This study was a pilot, safety, and pharmacokinetic study of MB-102 versus iohexol and the use of the non-invasive optical renal function monitor (ORFM) device in normal and compromised renal function participants with different skin color types.
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Number of Participants With Treatment-Emergent Adverse Events
Timeframe: From the time of dosing through the follow-up visit, up to 10 days