Subject with a history of alcohol abuse or currently drinks in excess of 28 units per week (males), or has a positive breath alcohol test at the Screening visit or on Day 1.

• Subject has a Heat pain tolerance threshold (HPTT) of = 50°C at screening.

• Subjects who do not develop erythema at the highest intensity of UV-B light used to establish Minimum erythema dose (MED).

• Known allergy or intolerance to capsaicin or hot peppers.

• Subjects who have any skin trauma, scars or other skin disorder or tattoos on their forearms or on the front of their thighs.

• Subject with active chronic pain conditions or a history of chronic pain conditions.

• Any condition that might interfere with the absorption, distribution, metabolism, and/or excretion of drugs.

• Previous ingestion of ICA-105665.

• Considering or scheduled to undergo any surgical procedure during the duration of the study.

• Prolonged QT/QTc interval (repeatedly = 450 msec). Received any agent known to alter hepatic or renal clearance (e.g., erythromycin, cimetidine, barbiturates, phenothiazines, clarithromycin, troleandomycin, ketoconazole, miconazole, fluconazole, itraconazole, etc.) for a period of 30 days prior to Day 1.

• History of risk factors for Torsades de Pointes (family history of long QT syndrome, heart failure, hypokalemia).

• Subject is unable to tolerate being blindfolded.

• Subject has participated in a clinical study involving capsaicin within 1 year of the Screening visit.

• Subject has a history of skin cancer.

• Subject has a clinically significant history of anemia.