Study of Seraprevir in Combination With Sofosbuvir in Chronic Genotype 1 Hepatitis C Virus Infection Patients
- Registration Number
- NCT04001608
- Lead Sponsor
- Ginkgopharma CO., LTD
- Brief Summary
This study was to assess the safety and efficacy of Seraprevir in combination with sofosbuvir administered for 12 weeks in patients with Hepatitis C (HCV) genotype1. Efficacy was assessed by the rate of sustained viral response (SVR) 12 weeks after the discontinuation of therapy (SVR12).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 206
- Hepatitis C virus (HCV) genotype 1 infection (confirmed at screening).
- HCVRNA greater than 10,000 IU/mL at screening.
- Participant must be willing and able to comply with the protocol requirements.
- weight was more than 40 kg.
- age is between 18-75,either sex.
- Co-infection with hepatitis B virus or human immunodeficiency virus (HIV).
- Infection with HCV non-genotype 1,or Infection with mixed genotype,or Genotype cannot be confirmed.
- Medical history of major functional organ transplantation.
- Suffering from serious blood system disease(such us Thalassemia/Sickle Cell Anemia).
- Participation in a clinical study within 3 months prior to first dose
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Seraprevir and sofosbuvir Seraprevir Subjects will receive oral tablets of Seraprevir 100mg twice a day along with oral tablet of sofosbuvir 400 mg,once a day from Day 1 up to Week 12. Seraprevir and sofosbuvir Sofosbuvir Subjects will receive oral tablets of Seraprevir 100mg twice a day along with oral tablet of sofosbuvir 400 mg,once a day from Day 1 up to Week 12.
- Primary Outcome Measures
Name Time Method Percentage of Participants Achieving a Sustained Virologic Response 12 Weeks After the Actual End of TreatmentοΌSVR12οΌ Posttreatment Week 12 SVR12 is defined as HCV RNA \< the lower limit of quantification (LLOQ; ie, \< 15 IU/mL) 12 weeks following the last dose of study drug.
- Secondary Outcome Measures
Name Time Method Percentage of Participants Achieving a On-treatment Virologic Response week 1,week 2,week 4,week8,week 12 Percentage of participants who achieved HCV RNA \<LLOQ at week 1,week 2,week 4,week8,week 12.
Percentage of Participants Achieving a Sustained Virologic Response 4 Weeks After the Actual End of Treatment (SVR4) Posttreatment Week 4 SVR4 is defined as HCV RNA \< LLOQ at 4 weeks following the last dose of study drug.
Trial Locations
- Locations (22)
The First Affiliated Hospital Of Guangxi Medical University
π¨π³Guangxi, Nanning, China
Traditional Chinese Medical Hospital Affiliated To Southwest Medical University
π¨π³Luzhou, Sichaun, China
The First Hospital Of Hebei Medical University
π¨π³Shijiazhuang, Hebei, China
Beijing Ditan Hospital,Capital Medical University
π¨π³Beijing, Beijing, China
The Sixth People's Hospital Of Zhengzhou
π¨π³Zhengzhou, Henan, China
Wuxi No.5 People's Hospital
π¨π³Wuxi, Jiangsu, China
Tongji Hospital Affiliated To Tongji Medical College Huazhong University Of Science And technology
π¨π³Wuhan, Hubei, China
Beijing Friendship Hospital,Capital Medical University
π¨π³Beijing, Beijing, China
Wuhan Medical Treatment Center
π¨π³Wuhan, Hubei, China
Chongqing Public Health Medical Center
π¨π³Chongqing, Chongqing, China
Chongqing Sanxia Center Hospital
π¨π³Chongqing, Chongqing, China
Affiliated Hospital Of Zunyi Medical University
π¨π³Zunyi, Guizhou, China
Beijing YouAn Hospital ,Capital Medical University
π¨π³Beijing, Beijing, China
Liuzhou General Hospital
π¨π³Liuzhou, Guangxi Zhuang Autonomous Region, China
The Affiliated Hospital OF Xuzhou Medical University
π¨π³Xuzhou, Jiangsu, China
The first hospital of JILIN university.
π¨π³Changchun, Jilin, China
Chengdu Public Health Medical Center
π¨π³Chendu, Sichuan, China
Sichuan Province General Hospital
π¨π³Chengdu, Sichuan, China
First Affiliated Hospital Of Xinjiang Medical University
π¨π³ΓrΓΌmqi, Xinjiang, China
Traditional Chinese Medical Hospital Uygur Autonomous Region
π¨π³ΓrΓΌmqi, Xinjiang, China
Huzhou Center Hospital
π¨π³Huzhou, Zhejiang, China
First Hospital Of Shanxi Medical University
π¨π³Taiyuan, Shanxi, China