Efficacy of All-Oral Anti-Viral Therapy for Symptomatic Hepatitis C Virus Infection-Related Cryoglobulinemia
2 other identifiers
interventional
10
1 country
1
Brief Summary
10 patients with chronic genotype 1 HCV infection and mixed cryoglobulinemia will be treated with Ledipasvir/Sofosbuvir 90mg/400 mg FDC once daily for 12 weeks (naïve subjects or non-cirrhotic treatment experienced subjects) or 24 weeks (treatment experienced subjects with cirrhosis). The researchers anticipate that approximately 20% of subjects may have cirrhosis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_2
Started Feb 2016
Typical duration for phase_2
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2016
CompletedFirst Submitted
Initial submission to the registry
July 3, 2016
CompletedFirst Posted
Study publicly available on registry
July 7, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 19, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
July 19, 2019
CompletedResults Posted
Study results publicly available
December 17, 2020
CompletedDecember 17, 2020
November 1, 2020
3.5 years
July 3, 2016
October 5, 2020
November 23, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Sustained Virologic Response (SVR)
Number of participants who attain SVR, ie, cleared HCV
2-4 weeks and 24 weeks after treatment
Response in Patients With Mixed Cryoglobulinemia (MC)
Response to medication in patients with MC categorized as either complete response (100% response) vs partial response (50% response).
up to 24 weeks after treatment
Study Arms (1)
Participant with Symptomatic Hepatitis C Virus Infection-Related Cryoglobulinemia
EXPERIMENTALParticipants treated with either Harvoni or Epclusa * Harvoni 90mg/400 mg FDC once daily. Subjects will take 1 tablet daily with or without food. * Epclusa 400mg/100mg 400mg/100mg FDC once daily
Interventions
12 weeks for naïve subjects or non-cirrhotic treatment experienced subjects; or 24 weeks for treatment experienced subjects with cirrhosis
once daily for 12 weeks (naïve subjects, non-cirrhotic treatment experienced or treatment experienced subjects with compensated cirrhosis) for genotype 1-6 subjects.
Eligibility Criteria
You may qualify if:
- Willing and able to provide written informed consent
- Male or female, age ≥18 years
- HCV RNA ≥ 15 IU/mL at Screening
- HCV genotype 1
- Chronic HCV infection (≥ 6 months) documented by prior medical history or liver biopsy
- Classification as treatment naïve or treatment experienced:
- Treatment naïve is defined as having never been exposed to approved or experimental HCV-specific direct-acting antiviral agents or prior treatment of HCV with interferon or ribavirin or DAAs (except for SOF-containing regimens).
- Treatment experienced is defined as prior treatment failure or relapse to a regimen containing interferon either with or without RBV or DAAs (except for SOF-containing regimens) that was completed at least 8 weeks prior to Baseline/Day 1.
- The subject's medical records must include sufficient detail of prior virologic failure to allow for categorization of prior response, as either:
- Non-Responder: Subject did not achieve undetectable HCV RNA levels while on treatment, or
- Relapse/Breakthrough: Subject achieved undetectable HCV RNA levels during treatment or within 4 weeks of the end of treatment but did not achieve SVR.
- Cirrhosis determination (approximately 20% of subjects may have cirrhosis) a. Cirrhosis is defined as any one of the following:
- i) Any previous liver biopsy showing cirrhosis (e.g., Metavir score = 4 or Ishak score ≥5) ii) FibroMeter® score \>0.442 or an AST:platelet ratio index (APRI) \>2 during Screening iii) Fibroscan with a result of \>12.5 kPa at any time prior to or during screening.
- b. Absence of cirrhosis is defined as any one of the following: i) Liver biopsy within 2 years of Screening showing absence of cirrhosis ii) FibroMeter® score \<0.442 or APRI ≤ 1 performed during Screening iii) Fibroscan with a result of ≤12.5 kPa within 6 months of Baseline/Day 1 Fibroscan results will supersede FibroMeter® /APRI; liver biopsy results will supersede Fibrotest® /APRI or Fibroscan results and be considered definitive.
- Liver imaging (ultrasound, CT scan or MRI) within 6 months of screening is required in patients with cirrhosis to exclude hepatocellular carcinoma (HCC)
- +32 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Icahn School of Medicine at Mount Sinailead
- Gilead Sciencescollaborator
Study Sites (1)
Icahn School of Medicine at Mount Sinai
New York, New York, 10029, United States
Related Publications (30)
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BACKGROUNDGorevic PD and Galanakis DK;
BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Peter D. Gorevic
- Organization
- Icahn School of Medicine at Mount Sinai
Study Officials
- PRINCIPAL INVESTIGATOR
Peter Gorevic, MD
Icahn School of Medicine at Mount Sinai
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
July 3, 2016
First Posted
July 7, 2016
Study Start
February 1, 2016
Primary Completion
July 19, 2019
Study Completion
July 19, 2019
Last Updated
December 17, 2020
Results First Posted
December 17, 2020
Record last verified: 2020-11
Data Sharing
- IPD Sharing
- Will not share