Sofosbuvir and Daclatasvir for Treating Hepatitis C in 200 Patients Co-infected With Human Immunodeficiency Virus (HIV200)
Primary Purpose
Hepatitis C Virus Infection, Response to Therapy of, Human Immunodeficiency Virus
Status
Completed
Phase
Phase 3
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
sofosbuvir and daclatasvir
Sponsored by
About this trial
This is an interventional treatment trial for Hepatitis C Virus Infection, Response to Therapy of
Eligibility Criteria
Inclusion Criteria:
- Positive qualitative hepatitis C virus RNA test on two occasions at least 6 months apart
- Positive human immunodeficiency virus test
Exclusion Criteria:
- Heart rate < 50/min,
- Taking amiodarone
- Renal failure
Sites / Locations
- Shariati Hospital
- Emam Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
sofosbuvir/daclatasvir
Arm Description
Once daily fixed-dose combination pill of sofosbuvir and daclatasvir for 12 weeks if the patient is non cirrhotic and for 24 weeks if cirrhotic
Outcomes
Primary Outcome Measures
The sustained viral response rate
Qualitative hepatitis C virus RNA polymerase chain reaction
Secondary Outcome Measures
Adverse drug events
Questionnaire
Full Information
NCT ID
NCT03369327
First Posted
December 6, 2017
Last Updated
February 19, 2019
Sponsor
Tehran University of Medical Sciences
Collaborators
RojanPharma Pharmaceutical Company
1. Study Identification
Unique Protocol Identification Number
NCT03369327
Brief Title
Sofosbuvir and Daclatasvir for Treating Hepatitis C in 200 Patients Co-infected With Human Immunodeficiency Virus
Acronym
HIV200
Official Title
Efficacy of a Fixed-Dose Combination Pill of Sofosbuvir and Daclatasvir in Treating Hepatitis C in 200 Patients Co-infected With Human Immunodeficiency Virus
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
September 1, 2018 (Actual)
Study Completion Date
December 1, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tehran University of Medical Sciences
Collaborators
RojanPharma Pharmaceutical Company
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In a multi-center study 200 patients co-infected with hepatitis C virus (HCV) and human immunodeficiency virus (HIV) will be treated with a fixed-dose combination pill combined of 400 mg sofosbuvir and 30, 60, or 90 mg of daclatasvir - depending on the particular antiretroviral treatment (ART) being used by the patient. The treatment duration will be 12 weeks for subjects without cirrhosis and 24 weeks for those with cirrhosis.
Detailed Description
To achieve the goal of elimination of hepatitis C in 2030 as set forward by the world health organization (WHO) a main group requiring treatment are subjects co-infected with HIV. These subjects offer a particular challenge as they are receiving ART which frequently interferes with hepatitis treatment. The number of pills they are already taking also limits the compliance of these patients.
In order to evaluate the efficacy of a fixed-dose combination pill combined of 400 mg sofosbuvir and 30, 60, or 90 mg of daclatasvir - depending on the particular ART medicine being used by the patient - a multi-center study of 200 co-infected patients has been designed.
The treatment duration will be 12 weeks for subjects without cirrhosis and 24 weeks for those with cirrhosis.
The study is one of the pilots being run for hepatitis C elimination in Iran.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C Virus Infection, Response to Therapy of, Human Immunodeficiency Virus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
232 (Actual)
8. Arms, Groups, and Interventions
Arm Title
sofosbuvir/daclatasvir
Arm Type
Experimental
Arm Description
Once daily fixed-dose combination pill of sofosbuvir and daclatasvir for 12 weeks if the patient is non cirrhotic and for 24 weeks if cirrhotic
Intervention Type
Drug
Intervention Name(s)
sofosbuvir and daclatasvir
Other Intervention Name(s)
Sovodak 30/400, Sovodak 60/400, Sovodak 90/400
Intervention Description
Depending on the ART received by each patient one of the fixed-dose combination pills below will be used:
Daclatasvir 30 mg and sofosbuvir 400 mg
Daclatasvir 60 mg and sofosbuvir 400 mg
Daclatasvir 90 mg and sofosbuvir 400 mg
Primary Outcome Measure Information:
Title
The sustained viral response rate
Description
Qualitative hepatitis C virus RNA polymerase chain reaction
Time Frame
12 weeks after end of treatment
Secondary Outcome Measure Information:
Title
Adverse drug events
Description
Questionnaire
Time Frame
weeks 2, 4, 8, 12 and 24
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Positive qualitative hepatitis C virus RNA test on two occasions at least 6 months apart
Positive human immunodeficiency virus test
Exclusion Criteria:
Heart rate < 50/min,
Taking amiodarone
Renal failure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reza Malekzadeh
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Study Chair
Facility Information:
Facility Name
Shariati Hospital
City
Tehran
ZIP/Postal Code
14117
Country
Iran, Islamic Republic of
Facility Name
Emam Hospital
City
Tehran
Country
Iran, Islamic Republic of
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33930223
Citation
Dehghan Manshadi SA, Merat S, Mohraz M, Rasoolinejad M, Sali S, Mardani M, Tabarsi P, Somi MH, Sedghi R, Tayeri K, Nikbin M, Karimi J, Sharifi AH, Kalantari S, Norouzi A, Merat D, Malekzadeh Z, Mirminachi B, Poustchi H, Malekzadeh R. Single-pill sofosbuvir and daclatasvir for treating hepatis C in patients co-infected with human immunodeficiency virus. Int J Clin Pract. 2021 Aug;75(8):e14304. doi: 10.1111/ijcp.14304. Epub 2021 May 17.
Results Reference
derived
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Sofosbuvir and Daclatasvir for Treating Hepatitis C in 200 Patients Co-infected With Human Immunodeficiency Virus
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