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  1. Article ; Online: Effects of trientine and penicillamine on intestinal copper uptake: A mechanistic 64 Cu PET/CT study in healthy humans.

    Kirk, Frederik Teicher / Munk, Ditte Emilie / Swenson, Eugene Scott / Quicquaro, Adam Michael / Vendelbo, Mikkel Holm / Schilsky, Michael L / Ott, Peter / Sandahl, Thomas Damgaard

    Hepatology (Baltimore, Md.)

    2023  Volume 79, Issue 5, Page(s) 1065–1074

    Abstract: Background and aims: Trientine (TRI) and D-penicillamine (PEN) are used to treat copper overload in Wilson disease. Their main mode of action is thought to be through the facilitation of urinary copper excretion. In a recent study, TRI was noninferior ... ...

    Abstract Background and aims: Trientine (TRI) and D-penicillamine (PEN) are used to treat copper overload in Wilson disease. Their main mode of action is thought to be through the facilitation of urinary copper excretion. In a recent study, TRI was noninferior to PEN despite lower 24-hour urinary copper excretion than PEN. We tested whether TRI and/or PEN also inhibit intestinal copper absorption.
    Approach and results: Sixteen healthy volunteers were examined with positron emission tomography (PET)/CT 1 and 15 hours after an oral Copper-64 ( 64 Cu) dose. They then received 7 days of either PEN or TRI (trientine tetrahydrochloride), after which the 64 Cu PET/CT scans were repeated. Venous blood samples were also collected. Pretreatment to posttreatment changes of the hepatic 64 Cu uptake reflect the effect of drugs on intestinal absorption. 64 Cu activity was normalized to dose and body weight and expressed as the mean standard uptake value. TRI (n=8) reduced hepatic 64 Cu activity 1 hour after 64 Cu dose from 6.17 (4.73) to 1.47 (2.97) standard uptake value, p <0.02, and after 15 hours from 14.24 (3.09) to 6.19 (3.43), p <0.02, indicating strong inhibition of intestinal 64 Cu absorption. PEN (n=8) slightly reduced hepatic standard uptake value at 15 hours, from 16.30 (5.63) to 12.17 (1.44), p <0.04.
    Conclusions: In this mechanistic study, we show that TRI inhibits intestinal copper absorption, in addition to its cupriuretic effect. In contrast, PEN has modest effects on the intestinal copper absorption. This may explain why TRI and PEN are equally effective although urinary copper excretion is lower with TRI. The study questions whether the same therapeutic targets for 24-hour urinary excretion apply to both drugs.
    MeSH term(s) Humans ; Penicillamine/pharmacology ; Penicillamine/therapeutic use ; Trientine/pharmacology ; Trientine/therapeutic use ; Copper ; Positron Emission Tomography Computed Tomography ; Copper Radioisotopes/therapeutic use ; Hepatolenticular Degeneration/drug therapy ; Positron-Emission Tomography
    Chemical Substances Penicillamine (GNN1DV99GX) ; Trientine (SJ76Y07H5F) ; Copper (789U1901C5) ; Copper-64 ; Copper Radioisotopes
    Language English
    Publishing date 2023-12-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604603-4
    ISSN 1527-3350 ; 0270-9139
    ISSN (online) 1527-3350
    ISSN 0270-9139
    DOI 10.1097/HEP.0000000000000708
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  2. Article ; Online: Prevention of neonatal hepatitis B virus transmission.

    Bleich, Lauren M / Swenson, Eugene S

    Journal of clinical gastroenterology

    2014  Volume 48, Issue 9, Page(s) 765–772

    Abstract: Hepatitis B virus (HBV) vertical transmission remains a worldwide issue but is fairly uncommon in the western world due to routine screening and vaccination. Universal screening of pregnant women during the second trimester facilitates interruption of ... ...

    Abstract Hepatitis B virus (HBV) vertical transmission remains a worldwide issue but is fairly uncommon in the western world due to routine screening and vaccination. Universal screening of pregnant women during the second trimester facilitates interruption of mother-to-child transmission (MTCT) by identifying HBV-infected mothers for whom intervention may reduce MTCT risk. HBV DNA level is the single most important predictor of MTCT. Other risk factors include HBeAg, HBe Ab, anti-HB core IgG, and HIV status. Current recommendations for infants born to HBsAg-positive mothers include administration of HBIG within 12 hours of birth and first dose of HBV vaccine within 24 hours of birth. Antiviral therapy is recommended in the third trimester of pregnancy in a subset of patients based on HBeAg and HBV DNA status for prophylaxis of MTCT, although discontinuation of antivirals after delivery is associated with significant increased risk of flares. This article outlines the data for prevention of vertical transmission of HBV.
    MeSH term(s) Antiviral Agents/administration & dosage ; DNA, Viral/blood ; Drug Administration Schedule ; Female ; HIV Infections ; Hepatitis B virus/genetics ; Hepatitis B virus/isolation & purification ; Hepatitis B, Chronic/prevention & control ; Hepatitis B, Chronic/transmission ; Humans ; Infant, Newborn ; Infectious Disease Transmission, Vertical/prevention & control ; Pregnancy ; Pregnancy Complications, Infectious/prevention & control ; Prenatal Diagnosis
    Chemical Substances Antiviral Agents ; DNA, Viral
    Language English
    Publishing date 2014-10
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 448460-5
    ISSN 1539-2031 ; 0192-0790
    ISSN (online) 1539-2031
    ISSN 0192-0790
    DOI 10.1097/MCG.0000000000000115
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  3. Article ; Online: Effects of tetrathiomolybdate on copper metabolism in healthy volunteers and in patients with Wilson disease.

    Kirk, Frederik Teicher / Munk, Ditte Emilie / Swenson, Eugene Scott / Quicquaro, Adam Michael / Vendelbo, Mikkel Holm / Larsen, Agnete / Schilsky, Michael L / Ott, Peter / Sandahl, Thomas Damgaard

    Journal of hepatology

    2023  Volume 80, Issue 4, Page(s) 586–595

    Abstract: Background & aims: In Wilson disease (WD), copper accumulates in the liver and brain causing disease. Bis-choline tetrathiomolybdate (TTM) is a potent copper chelator that may be associated with a lower risk of inducing paradoxical neurological ... ...

    Abstract Background & aims: In Wilson disease (WD), copper accumulates in the liver and brain causing disease. Bis-choline tetrathiomolybdate (TTM) is a potent copper chelator that may be associated with a lower risk of inducing paradoxical neurological worsening than conventional therapy for neurologic WD. To better understand the mode of action of TTM, we investigated its effects on copper absorption and biliary excretion.
    Methods: In a double-blind randomized setting, hepatic
    Results: In healthy volunteers, TTM reduced intestinal
    Conclusions: While we did not show an increase in biliary excretion of
    Impact and implications: Bis-choline tetrathiomolybdate (TTM) is an investigational copper chelator being developed for the treatment of Wilson disease. In animal models of Wilson disease, TTM has been shown to facilitate biliary copper excretion. In the present human study, TTM surprisingly did not facilitate biliary copper excretion but instead reduced intestinal copper uptake to a clinically significant degree. Our study builds on our understanding of human copper metabolism and the mechanism of action of TTM.
    MeSH term(s) Animals ; Humans ; Hepatolenticular Degeneration/drug therapy ; Hepatolenticular Degeneration/metabolism ; Copper/metabolism ; Positron Emission Tomography Computed Tomography ; Healthy Volunteers ; Chelating Agents/pharmacology ; Choline ; Molybdenum
    Chemical Substances Copper (789U1901C5) ; tetrathiomolybdate (91U3TGV99T) ; Chelating Agents ; Choline (N91BDP6H0X) ; Molybdenum (81AH48963U)
    Language English
    Publishing date 2023-12-10
    Publishing country Netherlands
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 605953-3
    ISSN 1600-0641 ; 0168-8278
    ISSN (online) 1600-0641
    ISSN 0168-8278
    DOI 10.1016/j.jhep.2023.11.023
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  4. Article ; Online: Corrigendum to "Rondeau E, Scully M, Ariceta G, Barbour T, Cataland S, Heyne N, Miyakawa Y, Ortiz S, Swenson E, Vallee M, Yoon S-S, Kavanagh D and Haller H; on behalf of the 311 Study Group. The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment." Kidney Int. 2020;97:1287-1296.

    Rondeau, Eric / Scully, Marie / Ariceta, Gema / Barbour, Tom / Cataland, Spero / Heyne, Nils / Miyakawa, Yoshitaka / Ortiz, Stephan / Swenson, Eugene / Vallee, Marc / Yoon, Sung-Soo / Kavanagh, David / Haller, Hermann

    Kidney international

    2021  Volume 99, Issue 5, Page(s) 1244

    Language English
    Publishing date 2021-03-23
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2021.03.008
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  5. Article: An HCV-positive recipient of an HCV-positive donor liver successfully treated before and immediately after liver transplant with daclatasvir, sofosbuvir, and ribavirin.

    Poordad, Fred / Lawitz, Eric / Gutierrez, Julio A / Guerrero, Juan / Speeg, Kermit / Swenson, Eugene S

    Clinical case reports

    2017  Volume 5, Issue 4, Page(s) 371–375

    Abstract: This case suggests that initiation of HCV therapy immediately after liver transplantation with well-tolerated, all-oral regimens may achieve a virologic cure in HCV-positive recipients, thus preventing post-transplant HCV recurrence and associated ... ...

    Abstract This case suggests that initiation of HCV therapy immediately after liver transplantation with well-tolerated, all-oral regimens may achieve a virologic cure in HCV-positive recipients, thus preventing post-transplant HCV recurrence and associated disease progression. This strategy may broaden utilization of HCV-positive donor livers, potentially including HCV-negative transplant recipients.
    Language English
    Publishing date 2017-02-03
    Publishing country England
    Document type Case Reports
    ZDB-ID 2740234-4
    ISSN 2050-0904
    ISSN 2050-0904
    DOI 10.1002/ccr3.841
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  6. Article ; Online: Erratum to "Rondeau E, Scully M, Ariceta G, Barbour T, Cataland S, Heyne N, Miyakawa Y, Ortiz S, Swenson E, Vallee M, Yoon S-S, Kavanagh D, Haller H; on behalf of the 311 Study Group. The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment" Kidney Int. 2020;97:1287-1296.

    Rondeau, Eric / Scully, Marie / Ariceta, Gema / Barbour, Tom / Cataland, Spero / Heyne, Nils / Miyakawa, Yoshitaka / Ortiz, Stephan / Swenson, Eugene / Vallee, Marc / Yoon, Sung-Soo / Kavanagh, David / Haller, Hermann

    Kidney international

    2020  Volume 98, Issue 6, Page(s) 1621

    Language English
    Publishing date 2020-11-12
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2020.11.001
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  7. Article ; Online: The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment.

    Rondeau, Eric / Scully, Marie / Ariceta, Gema / Barbour, Tom / Cataland, Spero / Heyne, Nils / Miyakawa, Yoshitaka / Ortiz, Stephan / Swenson, Eugene / Vallee, Marc / Yoon, Sung-Soo / Kavanagh, David / Haller, Hermann

    Kidney international

    2020  Volume 97, Issue 6, Page(s) 1287–1296

    Abstract: Ravulizumab is a long-acting C5 inhibitor engineered from eculizumab with increased elimination half-life, allowing an extended dosing interval from two to eight weeks. Here we evaluate the efficacy and safety of ravulizumab in adults with atypical ... ...

    Abstract Ravulizumab is a long-acting C5 inhibitor engineered from eculizumab with increased elimination half-life, allowing an extended dosing interval from two to eight weeks. Here we evaluate the efficacy and safety of ravulizumab in adults with atypical hemolytic uremic syndrome presenting with thrombotic microangiopathy. In this global, phase 3, single arm study in complement inhibitor-naïve adults (18 years and older) who fulfilled diagnostic criteria for atypical hemolytic uremic syndrome, enrolled patients received ravulizumab through a 26-week initial evaluation period. The primary endpoint was complete thrombotic microangiopathy response defined as normalization of platelet count and lactate dehydrogenase and 25% or more improvement in serum creatinine. Secondary endpoints included changes in hematologic variables and renal function. Safety was also evaluated. Ravulizumab treatment resulted in an immediate, complete, and sustained C5 inhibition in all patients. Complete thrombotic microangiopathy response was achieved in 53.6% of patients. Normalization of platelet count, lactate dehydrogenase and 25% or more improvement in serum creatinine was achieved in 83.9%, 76.8% and 58.9% of patients, respectively. Improvement in estimated glomerular filtration rate by one or more stage was achieved in 68.1% of patients by day 183. No unexpected adverse events were reported across a safety analysis set of 58 patients. Four deaths occurred (three within one month of study initiation, including one in a patient excluded based on eligibility criteria after the first dose) with none considered treatment-related by the study investigator. Thus, treatment with ravulizumab once every eight weeks resulted in rapidly improved hematologic and renal endpoints with no unexpected adverse events in adults with atypical hemolytic uremic syndrome.
    MeSH term(s) Adult ; Antibodies, Monoclonal, Humanized ; Atypical Hemolytic Uremic Syndrome/drug therapy ; Complement Inactivating Agents/adverse effects ; Complement System Proteins ; Humans ; Thrombotic Microangiopathies/diagnosis ; Thrombotic Microangiopathies/drug therapy
    Chemical Substances Antibodies, Monoclonal, Humanized ; Complement Inactivating Agents ; Complement System Proteins (9007-36-7) ; ravulizumab (C3VX249T6L)
    Language English
    Publishing date 2020-03-06
    Publishing country United States
    Document type Clinical Trial, Phase III ; Journal Article
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2020.01.035
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  8. Article ; Online: Short-duration treatment for chronic hepatitis C virus with daclatasvir, asunaprevir, beclabuvir and sofosbuvir (FOURward study).

    Sulkowski, Mark S / Flamm, Steve / Kayali, Zeid / Lawitz, Eric J / Kwo, Paul / McPhee, Fiona / Torbeyns, Anne / Hughes, Eric A / Swenson, Eugene S / Yin, Philip D / Linaberry, Misti

    Liver international : official journal of the International Association for the Study of the Liver

    2017  Volume 37, Issue 6, Page(s) 836–842

    Abstract: Background & aims: The phase 2, FOURward study (NCT02175966) investigated short-duration therapy (4/6 weeks) with four direct-acting antivirals (DAAs) with distinct mechanisms of action in patients infected with hepatitis C virus (HCV) genotype-1.: ... ...

    Abstract Background & aims: The phase 2, FOURward study (NCT02175966) investigated short-duration therapy (4/6 weeks) with four direct-acting antivirals (DAAs) with distinct mechanisms of action in patients infected with hepatitis C virus (HCV) genotype-1.
    Methods: Non-cirrhotic patients were randomized 1:1 to DCV-TRIO (fixed-dose daclatasvir 30 mg, asunaprevir 200 mg and beclabuvir 75 mg) twice-daily + sofosbuvir 400 mg once-daily for 4 or 6 weeks. The primary endpoint was sustained virological response at post-treatment Week 12 (SVR12). Patients without SVR12 were offered retreatment based on the DAA resistance profile at failure; patients with resistance to ≤1 DCV-TRIO component received DCV-TRIO + RBV for 12 weeks.
    Results: Twenty-eight patients with HCV genotype-1 were enrolled; 79% had genotype-1a infection and median baseline HCV-RNA levels were high (9 × 10
    Conclusions: Short-duration treatment with four DAAs with distinct mechanisms of action was insufficient for most patients with genotype-1 infection and high baseline viraemia. Non-SVR12 was not associated with emergence of NS3 or NS5B RAS and retreatment with DCV-TRIO + RBV for 12 weeks led to SVR in all patients.
    MeSH term(s) Adult ; Antiviral Agents/therapeutic use ; Benzazepines/therapeutic use ; Drug Therapy, Combination ; Female ; Hepacivirus/genetics ; Hepatitis C, Chronic/drug therapy ; Humans ; Imidazoles/therapeutic use ; Indoles/therapeutic use ; Isoquinolines/therapeutic use ; Male ; Middle Aged ; Sofosbuvir/therapeutic use ; Sulfonamides/therapeutic use ; Sustained Virologic Response ; United States ; Viral Load ; Young Adult
    Chemical Substances 8-cyclohexyl-N-((dimethylamino)sulfonyl)-1,1a,2,12b-tetrahydro-11-methoxy-1a-((3-methyl-3,8-diazabicyclo(3.2.1)oct-8-yl)carbonyl)cycloprop(d)indolo(2,1-a)(2)benzazepine-5-carboxamide ; Antiviral Agents ; Benzazepines ; Imidazoles ; Indoles ; Isoquinolines ; Sulfonamides ; daclatasvir (LI2427F9CI) ; asunaprevir (S9X0KRJ00S) ; Sofosbuvir (WJ6CA3ZU8B)
    Language English
    Publishing date 2017-02-02
    Publishing country United States
    Document type Clinical Trial, Phase II ; Journal Article ; Randomized Controlled Trial
    ZDB-ID 2102783-3
    ISSN 1478-3231 ; 1478-3223
    ISSN (online) 1478-3231
    ISSN 1478-3223
    DOI 10.1111/liv.13335
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  9. Article ; Online: Daclatasvir with sofosbuvir and ribavirin for hepatitis C virus infection with advanced cirrhosis or post-liver transplantation recurrence.

    Poordad, Fred / Schiff, Eugene R / Vierling, John M / Landis, Charles / Fontana, Robert J / Yang, Rong / McPhee, Fiona / Hughes, Eric A / Noviello, Stephanie / Swenson, Eugene S

    Hepatology (Baltimore, Md.)

    2016  Volume 63, Issue 5, Page(s) 1493–1505

    Abstract: Unlabelled: Chronic hepatitis C virus (HCV) infection with advanced cirrhosis or post-liver transplantation recurrence represents a high unmet medical need with no approved therapies effective across all HCV genotypes. The open-label ALLY-1 study ... ...

    Abstract Unlabelled: Chronic hepatitis C virus (HCV) infection with advanced cirrhosis or post-liver transplantation recurrence represents a high unmet medical need with no approved therapies effective across all HCV genotypes. The open-label ALLY-1 study assessed the safety and efficacy of a 60-mg once-daily dosage of daclatasvir (pan-genotypic NS5A inhibitor) in combination with sofosbuvir at 400 mg once daily (NS5B inhibitor) and ribavirin at 600 mg/day for 12 weeks with a 24-week follow-up in two cohorts of patients with chronic HCV infection of any genotype and either compensated/decompensated cirrhosis or posttransplantation recurrence. Patients with on-treatment transplantation were eligible to receive 12 additional weeks of treatment immediately after transplantation. The primary efficacy measure was sustained virologic response at posttreatment week 12 (SVR12) in patients with a genotype 1 infection in each cohort. Sixty patients with advanced cirrhosis and 53 with posttransplantation recurrence were enrolled; HCV genotypes 1 (76%), 2, 3, 4, and 6 were represented. Child-Pugh classifications in the advanced cirrhosis cohort were 20% A, 53% B, and 27% C. In patients with cirrhosis, 82% (95% confidence interval [CI], 67.9%-92.0%) with genotype 1 infection achieved SVR12, whereas the corresponding rates in those with genotypes 2, 3, and 4 were 80%, 83%, and 100%, respectively; SVR12 rates were higher in patients with Child-Pugh class A or B, 93%, versus class C, 56%. In transplant recipients, SVR12 was achieved by 95% (95% CI, 83.5%-99.4%) and 91% of patients with genotype 1 and 3 infection, respectively. Three patients received peritransplantation treatment with minimal dose interruption and achieved SVR12. There were no treatment-related serious adverse events.
    Conclusion: The pan-genotypic combination of daclatasvir, sofosbuvir, and ribavirin was safe and well tolerated. High SVR rates across multiple HCV genotypes were achieved by patients with post-liver transplantation recurrence or advanced cirrhosis.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Antiviral Agents/administration & dosage ; Drug Therapy, Combination ; Female ; Hepatitis C, Chronic/complications ; Hepatitis C, Chronic/drug therapy ; Hepatitis C, Chronic/virology ; Humans ; Imidazoles/administration & dosage ; Imidazoles/adverse effects ; Liver Cirrhosis/etiology ; Liver Transplantation/adverse effects ; Male ; Middle Aged ; Prospective Studies ; RNA, Viral/blood ; Recurrence ; Ribavirin/administration & dosage ; Ribavirin/adverse effects ; Sofosbuvir/administration & dosage ; Sofosbuvir/adverse effects
    Chemical Substances Antiviral Agents ; BMS-790052 ; Imidazoles ; RNA, Viral ; Ribavirin (49717AWG6K) ; Sofosbuvir (WJ6CA3ZU8B)
    Language English
    Publishing date 2016-05
    Publishing country United States
    Document type Clinical Trial, Phase III ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 604603-4
    ISSN 1527-3350 ; 0270-9139
    ISSN (online) 1527-3350
    ISSN 0270-9139
    DOI 10.1002/hep.28446
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  10. Article ; Online: Daclatasvir/asunaprevir/beclabuvir, all-oral, fixed-dose combination for patients with chronic hepatitis C virus genotype 1.

    Kao, Jia-Horng / Yu, Ming-Lung / Peng, Cheng-Yuan / Heo, Jeong / Chu, Chi-Jen / Chang, Ting-Tsung / Lee, Youn-Jae / Hu, Tsung-Hui / Yoon, Ki Tae / Paik, Seung Woon / Lim, Young Suk / Ahn, Sang Hoon / Isakov, Vasily / McPhee, Fiona / Hu, Wenhua / Scott Swenson, Eugene / Yin, Philip D / Treitel, Michelle

    Journal of gastroenterology and hepatology

    2017  Volume 32, Issue 12, Page(s) 1998–2005

    Abstract: Background and aim: This multinational (Taiwan, South Korea, Russia) phase 3 study evaluated the all-oral, ribavirin-free, fixed-dose combination (DCV-TRIO) of daclatasvir (NS5A inhibitor) 30 mg, asunaprevir (NS3 inhibitor) 200 mg, and beclabuvir (NS5B ... ...

    Abstract Background and aim: This multinational (Taiwan, South Korea, Russia) phase 3 study evaluated the all-oral, ribavirin-free, fixed-dose combination (DCV-TRIO) of daclatasvir (NS5A inhibitor) 30 mg, asunaprevir (NS3 inhibitor) 200 mg, and beclabuvir (NS5B inhibitor) 75 mg, in patients with chronic hepatitis C virus genotype-1 infection, with or without compensated cirrhosis.
    Methods: UNITY-4 (NCT02170727) was an open-label, two-cohort study in which 169 patients, treatment-naive (n = 138) or treatment-experienced (n = 31), received twice-daily DCV-TRIO for 12 weeks with 24 weeks of post-treatment follow-up. The primary efficacy end point was sustained virologic response at post-treatment week 12 (SVR12) in treatment-naive patients.
    Results: Eighty-eight (52%) patients were men, 81 (48%) Taiwanese, 78 (46%) Korean, and 10 (6%) Russian; 23 (14%) had compensated cirrhosis, and 52 (31%) were IL28B (rs1297860) non-CC genotype. Baseline resistance-associated NS5A polymorphisms (L31 and/or Y93) were detected in 25/165 (15%) patients with available genotype-1 sequencing data. SVR12 was achieved by 98.6% (136/138; 95% confidence interval: 94.9-99.8%) of treatment-naive and 100% (31/31; 95% confidence interval: 88.8-100%) of treatment-experienced patients. Both virologic failures were found to be infected with hepatitis C virus genotype-6g; 100% SVR12 was observed for genotype-1a (n = 8) and genotype-1b (n = 157). Two patients experienced serious adverse events. Eight (5%) patients experienced reversible grade 3/4 alanine aminotransferase or aspartate aminotransferase elevations, leading to discontinuation in four (2%); all achieved SVR12. There were no grade 3/4 total bilirubin increases and no deaths.
    Conclusions: Twelve weeks of DCV-TRIO was well tolerated and provided 100% SVR12 in treatment-naive and treatment-experienced patients with genotype-1 infection, with or without cirrhosis, including those with baseline NS5A-L31 or NS5A-Y93 resistance-associated substitutions.
    Language English
    Publishing date 2017-12
    Publishing country Australia
    Document type Journal Article
    ZDB-ID 632882-9
    ISSN 1440-1746 ; 0815-9319
    ISSN (online) 1440-1746
    ISSN 0815-9319
    DOI 10.1111/jgh.13796
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