Recruiting

Genvoya & Epclusa & Biktarvy

Sponsor:

Saskatchewan Health Authority - Regina Area

Code:

NCT03549312

Conditions

HIV-1-infection

Hepatitis C, Chronic

Methadone Dependence

Opioid Dependence

Bone Diseases, Metabolic

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Genvoya

Epclusa

Biktarvy

Study Details

Brief summary:

The study hypothesis is to determine the feasibility of switching HIV-HCV co-infected patients receiving methadone or buprenorphine/naloxone as opioid substitution therapy with suppressed HIV RNA viral load on current antiretroviral therapy to elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (E/C/F/TAF, Genvoya™) followed by 12 weeks of HCV antiviral therapy with sofosbuvir/velpatasvir (SOF/VEL, Epclusa™), followed then by switch to bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF, Biktarvy™) for an additional 48 weeks.

Conditions

HIV-1-infection

Hepatitis C, Chronic

Methadone Dependence

Opioid Dependence

Bone Diseases, Metabolic

Study ID

NCT03549312

Start date

Feb 1, 2018

Status verified date

Dec, 2019

Completion date

Jun 22, 2021

Anticipated

Primary completion date

Jul 21, 2020

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Male and Females, 18 years or older
2. HIV infected (ELISA with western blot confirmation)
3. HCV RNA positive for minimum of 6 months / Genotype 1-6
4. Prescribed a combination ART regimen (cART) that may include any DHHS recommended or alternative regimens, which the treating physician considers is appropriate for their patient, except E/C/F/TAF or B/F/TAF at any point previously.
5. HIV RNA ≤ 50 c/mL at screening and ≤ 200 c/mL for at least 3 months prior to screening.
6. CD4 ≥ 200 cells/uL at screening.
7. Stage 0 to 4 fibrosis.
8. On methadone or buprenorphine/naloxone as OST for at least 3 months prior to screening and deemed stable on OST by the investigator.
9. Treatment naïve to all anti-HCV therapy, or treatment experienced but with no previous exposure to NS5A inhibitors.
10. Ability to remain adherent to medications and study protocol as per investigator opinion
11. Must be willing and able to understand the requirements of study participation and provide signed and dated written informed consent prior to screening.
12. Female subjects are willing to use acceptable methods of birth control as defined in the protocol.

Exclusion Criteria:

1. Have received any anti-HCV therapy previously with NS5A inhibitors. Previous treatment regimens allowed may include pegylated interferon, ribavirin, 1st generation NS3/NS4 protease inhibitors (telaprevir or boceprevir), and sofosbuvir.
2. Have any evidence of decompensated liver disease including ascites, esophageal or gastric variceal bleeding, hepatic encephalopathy, or other symptoms suggestive of advanced liver disease. For cirrhotic patients with Child-Pugh Class B or C or with Pugh-Turcotte (CPT) score greater than 6 must be excluded.
3. Co-infection with hepatitis B.
4. Has cirrhosis and liver imaging within 6 months of Day 1 showing evidence of hepatocellular carcinoma (HCC), or is under evaluation for HCC.
5. Concomitant use of drugs with contraindication or drug-interactions with E/C/F/TAF on Day 1 visit or B/F/TAF on Week 48/0E visit. However, the use of any concomitant drugs with contraindication with SOF/VEL are to be stopped during the weeks of treatment (i.e. week 12-24), and only after the Principal Investigator's permission, may the use of these drugs may be continued or restarted after week 24 visit (i.e. end of SOF/VEL therapy).
6. Have any active contraindication to the use of methadone, as listed in the product monograph for methadone and listed below, unless deemed acceptable based on the Principal Investigator's judgement:

1. Patients who are hypersensitive to the active substance (methadone hydrochloride) or other opioid analgesics or to any ingredient in the formulation.
2. Patients with a known or suspected mechanical gastrointestinal obstruction.
3. Patients with a suspected surgical abdomen.
4. Patients with acute asthma or other obstructive airway, and status asthmaticus.
5. Patients with acute respiratory depression, elevated carbon dioxide levels in the blood, and corpulmonale.
6. Patients with acute alcoholism, delirium tremors, and convulsive disorders.
7. Patients with severe central nervous system depression, increased cerebrospinal or intracranial pressure, and head injury.
8. Patients taking monoamine oxidase (MAO) inhibitors (or within 14 days of such therapy).
9. Patients with diarrhea associated with pseudomembranous colitis caused by cephalosporins, lincomycins (including topical clindamycin) or penicillin, or to patients having diarrhea caused by poisoning, until toxic material has been eliminated from the gastrointestinal tract.
7. Concomitant use of alcohol to a degree deemed by the investigator to be dangerous in conjunction with administration of methadone.
8. Has documented historic resistance to any of the components of E/C/F/TAF or B/F/TAF.
9. Has an eGFR (by MDRD equation) < 30 mL/min/1.73m2.
10. Is pregnant, breast-feeding, or planning or suspected to get pregnant.
11. Has any reason, in the opinion of the investigator, which would make the candidate inappropriate for participation in an investigative study involving oral medications.
12. Involved in any other interventional HIV or HCV study during the study period.

Study Design

Enrollment

25 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Switch to Genvoya Followed By HCV Therapy Then Start Biktarvy

Oral Genvoya 150/150/200/10 mg \& Epclusa 400/100 mg once daily. Once completed HCV therapy, switch anti-retroviral treatment to Oral Biktarvy 50/200/25 mg.

Interventions

Genvoya

Switching to Genvoya for 48 weeks in patients with HIV/HCV co-infection and stably suppressed HIV RNA, prior to starting HCV treatment, while receiving methadone or buprenorphine/naloxone as opioid substitution therapy.

Plasma HIV-1 RNA < 50 copies/mL at weeks 4, 12, 24, 36 and 48.

Epclusa

HCV therapy with direct-acting-antiviral therapy with Epclusa in HIV-HCV co-infected patients with suppressed HIV RNA, receiving methadone as opioid substitution therapy.

Plasma HCV RNA viral load at weeks 12, 24, 36, 48, 72 and 96.

Biktarvy

Switching to Biktarvy for 48 weeks in patients with HIV previously treated with Genvoya, stably supressed HIV RNA, while receiving methadone or buprenorphine/naloxone as opioid substitution therapy.

Plasma HIV-1 RNA < 50 copies/mL at weeks 52, 60, 72, 84 and 96.

Primary outcome measure

  • Feasibility assessment: participants approached, screened and enrolled in the study along with completed study visits [ Time Frame: Up to 48 weeks on Genvoya and 12 weeks of Epclusa and 48 weeks of Biktarvy ]
  • Assessment of incidence of screen failures [ Time Frame: Week 96 ]
  • Adherence [ Time Frame: Week 96 ]

Central Contacts and Locations

Locations

Saskatchewan Health Authority

Recruiting

Regina, Saskatchewan, Canada, S4P 0W5

Contacts

Principal Investigator:

Alexander Wong, MD

More Information

Sponsor

Saskatchewan Health Authority - Regina Area

Last update posted

Dec 24, 2019

Last verified

Dec, 2019

Keywords

  • HIV
  • Hepatitis C
  • Methadone
  • HIV/HCV Co-Infection
  • Opioid Substitution Therapy
  • Buprenorphine/Naloxone

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Saskatchewan Health Authority - Regina Area on 2019-12-24.