U.S., Feb. 4 -- ClinicalTrials.gov registry received information related to the study (NCT07384936) titled 'Topefilgrastim Injection in the Treatment of High-Risk Pregnant Patients With Preeclampsia' on Jan. 19.
Brief Summary: This study is an open-label, prospective investigation designed to enroll 100 high-risk pregnant subjects with preeclampsia (PE). Participants will be allocated in a 2:2:1 ratio to one of three groups: the Topefilgrastim 0.5mg/biweekly group, the Topefilgrastim 1mg/biweekly group, or the control group, based on investigator judgment and patient preference. The overall study consists of three parts: a screening period, a treatment period, and a follow-up period.
Study Start Date: Jan. 31
Study Type: INTERVENTIONAL
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