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Department

Toxicology

Preferred Sample Type

Teriflunomide (A77 1726, leflunomide metabolite)

Suitable Specimen Types

  • Serum
  • EDTA Plasma
  • Li Hep Plasma
50 ul of plasma or serum.

Specimen Transport

Usual

Sample Processing in Laboratory

Centrifuge and place in toxicology box in cold room.

Sample Preparation

Centrifuge

Turnaround Time

3 working days

Sample Stability

4 ºC

Teriflunomide (A77 1726, leflunomide metabolite)

General Information

Leflunomide is an immunomodulatory drug which functions by inhibiting the mitochondrial enzyme dihydroorotate dehydrogenase (DHODH), which plays a key role in the de novo synthesis of the uridine monophosphate (rUMP), which is required for the synthesis of DNA and RNA. Hence leflunomide inhibits the reproduction of rapidly dividing cells, especially lymphocytes. It is approved for use in moderate-to-severe rheumatoid arthritis and psoriatic arthritis but has also shown to be of use in a number of other diseases such as Systemic lupus erythematosus, Crohn's disease, sarcoidosis and viral nephropathy.

Teriflunomide is the active metabolite of leflunomide (leflunomide is a pro-drug) and is marketed as a drug in its own right (trade name Aubagio, marketed by Sanofi, also known as A77 1726) for the treatment of multiple sclerosis.

This assay is for the measurement of teriflunomide for monitoring of leflunomide and teriflunomide treatment. There is no clinical utility in measurement of leflunomide.

Patient Preparation

Take sample pre-dose (trough).

Notes

This test is designed for the therapeutic drug monitoring of teriflunomide/leflunomide levels to ensure adequate dosage. This test is not meant to monitor the elimination of teriflunomide in women of childbearing potential who discontinue teriflunomide. This service is available via Eurofins (Sanofi-Aventis kit)

Reference Range

Therapeutic targets remain only loosely defined and appear to vary depending on the purpose of therapy. A reference range of 18 - 63 mg/L has been suggested. Adverse reactions to leflunomide do not correlate well with serum drug concentration, but include diarrhoea, hypertension, and liver toxicity. 

Please contact the laboratory for more information.

Specifications

  • EQA Scheme?: No