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CBP-4888 Use to tREat PreEclampsia (CUREPE-01) An open-label, dose finding study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single ascending subcutaneous doses of CBP-4888 in hospitalized participants with preterm preeclampsia receiving standard of care, expectant management.

Project: Research

Project Details

StatusNot started

Clinical Trial Phase

  • External Sponsor
  • Phase I