Authors:
Moreland, LW
McCabe, DP
Caldwell, JR
Sack, M
Weisman, M
Henry, G
Seely, JE
Martin, SW
Yee, CL
Bendele, AM
Frazier, JL
Kohno, T
Cosenza, ME
Lyons, SA
Dayer, JM
Cohen, AM
Edwards, CK
Citation: Lw. Moreland et al., Phase I/II trial of recombinant methionyl human tumor necrosis factor binding protein PEGylated dimer in patients with active refractory rheumatoid arthritis, J RHEUMATOL, 27(3), 2000, pp. 601-609
Authors:
Silbaugh, SA
Stengel, PW
Cockerham, SL
Froelich, LL
Bendele, AM
Spaethe, SM
Sofia, MJ
Sawyer, JS
Jackson, WT
Citation: Sa. Silbaugh et al., Pharmacologic actions of the second generation leukotriene B-4 receptor antagonist LY293111: in vivo pulmonary studies, N-S ARCH PH, 361(4), 2000, pp. 397-404
Authors:
Bendele, AM
Chlipala, ES
Scherrer, J
Frazier, J
Sennello, G
Rich, WJ
Edwards, CK
Citation: Am. Bendele et al., Combination benefit of treatment with the cytokine inhibitors interleukin-1 receptor antagonist and PEGylated soluble tumor necrosis factor receptor type I in animal models of rheumatoid arthritis, ARTH RHEUM, 43(12), 2000, pp. 2648-2659
Authors:
Davis, MW
Feige, U
Bendele, AM
Martin, SW
Edwards, CK
Citation: Mw. Davis et al., Treatment of rheumatoid arthritis with PEGylated recombinant human solubletumour necrosis factor receptor type I: a clinical update, ANN RHEUM D, 59, 2000, pp. 41-43
Authors:
Bendele, AM
McComb, J
Gould, T
Frazier, J
Chlipala, ES
Seely, J
Kieft, G
Wolf, J
Edwards, CK
Citation: Am. Bendele et al., Combination benefit of PEGylated soluble tumor necrosis factor receptor type I (PEG sTNF-RI) and dexamethasone or indomethacin in adjuvant arthritic rats, INFLAMM RES, 48(8), 1999, pp. 453-460
Authors:
Bendele, AM
McComb, J
Gould, T
Frazier, J
Chlipala, E
Seely, J
Kieft, G
Edwards, CK
Citation: Am. Bendele et al., Effects of PEGylated soluble tumor necrosis factor receptor type I (PEG sTNF-RI) alone and in combination with methotrexate in adjuvant arthritic rats, CLIN EXP RH, 17(5), 1999, pp. 553-560
Authors:
Black, LE
Bendele, AM
Bendele, RA
Zack, PM
Hamilton, M
Citation: Le. Black et al., Regulatory decision strategy for entry of a novel biologic therapeutic with a clinically unmonitorable toxicity into clinical trials: Pre-IND meetings and a case example, TOX PATHOL, 27(1), 1999, pp. 22-26