Treatment of moderate‐to‐severe canine atopic dermatitis with modified‐release mycophenolate (OKV‐1001): A pilot open‐label, single‐arm multicentric clinical trial
Background Mycophenolate is an immunomodulating agent successfully used for the treatment of moderate‐to‐severe atopic dermatitis (AD) in people. Mycophenolate is an effective steroid‐sparing treatment option for use in dogs with inflammatory skin diseases. Objective To evaluate whether once‐daily m...
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Veröffentlicht in: | Veterinary dermatology 2024-12, Vol.35 (6), p.652-661 |
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Zusammenfassung: | Background
Mycophenolate is an immunomodulating agent successfully used for the treatment of moderate‐to‐severe atopic dermatitis (AD) in people. Mycophenolate is an effective steroid‐sparing treatment option for use in dogs with inflammatory skin diseases.
Objective
To evaluate whether once‐daily modified‐release mycophenolate (OKV‐1001) is safe and effective for treating moderate‐to‐severe canine AD.
Animals
Client‐owned atopic dogs (n = 9) were enrolled.
Materials and Methods
In an open‐label multicentre pilot study, OKV‐1001 (30 mg/kg every 24 h) was given orally for ≤84 days. Concomitant tapering doses of glucocorticoids were administered up to Day (D)28. Clinicians assessed Canine Atopic Dermatitis Extent and Severity Index, 4th iteration (CADESI‐04) on D0, D14, D28, D56 and D84. Body weight and clinical pathological parameters were measured at baseline and at the end of the study.
Results
Treatment with OKV‐1001 combined with glucocorticoids significantly reduced the severity of AD within two weeks in seven of nine (77.8%) dogs. The mean percentage change from baseline in the CADESI‐04 score was 29% (p = 0.009) at D14 (n = 9), 39% (p = 0.008) at D28 (n = 9) and 49% (p = 0.03) at D56 (n = 7) at which point glucocorticoids had been withdrawn. In two dogs the improvement in CADESI‐04 was 62% and 23% (respectively) on D84. No significant adverse events including clinical pathological findings were reported.
Conclusions and Clinical Relevance
Modified‐release mycophenolate (OKV‐1001) may represent a promising alternative treatment option for dogs with moderate‐to‐severe AD. The safety and efficacy profile of OKV‐1001 will need to be established in larger, placebo‐controlled clinical trials.
Zusammenfassung
Hintergrund
Mycophenolate ist ein immunmodulatorischer Wirkstoff, der erfolgreich bei der Behandlung von mittlerer‐bis‐schwerer atopischer Dermatitis (AD) des Menschen eingesetzt wird. Mycophenolate ist eine wirksame Steroide‐sparende Behandlungsoption zum Einsatz bei Hunden mit entzündlichen Hauterkrankungen.
Ziel
Das Ziel dieser Studie war die Feststellung, ob einmal täglich eingesetztes modifiziertes Mycophenolat (OKV‐1001) bei der Behandlung von mittlerer‐bis‐schwerer AD des Hundes sicher und effektiv ist.
Tiere
Es wurden atopische Hunde (n = 9) in Privatbesitz in die Studie aufgenommen.
Materialien und Methoden
In einer offenen Multicenter Pilotstudie wurde OKV‐1001 (30 mg/kg alle 24 h) per os für ≤84 Tage verabreicht. Es wurden gleichzeitig aussc |
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ISSN: | 0959-4493 1365-3164 1365-3164 |
DOI: | 10.1111/vde.13283 |