Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia

NCT: NCT06580405 · NOT_YET_RECRUITING

NCT IDNCT06580405
StatusNOT_YET_RECRUITING
Start Date2026-10-01
Completion2029-11-30
SponsorKaneka Medical America LLC (INDUSTRY)
First posted
Last updated

Brief Summary

The study will primarily evaluate safety of the KNP-1000 apheresis system for pregnant women and their fetuses diagnosed with preeclampsia with severe features between 23- and 32-weeks' gestation (very preterm).

Frequently Asked Questions

What is A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia?

A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia is a clinical trial registered under NCT06580405. Current status: NOT_YET_RECRUITING.

What is the status of NCT06580405?

The current status of NCT06580405 (A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia) is: NOT_YET_RECRUITING.

When did A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia start?

A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia started on 2026-10-01.

Related Devices

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.