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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

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Trial Profile

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

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 15 Jan 2026

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At a glance

  • Drugs CBP-4888 (Primary)
  • Indications Preeclampsia
  • Focus Adverse reactions
  • Sponsors Comanche Biopharma

Most Recent Events

  • 22 Dec 2025 Status changed from not yet recruiting to recruiting.
  • 15 Dec 2025 Status changed from planning to not yet recruiting.
  • 22 Jan 2024 New trial record

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