CD40 ligand antagonist dazodalibep in Sjögren's disease: a randomized, double-blinded, placebo-controlled, phase 2 trial

被引:6
|
作者
St. Clair, E. William [1 ]
Baer, Alan N. [2 ]
Ng, Wan-Fai [3 ,4 ,5 ,6 ]
Noaiseh, Ghaith [7 ]
Baldini, Chiara [8 ]
Tarrant, Teresa K. [1 ,9 ]
Papas, Athena [10 ]
Devauchelle-Pensec, Valerie [11 ,12 ]
Wang, Liangwei [13 ]
Xu, Wenjing [13 ]
Pham, Tuyet-Hang [13 ]
Sikora, Keith [13 ]
Rees, William A. [13 ]
Alevizos, Ilias [13 ]
机构
[1] Duke Univ, Dept Med, Div Rheumatol & Immunol, Durham, NC 27708 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD USA
[3] Newcastle Univ, Translat & Clin Res Inst, Newcastle Upon Tyne, England
[4] Newcastle Tyne Hosp NHS Fdn Trust, NIHR Newcastle Biomed Res Ctr, Newcastle Upon Tyne, England
[5] Newcastle Tyne Hosp NHS Fdn Trust, NIHR Newcastle Clin Res Facil, Newcastle Upon Tyne, England
[6] Univ Coll Cork, HRB Clin Res Facil, Cork, Ireland
[7] Univ Kansas, Dept Med, Div Allergy Clin Immunol & Rheumatol, Kansas City, KS USA
[8] Univ Pisa, Dept Clin & Expt Med, Rheumatol Unit, Pisa, Italy
[9] Durham Vet Adm Hosp, Durham, NC USA
[10] Tufts Sch Dent Med, Div Oral Biol, Boston, MA USA
[11] Brest Univ Hosp, Dept Rheumatol, Brest, France
[12] INSERM U1227, Brest, France
[13] Amgen Inc, Thousand Oaks, CA USA
关键词
PRIMARY SJOGRENS-SYNDROME; DRY EYE SYMPTOMS; PILOCARPINE; EXPRESSION; MOUTH;
D O I
10.1038/s41591-024-03009-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sj & ouml;gren's disease (SjD) is a chronic, systemic autoimmune disease with no approved disease-modifying therapies. Dazodalibep (DAZ), a novel nonantibody fusion protein, is a CD40 ligand antagonist that blocks costimulatory signals between T and B cells and antigen-presenting cells, and therefore may suppress the wide spectrum of cellular and humoral responses that drive autoimmunity in SjD. This study was a phase 2, randomized, double-blinded, placebo (PBO)-controlled trial of DAZ with a crossover stage in two distinct populations of participants with SjD. Population 1 had moderate-to-severe systemic disease activity and population 2 had an unacceptable symptom burden and limited systemic organ involvement. All participants had a diagnosis of SjD, with 21.6% and 10.1% having an associated connective tissue disease (rheumatoid arthritis or systemic lupus erythematosus) in populations 1 and 2, respectively. The remaining participants would be considered as having primary Sj & ouml;gren's syndrome. The primary endpoint for population 1 (n = 74) was the change from baseline in the European League Against Rheumatism Sj & ouml;gren's Syndrome Disease Activity Index at day 169. The primary endpoint for population 2 (n = 109) was the change from baseline in the European League Against Rheumatism Sj & ouml;gren's Syndrome Patient Reported Index at day 169. The primary endpoints (least squares mean +/- standard error) were achieved with statistical significance for both population 1 (DAZ, -6.3 +/- 0.6; PBO, -4.1 +/- 0.6; P = 0.0167) and population 2 (DAZ, -1.8 +/- 0.2; PBO, -0.5 +/- 0.2; P = 0.0002). DAZ was generally safe and well tolerated. Among the most frequently reported adverse events were COVID-19, diarrhea, headache, nasopharyngitis, upper respiratory tract infection, arthralgia, constipation and urinary tract infection. In summary, DAZ appears to be a potential new therapy for SjD and its efficacy implies an important role for the CD40/CD40 ligand pathway in its pathogenesis. ClinicalTrials.gov identifier: NCT04129164. In a phase 2 trial of dazodalibep, a CD40 ligand, with a crossover stage in two distinct populations of patients with Sj & ouml;gren's disease, the compound was well tolerated and led to significantly improved disease activity.
引用
收藏
页码:1583 / 1592
页数:28
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