Zobrazeno 1 - 10
of 11
pro vyhledávání: '"M E Lebsack"'
Publikováno v:
Arthritis & Rheumatism. 39:1092-1101
Objective. To preliminarily evaluate the safety and efficacy of different dose levels and dosing frequencies of recombinant human interleukin-1 receptor antagonist (rHuIL-1Ra) in the treatment of patients with rheumatoid arthritis (RA). Methods. One
Autor:
Julie M. Vose, James R. Anderson, L. Garrison, M. E. Lebsack, J. E. Anderson, Philip J. Bierman, Frederick R. Appelbaum, James O. Armitage
Publikováno v:
Journal of Clinical Oncology. 14:520-526
PURPOSE A phase I/II study of PIXY321 following high-dose therapy (HDT) and autologous bone marrow transplantation (ABMT) was conducted to evaluate the safety and clinical potential of this agent. PATIENTS AND METHODS Fifty patients with Hodgkin's di
Autor:
Margaret Chrymko, M. E. Lebsack, Ralph Abadier, Kathleen A. Stringer, Donald F. Switzer, Allen J. Sedman
Publikováno v:
The Journal of Clinical Pharmacology. 31:607-610
The effect of administration of pirmenol, an extensively metabolized and plasma protein-bound antiarrhythmic agent, was evaluated in ten patients on chronic warfarin therapy. After a 3-week baseline period and 7 days of placebo administration, patien
Autor:
C Nichols, C F LeMaistre, A Smith, M Lange, J. E. Anderson, J M Fernandez Ranada, Julie M. Vose, W Longo, L. Garrison, E A Copelan, A Granena, A N Pandite, D L Topolsky, T Ahmed, R. B. Geller, I Tabbara, P. J. Bierman, Patrick J. Stiff, M W Schuster, R A Beveridge, M. E. Lebsack, A. Keating
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 15(4)
PURPOSE A phase III trial to compare PIXY321 with granulocyte-macrophage colony-stimulating factor (GM-CSF) following high-dose therapy and autologous bone marrow transplant (ABMT) was conducted to evaluate the time to hematopoietic recovery. PATIENT
Publikováno v:
Arthritis and rheumatism. 39(7)
To preliminarily evaluate the safety and efficacy of different dose levels and dosing frequencies of recombinant human interleukin-1 receptor antagonist (rHuIL-1Ra) in the treatment of patients with rheumatoid arthritis (RA).One hundred seventy-five
Autor:
Linda Welage, Jerome J. Schentag, David E. Nix, Allyn Norman, M. E. Lebsack, Bruce Ryerson, Roger D Toothaker, Allen J Sedman
Publikováno v:
Clinical pharmacology and therapeutics. 52(3)
The effect of gastric acidity on the oral absorption of the quinolone antibiotic enoxacin was evaluated in 12 healthy volunteers. In a randomized, crossover design, single 400 mg oral enoxacin doses were administered on four occasions: alone, after 5
Autor:
Tsun Chang, M. E. Lebsack, Alien L. Goidfarb, Allen J. Sedman, Anne B. Cetnarowski-Cropp, Kathleen A. Stringer, Louis L. Raduiovic, Howard N. Bockbrader
Publikováno v:
Journal of clinical pharmacology. 32(1)
The potential for a drug—drug interaction between pirmenol, an extensively metabolized antiarrhythmic agent, and cimetidine, an inhibitor of hepatic drug-metabolizing enzymes, was evaluated in eight healthy adults. A single 150-mg oral dose of pirm
Publikováno v:
Biochemical pharmacology. 30(7)
Autor:
M E, Lebsack, A D, Anderson
Publikováno v:
Research communications in chemical pathology and pharmacology. 26(2)
The in vivo inhibition of low Km mitochondrial aldehyde dehydrogenase (AlDH) activity by pargyline was not maximal until more than 30 minutes after i.p. injection. Enzyme activity returned to control levels within 36 hours of drug injection but the r
Autor:
Thaddeus H. Grasela, A W Kinkel, J H Wilton, R W Schultz, A J Sedman, D J Thomas, M E Lebsack, Jerome J. Schentag
Publikováno v:
Antimicrobial agents and chemotherapy. 33(5)
Ten normal volunteers participated in a randomized, five-way crossover study to determine the effect of concurrent enoxacin and antacid or ranitidine administration on enoxacin absorption. The bioavailability of a single oral 400-mg enoxacin dose was