[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100586126":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":28,"centralContacts":29,"locations":35,"responsibleParty":62,"collaborators":28,"id":64,"slug":28,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":28,"eligibilityCriteria":69,"healthyVolunteers":70,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":28,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":28,"overallStatus":38,"whyStopped":28,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"Atea Pharmaceuticals, Inc.","INDUSTRY",[8,14,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Group 1 - Severe Renal Impairment","EXPERIMENTAL","Single dose Bemnifosbuvir (BEM)\u002FRuzasvir (RZR) as a fixed-dose combination",[13],"Drug: Bemnifosbuvir (BEM)\u002FRuzasvir (RZR) as a fixed-dose combination",{"label":15,"type":10,"description":11,"interventionNames":16},"Group 2 - Severe Hepatic Impairment",[13],{"label":18,"type":10,"description":11,"interventionNames":19},"Group 3 - Matched Healthy Subjects",[13],[21],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DRUG","Bemnifosbuvir (BEM)\u002FRuzasvir (RZR) as a fixed-dose combination","A single dose of BEM\u002FRZR will be administered",[9,15,18],[27],"AT-527 (BEM) and AT-038 (RZR)",null,[30],{"name":31,"role":32,"phone":33,"phoneExt":28,"email":34},"Atea Study Clinical Trials Administrator","CONTACT","888-481-1607","ateaclinicaltrials@ateapharma.com",[36,52],{"facility":37,"status":38,"city":39,"state":40,"zip":41,"country":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Atea Study Site","RECRUITING","Orlando","Florida","32809","United States",{"type":44,"coordinates":45},"Point",[46,47],-81.37924,28.53834,{"lat":47,"lon":46},[50],{"name":37,"role":32,"phone":33,"phoneExt":28,"email":51},"AteaClinicalTrials@ateapharma.com",{"facility":37,"status":38,"city":53,"state":40,"zip":54,"country":42,"cosmosGeoPoint":55,"geoPoint":59,"contacts":60},"Tampa","33603",{"type":44,"coordinates":56},[57,58],-82.45843,27.94752,{"lat":58,"lon":57},[61],{"name":37,"role":32,"phone":33,"phoneExt":28,"email":51},{"type":63,"investigatorFullName":28,"investigatorTitle":28,"investigatorAffiliation":28,"oldNameTitle":28,"oldOrganization":28},"SPONSOR","100586126",false,"NCT06911320","Study of Bemnifosbuvir\u002FRuzasvir as a Fixed-dose Combination in Subjects With Normal or Severely Impaired Renal or Hepatic Function","A Phase 1, Open-Label, Parallel-Group, Single-Dose Study to Evaluate the Safety and Pharmacokinetics of Bemnifosbuvir and Ruzasvir Administered as a Fixed-Dose Combination in Adult Participants With Severe Renal or Hepatic Impairment in Comparison to Healthy Participants","Inclusion Criteria:\n\n* Must agree to use two methods of birth control from Screening through 90 days after administration of the last dose of study drug\n* Females must have a negative pregnancy test at Screening and prior to dosing\n* BMI of 18.5 to 43.0 kg\u002Fm2\n* Willing to comply with the study requirements and to provide written informed consent\n\nRenal Impaired Subjects (Group 1):\n\n* Considered stable in the judgement of an Investigator\n* Presence of severe renal impairment or kidney failure (as defined by eGFR\\\u003C 30 mL\u002F min)\n\nHepatic Impaired Subjects (Group 2):\n\n* Considered stable for at least 1 month prior to Screening, as per the judgement of an Investigator\n* Presence of severe hepatic impairment (Child-Pugh Class C: score of 10 to 15).\n\nSubjects with Normal Hepatic and Renal Function (Group 3):\n\n* Medically healthy, in the opinion of an Investigator\n* Must match by gender, age (± 10 years), and BMI (within 20%) to the pooled mean values of subjects with severe renal and hepatic impairment\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding\n* Infected with hepatitis B virus, hepatitis C virus or HIV\n* Abuse of alcohol or drugs\n* Use of other investigational drugs within 28 days of dosing\n* Other clinically significant medical conditions or laboratory abnormalities\n\nRenal and Hepatic Impaired Subjects (Group 1 and 2):\n\n* Presence of poorly controlled Type 1 or Type 2 diabetes as defined by Hemoglobin A1c \\> 10%\n* Undergoing any method of dialysis\n* Subjects requiring treatment for hepatic impairment or other chronic disease must be on a stable treatment plan\n\nRenal Impaired Subjects (Group 1):\n\n* History of renal transplant\n* Concurrent use of medications known to affect the elimination of serum creatinine\n\nHepatic Impaired Subjects (Group 2):\n\n* History of liver transplant\n* Evidence of hepatic carcinoma presence at Screening",true,"ALL","18 Years","80 Years",{"count":75,"type":76},28,"ESTIMATED","INTERVENTIONAL",[79],"PHASE1","To Assess the Effect of Severe Hepatic or Renal Impairment on the Pharmacokinetics of Bemnifosbuvir\u002FRuzasvir After a Single Dose",[82,83,84],"Healthy Volunteer Study","Hepatic Impairment","Renal Impairment","2026-04-08",{"date":87,"type":88},"2026-04-13","ACTUAL",{"date":90,"type":88},"2025-04-09",{"date":92,"type":76},"2026-05",{"name":5,"class":6},2]