Condition: Familial Chylomicronemia Syndrome (FCS) · Sponsor: CorrectSequence Therapeutics Co., Ltd
This is an open-label, single-arm, dose-escalation Phase I clinical trial to evaluate the safety, tolerability, pharmacodynamics (PD), and pharmacokinetics (PK) of CS-121, an in vivo base editing therapy delivered by lipid nanoparticles targeting APOC3, in adult participants (18-55 years) with familial chylomicronemia syndrome (FCS).
This description comes directly from the study's public registry record.
Yaliang Li · +8618621046122 · yaliang.li@correctsequence.com
Always discuss trial participation with your own doctor first.
| The First Affiliated Hospital of Anhui Medical University | Hefei, Anhui, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07176923