Ignite Creation Date:
2025-12-24 @ 2:13 PM
Ignite Modification Date:
2025-12-25 @ 4:05 PM
Study NCT ID:
NCT00885495
Status:
COMPLETED
Last Update Posted:
2022-02-11
First Post:
2009-04-20
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Darunavir/Ritonavir and Rosuvastatin Pharmacokinetic Study
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D015658', 'term': 'HIV Infections'}, {'id': 'D050171', 'term': 'Dyslipidemias'}], 'ancestors': [{'id': 'D000086982', 'term': 'Blood-Borne Infections'}, {'id': 'D003141', 'term': 'Communicable Diseases'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D015229', 'term': 'Sexually Transmitted Diseases, Viral'}, {'id': 'D012749', 'term': 'Sexually Transmitted Diseases'}, {'id': 'D016180', 'term': 'Lentivirus Infections'}, {'id': 'D012192', 'term': 'Retroviridae Infections'}, {'id': 'D012327', 'term': 'RNA Virus Infections'}, {'id': 'D014777', 'term': 'Virus Diseases'}, {'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D007153', 'term': 'Immunologic Deficiency Syndromes'}, {'id': 'D007154', 'term': 'Immune System Diseases'}, {'id': 'D052439', 'term': 'Lipid Metabolism Disorders'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000069454', 'term': 'Darunavir'}, {'id': 'D019438', 'term': 'Ritonavir'}, {'id': 'D000068718', 'term': 'Rosuvastatin Calcium'}], 'ancestors': [{'id': 'D013449', 'term': 'Sulfonamides'}, {'id': 'D000577', 'term': 'Amides'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D002219', 'term': 'Carbamates'}, {'id': 'D000144', 'term': 'Acids, Acyclic'}, {'id': 'D002264', 'term': 'Carboxylic Acids'}, {'id': 'D013450', 'term': 'Sulfones'}, {'id': 'D013457', 'term': 'Sulfur Compounds'}, {'id': 'D005663', 'term': 'Furans'}, {'id': 'D006573', 'term': 'Heterocyclic Compounds, 1-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D013844', 'term': 'Thiazoles'}, {'id': 'D001393', 'term': 'Azoles'}, {'id': 'D005464', 'term': 'Fluorobenzenes'}, {'id': 'D006845', 'term': 'Hydrocarbons, Fluorinated'}, {'id': 'D006846', 'term': 'Hydrocarbons, Halogenated'}, {'id': 'D006838', 'term': 'Hydrocarbons'}, {'id': 'D011743', 'term': 'Pyrimidines'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'carl.fichtenbaum@uc.edu', 'phone': '513-584-6361', 'title': 'Dr. Carl J. Fichtenbaum', 'organization': 'University of Cincinnati College of Medicine'}, 'certainAgreement': {'piSponsorEmployee': False, 'restrictiveAgreement': False}, 'limitationsAndCaveats': {'description': 'No clinical outcome data beyond 7 days is available. Cannot necessarily extrapolate directly to persons with HIV.'}}, 'adverseEventsModule': {'eventGroups': [{'id': 'EG000', 'title': 'Darunavir+Ritonavir', 'description': 'Darunavir 600 mg and ritonavir 100 mg twice daily x 7 days', 'otherNumAtRisk': 15, 'otherNumAffected': 6, 'seriousNumAtRisk': 15, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Rosuvastatin', 'description': 'Rosuvastatin 10 mg daily x 7 days', 'otherNumAtRisk': 14, 'otherNumAffected': 4, 'seriousNumAtRisk': 14, 'seriousNumAffected': 0}, {'id': 'EG002', 'title': 'Darunavir, Ritonavir and Rosuvastatin', 'description': 'Darunavir 600 mg and Ritonavir 100 mg twice daily with Rosuvastatin 10 mg daily x 7 days', 'otherNumAtRisk': 12, 'otherNumAffected': 4, 'seriousNumAtRisk': 12, 'seriousNumAffected': 0}], 'otherEvents': [{'term': 'Headache', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 1}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 1}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Nausea', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Diarrhea', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 4}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 0}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Skin Rash', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 3}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 0}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Elevated AST', 'notes': 'Grade I \\< 2 x ULN', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 2}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 1}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 1}], 'organSystem': 'Hepatobiliary disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Muscle Weakness', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 1}], 'organSystem': 'Musculoskeletal and connective tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Sinus congestion', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 1}], 'organSystem': 'Respiratory, thoracic and mediastinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Upper respiratory infection', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 1}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 0}], 'organSystem': 'Respiratory, thoracic and mediastinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Elevated CPK', 'notes': 'Grade I \\< 3 x ULN', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 2}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 0}], 'organSystem': 'Musculoskeletal and connective tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Anemia', 'notes': 'Grade I: 10-12 gm/dL', 'stats': [{'groupId': 'EG000', 'numAtRisk': 15, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 14, 'numAffected': 1}, {'groupId': 'EG002', 'numAtRisk': 12, 'numAffected': 0}], 'organSystem': 'Blood and lymphatic system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}], 'frequencyThreshold': '1'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Cmax of Rosuvastatin', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}, {'value': '12', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Rosuvastatin', 'description': 'Rosuvastatin 10 mg daily for 7 days.'}, {'id': 'OG001', 'title': 'Rosuvastatin-Darunavir-Ritonavir', 'description': 'Rosuvastatin 10 mg daily, Darunavir 600 mg and Ritonavir 100 mg twice daily for 7 days'}], 'classes': [{'categories': [{'measurements': [{'value': '6.70', 'groupId': 'OG000', 'lowerLimit': '5.26', 'upperLimit': '8.53'}, {'value': '16.32', 'groupId': 'OG001', 'lowerLimit': '11.78', 'upperLimit': '22.61'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': '7 days', 'unitOfMeasure': 'ng/mL', 'dispersionType': '90% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Analysis of 12 subjects who completed all 3 PK visits'}, {'type': 'PRIMARY', 'title': 'AUC of Rosuvastatin', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}, {'value': '12', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Rosuvastatin', 'description': 'Rosuvastatin 10 mg daily for 7 days.'}, {'id': 'OG001', 'title': 'Rosuvastatin-Darunavir-Ritonavir', 'description': 'Rosuvastatin 10 mg daily, Darunavir 600 mg and Ritonavir 100 mg twice daily for 7 days'}], 'classes': [{'categories': [{'measurements': [{'value': '108.96', 'groupId': 'OG000', 'lowerLimit': '83.85', 'upperLimit': '141.6'}, {'value': '161.24', 'groupId': 'OG001', 'lowerLimit': '124.62', 'upperLimit': '208.59'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': '7 days', 'unitOfMeasure': 'ng*hr/mL', 'dispersionType': '90% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Analysis of 12 subjects who completed all 3 PK visits'}, {'type': 'SECONDARY', 'title': 'To Investigate the Effect of Rosuvastatin on the Steady State Pharmacokinetics of Darunavir/Ritonavir.', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Darunavir/Ritonavir+Rosuvastatin', 'description': 'Combination of all three medications'}], 'classes': [{'title': 'Darunavir Cmin with Rosuvastatin', 'categories': [{'measurements': [{'value': '2744', 'groupId': 'OG000', 'lowerLimit': '2157', 'upperLimit': '3492'}]}]}, {'title': 'Darunavir Cmin absent Rosuvastatin', 'categories': [{'measurements': [{'value': '3235', 'groupId': 'OG000', 'lowerLimit': '2759', 'upperLimit': '3794'}]}]}, {'title': 'Ritonavir Cmin absent Rousuvastatin', 'categories': [{'measurements': [{'value': '194', 'groupId': 'OG000', 'lowerLimit': '142', 'upperLimit': '266'}]}]}, {'title': 'Ritonavir Cmin with Rousuvastatin present', 'categories': [{'measurements': [{'value': '148', 'groupId': 'OG000', 'lowerLimit': '107', 'upperLimit': '204'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': '45 days', 'description': 'Geometric mean of the Concentration minimum of darunavir and ritonavir in the presence and absence of rosuvastatin.', 'unitOfMeasure': 'ng/mL', 'dispersionType': '90% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants taking all three medications'}, {'type': 'SECONDARY', 'title': 'To Compare the Change in Low-density Lipoprotein (LDL) Cholesterol With Rosuvastatin Therapy Alone, Darunavir/Ritonavir Therapy Alone and With the Co-administration of Rosuvastatin and Darunavir/Ritonavir.', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}, {'value': '12', 'groupId': 'OG001'}, {'value': '12', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Rosuvastatin Alone', 'description': 'LDL values with rosuvastatin administration'}, {'id': 'OG001', 'title': 'Darunavir/Ritonavir', 'description': 'LDL values with darunavir/ritonavir administration'}, {'id': 'OG002', 'title': 'Rosuvastatin+Darunavir/Ritonavir', 'description': 'LDL values with all three medications'}], 'classes': [{'categories': [{'measurements': [{'value': '85', 'groupId': 'OG000', 'lowerLimit': '55', 'upperLimit': '96'}, {'value': '115', 'groupId': 'OG001', 'lowerLimit': '85', 'upperLimit': '148'}, {'value': '80', 'groupId': 'OG002', 'lowerLimit': '69', 'upperLimit': '101'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': '45 days', 'description': 'LDL values', 'unitOfMeasure': 'mg/dL', 'dispersionType': 'Inter-Quartile Range', 'reportingStatus': 'POSTED', 'populationDescription': 'Individuals taking medications with measurements of LDL'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'B-Darunavir+Ritonavir Initial Arm', 'description': 'Darunavir+ritonavir x 7 days; Rosuvastatin x 7 days; Combination x 7 days'}, {'id': 'FG001', 'title': 'A-Rosuvastatin Initial Arm', 'description': 'Rosuvastatin x 7 days; darunavir+ritonavir x 7 days; Combination x 7 days'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '8'}, {'groupId': 'FG001', 'numSubjects': '9'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '6'}, {'groupId': 'FG001', 'numSubjects': '6'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '3'}]}], 'dropWithdraws': [{'type': 'Adverse Event', 'reasons': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '2'}]}, {'type': 'Protocol Violation', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '1'}]}, {'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}], 'recruitmentDetails': 'Subjects were recruited from the community between September 2008 and March 2009', 'preAssignmentDetails': '1 subject was excluded based upon elevated triglyceride level prior to randomization'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'BG000'}, {'value': '9', 'groupId': 'BG001'}, {'value': '17', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': 'B-Darunavir+Ritonavir Initial Arm', 'description': 'Darunavir+ritonavir x 7 days; Rosuvastatin x 7 days; Combination x 7 days'}, {'id': 'BG001', 'title': 'A-Rosuvastatin Initial Arm', 'description': 'Rosuvastatin x 7 days; darunavir+ritonavir x 7 days; Combination x 7 days'}, {'id': 'BG002', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Categorical', 'classes': [{'categories': [{'title': '<=18 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Between 18 and 65 years', 'measurements': [{'value': '8', 'groupId': 'BG000'}, {'value': '9', 'groupId': 'BG001'}, {'value': '17', 'groupId': 'BG002'}]}, {'title': '>=65 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '28', 'spread': '11', 'groupId': 'BG000'}, {'value': '28', 'spread': '10', 'groupId': 'BG001'}, {'value': '28', 'spread': '10', 'groupId': 'BG002'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '3', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '8', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '5', 'groupId': 'BG000'}, {'value': '4', 'groupId': 'BG001'}, {'value': '9', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '8', 'groupId': 'BG000'}, {'value': '9', 'groupId': 'BG001'}, {'value': '17', 'groupId': 'BG002'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1', 'PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'CROSSOVER'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 17}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2009-01'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-01', 'completionDateStruct': {'date': '2010-08', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2022-01-19', 'studyFirstSubmitDate': '2009-04-20', 'resultsFirstSubmitDate': '2011-03-24', 'studyFirstSubmitQcDate': '2009-04-21', 'lastUpdatePostDateStruct': {'date': '2022-02-11', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2021-12-20', 'studyFirstPostDateStruct': {'date': '2009-04-22', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2022-01-19', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2010-04', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Cmax of Rosuvastatin', 'timeFrame': '7 days'}, {'measure': 'AUC of Rosuvastatin', 'timeFrame': '7 days'}], 'secondaryOutcomes': [{'measure': 'To Investigate the Effect of Rosuvastatin on the Steady State Pharmacokinetics of Darunavir/Ritonavir.', 'timeFrame': '45 days', 'description': 'Geometric mean of the Concentration minimum of darunavir and ritonavir in the presence and absence of rosuvastatin.'}, {'measure': 'To Compare the Change in Low-density Lipoprotein (LDL) Cholesterol With Rosuvastatin Therapy Alone, Darunavir/Ritonavir Therapy Alone and With the Co-administration of Rosuvastatin and Darunavir/Ritonavir.', 'timeFrame': '45 days', 'description': 'LDL values'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['HIV', 'dyslipidemia', 'statins', 'protease inhibitors'], 'conditions': ['HIV Infections']}, 'descriptionModule': {'briefSummary': 'This is a phase I, open-label, controlled drug interaction study to determine the effects of darunavir plus ritonavir on the pharmacokinetics of the hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, rosuvastatin, in HIV-1-seronegative subjects.', 'detailedDescription': 'Twelve HIV-negative healthy volunteers will be randomized to one of two groups. Group 1 would receive rosuvastatin 10mg daily (Treatment A) in interval 1 for 7 days, followed by a washout period of at least 7 days. In interval 2, darunavir/ritonavir 600/100mg bid (Treatment B) would be administered for 7 days, followed by another 7 day washout period. Lastly, in interval 3 subjects will administer darunavir/ritonavir and rosuvastatin (Treatment C) for total of 7 days. Group 2 will administer Treatment B in interval 1 for 7 days, followed by a washout period of 7 days, then treatment A in interval 2 for 7 days followed by another 7 day washout period. Group 2 would then co-administer rosuvastatin and darunavir/ritonavir for the last 7 days. Intensive PK sampling will be performed on day 7, 21 and 35 following a meal.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Absence of HIV-1/HIV-2 infection as documented by a licensed ELISA test kit within 21 days prior to study entry.\n2. Male or female subjects, aged ≥ 18 and ≤ 60 years\n3. Weight ≥50 kg and a Body Mass Index (\\[BMI\\], weight in kg divided by the square of height in meters) ≥18.0 and ≤ 35.0 kg/m2. Refer to Appendix I.\n4. Informed Consent Form (ICF) signed voluntarily before the first trial-related activity.\n5. Able to comply with protocol requirements.\n6. Healthy on the basis of a medical evaluation that reveals the absence of any clinically relevant abnormality and includes a physical examination, medical history, vital signs, and the results of blood tests and a urinalysis carried out at screening.\n\nExclusion Criteria:\n\n1. History or evidence of current use of alcohol, barbiturate, amphetamine, recreational or narcotic drug use, which in the investigator\'s opinion would compromise subject\'s safety and/or compliance with the trial procedures.\n2. Currently active significant gastrointestinal, cardiovascular, neurologic, psychiatric, metabolic, renal, hepatic, respiratory, inflammatory, or infectious disease, that in the opinion of the investigator would represent a contraindication to study enrollment.\n3. Creatinine clearance of ≤ 60mL/min.\n4. Currently significant diarrhea, gastric stasis, or constipation that in the investigator\'s opinion could influence drug absorption or bioavailability.\n5. eruptions, drug allergies, food allergy, dermatitis, eczema, psoriasis, or urticaria, that in the opinion of the investigator would represent a contraindication to study enrollment.\n6. Previously demonstrated clinically significant allergy or hypersensitivity to any of the excipients of the medications administered in the trial.\n7. History of significant drug allergy such as, but not limited to, sulphonamides and penicillins. Prezista is a sulphonamide. The potential for cross-sensitivity between drugs in the sulphonamide class and Prezista in HIV-negative subjects is unknown.\n8. Use of concomitant medication, including investigational, prescription, and over-the-counter products and dietary supplements with the following exceptions: aspirin, acetaminophen, anti-histamines such as diphenhydramine, inhalers for asthma, daily multivitamins, mineral supplements and hormonal oral contraceptives. Concomitant medication other than those listed above must have been discontinued at least 7 days before study entry.\n9. Female subjects of childbearing potential without use of effective nonhormonal birth control methods, or not willing to continue practicing these birth control methods for at least 30 days after the end of the treatment period; Note: Estrogen-based hormonal contraception may not be reliable when taking Prezista, therefore to be eligible for this trial, women of childbearing potential should either:\n\n * use a double barrier method to prevent pregnancy (i.e., using a condom with either diaphragm or cervical cap);\n * use non-estrogen hormonal based contraceptives in combination with a barrier contraceptive (i.e., male condom, diaphragm or cervical cap, or female condom);\n * use a intrauterine device in combination with a barrier contraceptive (i.e., male condom, diaphragm or cervical cap, or female condom);\n * be not sexually active, or have a vasectomized partner (confirmed sterile).\n\n Women with tubal ligation are required to use one non-hormonal contraceptive method.\n\n Women who are postmenopausal for at least 2 years, and women with total hysterectomy are considered of non-childbearing potential.\n10. A positive pregnancy test or breast feeding at screening.\n11. Participation in an investigational drug trial within 90 days prior to the first intake of trial medication.\n12. Donation of blood or plasma within 60 days preceding the first trial-related blood drawing.\n13. Subjects with the following laboratory abnormalities at screening as defined by the Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events ("DAIDS grading table") and in accordance with the normal ranges of the trial clinical laboratory:\n\n * serum creatinine grade 1 or greater (≥ 1.1 x upper limit of laboratory normal range \\[ULN\\]);\n * lipase or pancreatic amylase grade 1 or greater (≥ 1.1 x ULN);\n * hemoglobin grade 1 or greater (≤ 10.9 g/dL)\n * platelet count grade 1 or greater (≤ 124.999 x 109/L);\n * absolute neutrophil count grade 1 or greater (≤ 1.3 x 109/L);\n * aspartate aminotransferase (AST) or alanine aminotransferase (ALT) grade 1 or greater (≥ 1.25 x ULN);\n * total bilirubin grade 1 or greater (≥ 1.1 x ULN),\n * any other laboratory abnormality of grade 2 or above'}, 'identificationModule': {'nctId': 'NCT00885495', 'briefTitle': 'Darunavir/Ritonavir and Rosuvastatin Pharmacokinetic Study', 'organization': {'class': 'OTHER', 'fullName': 'University of Cincinnati'}, 'officialTitle': 'The Effects of Darunavir Plus Ritonavir on the Pharmacokinetics and Pharmacodynamics of Rosuvastatin', 'orgStudyIdInfo': {'id': 'IDC 40'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'B', 'description': 'Darunavir+ritonavir x 7 days; Rosuvastatin x 7 days; Combination x 7 days', 'interventionNames': ['Drug: darunavir, ritonavir, rosuvastatin']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'A', 'description': 'Rosuvastatin x 7 days; darunavir+ritonavir x 7 days; Combination x 7 days', 'interventionNames': ['Drug: rosuvastatin, darunavir, ritonavir']}], 'interventions': [{'name': 'darunavir, ritonavir, rosuvastatin', 'type': 'DRUG', 'otherNames': ['Prezista', 'Norvir', 'Crestor'], 'description': 'darunavir 600 mg twice daily for 7 days ritonavir 100 mg twice daily for 7 days rosuvastatin 10 mg once daily for 7 days Combination of all three drugs for 7 days', 'armGroupLabels': ['B']}, {'name': 'rosuvastatin, darunavir, ritonavir', 'type': 'DRUG', 'otherNames': ['Prezista', 'Norvir', 'Crestor'], 'description': 'rosuvastatin 10 mg daily for 7 days; darunavir 600 mg twice daily for 7 days with ritonavir 100 mg twice daily for 7 days; Combination of all three for 7 days', 'armGroupLabels': ['A']}]}, 'contactsLocationsModule': {'locations': [{'zip': '45267', 'city': 'Cincinnati', 'state': 'Ohio', 'country': 'United States', 'facility': 'University of Cincinnati AIDS Clinical Trials Unit', 'geoPoint': {'lat': 39.12711, 'lon': -84.51439}}], 'overallOfficials': [{'name': 'Carl J Fichtenbaum, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Cincinnati'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of Cincinnati', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Professor', 'investigatorFullName': 'Carl J. Fichtenbaum', 'investigatorAffiliation': 'University of Cincinnati'}}}}