| Eligibility |
Inclusion Criteria:
1. Normal healthy volunteers with an age of 18 to 65 years inclusive at the time of
informed consent.
2. Participants can be of any ethnicity or race, excluding Asian by self-declaration. For
the purposes of this protocol, Asian is defined as a person having origins in any of
the original peoples of the Far East, Southeast Asia, or the Indian subcontinent,
including for example, Cambodia, China, India, Japan, Korea, Malaysia, Pakistan,
Philippines, Thailand, and Vietnam. If an individual identifies as mixed race,
exclusion will occur if the proportion of self-declaration as Asian exceeds 25%.
3. Participants must be in good general health, in the opinion of the Investigator, with
no significant medical history (ie, history of childhood asthma [resolved] is
acceptable; history of depression [non-hospitalised, medicated] or migraines is not
acceptable), and no clinically significant abnormalities on physical examination at
Screening and/or before administration of the initial dose of IP.
4. Participants must have documented evidence of receipt of licensed COVID-19
vaccinations as per the current Australian Technical Advisory Group on Immunisation
(ATAGI) guidelines and be fully vaccinated as per local guidelines.
5. Participants must have a BMI between > 18.0 and < 32.0 kg/m2 at Screening.
6. Participants must have clinical laboratory values within normal range as specified by
the testing laboratory, unless deemed not clinically significant by the Investigator
or delegate. A single repeat test can be performed for clinically significant abnormal
values, at the discretion of the Investigator.
7. Participants must be a non-smoker and must not have used any tobacco products within 2
months prior to Screening, or if a smoker, they must smoke no more than 2 cigarettes
or equivalent per week.
8. Participants must have no relevant dietary restrictions (restrictions that would
prevent consumption of the standard meals to be provided), and be willing to consume
standard meals provided.
9. Females must be non-pregnant and non-lactating, and must use an acceptable, highly
effective double contraception from Screening until 30 days after last dose of IP,
including the follow-up period. Double contraception is defined as a condom AND one
other form of the following:
- Established hormonal contraception (with approved oral contraceptive pills
[OCPs], long-acting implantable hormones, injectable hormones);
- A vaginal ring or an intrauterine device (IUD);
- Documented evidence of surgical sterilisation at least 6 months prior to
Screening (eg, tubal occlusion, hysterectomy, bilateral salpingectomy, or
bilateral oophorectomy for women or vasectomy for men, provided the male partner
is a sole partner).
Women not of childbearing potential must be post-menopausal for = 12 months.
Post-menopausal status will be confirmed through testing of follicle-stimulating
hormone (FSH) levels = 40 IU/L at Screening for amenorrhoeic female participants.
Females who are abstinent from heterosexual intercourse will also be eligible.
Periodic abstinence (eg, calendar, ovulation, symptothermal, post-ovulation methods)
and withdrawal are not considered highly effective methods of birth control.
Participant complete abstinence for the duration of the study and for 1 month after
the last study treatment is acceptable.
Female participants who are in exclusively same-sex relationships are not required to
use contraception.
Woman of childbearing potential (WOCBP) must have a negative pregnancy test at
Screening and Day 1 and be willing to have additional pregnancy tests as required
throughout the study.
Males must be surgically sterile (> 30 days since vasectomy with no viable sperm),
abstinent, or if engaged in sexual relations with a WOCBP, the participant and his
partner must be surgically sterile (eg, tubal occlusion, hysterectomy, bilateral
salpingectomy, bilateral oophorectomy) or using an acceptable, highly effective
contraceptive method from Screening until study completion, including the follow-up
period, and for at least 90 days post final dose. Acceptable methods of contraception
include the use of condoms and the use of an effective contraceptive for the female
partner that includes: OCPs, long-acting implantable hormones, injectable hormones, a
vaginal ring, or an IUD. Participants with same-sex partners (abstinence from
penile-vaginal intercourse) are eligible when this is their preferred and usual
lifestyle.
10. Male participants must not donate sperm for at least 90 days after the last dose of
IP, and female participants must not donate ovum for at least 30 days after the last
dose of IP.
Exclusion Criteria:
1. Use of any IP or investigational medicinal device within 30 days prior to treatment,
or 5 half-lives of the product, whichever is the longest.
2. Prior or ongoing medical conditions, medical history, physical findings, or laboratory
abnormality that, in the Investigator's opinion, could adversely affect the safety of
the participant or confound treatment assessment.
3. Allergy or hypersensitivity to the IP or any of its constituents.
4. History of allergic or anaphylactic reactions that are considered severe in the
opinion of the Investigator (with the allowance of well-managed allergies such as
allergic rhinitis, eczema, stinging insect allergies, and pollen allergies).
5. Any history of cardiac disease.
6. Abnormal ECG findings at Screening that are considered by the Investigator to be
clinically significant.
7. Use of or anticipated use of any prescription drugs (other than hormonal
contraception; OCPs, long-acting implantable hormones, injectable hormones, a vaginal
ring, or an IUD), over-the-counter (OTC) medication, herbal remedies, supplements, or
vitamins 2 weeks prior to dosing and during course of study without prior approval of
the Investigator and MM. Simple analgesics (paracetamol, nonsteroidal
anti-inflammatory drugs [NSAIDs]) are permitted at 1 or 2 therapeutic doses per week
at the discretion of the Investigator.
8. Pregnant or lactating at Screening or planning to become pregnant (self or partner) at
any time during the study, including the follow-up period.
9. Presence of any underlying physical or psychological medical condition that, in the
opinion of the Investigator, would make it unlikely that the participant will comply
with the protocol or complete the study per protocol.
10. Blood donation or significant blood loss within 60 days prior to the first IP
administration.
11. Plasma donation within 7 days prior to the first IP administration.
12. Fever (body temperature > 38°C) or symptomatic viral or bacterial infection within 2
weeks prior to Screening.
13. History of malignancy, except for non-melanoma skin cancer, excised more than 2 years
ago and cervical intraepithelial neoplasia that has been successfully cured more than
5 years prior to Screening.
14. History or presence of a condition associated with significant immunosuppression
(significant in the opinion of the Investigator).
15. History of life-threatening infection (eg, meningitis).
|
