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eGFR Evolution in HCV Patients Receiving SOF-based or SOF-free DAAs

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National Taiwan University

Status

Completed

Conditions

Hepatitis C
Renal Disease
Viral Hepatitis C

Treatments

Drug: Elbasvir / Grazoprevir Oral Tablet
Drug: Ombitasvir/paritaprevir/ritonavir
Drug: Sofosbuvir / Velpatasvir Oral Tablet
Drug: Glecaprevir and Pibrentasvir
Drug: Sofosbuvir Tablets
Drug: Sofosbuvir and Ledipasvir

Study type

Observational

Funder types

Other

Identifiers

NCT04047680
201509009RINB

Details and patient eligibility

About

Data regarding the nephrotoxicity of sofosbuvir (SOF) remain controversial. The investigators compared the changes of estimated glomerular filtration rate (eGFR) in patients with chronic hepatitis C virus (HCV) infection receiving SOF-based or SOF-free direct acting antivirals (DAAs).

Full description

Chronic hepatitis C virus (HCV) infection is a major health problem that affects 71 million people worldwide. Patients with chronic HCV infection may present with various hepatic and extrahepatic manifestations which lead to substantial morbidity and mortality. In contrast, the long-term health outcome improves following successful HCV eradication by antiviral therapies.

Owing to the excellent efficacy and safety as well as the short treatment duration, the use of interferon (IFN)-free direct acting antivirals (DAAs) has become the standard-of-care for managing HCV. Sofosbuvir (SOF) is a pyrimidine nucleotide analogue which acts as the HCV ribonucleic acid (RNA) chain terminator by inhibiting HCV non-structural protein 5B (NS5B) RNA-dependent RNA polymerase following intrahepatic activation to uridine triphosphate form. Dephosphorylation results in the formation of inactive metabolite (GS-331007) that undergoes extensive renal excretion. Clinically, SOF is administered once-daily with pangenotypic potency, well tolerability and a high genetic barrier to drug resistance. Furthermore, SOF can be used in combination with NS3/4A protease inhibitors (PIs), NS5A inhibitors, and/or ribavirin (RBV) to achieve high rates of sustained virologic response (SVR). Therefore, applying SOF-based DAAs for HCV is welcome to most treating physicians.

Following the widespread use of SOF-based DAAs for treating HCV in different populations, a large-scale real-world HCV-TARGET study enrolling 1,789 patients indicated that patients with a baseline eGFR ≤ 45 mL/min/1.73m2 were associated with a higher risk of worsening renal function than those with a baseline eGFR > 45 mL/min/1.73m2 following SOF-based DAAs. Moreover, three retrospective studies showed that SOF-based DAAs negatively affected the on-treatment and off-therapy eGFR. On the contrary, other studies showed that the use of SOF-based DAAs did not worsen the eGFR. Because most studies were retrospective in nature without protocol-defined time point for eGFR assessment or patient election, and did not enroll patients receiving SOF-free DAAs as the controls, the investigators thus conducted a prospective study to evaluate the evolution of eGFR in patients with chronic HCV infection receiving SOF-based or SOF-free DAAs.

Enrollment

441 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic HCV patients receiving SOF-based or SOF-free DAAs for 12 weeks

Exclusion criteria

  • Decompensated cirrhosis (Child-Pugh B or C)
  • Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73m2
  • Active hepatocellular carcinoma (HCC)
  • Organ transplantation
  • Hepatitis B virus (HBV) co-infection
  • Human immunodeficiency virus (HIV) co-infection
  • Not received off-therapy follow-up till week 24

Trial design

441 participants in 2 patient groups

SOF-based DAAs
Description:
Patients receiving sofosbuvir (SOF)-based direct acting antiviral agents (DAAs) for 12 weeks
Treatment:
Drug: Sofosbuvir and Ledipasvir
Drug: Sofosbuvir Tablets
Drug: Sofosbuvir / Velpatasvir Oral Tablet
SOF-free DAAs
Description:
Patients receiving sofosbuvir (SOF)-free direct acting antiviral agents (DAAs) for 12 weeks
Treatment:
Drug: Glecaprevir and Pibrentasvir
Drug: Ombitasvir/paritaprevir/ritonavir
Drug: Elbasvir / Grazoprevir Oral Tablet

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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