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Volumn 15, Issue 1, 2001, Pages 33-45
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Phase I/II dose escalation and randomized withdrawal study with add-on azodicarbonamide in patients failing on current antiretroviral therapy
a,g b b a c c c d e e f
e
Hubriphar SA
(Belgium)
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Author keywords
[No Author keywords available]
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Indexed keywords
ANTIRETROVIRUS AGENT;
AZOFORMAMIDE;
UNCLASSIFIED DRUG;
UREA DERIVATIVE;
ZINC FINGER PROTEIN;
ACQUIRED IMMUNE DEFICIENCY SYNDROME;
ADULT;
ANTIMICROBIAL THERAPY;
ARTICLE;
CLINICAL ARTICLE;
CLINICAL TRIAL;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
DOSE RESPONSE;
DOUBLE BLIND PROCEDURE;
DRUG EFFICACY;
DRUG SAFETY;
FEMALE;
HUMAN;
HUMAN IMMUNODEFICIENCY VIRUS 1;
HUMAN IMMUNODEFICIENCY VIRUS INFECTION;
LYMPHOCYTE COUNT;
MALE;
MAXIMUM ALLOWABLE CONCENTRATION;
PHASE 1 CLINICAL TRIAL;
PHASE 2 CLINICAL TRIAL;
PHENOTYPE;
PRACTICE GUIDELINE;
PRIORITY JOURNAL;
RANDOMIZED CONTROLLED TRIAL;
TREATMENT OUTCOME;
ACQUIRED IMMUNODEFICIENCY SYNDROME;
ADULT;
ANTI-HIV AGENTS;
AZO COMPOUNDS;
CD4 LYMPHOCYTE COUNT;
CD4-CD8 RATIO;
CONSUMER PRODUCT SAFETY;
DOUBLE-BLIND METHOD;
HIV-1;
HUMANS;
MALE;
MIDDLE AGED;
TREATMENT FAILURE;
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EID: 0035808584
PISSN: 02699370
EISSN: None
Source Type: Journal
DOI: 10.1097/00002030-200101050-00007 Document Type: Article |
Times cited : (45)
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References (44)
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