| Eligibility |
Inclusion Criteria:
1. Must have given written informed consent before any study-related activities are
carried out and must be able to understand the full nature and purpose of the trial,
including possible risks and adverse effects.
2. Adult males and females, 18 to 55 years of age (inclusive) at screening.
3. Body mass index = 18.0 and = 30.0 kg/m2, with a body weight (to 1 decimal place) = 50
kg at screening.
4. Be non-smokers (including tobacco, e-cigarettes and marijuana) for at least 3 months
prior to first study drug administration and have a negative test for cotinine at the
screening visit and at check- in on Day -1.
5. Medically healthy without clinically significant abnormalities (in the opinion of the
PI) at the screening visit and prior to dosing at the timepoints indicated in the
Schedules of Assessments (SoA), including:
1. Physical examination without any clinically significant findings;
2. Systolic blood pressure in the range of 90 to 140 mmHg (inclusive) and diastolic
blood pressure in the range of 40 to 90 mmHg (inclusive) after 5 minutes in
supine (or semi- supine) position;
3. Heart rate in the range of 40 to 100 bpm (inclusive) after 5 minutes rest in
supine (or semi- supine) position;
4. Body temperature (tympanic or oral) in the range 35.5°C to 37.5°C (inclusive);
5. No clinically significant findings in serum chemistry, haematology, coagulation,
and urinalysis tests (any of the routine laboratory test may be repeated at the
discretion of the PI);
6. Triplicate 12-lead ECG (taken after the volunteer has been supine (or
semi-supine) for at least 5 minutes) with a QT interval corrected using the
Fridericia method (QTcF) = 450 msec for males and = 470 msec for females and no
clinically significant abnormalities.
6. Female volunteers must:
a. Be of nonchildbearing potential i.e., be surgically sterilised (hysterectomy,
bilateral salpingectomy, bilateral oophorectomy at least 6 weeks before screening) or
be postmenopausal, where menopause is defined as 12 months of amenorrhea in the
absence of other biological causes. Females under the age of 55 years must have a
documented serum follicle-stimulating hormone (FSH) level > 40mIU/mL to confirm
menopause (females who are taking Hormone Replacement Therapy (HRT) should provide
evidence that they are post-menopausal or should be excluded as their post-menopausal
status cannot be confirmed by measuring FSH - alternatively they would need to stop
HRT to allow FSH to be measured).
b. If of childbearing potential (defined as any female who has experienced menarche
and who has not undergone surgical sterilisation and is not postmenopausal), the
participant:
- Must have a negative serum test at the screening visit and a negative urine
pregnancy test within 24 hours prior to the start of study drug;
- Must not be breastfeeding, lactating or planning pregnancy during the study
period;
- Must agree not to attempt to become pregnant;
- If not exclusively in same-sex relationships, must agree to use adequate
contraception (which is defined as use of a condom by the male partner combined
with use of a highly effective method of contraception by the female partner;
refer to Appendix 5. Highly Effective Forms of Contraception) after signing
consent, during the study, and at least 30 days after the EoS visit;
- Must agree to not donate ova for at least 30 days after the EoS visit.
7. Male participants, if not surgically sterilised, must agree to:
1. Not donate sperm after signing consent, during the study, and at least 90 days
after the EoS visit;
Exclusion Criteria:
1. History or presence of significant cardiovascular, pulmonary, hepatic, renal,
haematological, gastrointestinal, endocrine, immunologic, dermatologic or neurological
disease, including any acute illness or major surgery within the past 3 months
determined by the PI to be clinically significant (participants with resolved
childhood asthma may be included in the study).
2. Current infection that requires systemically absorbed antibiotic, antifungal,
antiparasitic or antiviral medications.
3. Suffer from frequent or recurrent infections (defined as =3 occurrences in the 12
months preceding first study drug administration or 2 occurrences in the 6 months
preceding first study drug administration).
4. Any history of malignant disease in the last 10 years (excludes surgically resected
skin squamous cell or basal cell carcinoma).
5. Presence of clinically relevant immunosuppression from, but not limited to,
immunodeficiency conditions such as common variable hypogammaglobulinemia.
6. Use of or plans to use systemic immunosuppressive (e.g., corticosteroids,
methotrexate, azathioprine, cyclosporine) or immunomodulating medications (e.g.,
interferon) during the study or within 3 months prior to the first study drug
administration (prior use of nasal sprays for hayfever may be permitted if used > 30
days prior to study drug administration or alternatively at the discretion of the PI).
7. History of risk factors for torsade de pointes (including a family history of long QT
syndrome or sudden cardiac death) or a known arrythmia.
8. Liver function test results elevated more than 1.5-fold above the upper limit of
normal (ULN) for gamma glutamyl transferase (GGT), bilirubin (total, conjugated and
unconjugated), alkaline phosphatase (ALP), aspartate aminotransferase (AST) or alanine
aminotransferase (ALT). Volunteers with ALP and/or ALT/AST above the limits specified
may be included, at the discretion of the PI, if the levels are unaccompanied by
clinical signs and are determined to be normal variants.
9. Positive test results for active human immunodeficiency virus (HIV), hepatitis B
surface antigen (HBsAg), hepatitis C virus (HCV) antibodies or Quantiferon Gold®
(Tuberculosis (TB) infection) at the screening visit.
10. Presence or having sequelae of gastrointestinal, liver, kidney, or other conditions
known to interfere with the absorption, distribution, metabolism, or excretion of
drugs (prior gall bladder and/or appendix removal is not exclusionary if the procedure
was undertaken = 3 months prior to study drug administration; if less than 3 months,
history of such procedures may still be considered not exclusionary if it is deemed
appropriate by the PI).
11. Estimated creatinine clearance (CrCl) < 60 mL/min using the Cockcroft-Gault formula or
serum creatinine more than 1.5-fold above the ULN.
History of substance abuse or alcohol abuse within 12 weeks prior to the screening visit
(defined as more than an average of 14 standard drinks per week or regular consumption of
more than 4 standard drinks on any one day; where 1 standard drink is 10 g of pure alcohol
and is equivalent to 285 mL beer [4.9% Alc./Vol], 100 mL wine [12% Alc./Vol], 30 mL spirit
[40% Alc./Vol]).
13. Positive drugs of abuse or alcohol breath test results at the screening visit or at
check-in (Day -1).
14. Use of any prescription or over-the-counter medication (including herbal products, and
hormone supplements) within 10 days or 5 half-lives of the medication (whichever is longer)
prior to the first study drug administration - exceptions include occasional use of
paracetamol (doses of 500 mg up to every 6 hours or 2 g per day maximum for no more than 3
consecutive days), ibuprofen (doses of 400 mg up to every 6 hours or 1.2 g per day maximum
for no more than 3 consecutive days), topical ointments, and vitamins or dietary
supplements.
15. Demonstrated clinically significant (required intervention, e.g., emergency room visit,
epinephrine administration) allergic reactions (e.g., food, drug, or atopic reactions,
asthmatic episodes) which, in the opinion of the PI, would interfere with the volunteer's
ability to participate in the trial.
16. Known hypersensitivity to any of the study drug ingredients. 17. Use of any
vaccinations within 14 days (within 4 weeks for live virus vaccines) prior to the first
study drug administration.
18. For women of childbearing potential, a positive serum pregnancy test at the screening
visit or a positive urine pregnancy test (with confirmatory serum pregnancy test) at
check-in (Day -1).
19. Females who are breastfeeding or planning to breast feed at any time during the study.
20. Donation of blood or plasma within 30 days prior to first study drug administration, or
loss of whole blood of more than 500 mL within 30 days prior to first study drug
administration, or receipt of a blood transfusion within 1 year of first study drug
administration.
21. Treatment with an investigational drug in another clinical trial within 60 days or 5
half-lives of the other investigational drug (whichever is longer) prior to the first
administration of study drug in this trial.
22. Any other condition or prior therapy that in the opinion of the PI would make the
volunteer
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