Abstract | OBJECTIVE: MATERIALS AND METHODS: RESULTS: Three out of four patients responded to infliximab treatment, while two of them retained the response during a two-year follow up. A higher dose regimen (5 mg/kg), however, was eventually warranted for two of the responders. No major side effects were noted. CONCLUSIONS:
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Authors | Zaharenia Th Karageorgaki, Clio P Mavragani, Matthilde A Papathanasiou, Fotini N Skopouli |
Journal | Clinical rheumatology
(Clin Rheumatol)
Vol. 26
Issue 6
Pg. 984-7
(Jun 2007)
ISSN: 0770-3198 [Print] Germany |
PMID | 16633710
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Antibodies, Monoclonal
- Antirheumatic Agents
- Tumor Necrosis Factor-alpha
- Infliximab
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Topics |
- Adolescent
- Adult
- Antibodies, Monoclonal
(adverse effects, therapeutic use)
- Antirheumatic Agents
(adverse effects, therapeutic use)
- Female
- Follow-Up Studies
- Humans
- Infliximab
- Takayasu Arteritis
(drug therapy)
- Treatment Outcome
- Tumor Necrosis Factor-alpha
(adverse effects, antagonists & inhibitors)
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