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Volumn 22, Issue 5, 2001, Pages 485-502
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Considerations in the evaluation of surrogate endpoints in clinical trials: Summary of a National Institutes of Health Workshop
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Author keywords
Biomarkers; Meta analysis; Surrogate endpoints
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Indexed keywords
ANTIRETROVIRUS AGENT;
BIOCHEMICAL MARKER;
CD4 ANTIGEN;
NELFINAVIR;
VIRUS RNA;
ZIDOVUDINE;
ACQUIRED IMMUNE DEFICIENCY SYNDROME;
CLINICAL RESEARCH;
CLINICAL TRIAL;
CONFERENCE PAPER;
DATA BASE;
DIAGNOSTIC VALUE;
DISEASE MARKER;
EARLY DIAGNOSIS;
EVALUATION;
GENOME;
HEALTH CARE ORGANIZATION;
HUMAN;
MATHEMATICAL ANALYSIS;
META ANALYSIS;
METHODOLOGY;
PERSONNEL;
PREDICTION;
PROGNOSIS;
REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;
STATISTICAL MODEL;
T LYMPHOCYTE;
TECHNOLOGY;
TRAINING;
TREATMENT OUTCOME;
VIRUS LOAD;
VIRUS TRANSMISSION;
WORKSHOP;
ANTIVIRAL AGENTS;
BIOLOGICAL MARKERS;
BIOTECHNOLOGY;
CLINICAL TRIALS;
CONSENSUS DEVELOPMENT CONFERENCES;
DISEASE TRANSMISSION, VERTICAL;
FEMALE;
GENOMICS;
HIV INFECTIONS;
HIV-1;
HUMANS;
META-ANALYSIS;
NATIONAL INSTITUTES OF HEALTH (U.S.);
PREDICTIVE VALUE OF TESTS;
PREGNANCY;
RESEARCH DESIGN;
RNA, VIRAL;
UNITED STATES;
VIRAL LOAD;
ZIDOVUDINE;
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EID: 0034802767
PISSN: 01972456
EISSN: None
Source Type: Journal
DOI: 10.1016/S0197-2456(01)00153-2 Document Type: Conference Paper |
Times cited : (370)
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References (18)
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