TY - JOUR
T1 - Etanercept
T2 - Efficacy and safety for approved indications
AU - Kerensky, Todd A.
AU - Gottlieb, Alice B.
AU - Yaniv, Shimrat
AU - Au, Shiu Chung
N1 - Funding Information:
This manuscript has been funded by Tufts Medical Center, Department of Dermatology. A Gottlieb currently has consulting/advisory board agreements with the following: Abbott Laboratories, Actelion, Alnylam, Amgen, Beiersdorf, Inc., Astellas Pharma US, Inc., BIND Biosciences, Inc., Canfite, Celgene Corp., Centocor Ortho Biotech, Inc., Cytokine Pharmasciences, DermiPsor, Incyte Corp., Merck & Co., Inc., Novo Nordisk A/S, Ono, Pfizer, Inc., Pharmaceutical Product Development (PPD), Inc., Puretech, Schering-Plough Corp., and UCB. She is also the principal investigator for research/educational grants awarded to Tufts Medical Center from Abbott Laboratories, Amgen, Celgene, Centocor Ortho Biotech, Immune Control, Novo Nordisk, Pfizer and UCB. The remaining authors declare no conflict of interests.
PY - 2012/1
Y1 - 2012/1
N2 - Introduction: Etanercept is a tumor necrosis factor alpha (TNF-α) inhibitor, which is approved for the treatment of immune-mediated inflammatory conditions including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), psoriatic arthritis (PsA), ankylosing spondylitis (AS) and psoriasis (PsO). Areas covered: Clinical efficacy and safety data of etanercept for the approved indications are reviewed in this paper. Data were obtained from published clinical trials, registries, post-marketing data as well as information provided by Amgen. Expert opinion: Etanercept is a generally well-tolerated treatment for the approved inflammatory diseases. The most common adverse effect of etanercept treatment is injection site reaction, which is generally self-limiting and often does not require treatment. Etanercept may be associated with an increased risk for infection, the development of malignancy, demyelinating disease and congestive heart failure. Fewer patients withdraw from etanercept due to adverse events than with other biologics. For pediatric patients, there are more data for etanercept than other biologics, and etanercept may have lower rates for the development of malignancy.
AB - Introduction: Etanercept is a tumor necrosis factor alpha (TNF-α) inhibitor, which is approved for the treatment of immune-mediated inflammatory conditions including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), psoriatic arthritis (PsA), ankylosing spondylitis (AS) and psoriasis (PsO). Areas covered: Clinical efficacy and safety data of etanercept for the approved indications are reviewed in this paper. Data were obtained from published clinical trials, registries, post-marketing data as well as information provided by Amgen. Expert opinion: Etanercept is a generally well-tolerated treatment for the approved inflammatory diseases. The most common adverse effect of etanercept treatment is injection site reaction, which is generally self-limiting and often does not require treatment. Etanercept may be associated with an increased risk for infection, the development of malignancy, demyelinating disease and congestive heart failure. Fewer patients withdraw from etanercept due to adverse events than with other biologics. For pediatric patients, there are more data for etanercept than other biologics, and etanercept may have lower rates for the development of malignancy.
KW - Ankylosing spondylitis
KW - Behçet's disease
KW - Etanercept
KW - Juvenile idiopathic arthritis
KW - Psoriasis
KW - Psoriatic arthritis
KW - Rheumatoid arthritis
KW - Tumor necrosis factor alpha inhibitors
UR - http://www.scopus.com/inward/record.url?scp=84555190222&partnerID=8YFLogxK
U2 - 10.1517/14740338.2012.633509
DO - 10.1517/14740338.2012.633509
M3 - Article
C2 - 22074366
AN - SCOPUS:84555190222
SN - 1474-0338
VL - 11
SP - 121
EP - 139
JO - Expert Opinion on Drug Safety
JF - Expert Opinion on Drug Safety
IS - 1
ER -