A phase 2 trial investigating the efficacy and safety of the mPGES-1 inhibitor vipoglanstat in systemic sclerosis-related Raynaud's

Author:

Tornling Göran12,Edenius Charlotte23,Pauling John D456,Denton Christopher P7ORCID,Olsson Anna2,Kowalski Jan8,Murray Andrea9ORCID,Anderson Marina1011,Bhat Smita12,Del Galdo Francesco13ORCID,Hall Frances14,Korkosz Mariusz1516,Krasowska Dorota17,Olas Jacek18,Smith Vanessa1920ORCID,van Laar Jacob M21ORCID,Vonk Madelon C22,Wojteczek Anna2324,Herrick Ariane L9ORCID

Affiliation:

1. Respiratory Medicine Division, Department of Medicine Solna, Karolinska Institutet , Stockholm, Sweden

2. Gesynta Pharma AB , Stockholm, Sweden

3. Rheumatology Division, Department of Medicine Solna, Karolinska Institutet , Stockholm, Sweden

4. Department of Rheumatology, North Bristol NHS Trust , Bristol, UK

5. Musculoskeletal Research Unit, Translational Health Sciences, Bristol Medical School, University of Bristol , Bristol, UK

6. Royal National Hospital for Rheumatic Diseases (part of the Royal United Hospitals NHS Foundation Trust) , Bath, UK

7. Centre for Rheumatology, Royal Free Hospital and University College London , London, UK

8. JK Biostatistics AB , Stockholm, Sweden

9. Centre for Musculoskeletal Research, The University of Manchester, Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre , Manchester, UK

10. Aintree University Hospital, Liverpool University Hospitals NHS Trust , Liverpool, UK

11. Lancaster Medical School, Lancaster University , Lancaster, UK

12. Ninewells Hospital and Medical School , Dundee, UK

13. Leeds Institute of Rheumatology & Musculoskeletal Medicine, and NIHR Leeds Biomedical Research Centre, University of Leeds , Leeds, UK

14. Cambridge University Hospitals NHS Foundation Trust , Cambridge, UK

15. Centrum Medyczne Pratia MCM Krakow , Krakow, Poland

16. Jagiellonian University Medical College , Krakow, Poland

17. Department of Dermatology, Venereology and Pediatric Dermatology Medical University of Lublin , Poland

18. Małopolskie Centrum Kliniczne , Kraków, Poland

19. Department of Internal Medicine, Ghent University , Ghent, Belgium

20. Department of Rheumatology, Ghent University Hospital, Ghent, Belgium; Unit for Molecular Immunology and Inflammation, VIB Inflammation Research Center (IRC) , Ghent, Belgium

21. University Medical Center Utrecht , Utrecht, The Netherlands

22. Department of Rheumatology, Radboud University Medical Center , Nijmegen, The Netherlands

23. Early Phase Clinical Trials Centre, Medical University of Gdańsk , Gdańsk, Poland

24. Department of Rheumatology, Clinical Immunology, Geriatrics and Internal Medicine, Medical University of Gdańsk , Gdańsk, Poland

Abstract

Abstract Objective Our objective was to test the hypothesis, in a double-blind, placebo-controlled study that vipoglanstat, an inhibitor of microsomal prostaglandin E synthase-1 (mPGES-1), which decreases prostaglandin E2 (PGE2) and increases prostacyclin biosynthesis, improves RP. Methods Patients with SSc and ≥7 RP attacks during the last screening week prior to a baseline visit were randomized to 4 weeks treatment with vipoglanstat 120 mg or placebo. A daily electronic diary captured RP attacks (duration and pain) and Raynaud’s Condition Score, with change in RP attacks/week as the primary end point. Cold challenge assessments were performed at baseline and end of treatment. Exploratory end points included patients’ and physicians’ global impression of change, Assessment of Scleroderma-associated Raynaud’s Phenomenon questionnaire, mPGES-1 activity, and urinary excretion of arachidonic acid metabolites. Results Sixty-nine subjects received vipoglanstat (n = 33) or placebo (n = 36). The mean weekly number of RP attacks [baseline; vipoglanstat 14.4 (S.D. 6.7), placebo 18.2 (12.6)] decreased by 3.4 (95% CI –5.8; –1.0) and 4.2 (–6.5; –2.0) attacks per week (P = 0.628), respectively. All patient-reported outcomes improved, with no difference between the groups. The mean change in recovery of peripheral blood flow after the cold challenge did not differ between the study groups. Vipoglanstat fully inhibited mPGES-1, resulting in 57% reduction of PGE2 and 50% increase of prostacyclin metabolites in the urine. Vipoglanstat was safe and well tolerated. Conclusion Although vipoglanstat was safe, and well tolerated in a dose achieving full inhibition of mPGES-1, it was ineffective in SSc-related RP. Further development and evaluation of vipoglanstat will therefore be in other diseases where mPGES-1 plays a pathogenetic role. Trial registration ClinicalTrials.gov, https://www.clinicaltrials.gov, NCT0474420.

Funder

Gesynta Pharma AB

Publisher

Oxford University Press (OUP)

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