Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Males of any race, between 35 and 65 years of age, inclusive, at screening.
Body mass index between 18.0 and 32.0 kg/m2, inclusive, at screening.
In good health, determined by no clinically significant findings from medical history, physical examination, 12-lead ECG, vital signs measurements, and clinical laboratory evaluations (congenital nonhemolytic hyperbilirubinemia [eg, Gilbert's syndrome] is acceptable) at screening or check-in as assessed by the Investigator (or designee).
Will agree to use contraception as detailed in Section 7.6.
History of a minimum of 1 bowel movement per day.
Able to comprehend and willing to sign an Inform Consent Form and to abide by the study restrictions.

Exclusion Criteria:

Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, haematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder, as determined by the Investigator (or designee).
History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the Investigator (or designee).
History of dermatological conditions within the 6 months prior to dosing, such as rash, pruritus, and dermatitis, as determined by the Investigator (or designee).
History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy and hernia repair will be allowed). Cholecystectomy is acceptable.
History of alcoholism or drug/chemical abuse within 2 years prior to check-in.

Alcohol consumption of >28 units per week for males. One unit of alcohol equals

½ pint (285 mL) of beer or lager, 1 glass (125 mL) of wine, or 1/6 gill (25 mL) of spirits.

Positive alcohol breath test or positive urine cotinine test result, or positive urine drug screen (confirmed by repeat) at screening or check-in.
Positive hepatitis panel and/or positive human immunodeficiency virus test (Appendix 3).
Participation in a clinical study involving administration of an investigational drug (new chemical entity) in the past 3 months prior to check-in.
Use or intend to use any medications/products known to alter drug absorption, metabolism, or elimination processes, including St. John's wort, within 30 days prior to check-in, unless deemed acceptable per Investigator (or designee) and Sponsor decision.
Use or intend to use any prescription medications/products within 14 days prior to check-in, unless deemed acceptable by the Investigator (or designee).
Use or intend to use slow-release medications/products considered to still be active within 14 days prior to check-in, unless deemed acceptable by the Investigator (or designee).
Use or intend to use any nonprescription medications/products including vitamins, minerals, and phytotherapeutic/herbal/plant-derived preparations within 7 days prior to check-in, unless deemed acceptable per Investigator (or designee) and Sponsor decision.
Use of tobacco- or nicotine-containing products within 3 months prior to check-in.
Receipt of blood products within 2 months prior to check-in.
Donation of blood from 3 months prior to screening, plasma from 2 weeks prior to screening, or platelets from 6 weeks prior to screening.
Poor peripheral venous access.
Have previously completed or withdrawn from this study or any other study investigating BNZ, and have previously received the investigational product.
Subjects with exposure to significant diagnostic or therapeutic radiation (eg, serial X-ray, computed tomography scan, barium meal) or current employment in a job requiring radiation exposure monitoring within 12 months prior to check-in.
Subjects who have participated in any clinical trial involving a radiolabelled investigational product within 12 months prior to check-in.
Subjects who, in the opinion of the Investigator (or designee), should not participate in this study.