Systemic sclerosis & Raynaud's

Co prescription of anti-acid therapy reduces the bioavailability of mycophenolate mofetil in systemic sclerosis patients: A crossover trial

Semin Arthritis RheumPublished Randomised controlled trial

Authors' conclusion

Co-administration of PPI or HRB can significantly reduce the bioavailability of MMF in patients with SSc.

Study context

Population
Systemic sclerosis (SSc) patients on a stable dose of mycophenolate mofetil (MMF) (1.5–3 g)
Participants
20 patients
Comparison
MMF alone vs MMF plus ranitidine vs MMF plus esomeprazole
  • MMF alonen = 20reference
  • Ranitidinen = 20
  • Esomeprazolen = 20
Primary endpoint
12-hour AUC of mycophenolic acid (MPA) levels
Follow-up
End of each month
Methodological detailssequential crossover
  • Sequential crossover

Primary result

As reported in the abstract

Mean 12-hour AUC of MPA, reduction vs MMF alone

Mean difference

22.28 μg h ml-1

Esomeprazole · 32.7% reduction in mean AUC Mycophenolic Acid (MPA)

Mean difference

14.93 μg h ml-1

Ranitidine · 21.97% reduction in MPA AUC

Further findings

Total gastrointestinal (GI) score · end of each month

Addition of ranitidine or esomeprazole resulted in significant reduction in total GI score

Original publication

Co prescription of anti-acid therapy reduces the bioavailability of mycophenolate mofetil in systemic sclerosis patients: A crossover trial. Semin Arthritis Rheum. Published 28 September 2023. doi:10.1016/j.semarthrit.2023.152270

Composed by AI from the published abstract and checked against it. How Briefs are made →

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