Dose-range and dose-frequency study of recombinant human interleukin-1 receptor antagonist in patients with rheumatoid arthritis

Arthritis and Rheumatism

Volumn 39, Issue 7, 1996, Pages 1092-1101

  Campion, G V ^a   Lebsack, M E ^a   Lookabaugh, J ^a,b   Gordon, G ^a   Catalano, M ^a  

^a AMGEN INC   (United States)

^b Boulder Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

INTERLEUKIN 1 RECEPTOR BLOCKING AGENT;

ADULT; AGED; ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DOSE CALCULATION; DOSE RESPONSE; DOUBLE BLIND PROCEDURE; DRUG EFFICACY; ERYTHEMA; FEMALE; HUMAN; IMMUNOTHERAPY; INJECTION PAIN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PRURITUS; RANDOMIZED CONTROLLED TRIAL; RHEUMATOID ARTHRITIS; SUBCUTANEOUS DRUG ADMINISTRATION; TREATMENT PLANNING;

ANTIBODIES; ARTHRITIS, RHEUMATOID; DOUBLE-BLIND METHOD; DRUG ADMINISTRATION SCHEDULE; FEMALE; HUMANS; INJECTIONS, SUBCUTANEOUS; INTERLEUKIN 1 RECEPTOR ANTAGONIST PROTEIN; MALE; MIDDLE AGED; QUALITY OF LIFE; RECEPTORS, INTERLEUKIN-1; RECOMBINANT PROTEINS; SEVERITY OF ILLNESS INDEX; SIALOGLYCOPROTEINS; TREATMENT OUTCOME;

EID: 0029943271     PISSN: 00043591     EISSN: None     Source Type: Journal    
DOI: 10.1002/art.1780390704     Document Type: Article

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