Condition: sFlt1 Mediated Preterm Preeclampsia · Preeclampsia · Preterm Preeclampsia · Sponsor: Comanche Biopharma
This study is a dose finding study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of subcutaneous CBP-4888 in hospitalized participants with Preterm Preeclampsia receiving Standard of Care, Expectant Management. Eligible participants are between 26 +0/7 and 35 +6/7 weeks gestational age and clinically appropriate for inpatient expectant management. Eligible participants will receive standard of care expectant management for their pregnancy with the only study interventions being one subcutaneous dose of CBP-4888. Participants will: * receive a single subcutaneous injection dose of CBP-4888 and will be followed through delivery and for 42 days (+14 days) after delivery. Participants will be followed through 6 weeks post delivery. * Infants will be evaluated immediately postpartum and then followed through 24 months of age with standard infant and pediatric assessments with phone calls made to parents.
This description comes directly from the study's public registry record.
Aparna Shah, MD · 248-520-7361 · ashah@comanchebiopharma.com
Always discuss trial participation with your own doctor first.
| The Royal Women's Hospital | Parkville, Victoria, Australia | Recruiting |
| Monash University | Melbourne, Australia | Recruiting |
| Royal Melbourne | Melbourne, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07282171