Abstract | INTRODUCTION: AREAS COVERED: Analysis of available clinical trial data on GM-CSF receptor-α antibody and medical literature search using MEDLINE for molecular mechanisms of pathogenesis of RA and its treatment forms the basis of this expert opinion review. The mavrilimumab Phase II double blind, randomized, placebo-controlled ascending dose trial demonstrated statistically significant achievement of primary and secondary end points in patients with moderate RA. The trial demonstrated significant clinical benefit in the 100 mg mavrilimumab cohort compared to the placebo group. EXPERT OPINION: The novel molecular targeting mechanism of mavrilimumab together with its demonstrated clinical efficacy, tolerability and safety profile in Phase II clinical trials in moderate RA, suggests significant potential utility for this drug to induce clinical remission, reduce flares and improve morbidity and mortality in patients with RA.
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Authors | Jagdish R Nair, Steven W Edwards, Robert J Moots |
Journal | Expert opinion on biological therapy
(Expert Opin Biol Ther)
Vol. 12
Issue 12
Pg. 1661-8
(Dec 2012)
ISSN: 1744-7682 [Electronic] England |
PMID | 23094973
(Publication Type: Journal Article, Review)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
- mavrilimumab
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Topics |
- Antibodies, Monoclonal
(immunology, therapeutic use)
- Antibodies, Monoclonal, Humanized
- Arthritis, Rheumatoid
(drug therapy)
- Clinical Trials as Topic
- Humans
- Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
(immunology)
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