| Eligibility |
Inclusion Criteria:
1. Provide signed informed consent prior to study entry.
2. Males and females aged 18 to 55 years at the time of consent.
3. Body mass index (BMI) = 18 and = 32 kg/m2.
4. Agree to abstain from alcohol intake from 48 hours before first IP administration
through to discharge from the CRU.
5. Agree to abstain from all caffeine- and xanthine-containing products (e.g., coffee,
tea, cola drinks, chocolate) for 48 hours before first IP administration through to
discharge from the CRU.
6. Have a negative urine drug screen/alcohol breath test at Day -1 (Admission). Repeat
urine drug screens will be permitted for suspected false positive results.
7. Use of acceptable contraception.
8. Males must not donate sperm for at least 90 days after the last dose of study drug.
9. Females of childbearing potential must have a negative serum pregnancy test at
Screening and a negative urine or serum pregnancy test on Day -1. If a urine test is
conducted and it is positive, a serum pregnancy test must also be performed for
confirmation. Females not of childbearing potential must be postmenopausal (defined as
cessation of regular menstrual periods for at least 12 months), confirmed by
follicle-stimulating hormone (FSH) level > 40 mIU/mL at Screening.
10. In good general health, in the opinion of the Principal Investigator (PI), with no
significant medical history, have no clinically significant abnormalities on physical
examination at Screening, and/or before administration of the initial dose of study
drug.
11. Have clinical laboratory values within normal ranges.
Exclusion Criteria:
1. Active smoker and/or user of nicotine-containing products (i.e., have not used
nicotine-containing products within the previous 3 months).
2. Human immunodeficiency virus (HIV) antibody positive.
3. Hepatitis B surface antigen (HBsAg) positive or Hepatitis C virus (HCV) positive.
4. Presence of any underlying or clinically significant physical or psychological medical
condition (e.g., hypertension, elevated cholesterol/triglycerides, asthma, or
diabetes) that, in the opinion of the PI, would make it unlikely that the subject will
complete the study per protocol.
5. History or presence of alcohol or drug abuse (including recreational marijuana use)
within the 2 years prior to the first IP administration, and unwillingness to be
totally abstinent during the period of confinement.
6. Blood donation or significant blood loss within 30 days prior to the first study drug
administration.
7. Plasma donation within 7 days prior to the first study drug administration.
8. Administration of IP in another trial within 30 days prior to the first IP
administration, or 5 half-lives, whichever is longer.
9. Females who are pregnant or breastfeeding.
10. Surgery within the past 3 months prior to the first IP administration determined by
the PI to be clinically relevant.
11. Consumption of any nutrients known to modulate cytochrome P450 3A4 (CYP3A4) or any
strong inhibitors or inducers of CYP3A4, starting from 14 days prior to the first dose
of IP on Day 1 and until the EOS assessments.
12. Consumption of cruciferous vegetables or chargrilled meat more than 3 × per week in
the previous 2 weeks.
13. Inability to refrain from consumption of grapefruit and Seville oranges or St. John's
Wort within 14 days prior to the first dose of IP on Day 1 and until the EOS
assessments.
14. Failure to satisfy the PI of fitness to participate for any other reason.
15. Active infection (diagnosed or suspected) or history of recurrent infections.
16. Active malignancy and/or history of malignancy in the past 5 years, except for
completely excised non-melanoma skin carcinomas or low grade cervical intraepithelial
neoplasia.
17. Serious local infection or systemic infection within 3 months requiring antibiotic
treatment.
18. Any acute illness within 30 days prior to Day 1.
19. Use of any prescription or over-the-counter (OTC) medication (except for paracetamol
and approved contraceptives) within 5 days or 5 half-lives (whichever is longer) prior
to dosing and during course of study without prior approval of the Investigator and
Medical Monitor. Simple analgesia (paracetamol) may be permitted at the discretion of
the Investigator.
20. For all participants, the use of any estrogen-containing products (e.g.,
contraceptives, patch, cream, implants) within 14 days prior to the first study drug
administration and until the EOS assessments.
21. Inability to refrain from vaccinations within 14 days of the first dose of IP and
until the EOS assessments.
22. History of allergy or intolerance to any IP or IP constituents used on study or any
clinically significant drug allergy as per the PIs judgment.
23. History of anaphylaxis or other severe allergic reaction to drug, food, toxin, or
other exposure.
24. Any surgical or medical condition that could interfere with the absorption,
distribution, metabolism, or excretion of the IP.
25. Any evidence of cardiac disease or clinically significant abnormalities on ECG.
26. Systolic blood pressure (BP) > 150 mmHg or < 80 mmHg or diastolic BP > 90 mmHg or < 50
mmHg at Screening with one repeat allowed per the PIs discretion at Screening and Day
-1.
27. Heart rate < 40 bpm or > 100 bpm at Screening with one repeat allowed per the PIs
discretion at Screening and Day -1.
28. Diets that could alter metabolism (i.e., high protein, Slim Fast®, Nutrisystem®, etc.)
within 7 days prior to dosing on Day 1.
29. Weight loss or gain of = 10% in the 30 days prior to dosing.
30. Strenuous exercise, including weightlifting, (> 5 × per week) within 2 weeks prior to
first IP administration on Day 1.
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