Condition: End Stage Kidney Disease (ESKD) · Sponsor: CSL Behring
This is a phase 1b, partial-blind (Sponsor unblinded), randomized, multicenter, placebo-controlled study. The primary objective of this study is to evaluate the pharmacokinetics (PK) of CSL300 after single and multiple doses in Chinese participants with end stage kidney disease (ESKD) undergoing dialysis.
This description comes directly from the study's public registry record.
Trial Registration Coordinator · +16108784697 · clinicaltrials@cslbehring.com
Always discuss trial participation with your own doctor first.
| Peking University People's Hospital | Beijing, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07619820