Showing a trial related to 

Closing Soon

Drug for Chronic Hepatitis C, sponsored by AbbVie

Get in touch This trial recruits from May 2016 for 65 weeks

Julie Knapik, MS

Phone: 816-524-0542

Email: julie.knapik@abbvie.com

Eligibility Criteria

Age: From 18 Years To 99 Years

Gender: Both

Inclusion Criteria

  • Male or female, at least 18 years of age at time of screening.

  • Screening laboratory result indicating HCV GT1 - 6 infection.

  • Subject is a recipient of a cadaveric or living donor liver transplant which was a consequence of HCV infection at least 3 months prior to screening Or Subject received a cadaveric or living donor kidney at least 3 months before screening.

  • Subjects must be documented as non-cirrhotic.

  • Subject is currently taking a stable immunosuppression regimen based on tacrolimus, sirolimus, everolimus, mycophenolate mofetil, azathioprine, and/or cyclosporine.

Exclusion Criteria

  • Female subject who is pregnant, breastfeeding or is considering becoming pregnant during the study or for approximately 30 days after the last dose of study drug.

  • Clinical history of fibrosing cholestatic hepatitis post-transplant.

  • Re-transplantation of the liver or kidney.

  • Steroid resistant rejection of the transplanted liver or kidney, or a history of rejection treated with high dose steroid within 3 months of screening.

  • History of post-transplant complications related to hepatic or renal vasculature.

NCT02692703

A Single-Arm, Open-Label, Multicenter Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Liver or Post-Renal Transplant Recipients With Chronic Hepatitis C Virus Genotype 1 - 6 Infection (MAGELLAN-2)

A Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Liver or Post-Renal Transplant Recipients With Chronic Hepatitis C Virus (MAGELLAN-2)

View record on ClinicalTrials.gov