A Non-Interventional Study of RoActemra/Actemra (Tocilizumab) in Patients With Moderate to Severe Rheumatoid Arthritis

Mise à jour : Il y a 4 ans
Référence : NCT01670045

Femme et Homme

  • | Pays :
  • Indonesia
  • | Organes :
  • -
  • | Spécialités :
  • -

Extrait

This multi-center observational study will evaluate the use and efficacy of RoActemra/Actemra (tocilizumab) in patients with moderate to severe rheumatoid arthritis. Eligible patients initiated on RoActemra/Actemra treatment according to the licensed label will be followed for 6 months.


Critère d'inclusion

  • Rheumatoid Arthritis

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