ABBVIE INITIATES ENROLLMENT OF SIX GLOBAL PHASE 3 CLINICAL STUDIES FOR ONCE-DAILY, PAN-GENOTYPIC HEPATITIS C REGIMEN

ABBVIE INITIATES ENROLLMENT OF SIX GLOBAL PHASE 3 CLINICAL STUDIES FOR ONCE-DAILY, PAN-GENOTYPIC HEPATITIS C REGIMEN

- THE ENDURANCE AND EXPEDITION PHASE 3 CLINICAL STUDIES EVALUATE THE INVESTIGATIONAL REGIMEN OF ONCE-DAILY CO-FORMULATED ABT-493 AND ABT-530 IN PATIENTS WITH HEPATITIS C GENOTYPES 1-6

- NEW INVESTIGATIONAL REGIMEN EVALUATES TREATMENT DURATIONS OF 12 WEEKS AND AS SHORT AS EIGHT WEEKS IN GENOTYPE 1 PATIENTS

Jan 11, 2016

NORTH CHICAGO, Ill., Jan. 11, 2016 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global biopharmaceutical company, today announced the initiation of six global Phase 3 clinical studies evaluating the safety and efficacy of its all-oral, once-daily, ribavirin-free investigational hepatitis C virus (HCV) regimen, ABT-493, an NS3/4A protease inhibitor, and ABT-530, an NS5A inhibitor, in patients with genotypes 1-6 (GT1-6) chronic HCV infection.

"We believe AbbVie's work in hepatitis C has contributed to the transformation of HCV care over the last few years," said Michael Severino, M.D., executive vice president, research and development and chief scientific officer, AbbVie. "Our journey continues with the initiation of these Phase 3 studies, which we hope will help us meet the needs of an even broader range of patients living with hepatitis C."

The ENDURANCE and EXPEDITION studies are part of AbbVie's Phase 3 HCV pipeline program and will recruit approximately 1,600 patients globally, from over 250 study sites and in 27 countries. The primary efficacy endpoint of all six studies is rate of sustained virologic response at 12 weeks post-treatment (SVR12).

The four ENDURANCE studies evaluate AbbVie's investigational regimen in patients without cirrhosis for up to 12 weeks. ENDURANCE-1 compares SVR in GT1 chronic HCV infected patients who received ABT-493/ABT-530 treatment durations of 12 weeks and as short as eight weeks. ENDURANCE-2 evaluates AbbVie's investigational regimen versus placebo in GT2 chronic HCV infected patients. ENDURANCE-3 compares AbbVie's investigational regimen with sofosbuvir/daclatasvir in treatment-naïve patients with GT3 chronic HCV infection. ENDURANCE-4 evaluates GT4-6 chronic HCV infected patients.

The EXPEDITION trials evaluate AbbVie's investigational regimen for 12 weeks in difficult to treat patient populations with chronic HCV infection. EXPEDITION-1 evaluates AbbVie's investigational regimen in GT1, 2, 4-6 chronic HCV infected patients with compensated cirrhosis (Child-Pugh A). EXPEDITION-4 evaluates GT1-6 chronic HCV infected patients with severe renal impairment and end-stage renal disease, with or without compensated cirrhosis.

More information on the studies is available at www.clinicaltrials.gov (NCT02604017, NCT02640482, NCT02640157, NCT02636595, NCT02642432, NCT02651194).

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