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Volumn 4, Issue 4, 2015, Pages e76-e83
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Pharmacokinetics and 48-week safety and efficacy of raltegravir for oral suspension in human immunodeficiency virus type-1-infected children 4 weeks to 2 years of age
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Author keywords
Pediatric HIV; Raltegravir; Treatment
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Indexed keywords
INTEGRASE INHIBITOR;
PROTEINASE INHIBITOR;
RALTEGRAVIR;
RNA DIRECTED DNA POLYMERASE;
VIRUS RNA;
ACQUIRED IMMUNE DEFICIENCY SYNDROME;
ANTIBIOTIC RESISTANCE;
ARTICLE;
CD4 LYMPHOCYTE COUNT;
CHILD;
DRUG EFFICACY;
DRUG SAFETY;
FEMALE;
HIGHLY ACTIVE ANTIRETROVIRAL THERAPY;
HUMAN;
HUMAN IMMUNODEFICIENCY VIRUS 1 INFECTION;
IMMUNE RECONSTITUTION INFLAMMATORY SYNDROME;
IMMUNE RESPONSE;
INFANT;
MAJOR CLINICAL STUDY;
MALE;
MAXIMUM PLASMA CONCENTRATION;
MOTHER TO CHILD VIRUS TRANSMISSION;
MULTICENTER STUDY;
NEWBORN;
OPEN STUDY;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
RASH;
SENSITIVITY ANALYSIS;
TIME TO MAXIMUM PLASMA CONCENTRATION;
VIRUS TRANSMISSION;
CLINICAL TRIAL;
HIV INFECTIONS;
HUMAN IMMUNODEFICIENCY VIRUS 1;
ORAL DRUG ADMINISTRATION;
PHASE 1 CLINICAL TRIAL;
PHASE 2 CLINICAL TRIAL;
ADMINISTRATION, ORAL;
CHILD, PRESCHOOL;
FEMALE;
HIV INFECTIONS;
HIV-1;
HUMANS;
INFANT;
MALE;
RALTEGRAVIR POTASSIUM;
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EID: 85006213867
PISSN: 20487193
EISSN: 20487207
Source Type: Journal
DOI: 10.1093/jpids/piu146 Document Type: Article |
Times cited : (30)
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References (11)
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