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| ID | Type | Description | Link |
|---|---|---|---|
| 2015-005453-13 | EudraCT Number |
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Impossibility of supplying the medication in research of the study by the pharmaceutical company that gave it to the trial
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Pilot, single center, open-label study to evaluate the efficacy and tolerability of Grazoprevir and Elbasvir in HCV GT1 and 4 liver transplant recipients.30 liver transplant recipients with hepatitis C recurrence.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Genotype 1B | Experimental | treatment 12 weeks |
|
| Genotype 1A and 4 | Experimental | treatment 16 weeks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Grazoprevir 100 mg/day | Drug | Grazoprevir 100 mg/ day 12 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Sustained virological response | Sustained virological response 12 w (SVR24) defined as HCV-RNA undetectable at post-treatment week 12. | 12 weeks post-treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Sustained virological response | Sustained virological response 12 ( SVR12) defined as HCV-RNA undetectable at post-treatment weeks 4 and , 24 respectively. | 4 weeks and 24 weeks post-treatment |
| To evaluate the beneficial effects of antiviral therapy on renal function. |
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Inclusion Criteria:
Exclusion Criteria:
Genotype 2, 3, 5 or 6 infection.
Decompensated cirrhosis defined by the presence of actual or previous history of clinical decompensation including ascites, hepatic encephalopathy, variceal bleeding or spontaneous bacterial peritonitis, or a Child-Pugh B or C.
Hepatocellular carcinoma after liver transplantation.
Total bilirubin > 3 mg/dL.
Immunosuppression with cyclosporine or an mTOR inhibitor (everolimus or sirolimus).
Severe extrahepatic diseases: cardiovascular, respiratory, cerebrovascular and poorly controlled diabetes.
Platelets < 75 x 109 cells/L.
Neutrophil count < 0.5 x 109 cells/L.
Hemoglobin < 9 g/dL.
Albumin < 3g/dL.
HIV infection.
Hepatitis B infection.
Active intake of toxic amounts of alcohol or recreational drugs.
Females who are pregnant, become to be pregnant or breastfeeding or males whose partners are pregnant, become to be pregnant or breastfeeding.
Intake of disallowed medications including(but not limited to):
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| Elbasvir 50 mg/d | Drug | Elbasvir 50 mg/day 12 weeks |
|
|
| Grazoprevir 100 mg/day | Drug | Grazoprevir 100 mg/day 16 weeks |
|
|
| Elbasvir 50 mg/day | Drug | Elbasvir 50 mg/d 16 weeks |
|
|
| Ribavirin 1200 mg/day | Drug | Ribavirin 1200 mg/day 16 weeks |
|
|
creatinine sample analyses blood analyses in all visits |
| 24 weeks post-treatment |
| To assess the impact of therapy in kidney function. | Elevation Transaminases blood analyses in all visits | 24 weeks post-treatment |
| Tolerability of this combination in liver transplant recipients. | Serious advers events evaluation | Every visit |
| ID | Term |
|---|---|
| D006526 | Hepatitis C |
| ID | Term |
|---|---|
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
| D006525 | Hepatitis, Viral, Human |
| D014777 | Virus Diseases |
| D018178 | Flaviviridae Infections |
| D012327 | RNA Virus Infections |
| D006505 | Hepatitis |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
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| ID | Term |
|---|---|
| C578009 | grazoprevir |
| C000589335 | elbasvir |
| D012254 | Ribavirin |
| ID | Term |
|---|---|
| D012263 | Ribonucleosides |
| D009705 | Nucleosides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
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