Safety and Pharmacokinetics of VNRX-5133 in the Epithelial Lining Fluid of Healthy Adult Subjects

NCT ID: NCT03870490

Last Updated: 2019-05-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-03-14
• Study Completion Date: 2019-04-01

Brief Summary

This is a single-center, open-label study to assess safety and pharmacokinetics of VNRX-5133 and cefepime in the epithelial lining fluid in healthy adult male and female subjects.

Conditions

Healthy Subjects

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Healthy Subjects

VNRX-5133 + cefepime

Group Type: EXPERIMENTAL

VNRX-5133 + cefepime

Intervention Type: DRUG

IV infusion (3 doses)

Interventions

VNRX-5133 + cefepime

IV infusion (3 doses)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Willing to participate in the trial, give written informed consent, and comply with the trial restrictions
• Gender: male or female with a negative serum pregnancy test (β-human chorionic gonadotropin [β-hCG]) at Screening and Day -1; females may be of childbearing potential or of nonchildbearing potential
• Age: ≥18 years at Screening
• Weight: ≥50 kg
• Body mass index (BMI): ≥18 kg/m2 and <30 kg/m2
• Normal blood pressure (BP), defined as a systolic value ≥90 mm Hg and ≤140 mm Hg and a diastolic value <90 mm Hg (Screening and Day -1)
• All values for hematology and clinical chemistry tests of blood and urine are either within normal limits of laboratory reporting range (WNL) or defined as permitted exceptions
• Ability and willingness to abstain from alcohol, from 48 hours (2 days) prior to admission to the Clinical Research Center (CRC) until discharge from the CRC
• Males who are not surgically sterilized and females of childbearing potential must agree to use highly effective methods of contraception during this trial and for 90 days after the last dose of study drug
• All over-the-counter (OTC) medications, health supplements, and herbal remedies (eg, St. John's Wort extract) must have been stopped at least 14 days prior to admission to the CRC
• Suitable veins for cannulation/multiple venipunctures as assessed by the Investigator at Screening

Exclusion Criteria

• Employee of the Contract Research Organization (CRO), CRC, or the Sponsor
• Female who is pregnant, lactating, or at risk of becoming pregnant during this trial or within 90 days after the last dose of study drug
• Male with a female partner who is pregnant or lactating during this trial or planning to attempt to become pregnant during this trial or within 90 days after the last dose of study drug
• Use of any investigational drug or device within 30 days prior to Screening (90 days for an injectable biological agent)
• Presence of a congenital or acquired immunodeficiency syndrome
• Any evidence or history of clinically significant medical abnormalities on PE or laboratory assessment
• Clinically significant ECG abnormality
• Sitting systolic BP >140 mm Hg or diastolic BP >90 mm Hg on a single measurement following at least 5 minutes of rest at Screening
• History of drug allergy of a severity that required urgent medical treatment such as treatment with epinephrine in an Emergency Department
• History of any hypersensitivity reaction following administration of a cephalosporin, penicillin, or other β-lactam antibacterial drug or any component of VNRX-5133 for injection formulation
• History of hypersensitivity to lidocaine, midazolam, fentanyl, or other topical anesthetics/opioids in similar classes to these agents
• Use of prescription or nonprescription drugs, vitamins, or dietary supplements within 14 days prior to the first dose of study drug
• History of donation of >450 mL of blood within 60 days prior to first dose of study drug or planned donation before 30 days has elapsed since final dose of study drug
• Plasma or platelet donation within 7 days of first dose of study drug or planned donation during this trial
• Current suspected drug or alcohol abuse as specified in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision criteria
• Recent history of alcohol consumption exceeding 7 drinks/week for females or 14 drinks/week for men (1 standard drink=5 ounces of wine or 12 ounces of beer or 1.5 ounces of hard liquor) within 6 months before Screening
• Use of tobacco- or nicotine-containing products from Screening through Check Out

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institutes of Health (NIH)

NIH

Sponsor Role: collaborator

Venatorx Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Hartford Hospital

Hartford, Connecticut, United States

Countries

United States

Other Identifiers

272201300019C-17-0-3

Identifier Type: NIH

Identifier Source: secondary_id

View Link

18-0001

Identifier Type: OTHER

Identifier Source: secondary_id

VNRX-5133-106

Identifier Type: -

Identifier Source: org_study_id