| Eligibility |
Inclusion Criteria:
1. Capable of giving signed informed consent as described in Section 10.1.3, which
includes compliance with the requirements, prohibitions and restrictions listed in the
informed consent form (ICF) and in this protocol.
2. Subject has been informed both verbally and in writing about the objectives of the
clinical trial, the methods, the anticipated benefits and potential risks and the
discomfort to which he/she may be exposed, and has given written consent to
participation in the trial prior to trial start and any trial-related procedure.
3. Study participant must be at least 18 years of age and not older than 55 years of age
at the time of signing the ICF.
4. Non-smokers or ex-smokers who had stopped smoking for at least 5 years prior to start
of the clinical study.
5. In good physical and mental health as determined on the basis of medical history and
general physical examination performed at screening.
6. Hematology and chemistry parameters, pulse rate and/or blood pressure, and ECG within
the reference range for the population studies, or showing no clinically relevant
deviations, as judged by the Investigator (Note that some defined clinical laboratory
parameters must not exceed the upper limit of reference range - see Exclusion
Criterion #3).
7. Negative urine test for selected drugs of abuse at screening and upon check-in at the
clinical site. Note: Subjects should not consume poppy-seeds within 72 h before
screening and before each urine drug screening because this can falsify the results of
the opiate urine drug test.
8. Negative alcohol breath test at screening and upon check-in at the clinical site.
9. Negative hepatitis panel (including hepatitis B surface antigen [HBsAg] and
anti-hepatitis C virus [HCV] antibodies) and negative human immunodeficiency virus
(HIV) antibody screens and negative SARS-CoV-2 PCR test.
10. Body weight at least 70 kg for males and 60 kg for females and have a body mass index
(BMI) = 18.0 kg/m2 and < 29.9 kg/m2.
11. Male or female. Pregnancy and Contraception
12. Female subjects must be of non-childbearing potential, as follows.
A female study participant is eligible to participate if she is not pregnant or
breastfeeding, and one of the following conditions applies:
1. At least 1 year post-menopausal (amenorrhea >12 months in the absence of an
alternative medical cause and follicle-stimulating hormone >30 mIU/mL in women not
using hormonal contraception or hormonal replacement therapy) prior to screening;
2. Surgically sterile (bilateral oophorectomy, hysterectomy, bilateral salpingectomy, or
bilateral tubal ligation).
To protect partners from possible exposure to study medication in semen, male subjects must
use a condom during the study, even if they have had a vasectomy or their partner is not of
childbearing potential, and they must not plan to father a child, or donate sperm, during
the study, and for 4 months after their final dose of study medication. Note: medically
acceptable methods of contraception that may be used by the partner include combined oral
contraceptive, contraceptive vaginal ring, contraceptive injection, intrauterine device,
and etonogestrel implant.
Exclusion Criteria:
1. Clinically relevant abnormal history, physical findings, ECG, or laboratory values at
the pre-study screening assessment that could interfere with the objectives of the
study or the safety of the subject. Note: Blood pressure and heart rate at the
screening examination outside the ranges 90- 139 mmHg systolic, 50-89 mmHg diastolic;
heart rate 50-90 bpm are considered as exclusion criteria.
2. QTc interval of ECG above the upper limit of reference range at screening. The
following commonly accepted reference range will be taken as a basis: Men: QTc = 440
ms; Women: QTc = 460 ms.
3. Aspartate aminotransferase [AST], alanine aminotransferase [ALT], alkaline phosphatase
[AP], glutamate dehydrogenase [GLDH], gamma glutamyl transpeptidase [?-GT]) above the
upper limit of the reference range.
4. Presence of acute or chronic illness or history of chronic illness sufficient to
invalidate the subject's participation in the study or make it unnecessarily
hazardous.
5. A condition that, in the opinion of the Investigator, could compromise the well-being
of the subject or course of the study, or prevent the subject from meeting or
performing any study requirements.
6. Impaired endocrine, thyroid, hepatic, respiratory or renal function, diabetes
mellitus, coronary heart disease, cancer, or history of any psychotic mental illness.
7. Respiratory tract infection within 4 weeks before the screening visit.
8. History of surgery or medical intervention, or planned surgery or medical
intervention, that could interfere with the objectives of the study or the safety of
the subject.
9. Presence or history of severe adverse reaction to any drug, or sensitivity to
components of the study medication.
10. Loss of more than 400 mL blood, e.g., as a blood donor, or donation of blood products,
during the 3 months before the study.
11. Positive fecal blood test at screening.
12. Active or latent parasitic infection, visit to a country with a high prevalence of
parasitic infections within 3 months before receiving study medication.
13. Use of any prescription or over-the-counter medicine, with the exception of
acetaminophen (paracetamol), within 14 days (or 5 half-lives, whichever is longer)
before the first dose of study medication as defined in Section 10.5.
14. Treatment with any known enzyme inducing or inhibiting agents (e.g., St. John's Wort
(Johanniskraut), barbiturates, phenothiazines, cimetidine, ketoconazole etc.) within
30 days before first administration of IMP or during the trial.
15. Presence or history of drug or alcohol abuse, or intake of more than 21 units (14
units for women) of alcohol weekly.
16. Receipt of a living vaccine within the 3 months, or mRNA or vector vaccine against
COVID-19 within 4 weeks before dosing, or planned vaccination during the study.
17. Currently participating in other clinical trials or previous treatment with an
investigational medicinal product within 5 half-lives or 30 days (whichever is longer)
prior to randomization.
18. Known allergy or hypersensitivity to the IMP (including excipients) or history of
severe adverse reaction to any drug, or sensitivity to components of the study
medication.
19. Study participant is pregnant or breastfeeding.
20. Subject has been committed to an institution by virtue of an order issued either by
the judicial or the administrative authorities.
21. Subject is an employee of the sponsor, or an employee of any third-party organization
involved into the clinical trial, or an employee of the clinical trial site, or is
dependent on the investigator.
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