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The biologic drug Actemra® to dramatically
increase the benefit of Rheumatoid Arthritis
          monotherapy treatment

  Good news for Rheumatoid Arthritis (RA) patients, as
  Actemra® (TOCILIZUMAB) shows superior results in
 reducing disease activity in patients when compared to
              Humira® (ADALIMUMAB)

         Graeser Associates International
Rheumatoid Arthritis patients are often treated with biological
drugs such as Actemra® or Humira®, usually combined with
methotrexate. However, due to methotrexate intolerance,
significant side effects or ineffectiveness, it is quite common to see
patients receiving biological monotherapy, i.e., a single biological
drug as the only therapy for their symptoms.
• From a recent study (Gabay et al., “TOCILIZUMAB (TCZ)
  MONOTHERAPY IS SUPERIOR TO ADALIMUMAB (ADA)
  MONOTHERAPY IN REDUCING DISEASE ACTIVITY IN
  PATIENTS WITH RHEUMATOID ARTHRITIS (RA): 24-WEEK
  DATA FROM THE PHASE 4 ADACTA TRIAL” Ann Rheum Dis
  2012;71(Suppl3):152) it is evident that patients receiving the
  Actemra® drug as monotherapy have had significant improvement
  in the reduction of the symptoms of the disease when compared to
  patients receiving Humira® after a 24 week period of treatment.
• From the 8th week and onwards, patients treated with Actemra®
  have demonstrated improvement in swollen and tender joint counts,
  ESR (Erythrocyte sedimentation rate, a common measure of
  inflammation) and patient global assessment, and statistical
  significance was also achieved in favor of Actemra® for the general
  disease remission and lower activity.
• The results of this research were presented at the EULAR (The
  European League Against Rheumatism) conference in Berlin
  in June 2012, and are considered a breakthrough which will
  enable physicians to better treat monotherapy patients
  suffering from polypharmacy side-effects and accordingly
  provide better care for this complex disease.
• In our next blog posts, Graeser Associates International will be
  providing you with the latest updates on biological drugs and
  biosimilars.

• We will also be providing powerpoint presentations, written
  reports, and short audio and video presentations through our
  Slideshare channel (www.slideshare.net/biosimilars). We will
  also be selling more detailed reports and longer audio and
  video presentations – please see our biosimilars product page
  for a list of products (www.biosimilars.me).
• Adv. Ariel Averbuch, RPh, is an advisor on
  IP, healthcare and business strategies at
  Graeser Associates International (GAI), an
  international health care intellectual property
  firm, and acts as Chairman at the
  Pharmaceutical Society of Israel (PSI). Adv.
  Averbuch has been a pharmacist for over 10
  years and is also a lawyer and a patent
  attorney (Israel), having extensive experience
  in the pharmaceutical field. Follow Ariel
  Averbuch on LinkedIn and Twitter:
  @ArielAverbuch. Follow our biosimilar
  communications on Twitter:
  @biosimilarsGAI. Email us at
  biosimilars@gai-ip.com.

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The biologic drug actemra® to dramatically increase the benefit of rheumatoid arthritis monotherapy treatment

  • 1. The biologic drug Actemra® to dramatically increase the benefit of Rheumatoid Arthritis monotherapy treatment Good news for Rheumatoid Arthritis (RA) patients, as Actemra® (TOCILIZUMAB) shows superior results in reducing disease activity in patients when compared to Humira® (ADALIMUMAB) Graeser Associates International
  • 2. Rheumatoid Arthritis patients are often treated with biological drugs such as Actemra® or Humira®, usually combined with methotrexate. However, due to methotrexate intolerance, significant side effects or ineffectiveness, it is quite common to see patients receiving biological monotherapy, i.e., a single biological drug as the only therapy for their symptoms.
  • 3. • From a recent study (Gabay et al., “TOCILIZUMAB (TCZ) MONOTHERAPY IS SUPERIOR TO ADALIMUMAB (ADA) MONOTHERAPY IN REDUCING DISEASE ACTIVITY IN PATIENTS WITH RHEUMATOID ARTHRITIS (RA): 24-WEEK DATA FROM THE PHASE 4 ADACTA TRIAL” Ann Rheum Dis 2012;71(Suppl3):152) it is evident that patients receiving the Actemra® drug as monotherapy have had significant improvement in the reduction of the symptoms of the disease when compared to patients receiving Humira® after a 24 week period of treatment. • From the 8th week and onwards, patients treated with Actemra® have demonstrated improvement in swollen and tender joint counts, ESR (Erythrocyte sedimentation rate, a common measure of inflammation) and patient global assessment, and statistical significance was also achieved in favor of Actemra® for the general disease remission and lower activity.
  • 4. • The results of this research were presented at the EULAR (The European League Against Rheumatism) conference in Berlin in June 2012, and are considered a breakthrough which will enable physicians to better treat monotherapy patients suffering from polypharmacy side-effects and accordingly provide better care for this complex disease.
  • 5. • In our next blog posts, Graeser Associates International will be providing you with the latest updates on biological drugs and biosimilars. • We will also be providing powerpoint presentations, written reports, and short audio and video presentations through our Slideshare channel (www.slideshare.net/biosimilars). We will also be selling more detailed reports and longer audio and video presentations – please see our biosimilars product page for a list of products (www.biosimilars.me).
  • 6. • Adv. Ariel Averbuch, RPh, is an advisor on IP, healthcare and business strategies at Graeser Associates International (GAI), an international health care intellectual property firm, and acts as Chairman at the Pharmaceutical Society of Israel (PSI). Adv. Averbuch has been a pharmacist for over 10 years and is also a lawyer and a patent attorney (Israel), having extensive experience in the pharmaceutical field. Follow Ariel Averbuch on LinkedIn and Twitter: @ArielAverbuch. Follow our biosimilar communications on Twitter: @biosimilarsGAI. Email us at biosimilars@gai-ip.com.