A Study to Evaluate the Effect of IV Doses of Rivipansel on Subjects With Renal Impairment and in Healthy Subjects
Completed · Phase 1
Conditions studied: Renal Impairment, Healthy
In brief
The purpose of this study is to determine the effect of renal impairment on rivipansel.
Key facts
- Study ID
- NCT02813798
- Run by
- GlycoMimetics Incorporated
- People needed
- 28
- Starts
- 2016-06-01
- Expected to finish
- 2018-02-01
- Last updated by the study team
- 2020-06-18
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Female subjects of non-childbearing potential or male subjects
- Body Mass Index (BMI) of 17.5 to 40.0 kg/m2
- Stable renal function
You may not qualify if…
- A positive urine drug screen for illicit drugs
- Treatment with an investigational drug within 30 days of the dose of study medication
- Pregnant females, breastfeeding female subjects and male subjects with partners currently pregnant
- Use of herbal supplements in the 28 days prior to the dose of study medication
- Blood donation (excluding plasma donation) of approximately 1 pint or more within 56 days prior to study medication
- Requiring dialysis
Where it is running
- Anaheim Clinical Trials, LLC — Anaheim, California, United States
- Avail Clinical Research, LLC — DeLand, Florida, United States
- Orlando Clinical Research Center — Orlando, Florida, United States
Full record on ClinicalTrials.gov
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