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Clinical Trial Design in Juvenile Idiopathic Arthritis.

Publication ,  Journal Article
Balevic, SJ; Becker, ML; Cohen-Wolkowiez, M; Schanberg, LE
Published in: Paediatr Drugs
October 2017

Randomized clinical trials provide the gold standard evidence base to guide clinical practice. Despite major advances in trial design, pediatric clinical trials are still difficult to perform and pose unique challenges, including the need to consider the impact of developmental changes in trial design. Advances within pediatric rheumatology combined with the need to comply with legislative requirements have driven new approaches to performing pediatric clinical trials such as utilization of large research networks, incorporation of patient and family stakeholders in the planning and implementation of clinical trials, and the development of novel trial designs. The expansion of available biological therapeutics that now includes biosimilar drugs highlights the important and difficult balance of providing new and cost-effective drugs to children while ensuring safety in a vulnerable population. Future advances in juvenile idiopathic arthritis (JIA) clinical trials will likely be the application of precision medicine based on biologic, rather than phenotypic, classification of JIA, with improved understanding of pediatric clinical pharmacology. Clinical trial simulations and comparative effectiveness studies are important supplements to traditional clinical trials, permitting efficient studies and results that are more generalizable.

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Published In

Paediatr Drugs

DOI

EISSN

1179-2019

Publication Date

October 2017

Volume

19

Issue

5

Start / End Page

379 / 389

Location

Switzerland

Related Subject Headings

  • Randomized Controlled Trials as Topic
  • Pediatrics
  • Humans
  • Drug Costs
  • Clinical Trials as Topic
  • Child
  • Arthritis, Juvenile
  • Antirheumatic Agents
  • 3214 Pharmacology and pharmaceutical sciences
  • 3213 Paediatrics
 

Citation

APA
Chicago
ICMJE
MLA
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Balevic, S. J., Becker, M. L., Cohen-Wolkowiez, M., & Schanberg, L. E. (2017). Clinical Trial Design in Juvenile Idiopathic Arthritis. Paediatr Drugs, 19(5), 379–389. https://doi.org/10.1007/s40272-017-0244-2
Balevic, Stephen J., Mara L. Becker, Michael Cohen-Wolkowiez, and Laura E. Schanberg. “Clinical Trial Design in Juvenile Idiopathic Arthritis.Paediatr Drugs 19, no. 5 (October 2017): 379–89. https://doi.org/10.1007/s40272-017-0244-2.
Balevic SJ, Becker ML, Cohen-Wolkowiez M, Schanberg LE. Clinical Trial Design in Juvenile Idiopathic Arthritis. Paediatr Drugs. 2017 Oct;19(5):379–89.
Balevic, Stephen J., et al. “Clinical Trial Design in Juvenile Idiopathic Arthritis.Paediatr Drugs, vol. 19, no. 5, Oct. 2017, pp. 379–89. Pubmed, doi:10.1007/s40272-017-0244-2.
Balevic SJ, Becker ML, Cohen-Wolkowiez M, Schanberg LE. Clinical Trial Design in Juvenile Idiopathic Arthritis. Paediatr Drugs. 2017 Oct;19(5):379–389.
Journal cover image

Published In

Paediatr Drugs

DOI

EISSN

1179-2019

Publication Date

October 2017

Volume

19

Issue

5

Start / End Page

379 / 389

Location

Switzerland

Related Subject Headings

  • Randomized Controlled Trials as Topic
  • Pediatrics
  • Humans
  • Drug Costs
  • Clinical Trials as Topic
  • Child
  • Arthritis, Juvenile
  • Antirheumatic Agents
  • 3214 Pharmacology and pharmaceutical sciences
  • 3213 Paediatrics