A Study to Evaluate the Effect of Age on the Pharmacokinetics, Safety and Tolerability of IV Rivipansel.
Completed · Phase 1
Conditions studied: Healthy
In brief
The purpose of this study is to evaluate the effect of age on PK, safety and tolerability of IV rivipansel.
Key facts
- Study ID
- NCT02998099
- Run by
- GlycoMimetics Incorporated
- People needed
- 16
- Starts
- 2017-01-01
- Expected to finish
- 2017-03-01
- Last updated by the study team
- 2020-06-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy female subjects of non-childbearing potential or healthy male subjects who are between the ages of 18-45 years or 65 years of age or older.
- Body mass index (BMI) of 17.5 to 40 kg/m2
You may not qualify if…
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at the time of dosing).
- Pregnant females; breastfeeding female subjects; male subjects with partners currently pregnant
- Treatment with another investigational drug within 30 days or 5 half-lives preceding the dose of study medication
- Blood donation within 60 days prior to dosing.
Where it is running
- Orlando Clinical Research Center — Orlando, Florida, United States
Full record on ClinicalTrials.gov
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