To calculate the efficacy and safety of ABT-493/ABT-530 for HCV in Japan, Randmised non-blinded multicenter trial

To calculate the efficacy and safety of ABT-493/ABT-530 for HCV in Japan, Randmised non-blinded multicenter trial - The efficacy and safety of ABT-493/ABT-530 for HCV genotype 1. (CERTAIN-1)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000022567

Enrollment

Registered

2016-06-01

Start date

2016-06-06

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCV

Interventions

ABT-493/ABT-530 treatment for 12 weeks. CH or LC. LDV/SOF treatment for 12 weeks. CH or LC.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: CH or LC

Exclusion criteria

Exclusion criteria: HCC

Design outcomes

Primary

Measure	Time frame
SVR of 12 weeks with after treatment	—

Countries

Japan

Contacts

Public ContactMichiharu Komatsu

Shinshu University of Medicine Gastroenterology

komichi@shinshu-u.ac.jp0263-37-2634

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026