Condition: Chronic Hepatitis D · Sponsor: Karolinska University Hospital
The aim is to assess the efficacy and specific safety in an observational study of patients with Chronic hepatitis D (CHD) with prospective follow-up, with antiviral treatment of 2 mg Bulevirtide (BLV) +/- PEG-IFNα-2a and +/- NA given as part of the patient's routine medical care. Also, explorative endpoints of biomarkers in peripheral blood, saliva, fecal sample and/or intrahepatic markers/signatures, and quality of life outcomes will be assessed.
This description comes directly from the study's public registry record.
Soo Aleman, MD, PhD · +46 72-595 72 25 · soo.aleman@regionstockholm.se
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| Karolinska University Hospital, Department of Infectious Diseases | Stockholm, Sweden | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06051045