Study to Assess the Safety and Pharmacokinetics of ATL-001 (Ciclopirox Olamine) in Healthy Volunteers

Exclusion Criteria

• •1. Current drug or alcohol dependence (excluding caffeine), based on self-report, including subjects who have been in a drug rehabilitation program
• •2. Current smoker or a history of using tobacco products within 3 months prior to Screening
• •3. Clinically significant abnormalities on physical examination, medical history, 12-lead ECG (i.e., QTc \> 440 ms for male subjects and \> 450 ms for female subjects), vital signs, or laboratory values, as judged by the investigator or designee
• •4. History or presence of any clinically significant illness (e.g., cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, musculoskeletal, or psychiatric) or any other condition, which in the opinion of the investigator would jeopardize the safety of the subject or the validity of the study results
• •5. Use of a non-prescription drug within 14 days prior to the first drug administration. Subjects who have taken over-the-counter medication may still be entered into the study, if in the opinion of the investigator or designee, the medication received will not interfere with the study procedures or data integrity or compromise the safety of the subject
• •6. Use of any prescription medications, recreational drugs, or natural health products (except vitamin or mineral supplements, acceptable forms of birth control, and hormone replacement) within 14 days prior to first drug administration or throughout the study, unless in the opinion of the investigator or designee, the product will not interfere with the study procedures or data integrity or compromise the safety of the subject
• •7. Use of any medication that interfere with the glucuronidation metabolic pathway within 14 days prior to first drug administration
• •8. Positive urine drug screen
• •9. Positive breath alcohol test. If a subject presents with positive breath alcohol test, the subject may be rescheduled at the discretion of the investigator or designee
• •10. Female subjects who are currently pregnant or lactating or who are planning to become pregnant within 60 days of last study drug administration
• •11. Known history of allergy or hypersensitivity to any component of the active drug or placebo
• •12. Positive for Hepatitis B, Hepatitis C, HIV or COVID-19
• •13. Treatment with any investigational drug within 30 days prior to first drug administration in the treatment phase
• •14. A subject who, in the opinion of the investigator or designee, is not considered to be suitable and is unlikely to comply with the study protocol for any reason