A Phase 1, Open-Label Study to Assess the Single-Dose Pharmacokinetics of Eravacycline in Subjects With Impaired Hepatic Function and Healthy Subjects

NCT02135302 | Completed Phase 1

• 1 other identifier: TP-434-013
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 3

Brief Summary

This is a multi-center, open-label clinical study to assess the single-dose PK of eravacycline in subjects with hepatic impairment and healthy subjects conducted at approximately 3 sites in the United States. This study includes an up to 21-day Screening Period, a 5-day Treatment Period, and an End of Study Visit occurring approximately 2 weeks (± 2 days) after initiation of study drug administration. Approximately 24 subjects will be enrolled: 18 subjects with impaired hepatic function (6 subjects who meet the criteria for each of the 3 Child-Pugh categories of mild \[5 - 6 points\], moderate \[7 - 9 points\], and severe \[10 - 15 points\]) and 6 healthy subjects without hepatic impairment. Healthy subjects will be matched to hepatically impaired subjects in gender, age, and body mass index (BMI). All subjects will be administered a single IV dose of eravacycline (1.5 mg/kg).

Conditions

Impaired Hepatic Function

Keywords

hepatic

Outcome Measures

Primary Outcomes (1)

• This study is being conducted to assess the pharmacokinetic (PK) profile of eravacycline

  To assess the pharmacokinetic (PK) profile of eravacycline after administration of a single intravenous (IV) dose (1.5 mg/kg) to subjects with mild, moderate, and severe impaired hepatic function compared with normal healthy subjects

  one year

Secondary Outcomes (1)

• Safety and tolerability of Eravacycline

  one year

Study Arms (2)

Impaired hepatic function

EXPERIMENTAL

A single 1.5 mg/kg dose of eravacycline will be administered intravenously on Day 1 as a 60 minute infusion to each hepatically impaired subject.

Drug: eravacycline

Healthy subjects

EXPERIMENTAL

A single 1.5 mg/kg dose of eravacycline will be administered intravenously on Day 1 as a 60 minute infusion to each healthy subject.

Drug: eravacycline

Interventions

eravacycline DRUG

Eravacycline (TP-434) is a parenteral and oral antibiotic of the tetracycline class that is highly active in vitro and in established animal infection models against both nosocomial and community-acquired methicillin-susceptible or -resistant Staphylococcus aureus strains, vancomycin-susceptible or -resistant Enterococcus faecium and Enterococcus faecalis, and penicillin-susceptible or -resistant strains of Streptococcus pneumoniae. In addition, eravacycline is highly active against clinically important species of Enterobacteriaceae (including those isolates that produce extended-spectrum β-lactamases and/or are carbapenem-resistant), Acinetobacter baumannii, and anaerobes.

Also known as: TP-434

Healthy subjects; Impaired hepatic function

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female subject aged ≥18 years at Screening;
• 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;
• 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;
• Female subjects of childbearing potential (including females with questionable postmenopausal status) must have a negative pregnancy test prior to dosing (Screening and Day -1);
• Has a body mass index of 17 kg/m2 to 40 kg/m2, inclusive;
• Has negative alcohol and illicit drug screens;
• Has a negative screen for Human immunodeficiency virus (HIV);
• Is able to understand and comply with study procedures and give written informed consent according to institutional and regulatory guidelines;
• Subjects with hepatic impairment:
• 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);
• 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:

You may not qualify if:

• Female subjects who are pregnant, breastfeeding, or planning to become pregnant during the course of the study;
• 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;
• Evidence of renal impairment with a creatinine clearance of \<50 mL/min/1.73m2 as measured by the Cockcroft Gault formula;
• 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;
• Has a history of alcoholism or drug abuse within 2 years prior to dosing;
• 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);
• Use of alcohol within 48 hours prior to dosing;
• Has had a major surgical procedure within 3 months prior to administration of study drug;
• Has known allergies to tetracycline antibiotic or related compounds, or a history of multiple adverse drug allergies of any origin;
• Has inadequate venous access;
• Donated \>500 mL of blood within 2 months prior to Screening;
• 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;
• Is a member of the clinical site personnel directly affiliated with this study;
• 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;
• Fails to comply with protocol requirements, or whose further participation in the study would be unsuitable to the subject, as determined by the investigator;

Sponsors & Collaborators

• Tetraphase Pharmaceuticals, Inc: lead

Study Sites (3)

Davita Clinical Research

Lakewood, Colorado, 800228, United States

Location

Orlando Clinical Research Center

Orlando, Florida, 32809, United States

Location

New Orleans Center for Clinical Research

Knoxville, Tennessee, 37920, United States

Location

MeSH Terms

Interventions

eravacycline

Study Officials

• William Smith, MD

  New Orleans Center for Clinical Research

  PRINCIPAL INVESTIGATOR

• Thomas Marbury, MD

  Orlando Clinical Research Center

  PRINCIPAL INVESTIGATOR

• Chris Galloway, MD

  Davia Clinical Research

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 5, 2014
• First Posted: May 9, 2014
• Study Start: October 1, 2013
• Primary Completion: February 1, 2014
• Study Completion: March 1, 2014
• Last Updated: December 17, 2021

Record last verified: 2021-12

Locations

US (3)