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A comprehensive approach to identify approved drugs and treatments for repositioning as therapies for systemic lupus erythematosus
Arthritis Research & Therapy volume 16, Article number: A51 (2014)
Development of new systemic lupus erythematosus (SLE) treatments has been slow. To accelerate the pace, an evidence-based approach was developed to find new lupus therapies amongst 6,800 compounds FDA approved for human use.
The Lupus Treatment List (LRxL) was constructed with intense input from the entire lupus community, including patients, and was used to prioritize therapies to be tested in small focused, biomarker-rich clinical trials (SLE Treatment Acceleration Trials (STAT)). All drugs widely used for lupus or known to be in development for lupus by Pharma/Biotech were excluded. Details of the project can be viewed online . A novel evidence-based composite scoring system was developed to rank the identified drugs/therapies numerically by scientific rationale, experience in lupus mice/human cells, previous clinical experience in autoimmunity, drug properties and adverse event profile.
Of the 157 therapies initially screened, more than 25 have an appropriate set of characteristics to consider for testing in clinical trials in lupus, including drugs targeting cellular metabolism, kinases, the immune system, HDACs, complement as well as cellular therapies and nondrug interventions.
This approach has not only identified unique candidates that could be useful in SLE and possibly other autoimmune/inflammatory conditions, but has also yielded a rigorous evidence-based process by which therapies can be usefully rated for possible clinical application to treat these conditions, thereby mitigating risk in drug development.
LrXL STAT. [http://www.linkedin.com/in/lrxlstat]
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Grammer, A.C., Ryals, M. & Lipsky, P.E. A comprehensive approach to identify approved drugs and treatments for repositioning as therapies for systemic lupus erythematosus. Arthritis Res Ther 16 (Suppl 1), A51 (2014). https://doi.org/10.1186/ar4667
- Clinical Trial
- Immune System
- Systemic Lupus Erythematosus
- Clinical Application
- Clinical Experience