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Study identifier: NCT06367465 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Feasibility and Acceptability of HCV Treatment in Pregnancy

Condition: Hepatitis C · Pregnancy Complications  ·  Sponsor: Washington University School of Medicine

PhaseN/A
Planned participants50
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Pregnant adults over the age of 18 who are seen in the Washington University obstetrics and gynecology, maternal fetal medicine or infectious diseases clinic or admitted to BJH with hepatitis C virus infection who have a history of past or current drug use Participant Duration: Approximately 1 year. Aims: Aim 1 - Evaluate adherence and treatment completion rates when glecaprevir-pibrentasvir is started during pregnancy for women who use drugs. Aim 2 - Evaluate patient experience with hepatitis C virus treatment during pregnancy.

This description comes directly from the study's public registry record.

Talk to the study team

Tracey Bach, MBA  ·  314-273-6075  ·  habrockt@wustl.edu

Laura Marks, MD, PhD  ·  marks@wustl.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Barnes Jewish HospitalSt Louis, Missouri, United StatesRecruiting
Washington UniveristySt Louis, Missouri, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06367465