Pilot Treatment as Prevention for HCV Among Persons Who Actively Inject Drugs (BYE-C)
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Fase 4
Kontakter og lokationer
Studiesteder
-
-
California
-
San Francisco, California, Forenede Stater, 94102
- Substance Use Research Unit
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- ≥18 years of age;
- 2 consecutive positive HCV RNA tests at least 6 months after estimated date of infection;
- HCV genotype 1;
- HCV RNA <6 million copies by Roche TaqMan Assay
- No evidence of hepatic cirrhosis (as determined by two indices: Fib4<3.25-an accurate test for detecting cirrhosis based on age, AST, ALT and platelets [sensitivity/specificity 76-100/82-91%], confirmed by the fibrosis-cirrhosis index (FCI)<1.25 based on ALT, bilirubin, albumin and platelets [sensitivity/specificity 86/100%]);
- Drug injection in past 30 days by self-report and physical exam evidence of injection drug use (e.g. track marks),
- injected with others in past 12 months by self-report;
- Lab values within acceptable range (platelets>50,000, creatinine clearance by Cockroft-Gault>30mL/min, hemoglobin >10g/dL, INR<1.5 x upper limit of normal (ULN) unless stable on anticoagulant regimen or known hemophilia, AST/ALT<10 x ULN);
- Able to speak English;
- No plans to leave San Francisco area for at least 9 months and either lives or works in San Francisco, or travels to San Francisco at least weekly;
- for women of childbearing age, pregnancy test negative, not actively nursing, and agree to use birth control during treatment (although LDV-SOF has a "B" rating, consistent with no known evidence of harm, treatment is not urgent for these patients so we will err on the side of caution).
Exclusion Criteria:
- HIV+ by rapid test or pooled viral load;
- HBV surface antigen +;
- Non-definitive HCV genotype results;
- Previously received treatment for HCV (interferon, ribavirin, or DAA);
- Taking medications that affect pharmacokinetics of LDV-SOF (proton-pump inhibitors, anticonvulsants [phenobarbital, phenytoin, carbamazepine, oxcarbazepine], rifamycins, rosuvastatin, herbs [St. John's wort, silymarin, echinacea]);
History of any of the following:
- Current gastrointestinal disorder or post-operative condition that could interfere with the absorption of the study drug
- History of hepatic decompensation (i.e., ascites, encephalopathy or variceal hemorrhage)
- History of solid organ or bone marrow transplantation.
- Current treatment for cancer
- Chronic liver disease for non HCV reason, except iron overload (e.g., Wilson's disease, alfa 1 antitrypsin deficiency, cholangitis);
- Use of any prohibited concomitant medications as described in Section 5.2 within 21 days of the Day 1 visit; and
- Known hypersensitivity to LDV, SOF, the metabolites, or formulation excipients.
- No other conditions that preclude study involvement as determined by PI.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Aktiv komparator: Modified Directly Observed Therapy
Ledipasvir/Sofosbuvir Fixed-Dose Combination (LDV-SOF) tablet (LDV 90mg/SOF 400mg) observed daily dosing (modified for non-observed Saturday and Sunday dosing) for 8 weeks
|
Motivational Interviewing-based risk reduction and medication adherence counseling
|
|
Aktiv komparator: Unobserved Dosing
Ledipasvir/Sofosbuvir Fixed-Dose Combination (LDV-SOF) tablet (LDV 90mg/SOF 400mg) provided weekly (7 tablets) for unobserved daily dosing for 8 weeks
|
Motivational Interviewing-based risk reduction and medication adherence counseling
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of people who inject drugs (PWIDs) with HCV who were recruited and retained
Tidsramme: 44 weeks
|
To determine the feasibility of treating active PWIDs for HCV with LDV-SOF by mDOT versus unobserved dosing based on proportion eligible and enrolled among those screened and completion rates overall and by arm.
|
44 weeks
|
|
Medication adherence to study drug
Tidsramme: 44 weeks
|
To evaluate the acceptability of mDOT versus unobserved dosing, the percent of treatment medication adherence to LDV-SOF, as measured by the percent of doses taken overall (observed and unobserved), will be assessed using DOT doses and weekend Wise Pill data for the mDOT arm, and WisePill data for the unobserved dosing arm.
|
44 weeks
|
|
Challenges of medication adherence
Tidsramme: 44 weeks
|
To assess through in-depth, semi-structured qualitative interviews, the challenges with time intensity required for mDOT versus unobserved dosing for PWIDs treated with LDV-SOF.
|
44 weeks
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
SVR (end-of-treatment response)
Tidsramme: 12 weeks
|
We will compare the proportion of participants with undetectable HCV RNA at week 8 and post-treatment week 12 between arms.
|
12 weeks
|
|
SOF/metabolite levels
Tidsramme: 8 weeks
|
SOF/metabolite-positivity rates will be calculated by week in both arms.
|
8 weeks
|
|
HCV relapse and reinfection
Tidsramme: 36 weeks
|
Among participants who achieve SVR, we will determine the proportion who experience HCV relapse and reinfection at post-treatment week 36, overall and by arm.
|
36 weeks
|
|
Social and injector networks of participants
Tidsramme: 44 weeks
|
We will characterize injector network sizes at baseline and follow-up through ACASI surveys.
|
44 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Efterforskere
Efterforskere
- Studieleder: Emily Behar, MS, San Francisco Department of Public Health
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Studieafslutning (Faktiske)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 1R34DA039333 (U.S. NIH-bevilling/kontrakt)
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