Expired Study
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Overland Park, Kansas 66211


Purpose:

The objective of this study is to evaluate the safety and tolerability of RNS60 administered intravenously to healthy subjects. 12 subjects will receive RNS60 or placebo at three escalating rates for 48 hours for each rate.


Criteria:

Inclusion Criteria: - Males between 18-55 years - Minimum body weight of 60 kg - BMI of 18-32 kg/m2 - Able to execute informed written consent Exclusion Criteria: - A chronic or acute disease that might interfere with the evaluation of the safety of RNS60 - Current or prior malignancies (excluding history of treated non-melanoma skin carcinoma) - Positive viral serology test for HBsAG, Hep C antibody, Hep A IgM, or HIV - Use of any prescription medications within 2 weeks of the first day of dosing - Significant organ dysfunction, including cardiac, renal, liver, CNS, pulmonary, vascular, GI, endocrine or metabolic - Treatment with monoclonal antibody therapy within 5 half-lives prior to the first dose of study medication - Treatment with any investigational drugs or therapies within 30 days (or 5 half-lives, whichever is greater) prior to the first dose of study medication - Abnormal pre-admission vital signs, physical exam, clinical laboratory, or any safety variable considered clinically significant for this population by the PI - Subject is considering or has scheduled any surgical procedure during participation in study - History of alcohol and/or dug abuse within 1 year prior to first dose of study medication - Subject has donated plasma or blood within 30 days prior to first dose of study medication - Subject requires treatment with any medications, either prescription or nonprescription, including dietary supplements or herbal medications, within 14 days prior to the first dose of study medication. Exceptions are nonprescription topical medications (that are not systemically absorbed), acetaminophen, or vitamins at recommended daily doses (not mega dose vitamins) - A positive qualitative urine drug or alcohol test - Concurrent enrollment in any other clinical trial - Subject is judged by PI or Medical Monitor to be inappropriate for the study - - Subject has Gilbert's syndrome - Subject has estimated creatinine clearance at screening of <90 mL/min.


NCT ID:

NCT01264783


Primary Contact:

Principal Investigator
Kelly Craven, M.D.
Quintiles


Backup Contact:

N/A


Location Contact:

Overland Park, Kansas 66211
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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