메뉴 건너뛰기




Volumn 3, Issue 3, 2006, Pages 157-164

Development and validation of a quasi-quantitative bioassay for neutralizing antibodies against CP-870,893

Author keywords

Assay validation; Bioassay; CP 870,893; Daudi cell line; Neutralizing antibody

Indexed keywords

CD40 ANTIGEN; CP 870893; IDIOTYPIC ANTIBODY; IMMUNOGLOBULIN ANTIBODY; IMMUNOGLOBULIN G2; MONOCLONAL ANTIBODY; NEUTRALIZING ANTIBODY; UNCLASSIFIED DRUG;

EID: 33747619436     PISSN: 1547691X     EISSN: 1547691X     Source Type: Journal    
DOI: 10.1080/15476910600901535     Document Type: Conference Paper
Times cited : (9)

References (10)
  • 1
    • 3343015039 scopus 로고    scopus 로고
    • The role of the CD40 pathway in the pathogenesis and treatment of cancer
    • Eliopoulos, A. G., and Young, L. S. 2004. The role of the CD40 pathway in the pathogenesis and treatment of cancer. Curr. Opin. Pharmacol. 4:306-307.
    • (2004) Curr. Opin. Pharmacol. , vol.4 , pp. 306-307
    • Eliopoulos, A.G.1    Young, L.S.2
  • 2
    • 23944447879 scopus 로고    scopus 로고
    • Validation of immunoassays used to assess immunogenicity to therapeutic monoclonal antibodies
    • Geng, D., Shanker, G., Schantz, A., Rajadhyaksha, M., Davis, H., and Wagner, C. 2005. Validation of immunoassays used to assess immunogenicity to therapeutic monoclonal antibodies. J. Pharm. Biomed. Anal. 39:264-275.
    • (2005) J. Pharm. Biomed. Anal. , vol.39 , pp. 264-275
    • Geng, D.1    Shanker, G.2    Schantz, A.3    Rajadhyaksha, M.4    Davis, H.5    Wagner, C.6
  • 5
    • 0037277480 scopus 로고    scopus 로고
    • Prospects for CD40-directed experimental therapy of human cancer
    • Tong, A. W., and Stone, M. J. 2003. Prospects for CD40-directed experimental therapy of human cancer. Cancer Gene Ther. 10:1-13.
    • (2003) Cancer Gene Ther. , vol.10 , pp. 1-13
    • Tong, A.W.1    Stone, M.J.2
  • 8
    • 27544454016 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, and Center for Biologics Evaluation and Research. 2005. Guidance for Industry. Premarketing Risk Assessment. Available at (http://www.fda.gov/cber/guidelines.htm).
    • (2005) Guidance for Industry. Premarketing Risk Assessment
  • 9
    • 33747611389 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, and Center for Biologics Evaluation and Research. 2006. Guidance for Industry. S8 Immunotoxicity Studies for Human Pharmaceuticals. Available at (http://www.fda.gov/cber/guidelines.htm).
    • (2006) Guidance for Industry. S8 Immunotoxicity Studies for Human Pharmaceuticals


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.