BENITIONSClinical Trial Intelligence

A Phase 1 Study of MP-424, Peginterferon Alfa 2b, and Ribavirin in Hepatitis C

Phase 1 Completed NCT00630058

ConditionHepatitis C
PhasePhase 1
SponsorTanabe Pharma Corporation
StatusCompleted
Enrollment20 participants
InterventionsMP-424(H), PEG-IFN-a-2b, RBV, MP-424 (L), PEG-IFN-a-2b, RBV
Start dateApr, 2008
Completion dateMar, 2009
Results postedJan 18, 2013

Summary

The purpose of this study is to assess the safety, pharmacokinetics, HCV RNA kinetics, and other viral characteristics after administration of two arms of MP-424 in combination with Peginterferon Alfa 2b (PEG-IFN-a-2b) and Ribavirin (RBV) to patients with chronic hepatitis C.

Cmax (Maximum Observed Concentration in Plasma) of MP-424

Data were collected at Day1 to Day85 · μg/mL

Group A (MP-424 High)1.62 ± 0.43 μg/mL
Group B (MP-424 Low)1.45 ± 0.83 μg/mL
Group A (MP-424 High)3.96 ± 1.10 μg/mL
Group B (MP-424 Low)3.06 ± 0.90 μg/mL
Group A (MP-424 High)3.67 ± 0.87 μg/mL
Group B (MP-424 Low)3.16 ± 1.10 μg/mL

Tmax (Time of Maximum Concentration in Plasma) of MP-424

Data were collected at Day1 to Day85 · hours

Group A (MP-424 High)2.51 hours
Group B (MP-424 Low)2.54 hours
Group A (MP-424 High)2.50 hours
Group B (MP-424 Low)2.45 hours
Group A (MP-424 High)3.24 hours
Group B (MP-424 Low)2.43 hours

AUC 0-8h (Area Under the Concentration-time Curve From Time Zero to 8 Hours) of MP-424

Data were collected at Day1 to Day85 · μg/mL

Group A (MP-424 High)7.53 ± 1.93 μg/mL
Group B (MP-424 Low)6.55 ± 3.73 μg/mL
Group A (MP-424 High)26.00 ± 6.77 μg/mL
Group B (MP-424 Low)19.94 ± 5.97 μg/mL
Group A (MP-424 High)25.00 ± 5.23 μg/mL
Group B (MP-424 Low)21.35 ± 6.88 μg/mL

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