[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100596043":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":22,"locations":31,"responsibleParty":178,"collaborators":180,"id":188,"slug":189,"hasResults":190,"nctId":191,"briefTitle":192,"officialTitle":193,"acronym":21,"eligibilityCriteria":194,"healthyVolunteers":190,"sex":195,"minAge":196,"maxAge":197,"enrollmentInfo":198,"targetDuration":21,"studyType":201,"phases":202,"briefSummary":205,"conditions":206,"keywords":208,"overallStatus":34,"whyStopped":21,"lastUpdateSubmitDate":212,"lastUpdatePostDateStruct":213,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":221},{"fullName":5,"class":6},"National Institute of Allergy and Infectious Diseases (NIAID)","NIH",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"GLE\u002FPIB","EXPERIMENTAL","Pregnant participants will take three (3) GLE\u002FPIB fixed-dose combination tablets orally once daily with food for eight weeks",[13],"Drug: Glecaprevir\u002Fpibrentasvir",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DRUG","Glecaprevir\u002Fpibrentasvir","100 mg glecaprevir and 40 mg pibrentasvir for a total daily dose of glecaprevir 300 mg\u002Fpibrentasvir 120 mg",[9],[9],null,[23,27],{"name":24,"role":25,"phone":21,"phoneExt":21,"email":26},"IMPAACT ClinicalTrials.gov Coordinator","CONTACT","impaact.ctgov@fstrf.org",{"name":28,"role":25,"phone":29,"phoneExt":21,"email":30},"Katie McCarthy","919-321-3326","kmccarthy@fhi360.org",[32,51,63,78,93,108,123,138,152,163],{"facility":33,"status":34,"city":35,"state":36,"zip":37,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"USC LA","RECRUITING","Los Angeles","California","90089","United States","US",{"type":41,"coordinates":42},"Point",[43,44],-118.24368,34.05223,{"lat":44,"lon":43},[47],{"name":48,"role":25,"phone":49,"phoneExt":21,"email":50},"Yvonne Morales, LVN","323-865-1561","ytr@usc.edu",{"facility":52,"status":53,"city":35,"state":36,"zip":54,"country":38,"countryCode":39,"cosmosGeoPoint":55,"geoPoint":57,"contacts":58},"David Geffen School of Medicine at UCLA","NOT_YET_RECRUITING","90095",{"type":41,"coordinates":56},[43,44],{"lat":44,"lon":43},[59],{"name":60,"role":25,"phone":61,"phoneExt":21,"email":62},"Misciel Macaraig, BA, CCRC","310-206-6369","mbmacaraig@mednet.ucla.edu",{"facility":64,"status":34,"city":65,"state":66,"zip":67,"country":38,"countryCode":39,"cosmosGeoPoint":68,"geoPoint":72,"contacts":73},"University of Colorado Denver","Aurora","Colorado","80045",{"type":41,"coordinates":69},[70,71],-104.83192,39.72943,{"lat":71,"lon":70},[74],{"name":75,"role":25,"phone":76,"phoneExt":21,"email":77},"Carrie Chambers, RN","720-777-4424","carrie.chambers@childrenscolorado.org",{"facility":79,"status":34,"city":80,"state":81,"zip":82,"country":38,"countryCode":39,"cosmosGeoPoint":83,"geoPoint":87,"contacts":88},"Univ. of Florida Jacksonville","Jacksonville","Florida","32209",{"type":41,"coordinates":84},[85,86],-81.65565,30.33218,{"lat":86,"lon":85},[89],{"name":90,"role":25,"phone":91,"phoneExt":21,"email":92},"Adnan Shabbir","904-244-3796","adnan.shabbir@jax.ufl.edu",{"facility":94,"status":34,"city":95,"state":96,"zip":97,"country":38,"countryCode":39,"cosmosGeoPoint":98,"geoPoint":102,"contacts":103},"Lurie Children's Hospital of Chicago","Chicago","Illinois","60614",{"type":41,"coordinates":99},[100,101],-87.65005,41.85003,{"lat":101,"lon":100},[104],{"name":105,"role":25,"phone":106,"phoneExt":21,"email":107},"Rasima Cehic, RN","312-227-8273","rcehic@luriechildrens..org",{"facility":109,"status":34,"city":110,"state":111,"zip":112,"country":38,"countryCode":39,"cosmosGeoPoint":113,"geoPoint":117,"contacts":118},"Johns Hopkins University Baltimore","Baltimore","Maryland","21287",{"type":41,"coordinates":114},[115,116],-76.61219,39.29038,{"lat":116,"lon":115},[119],{"name":120,"role":25,"phone":121,"phoneExt":21,"email":122},"Amanda Haines, BSN, RN","443-287-8888","ahaines8@jhmi.edu",{"facility":124,"status":34,"city":125,"state":126,"zip":127,"country":38,"countryCode":39,"cosmosGeoPoint":128,"geoPoint":132,"contacts":133},"SUNY Stony Brook","Stony Brook","New York","11794",{"type":41,"coordinates":129},[130,131],-73.14094,40.92565,{"lat":131,"lon":130},[134],{"name":135,"role":25,"phone":136,"phoneExt":21,"email":137},"Barsha Chakraborty, MPH","631-444-8225","barsha.chakraborty@stonybrookmedicine.edu",{"facility":139,"status":34,"city":140,"state":126,"zip":141,"country":38,"countryCode":39,"cosmosGeoPoint":142,"geoPoint":146,"contacts":147},"Bronx-Lebanon Hospital Center","The Bronx","10457",{"type":41,"coordinates":143},[144,145],-73.86641,40.84985,{"lat":145,"lon":144},[148],{"name":149,"role":25,"phone":150,"phoneExt":21,"email":151},"Martha Cavallo, PNP","718-960-1016","mcavallo@bronxcare.org",{"facility":153,"status":53,"city":140,"state":126,"zip":154,"country":38,"countryCode":39,"cosmosGeoPoint":155,"geoPoint":157,"contacts":158},"Jacobi Medical Center","10461",{"type":41,"coordinates":156},[144,145],{"lat":145,"lon":144},[159],{"name":160,"role":25,"phone":161,"phoneExt":21,"email":162},"Marlene Burey, RN, PNP","718-918-4783","marlene.burey@nychhc.org",{"facility":164,"status":34,"city":165,"state":166,"zip":167,"country":38,"countryCode":39,"cosmosGeoPoint":168,"geoPoint":172,"contacts":173},"Baylor College of Medicine\u002F\u002FTexas Children's Hospital","Houston","Texas","77030",{"type":41,"coordinates":169},[170,171],-95.36327,29.76328,{"lat":171,"lon":170},[174],{"name":175,"role":25,"phone":176,"phoneExt":21,"email":177},"Mariam Pontifes","832-822-1268","mepontif@texaschildrens.org",{"type":179,"investigatorFullName":21,"investigatorTitle":21,"investigatorAffiliation":21,"oldNameTitle":21,"oldOrganization":21},"SPONSOR",[181,183,185],{"name":182,"class":6},"Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)",{"name":184,"class":6},"National Institute of Mental Health (NIMH)",{"name":186,"class":187},"AbbVie","INDUSTRY","100596043","phase-1-study-of-the-pharmacokinetics-and-safety-of-glecaprevirpibrentasvir-initiated-in-pregnancy-in-women-with-hepatitis-c-with-and-without-hiv-100596043",false,"NCT07040319","Study of the Pharmacokinetics and Safety of Glecaprevir\u002FPibrentasvir Initiated in Pregnancy in Women With Hepatitis C With and Without HIV","Phase I\u002FII Study of the Pharmacokinetics and Safety of Glecaprevir\u002FPibrentasvir Initiated in Pregnancy in Women With Hepatitis C With and Without HIV","Inclusion Criteria:\n\n* Of legal age or circumstance to provide independent informed consent as determined by site standard operating procedures (SOPs) and consistent with institutional review board\u002Fethics committee (IRB\u002FEC) policies and procedures\n* Willing and able to provide written informed consent for their own and their infant's study participation\n* At entry, 16-45 years of age (inclusive)\n* At entry, gestational age of 14-32 weeks, defined as greater than 13 weeks plus six days and less than or equal to 32 completed weeks gestation, as determined by the site investigator based on best obstetric estimate\n* At screening and at study entry, no evidence of multiple gestation, fetal anomalies, or intrauterine fetal growth restriction, as determined by the site investigator based on ultrasound\n* At screening, detectable HCV RNA test result based on testing of a specimen collected within 30 days prior to entry\n* At screening, negative test results for hepatitis B surface antigen based on testing of a specimen collected within 30 days prior to entry\n* At screening (i.e., from specimens collected within 30 days prior to entry), has normal, grade 1, grade 2, or grade 3 results for the following\n\n  * Aspartate aminotransferase (AST) (\\\u003C10.0 x ULN)\n  * Alanine aminotransferase (ALT) (\\\u003C10.0 x ULN)\n* At screening (i.e., from specimens collected within 30 days prior to entry), has normal, grade 1, or grade 2 results for the following\n\n  * Hemoglobin (≥8.5 g\u002FdL)\n  * Creatinine (≤1.8 x ULN)\n* At screening (i.e., from specimens collected within 30 days prior to entry), has normal or grade 1 results for the following\n\n  * International normalized ratio (INR) (\\\u003C1.5 x ULN)\n  * Platelet count (≥100,000 cells\u002Fmm3)\n  * Total bilirubin (\\\u003C1.6 x ULN)\n* HIV status determined based on testing meeting the requirements specified in protocol\n* For pregnant participants living with HIV: has a suppressed HIV viral load (HIV-1 RNA below the limit of quantification of the assay) on an ARV regimen for at least 30 consecutive days prior to entry that does not include efavirenz, etravirine, cobicistat, or any protease inhibitor (e.g., atazanavir, darunavir, lopinavir, ritonavir), as determined by the site investigator based on available medical records\n* At entry, expects to remain in the geographic area of the study site during pregnancy and for 10 weeks postpartum (or for 20 weeks post-entry, depending on gestational age at entry), as determined by the site investigator based on pregnant participant report\n\nExclusion Criteria:\n\n* Any previous treatment for hepatitis C, including HCV DAAs or interferon-based treatment\n* High risk of preterm delivery, defined as either of the following:\n\n  * History of spontaneous preterm delivery at less than 34 weeks, as determined by the site investigator based on pregnant participant report and available medical records, or\n  * Shortened cervix less than 20 mm if noted on ultrasound during the current pregnancy, as determined by the site investigator based on available medical records\n* Receipt of any prohibited medication, within 14 days prior to entry, as determined by the site investigator based on pregnant participant report and available medical records\n* Any of the following liver-related conditions:\n\n  * Clinical diagnosis of acute hepatitis not otherwise attributable to hepatitis C with AST or ALT ≥2.5 x ULN\n  * Evidence of decompensated cirrhosis including history of or present variceal hemorrhage, ascites, spontaneous bacterial peritonitis, hepatic encephalopathy, hepatocellular carcinoma, hepatorenal syndrome, or hepatopulmonary syndrome\n* Has any other documented or suspected clinically significant medical condition or any other condition that, in the opinion of the site investigator, would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving study objectives","FEMALE","16 Years","45 Years",{"count":199,"type":200},30,"ESTIMATED","INTERVENTIONAL",[203,204],"PHASE1","PHASE2","This is a Phase I\u002FII, multi-site, open-label, single arm study to describe the pharmacokinetics (PK) and safety of glecaprevir\u002Fpibrentasvir (GLE\u002FPIB) initiated during pregnancy in women with hepatitis C virus (HCV) infection (acute or chronic) with or without HIV and to evaluate safety for their infants through 10 weeks postpartum.",[207],"Hepatitis C",[209,207,210,211],"HIV","Pregnancy","Glecaprevir\u002FPibrentasvir","2026-06-29",{"date":214,"type":215},"2026-07-01","ACTUAL",{"date":217,"type":215},"2026-06-25",{"date":219,"type":200},"2027-10-30",{"name":5,"class":6},10]