| Eligibility |
Inclusion Criteria:
1. Subject's written informed consent obtained prior to any study-related procedures.
2. Able to understand and comply with the requirements of the study, as judged by the
investigator or designee.
3. Men and women between 18-65 years inclusive
4. Female subjects must either be of non-childbearing potential or if of childbearing
potential, must not be pregnant or breast feeding and use a highly effective birth
control method during treatment and for 90 days following last dose
5. Male subjects must use highly effective contraception during treatment and for 90 days
following last administered dose
6. Subject must agree not to donate semen or ova/oocytes during the study and for 90 days
after the last dose of IMP
7. Body mass index (BMI) = 18 and = 32 kg/m2.
8. Subjects with normal hearing
9. Subjects must be in good health at the time of screening
Exclusion Criteria:
1. History or presence of any clinically relevant acute or chronic medical or psychiatric
condition that could interfere with the subject's safety.
2. History or presence of vestibular disorder including vertigo, dizziness or other
auditory impairment as judged by the investigator or designee.
3. After 10 minutes supine rest at the time of screening or prior to dosing, any vital
signs values outside the following ranges:
- Systolic blood pressure <90 or >150 mmHg, or
- Diastolic blood pressure <50 or >95 mmHg, or
- Pulse <40 or >90 bpm
4. Any clinically significant abnormalities in resting ECG at the time of screening or
pre-dose Day 1 including prolonged QTcF (>450 ms for males; >470 ms for females) and
cardiac arrhythmias, as judged by the Investigator or designee.
5. Clinically significant abnormalities in renal function:
- serum creatinine >ULN
- eGFR <60 mL/min or = 60mL/min with evidence of any kidney dysfunction (e.g.
proteinuria, or clinical findings as judged by the investigator)
6. Any clinically significant illness, medical/surgical procedure or trauma within 4
weeks of the first administration of IMP (Day 1).
7. Malignancy within the past five years with the exception of in situ removal of basal
cell carcinoma or resected benign colonic polyps.
8. Any planned major surgery within the duration of the study.
9. History of latent or active tuberculosis or a positive Quantiferon test at screening.
10. Females who are pregnant, breast feeding or plan to be pregnant during the study
period or 90 days after.
11. Female subjects with a positive serum or urine pregnancy test (minimum sensitivity 25
IU/L or equivalent units of human chorionic gonadotropin [HCG]) at screening and
within 24 h prior to the first administration of IMP.
12. Positive serum hepatitis B surface antigen (HBsAg), hepatitis C virus antibodies
(HCVAb) or human immunodeficiency virus (HIV) 1 and/or 2 antibodies at screening.
13. Positive PCR test for active COVID -19 tested within seven days prior to
administration of the IMP on Day 1.
14. History of any drug and/or alcohol abuse in the past two years prior to screening.
15. Regular alcohol consumption in males >21 units per week and females >14 units per
week.
16. Positive urine drugs of abuse test and/or alcohol breath test at screening or on
admission to the unit prior to administration of the IMP on Day -1 that cannot be
accounted for by concomitant medication in the opinion of the Investigator or
designee.
17. Current or previous use of tobacco, nicotine products or e-cigarettes in the past six
months.
18. Smoking history of > 5 pack years.
19. Positive urine cotinine test at screening or Day -1.
20. Use of any prescribed or non-prescribed medication including analgesics, herbal
remedies, vitamins and minerals within two weeks prior to the (first) administration
of IMP, except those listed below, at the discretion of the Investigator or designee:
- hormone replacement therapy (HRT)
- hormonal contraception
- occasional intake of paracetamol (maximum 2000 mg/day for 3 consecutive days)
- nasal decongestants without cortisone for a maximum of 10 days
- antihistamines for a maximum of 10 days
- anticholinergics for a maximum of 10 days
21. Use of antacids, PPIs or any medication that changes gastric pH within two weeks prior
to the first administration of IMP (Day 1).
22. Use of macrolide antibiotics within two weeks prior to the first administration of IMP
(Day 1)
23. Subjects who have received a live vaccine in the 28 days prior to Day 1.
24. Plasma donation within one month of screening or blood donation (or corresponding
blood loss) =400mL during the three months prior to screening.
25. Subjects who do not have suitable veins for multiple venepunctures/cannulation as
assessed by the investigator or designee at screen.
26. Subject has dietary restrictions incompatible with the diet that can be provided by
the study site, in the opinion of the Investigator or is unwilling to refrain from
consuming restricted foods and beverages during the study
27. Regular excessive caffeine consumption defined by a daily intake of >5 cups of
caffeine containing beverages.
28. Known history of intolerance or hypersensitivity to macrolides, EP395 or to any other
component of the formulation.
29. Known history of intolerance to lactose.
30. Clinically significant serious adverse reaction, allergy or serious hypersensitivity,
including to any drug or food, as judged by the Investigator or designee.
31. Involvement in the planning and conduct of the study (applies to all EpiEndo, CRO or
investigational site staff).
32. Participation in another clinical study with an experimental drug within three months
or 5 half-lives, whichever is shorter, before the administration of IMP.
33. Considered unsuitable for entry into the study in any other way at the discretion of
the principal investigator or designee, e.g. investigator considers the subject
unlikely to comply with study procedures, restrictions and requirements.
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