U.S., Nov. 20 -- ClinicalTrials.gov registry received information related to the study (NCT07235059) titled 'Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of OJR520 in Healthy Volunteers and Participants With Chronic Kidney Disease' on Nov. 14.
Brief Summary: The purpose of this first-in-human (FIH) study is to evaluate safety, tolerability, pharmacokinetic (PK) of OJR520.
Study Start Date: Nov. 18
Study Type: INTERVENTIONAL
Condition:
Chronic Kidney Disease
Intervention:
DRUG: OJR520
Participants will receive OJR520 in different dose levels.
OTHER: Placebo
Participants will receive OJR520 matching placebo.
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Novartis Pharmaceuticals
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