RIBAVIRIN PLUS INFERGEN FOR NAIVE CHRONIC HEPATITIS C

$0M01FY2000RRNIH

Scripps Research Institute, La Jolla CA

Investigators

Linked publications & trials

Paper 21743843 Paper 20729202 Paper 20671544 Paper 19725955 Paper 19638630 Paper 19601917 Paper 19380829 Paper 19201908 Paper 19110882 Paper 18572749 Paper 18032230 Paper 18000612 Paper 17707394 Paper 17566187 Paper 17417061 Paper 17286337 Paper 17196788 Paper 17167091 Paper 17087525 Paper 17085285 Paper 17072763 Paper 17069096 Paper 16824189 Paper 16764678 Paper 16704731 Paper 16540354 Paper 16472381 Paper 16447184 Paper 16440356 Paper 16420570 Paper 16274834 Paper 16249086 Paper 16210047 Paper 16152757 Paper 16099876 Paper 16086027 Paper 15993396 Paper 15957670 Paper 15885606 Paper 15869602 Paper 15857880 Paper 15845647 Paper 15820680 Paper 15809662 Paper 15809302 Paper 15797250 Paper 15737885 Paper 15722961 Paper 15717930 Paper 15699338 Paper 15596404 Paper 15582126 Paper 15564736 Paper 15563590 Paper 15545608 Paper 15538718 Paper 15528155 Paper 15520293 Paper 15476476 Paper 15466165 Paper 15461631 Paper 15456488 Paper 15447883 Paper 15389814 Paper 15378430 Paper 15324319 Paper 15322500 Paper 15316247 Paper 15307835 Paper 15274051 Paper 15258162 Paper 15254019 Paper 15246277 Paper 15229052 Paper 15226188 Paper 15225163 Paper 15223009 Paper 15220431 Paper 15192150 Paper 15181000 Paper 15178452 Paper 15163749 Paper 15158353 Paper 15158197 Paper 15146422 Paper 15123662 Paper 15123364 Paper 15100149 Paper 15054810 Paper 15031635 Paper 15008601 Paper 14982867 Paper 14726383 Paper 14714613 Paper 14660653 Paper 14636643 Paper 14633776 Paper 14613989 Paper 14607931 Paper 14572816

Abstract

This is a randomized, open-label, multicenter, parallel-group safety study in naive hepatitis C patients. Total of 40 subjects will be enrolled and will receive either 9 mcg of infergen daily or 9 mcg of infergen plus 1200/1000mg of ribavirin daily. Non-genotype I patients receiving combination therapy will be treated for 24 weeks. Genotype I patients will be treated for 48 weeks. Subjects completing treatment III will be followed for an additional 24 weeks to assess presence of sustained viral response. Primary endpoint is to assess the 12 week safety and tolerability profiles of infegen dministered with ribavirin and infergen in naive, chronic Hep C patient population.

View original record on NIH RePORTER →