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Phase 3 Completed N=496 Randomized Double-blind Treatment

Phase 3 Study of BI 207127 in Combination With Faldaprevir and Ribavirin for Treatment of Patients With Hepatitis C Infection, Including Patients Who Are Not Eligible to Receive Peginterferon: HCVerso2

Hepatitis C, Chronic
Source: ClinicalTrials.gov NCT01728324 ↗
Enrolled (actual)
496
Serious AEs
5.4%
Results posted
Feb 2016
Primary outcomePrimary: SVR12 Rates With Historical Control — 79.95; 76.68; 88.28; 70.78 percentage of participants — p=<0.0001

Summary

The aim of the study is to confirm efficacy and safety of treatment with 600 mg of BID BI 207127 in combination with 120 mg QD FDV and RBV for 16 or 24 weeks in target chronically infected HCV GT1b treatment naïve patients, including patients with compensated cirrhosis.

Outcome Measures

OutcomeResultp-value
PRIMARY
SVR12 Rates With Historical Control
79.95; 76.68; 88.28; 70.78 <0.0001 sig
PRIMARY
Comparisons of SVR12 Rates Across Treatment Arms
82.0; 75.6; 73.6 0.0532
SECONDARY
SVR4: Plasma HCV RNA Level <25 IU/mL at 4 Weeks After EOT.
83.9; 80.3; 77.8 0.1671
SECONDARY
SVR24: Plasma HCV RNA Level <25 IU/mL at 24 Weeks After EOT.
81.0; 74.2; 72.2 0.0447 sig
SECONDARY
Prognostic Value of SVR12 Predicting SVR24
99.0; 99.0; 98.0

Eligibility Criteria

Inclusion criteria

  • Chronic hepatitis C infection, diagnosed by positive anti-HCV antibodies and detected HCV RNA at screening
  • HCV infection of sub-GT1b confirmed by genotypic testing at screening.
  • HCV viral load =1, 000 IU/mL at randomisation.
  • Patients who have never been previously treated with any other HCV treatment regimen.

Exclusion criteria

  • HCV infection of mixed GT (1/2, 1/3, and 1/4) diagnosed by genotypic testing at screening.
  • HCV infection of sub-GT1a, mixed GT1a/1b, or undefined GT1.
  • Liver disease due to causes other than chronic HCV infection.
  • HIV infection.
  • Hepatitis B virus infection based on presence of HBs-Ag.
  • Confirmed or suspected active malignancy or history of malignancy within the last 5 years prior to screening.
  • History of illicit drug abuse other than cannabis or chronic alcohol abuse within 12 months prior to randomisation.
  • Subject is not willing to comply with the precautionary measures to prevent photosensitivity (avoid excessive sun exposure and use sun block on a daily basis).
  • Decompensated liver disease, or history of decompensated liver disease.
  • Clinical evidence of unstable cardiovascular disease which may further decompensate due to anemia.
  • Red blood cell disorders.
  • Body weight 125 kg.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01728324). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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