Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
In HIV-infected people with metabolic fatty liver disease and liver fibrosis of any degree, as measured by non-invasive testing, antiretroviral treatment that includes rilpivinire for 18 months results in a slowing of progression and/or reduction of fatty metabolic liver disease, attenuating inflammation and liver fibrosis.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dolutegravir (DTG) 50 mg/day + Rilpivirine (RPV) 25mg per day | Experimental | Dolutegravir (DTG) 50 mg/day + Rilpivirine (RPV) 25mg per day. They may be administered in combination as 50/25 mg/day tablets (Juluca 50/25) or separately as Dolutegravir 50 mg/d tablets together with Rilpivirine 25 mg/d tablets (Tivicay 50 + Edurant 25) |
|
| TDF 245 mg /day or TAF 25 mg /day + FTC 200 mg /day + RPV 25 mg / day | Experimental | Tenofovir disoproxil fumarate (TDF) 245 mg per day or Tenofovir alafenamide (TAF) 25 mg per day + Emtricitabina (FTC) 200 mg/d + Rilpivirina (RPV) 25 mg/d. They may be administered as single tablets (EVIPLERA 200 mg/25 mg/245 mg) or in combination forms where one tablet contains TDF/TAF and FTC and another RPV tablet (TDF/FTC + Edurant 25 or Descovy 25/200 + Edurant 25) |
|
| Continue with their previous treatment. Any previous HAART does not contain RILPIVIRINE. | Active Comparator | Patients who are randomised to this treatment arm will continue with the HAART they were receiving prior to signing the informed consent. As in arms 1 and 2, a change in the form of HAART administration (from a combined to a separate form and vice versa) will be allowed as long as the HAART components are respected. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dolutegravir (DTG) 50 mg/day + Rilpivirine (RPV) 25mg per day | Drug | DTG/RPV will be administered in combination as 50/25 mg/day tablets or separately as DTG 50 mg/d tablets together with RPV 25 mg/d tablets. There will be no problem if during the course of the study the patient is switched from the combined form to the separate form and vice versa as long as the HAART (Highly Active Antiretroviral Therapy) components are respected. |
| Measure | Description | Time Frame |
|---|---|---|
| To evaluate the efficacy of Rilpivirine (RPV) as part of the antiretroviral treatment regimen in VIH-infected people, to slow the progression and/or reduce liver fibrosis of any degree | To measure the no progression and/or regression of liver fibrosis: No change in liver stiffness as measured by ET (Transient Elastography) or FIB4 at the 18-month visit with respect to the baseline, the intervention group (branches 1 and 2) compared to the control group. | 18 months |
| To evaluate the efficacy of Rilpivirine (RPV) as part of the antiretroviral treatment regimen in VIH-infected people, to slow the progression and/or reduce liver fibrosis of any degree | Reduction in liver stiffness measured by ET or FIB4 at the 18-month visit from baseline in the intervention group (arms 1 and 2) versus the control group. | 18 months |
| Measure | Description | Time Frame |
|---|---|---|
| Efficacy of RPV in reducing liver fibrosis of any grade | To evaluate the efficacy of RPV in reducing liver fibrosis of any grade, as measured by non-invasive tests, in HIV-infected people:
Proportion of subjects with ET measurement < 5.2 kPa in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months from the start of treatment. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital Universitario Gregorio Marañon | Madrid | Spain | ||||
| Hospital universitario Infanta Leonor |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| Tenofovir disoproxil fumarate (TDF) 245 mg per day or Tenofovir alafenamide (TAF) 25 mg per day + Emtricitabine (FTC) 200 mg per day + Rilpivirine 25 mg per day | Drug | TDF 245 mg/d or TAF 25mg/d together with FTC 200 mg/d and RPV 25 mg/d. They may be administered as single tablets or in combination forms where one tablet contains TDF/TAF and FTC and another RPV tablet. There will be no problem if during the course of the study the patient is switched from the combined form to the separate form and vice versa as long as the HAART components are respected. |
|
| Continue with their previous treatment. Any previous HAART that does not contain Rilpivirine. | Drug | Patients who are randomised to this treatment arm will continue with the HAART they were receiving prior to signing the informed consent. As in arms 1 and 2, a change in the form of HAART administration (from a combined to a separate form and vice versa) will be allowed as long as the HAART components are respected. |
|
| 12-18 months |
| Efficacy of RPV in reducing liver fibrosis of any grade | Proportion of subjects with a FIB4 measurement < 1.3 in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months from the start of treatment. | 12-18 months |
| Efficacy of RPV in reducing liver fibrosis of any grade | The mean reduction in the APRI measure in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| Efficacy of RPV in reducing liver fibrosis of any grade | Proportion of subjects with an APRI measure < 0.5 in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months from the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | The mean reduction in the percentage of liver fat, measured by magnetic resonance imaging, which measures the proton density fraction of fat (MRI-PDFF), between the beginning and the end of the study comparing the intervention group (arms 1 and 2) vs control group | 18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | Difference in the proportion of responders between the intervention group (arms 1 and 2) at 18 months from the start of treatment, defined as those who achieve >30% reduction in hepatic steatosis measured by MRI-PDFF | 18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | Proportion of subjects with hepatic steatosis measured as MRI-PDFF > 5% steatosis in the intervention group (arms 1 and 2) compared to the control group at 18 months from the start of treatment | 18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | The mean reduction of the CAP measurement in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | The mean reduction in the FLI measurement in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | The mean reduction in the HSI measure in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months from the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | The mean reduction of the TyG measurement in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | Proportion of subjects with hepatic steatosis measured as CAP > 238 dB/m in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months from the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | The mean reduction in the FLI measurement in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | Proportion of subjects with hepatic steatosis measured as HSI score > 36 in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months from the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to reduce hepatic steatosis | Proportion of subjects with hepatic steatosis measured as TyG score > 8.38 in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months from the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | The mean reduction of the HOMA-IR value in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | Difference in the proportion of subjects with insulin resistance, measured as HOMA-IR >2.5 in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | Mean reduction in TyG (IR) measurement in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months from the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | Difference in the proportion of subjects with insulin resistance measured as TyG > 4.68 in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months from the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | The mean reduction in fasting blood glucose (mg/dL) in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months from the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | Difference in the proportion of subjects with fasting glycemia > 100 mg/dL in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the insulin resistance | The reduction in the measurement of abdominal circumference and waist ratio/in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatmen | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | The mean reduction in fasting triglycerides (mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | Difference in the proportion of subjects with hypertriglyceridemia (value > 150 mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | Mean reduction in fasting LDL cholesterol quantification (mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | Difference in the proportion of subjects with elevated LDL cholesterol (value > 130 mg/dL and value >100 mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months of start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | The mean increase in fasting HDL cholesterol quantification (mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | Difference in the proportion of subjects with elevated HDL cholesterol (value > 45 mg/dL in men and value > 50 mg/dL in women) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months from the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | The mean reduction in fasting non-LDL cholesterol quantification (mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment. | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to improve the lipid metabolism | Difference in the proportion of subjects with elevated non-LDL cholesterol (value > 160 mg/dL) in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months after the start of treatment | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the liver inflammation | The mean change in ALT value (IU/mL) in the intervention group (arms 1 and 2) vs. the control group at 12 and 18 months from baseline | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the liver inflammation | The mean change in AST value (IU/mL) in the intervention group (arms 1 and 2) versus the control group at 12 and 18 months from the baseline visit | 12-18 months |
| To evaluate the efficacy of Rilpivirine (RPV) to decrease the liver inflammation. | The change of the gene expression value of: IL1-beta, IL6, IL10, MCP1, PAI-1, TGF-alpha, TNF-alpha in PBMCs in the intervention group (arms 1 and 2) compared to the control group at 12 and 18 months compared to the baseline visit. | 12-18 months |
| Efficacy of RPV to reduce hepatic steatosis/fibrosis. | To assess the efficacy of RPV as part of the antiretroviral treatment regimen in HIV-infected individuals to reduce hepatic steatosis/fibrosis based on the presence of PNPLA3 and MBOAT7-TMC4 genetic polymorphisms. | 18 months |
| To characterise the effects of RPV on the expression of inflammatory and fibrogenic markers in peripheral blood mononuclear cells | . Analyse the gene expression of inflammatory and fibrogenic markers in peripheral blood polymorphonuclear cells by RT-PCR: IL1-gamma, IL6, IL10, MCP1, P AI-1, TGF-beta, TNF-alpha. | 18 months |
| To characterise the effects of RPV on the expression of inflammatory and fibrogenic markers in peripheral blood mononuclear cells | . Measurement of ALT, AST and GGT in plasma as markers of inflammation. | 18 months |
| Efficacy of RPV to reduce the progression to steatohepatitis | In previous studies it has shown that PNPLA3, TM6SF2, and MBOAT7-TMC4 polymorphisms are associated with elevated ALT levels and histologic parameters of nonalcoholic steatohepatitis and fibrosis severity. On the baseline visit will be collected biological samples for genetuic study. A 3 ml blood sample will be drawn into an EDTA tube at baseline visit for determination of PNPLA3 (C, G alleles) and MBOAT7-TMC4 (G, A alleles) genetic polymorphisms. | 18 months |
| Madrid |
| Spain |
| Hospital Universitario Infanta SofĂa | Madrid | Spain |
| Hospital Universitario La Paz | Madrid | Spain |
| ID | Term |
|---|---|
| D015658 | HIV Infections |
| D065626 | Non-alcoholic Fatty Liver Disease |
| ID | Term |
|---|---|
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
| D015229 | Sexually Transmitted Diseases, Viral |
| D012749 | Sexually Transmitted Diseases |
| D016180 | Lentivirus Infections |
| D012192 | Retroviridae Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D005234 | Fatty Liver |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| C562325 | dolutegravir |
| D000068696 | Rilpivirine |
| D000068698 | Tenofovir |
| C442442 | tenofovir alafenamide |
| D000068679 | Emtricitabine |
| C075889 | Racivir |
| ID | Term |
|---|---|
| D009570 | Nitriles |
| D009930 | Organic Chemicals |
| D011743 | Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D063065 | Organophosphonates |
| D009943 | Organophosphorus Compounds |
| D000225 | Adenine |
| D011687 | Purines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D003841 | Deoxycytidine |
| D003562 | Cytidine |
| D011741 | Pyrimidine Nucleosides |
| D003853 | Deoxyribonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
Not provided
Not provided