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Volumn 2, Issue 5, 2002, Pages 523-528

HIV entry inhibitors in clinical development

Author keywords

[No Author keywords available]

Indexed keywords

1,1' [1,4 PHENYLENEBIS(METHYLENE)]BIS(1,4,8,11 TETRAAZACYCLOTETRADECANE); 4 BENZOYL 1 [(4 METHOXY 1H PYRROLO[2,3 B]PYRIDIN 3 YL)OXOACETYL] 2 METHYLPIPERAZINE; 4 [(4 BROMOPHENYL)(ETHOXYIMINO)METHYL] 1' [(2,4 DIMETHYL 3 PYRIDINYL)CARBONYL] 4' METHYL 1,4' BIPIPERIDINE; AMD 3645; ANTIVIRUS AGENT; CD4 ANTIGEN; CD4 IMMUNOGLOBULIN; CD4 IMMUNOGLOBULIN G2; CHEMOKINE RECEPTOR CCR5; CHEMOKINE RECEPTOR CXCR4; ENFUVIRTIDE; GLYCOPROTEIN GP 120; PRO 140; PROTEINASE INHIBITOR; RNA DIRECTED DNA POLYMERASE INHIBITOR; T 1249; UNCLASSIFIED DRUG; ZIDOVUDINE;

EID: 0036790563     PISSN: 14714892     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1471-4892(02)00196-0     Document Type: Review
Times cited : (43)

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    • Clotet B, Lazzarin A, Cooper D, Reynes J, Arasteh K, Nelson M, Katlama C, Chung J, Fang L, Delehanty J, M Salgo M: Enfuvirtide (T-20) in combination with an optimized background (OB) regimen vs. OB alone in patients with prior experience or resistance to each of the three classes of approved antiretrovirals (ARVs) in Europe and Australia (TORO 2). Abstract LbOr19A of the 14th International AIDS Conference, 2002 July 7-12, Barcelona, Spain.
    • (2002)
    • Clotet, B.1    Lazzarin, A.2    Cooper, D.3    Reynes, J.4    Arasteh, K.5    Nelson, M.6    Katlama, C.7    Chung, J.8    Fang, L.9    Delehanty, J.M.10    Salgo, M.11


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.