| Eligibility |
Inclusion Criteria:
1. Male or female subject aged =18 years at Screening;
2. Eligible female subjects of childbearing potential with a non-sterilized male sexual
partner must agree to use 2 medically accepted, effective methods of birth control
(eg, hormonal contraceptive, barrier contraceptive with additional spermicide, or an
intrauterine device) beginning >30 days prior to study drug administration and
continuing until 7 days after the end of the study. Female subjects who are
postmenopausal must have been postmenopausal for >1 year if they wish not to use
contraceptives. If postmenopausal status is questionable, the subject's
follicle-stimulating hormone level must be checked and must be elevated and consistent
with postmenopausal levels (ie, >40 IU/L); otherwise these subjects must agree to use
contraceptives listed above;
3. Male subjects with sexual partners of childbearing potential must agree to use a
barrier contraceptive from the time of study drug administration through 7 days after
the end of the study;
4. Female subjects of childbearing potential (including females with questionable
postmenopausal status) must have a negative pregnancy test prior to dosing (Screening
and Day -1);
5. Has a body mass index of 17 kg/m2 to 40 kg/m2, inclusive;
6. Has negative alcohol and illicit drug screens;
7. Has a negative screen for Human immunodeficiency virus (HIV);
8. Is able to understand and comply with study procedures and give written informed
consent according to institutional and regulatory guidelines;
Subjects with hepatic impairment:
9. Has a positive diagnosis of liver cirrhosis that has been stable for 2 months and is
confirmed by imaging techniques, biopsy, or physical signs consistent with a clinical
diagnosis of liver cirrhosis (eg, liver firmness to palpation, splenic enlargement,
spider angiomata, palmar erythema, parotid hypertrophy, testicular atrophy,
gynecomastia);
10. Subjects with hepatic impairment must be categorized in 1 of the following:
- Mild hepatic impairment: has impaired but stable hepatic function as evidenced by
Child-Pugh Clinical Assessment Score of 5-6 at both Screening and Day -1;
- Moderate hepatic impairment: has impaired but stable hepatic function as
evidenced by Child-Pugh Clinical Assessment Score of 7-9 at both Screening and
Day -1; or
- Severe hepatic impairment: has impaired but stable hepatic function as evidenced
by Child-Pugh Clinical Assessment Score of 10-15 at both Screening and Day -1;
Healthy subjects without hepatic impairment:
11. Must be in good health as determined by screening medical history, physical
examination, vital signs, blood chemistry, hematology, glucose, and coagulation
performance at Screening;
12. Has a negative screen for hepatitis B (HBV) and hepatitis C (HCV); and
13. Should be matched to a subject with hepatic impairment in gender, age, and BMI.
Exclusion Criteria:
1. Female subjects who are pregnant, breastfeeding, or planning to become pregnant during
the course of the study;
2. Has a history or current evidence of clinically significant hematological, renal,
endocrine, pulmonary, gastrointestinal, cardiovascular, neurological, or psychiatric
disease that may pose a significant safety risk or diminish a subject's ability to
undergo all study procedures and assessments;
3. Evidence of renal impairment with a creatinine clearance of <50 mL/min/1.73m2 as
measured by the Cockcroft Gault formula;
4. Use of another investigational drug or device within 30 days prior to receiving
eravacycline (TP-434), or within at least 5 half-lives of the previous investigational
drug, whichever is longer;
5. Has a history of alcoholism or drug abuse within 2 years prior to dosing;
6. Has a typical weekly alcohol consumption of 14 alcoholic drinks. One drink is defined
as 1 glass of beer (approximately 10 oz to 12 oz) or 1 can (12 oz) of beer, 1 glass of
wine (approximately 4 oz to 5 oz), or 1 glass of distilled spirits (hard liquor)
containing 1 oz of the liquor (1 oz of liquid is approximately 30 mL);
7. Use of alcohol within 48 hours prior to dosing;
8. Has had a major surgical procedure within 3 months prior to administration of study
drug;
9. Has known allergies to tetracycline antibiotic or related compounds, or a history of
multiple adverse drug allergies of any origin;
10. Has inadequate venous access;
11. Donated >500 mL of blood within 2 months prior to Screening;
12. Has a change in dose or frequency of any new or chronic dose-adjusted prescription or
non-prescription medication, including vitamins or herbal medications, within 7 days
or 5 half-lives (if known), whichever is longer, within 2 weeks prior to dosing;
13. Is a member of the clinical site personnel directly affiliated with this study;
14. Has poor mental function or any other reason to expect subject difficulty in complying
with the requirements of the study in the judgment of the investigator;
15. Fails to comply with protocol requirements, or whose further participation in the
study would be unsuitable to the subject, as determined by the investigator;
16. Clinically significant abnormal electrocardiograms (ECGs) (QTcB or QTcF >500 msec);
Subjects with hepatic impairment:
17. Has active HCV or HBV and is receiving antiviral therapy (either prescribed or
herbal);
18. Has fluctuating or rapidly deteriorating hepatic function as indicated by clinical
and/or laboratory signs of hepatic impairment (advanced ascites, infection of ascites,
fever, or active gastrointestinal bleeding);
19. Has sodium levels 125 mmol/L;
20. Has platelets <40,000 × 109/L of blood or evidence of severe active or recent
bleeding;
21. Has refractory encephalopathy, as judged by the investigator, or significant central
nervous system disease (eg, dementia or seizures) which the investigator considers to
interfere with informed consent, conduct, completion, or results of this study, or
constitutes an unacceptable risk to the subject;
22. Has signs of active infection;
23. Has experienced esophageal variceal bleeding within the past 6 months;
24. Has a Transjugular Intrahepatic Portosystemic Shunt placement;
Subjects without hepatic impairment:
25. Has aspartate aminotransferase or alanine aminotransferase >1.5 × upper limit of
normal (ULN); alkaline phosphatase or bilirubin 1.5 × ULN (isolated bilirubin >1.5 ×
ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). A single
repeat is allowed for eligibility determination;
26. Has systolic blood pressure outside of the range of 90-160 mmHg, or diastolic blood
pressure outside the range of 45-100 mmHg, or heart rate outside the range of 50-100
bpm for female subjects or 45-100 bpm for male subjects;
27. Has a history of Gilbert's disease; or
28. Takes any concomitant medication, either prescribed or over-the-counter. This includes
use of any prescription or non-prescription medication, including vitamins or herbal
medications, within 7 days or 5 half-lives (if known), whichever is longer, prior to
dosing and within 24 hours after dosing, excluding hormonal contraceptives. The use of
acetaminophen, naproxen, and ibuprofen is permitted except for within 24 hours prior
to dosing.
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