A Randomized, Double-Blind, Phase 3 Safety and Efficacy Study of Ridinilazole Versus Vancomycin for Treatment of Clostridioides difficile Infection: Clinical Outcomes With Microbiome and Metabolome Correlates of Response

被引:6
作者
Okhuysen, Pablo C. [1 ,16 ]
Ramesh, Mayur S. [2 ]
Louie, Thomas [3 ]
Kiknadze, Nino [4 ]
Torre-Cisneros, Julian [5 ,11 ]
de Oliveira, Claudia Murta [6 ]
Van Steenkiste, Christophe [7 ,8 ]
Stychneuskaya, Alena [9 ]
Garey, Kevin W. [10 ]
Garcia-Diaz, Julia
Li, Jianling [12 ]
Duperchy, Esther
Chang, Betty Y. [12 ]
Sukbuntherng, Juthamas [12 ]
Montoya, Jose G. [12 ,13 ]
Styles, Lori [12 ]
Clow, Fong [12 ]
James, Danelle [12 ]
Dubberke, Erik R. [14 ]
Wilcox, Mark [15 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Houston, TX USA
[2] Henry Ford Hlth, Detroit, MI USA
[3] Univ Calgary, Foothills Med Ctr, Calgary, AB, Canada
[4] Aversi Clin, Tbilisi, Georgia
[5] Reina Sofia Univ Hosp, Univ Cordoba, IMIBIC, CIBERINFEC, Cordoba, Spain
[6] Santa Casa Belo Horizonte, Belo Horizonte, Brazil
[7] Algemeen Ziekenhuis Maria Middelares, Ghent, Belgium
[8] Univ Antwerp, Antwerp, Belgium
[9] Vitebsk Reg Clin Hosp Infect Dis, Vitebsk, BELARUS
[10] Univ Houston, Coll Pharm, Houston, TX USA
[11] Ochsner Hlth, New Orleans, LA USA
[12] Summit Therapeut, Menlo Pk, CA USA
[13] Palo Alto Med Fdn, Dr Jack S Remington Lab Specialty Diagnost, Palo Alto, CA USA
[14] Washington Univ, Sch Med, St Louis, MO USA
[15] Univ Leeds, Leeds Teaching Hosp, Sch Med, Leeds, England
[16] UT MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, 1515 Holcombe Blvd,Unit 1460, Houston, TX 77030 USA
关键词
ridinilazole; vancomycin; Clostridioides difficile; microbiome; bile acids; ANTIMICROBIAL SUSCEPTIBILITY; FIDAXOMICIN; SURVEILLANCE; THERAPY; CARE;
D O I
10.1093/cid/ciad792
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Exposure to antibiotics predisposes to dysbiosis and Clostridioides difficile infection (CDI) that can be severe, recurrent (rCDI), and life-threatening. Nonselective drugs that treat CDI and perpetuate dysbiosis are associated with rCDI, in part due to loss of microbiome-derived secondary bile acid (SBA) production. Ridinilazole is a highly selective drug designed to treat CDI and prevent rCDI.Methods In this phase 3 superiority trial, adults with CDI, confirmed with a stool toxin test, were randomized to receive 10 days of ridinilazole (200 mg twice daily) or vancomycin (125 mg 4 times daily). The primary endpoint was sustained clinical response (SCR), defined as clinical response and no rCDI through 30 days after end of treatment. Secondary endpoints included rCDI and change in relative abundance of SBAs.Results Ridinilazole and vancomycin achieved an SCR rate of 73% versus 70.7%, respectively, a treatment difference of 2.2% (95% CI: -4.2%, 8.6%). Ridinilazole resulted in a 53% reduction in recurrence compared with vancomycin (8.1% vs 17.3%; 95% CI: -14.1%, -4.5%; P = .0002). Subgroup analyses revealed consistent ridinilazole benefit for reduction in rCDI across subgroups. Ridinilazole preserved microbiota diversity, increased SBAs, and did not increase the resistome. Conversely, vancomycin worsened CDI-associated dysbiosis, decreased SBAs, increased Proteobacteria abundance (similar to 3.5-fold), and increased the resistome.Conclusions Although ridinilazole did not meet superiority in SCR, ridinilazole greatly reduced rCDI and preserved microbiome diversity and SBAs compared with vancomycin. These findings suggest that treatment of CDI with ridinilazole results in an earlier recovery of gut microbiome health. Clinical Trials Registration.Ri-CoDIFy 1 and 2: NCT03595553 and NCT03595566.Conclusions Although ridinilazole did not meet superiority in SCR, ridinilazole greatly reduced rCDI and preserved microbiome diversity and SBAs compared with vancomycin. These findings suggest that treatment of CDI with ridinilazole results in an earlier recovery of gut microbiome health. Clinical Trials Registration.Ri-CoDIFy 1 and 2: NCT03595553 and NCT03595566. In this phase 3 superiority study, ridinilazole, bactericidal bis-benzimidazole against C. difficile, versus vancomycin reduced recurrent disease by 53%, preserved microbiota diversity, increased secondary bile acids, did not increase resistome, but did not meet superiority in initial clinical response. Graphical Abstract https://tidbitapp.io/tidbits/test-7e5035e4-ad1b-417a-bee9-788b33377fe0
引用
收藏
页码:1462 / 1472
页数:11
相关论文
共 50 条
  • [21] The antipyretic efficacy and safety of propacetamol compared with dexibuprofen in febrile children: a multicenter, randomized, double-blind, comparative, phase 3 clinical trial
    Choi, Seung Jun
    Moon, Sena
    Choi, Ui Yoon
    Chun, Yoon Hong
    Lee, Jung Hyun
    Rhim, Jung Woo
    Lee, Jin
    Kim, Hwang Min
    Jeong, Dae Chul
    BMC PEDIATRICS, 2018, 18
  • [22] Efficacy and safety of tadalafil in a pediatric population with pulmonary arterial hypertension: phase 3 randomized, double-blind placebo-controlled study
    Ivy, Dunbar
    Bonnet, Damien
    Berger, Rolf
    Meyer, Gisela M. B.
    Baygani, Simin
    Li, Baohui
    PULMONARY CIRCULATION, 2021, 11 (03)
  • [23] A Randomized, Double-Blind, Active Control, Multicenter, Phase 3 Study to Evaluate the Efficacy and Safety of Liztox® versus Botox® in Post-Stroke Upper Limb Spasticity
    Ye, Dong Hyun
    Chun, Min Ho
    Park, Yoon Ghil
    Paik, Nam-Jong
    Lee, Shi-Uk
    Yoo, Seung Don
    Kim, Deog Young
    TOXINS, 2023, 15 (12)
  • [24] A Phase 3, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study Evaluating the Safety and Efficacy of Metronidazole Vaginal Gel 1.3% in the Treatment of Bacterial Vaginosis
    Schwebke, Jane R.
    Marrazzo, Jeanne
    Beelen, Andrew P.
    Sobel, Jack D.
    SEXUALLY TRANSMITTED DISEASES, 2015, 42 (07) : 376 - 381
  • [25] Pooled analysis of the phase 3 REVIVE trials: randomised, double-blind studies to evaluate the safety and efficacy of iclaprim versus vancomycin for treatment of acute bacterial skin and skin-structure infections
    Huang, David B.
    Corey, G. Ralph
    Holland, Thomas L.
    Lodise, Thomas
    O'Riordan, William
    Wilcox, Mark H.
    File, Thomas M., Jr.
    Dryden, Matthew
    Balser, Barbara
    Desplats, Eve
    Torres, Antoni
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2018, 52 (02) : 233 - 240
  • [26] Efficacy and Safety of Ocrelizumab in Active Proliferative Lupus Nephritis: Results From a Randomized, Double-Blind, Phase III Study
    Mysler, Eduardo F.
    Spindler, Alberto J.
    Guzman, Renato
    Bijl, Marc
    Jayne, David
    Furie, Richard A.
    Houssiau, Frederic A.
    Drappa, Jorn
    Close, David
    Maciuca, Romeo
    Rao, Kajal
    Shahdad, Saba
    Brunetta, Paul
    ARTHRITIS AND RHEUMATISM, 2013, 65 (09): : 2368 - 2379
  • [27] A Phase 3, Randomized, Double-Blind, Multicenter Study To Evaluate the Safety and Efficacy of Intravenous Iclaprim versus Vancomycin for Treatment of Acute Bacterial Skin and Skin Structure Infections Suspected or Confirmed To Be Due to Gram-Positive Pathogens (REVIVE-2 Study)
    Holland, Thomas L.
    O'Riordan, William
    McManus, Alison
    Shin, Elliot
    Borghei, Ali
    File, Thomas M., Jr.
    Wilcox, Mark H.
    Torres, Antoni
    Dryden, Matthew
    Lodise, Thomas
    Oguri, Toyoko
    Corey, G. Ralph
    McLeroth, Patrick
    Shukla, Rajesh
    Huang, David B.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (05)
  • [28] CLOVER (CLOstridium difficile Vaccine Efficacy tRial) Study: A Phase 3, Randomized Trial Investigating the Efficacy and Safety of a Detoxified Toxin A/B Vaccine in Adults 50 Years and Older at Increased Risk of Clostridioides difficile Infection
    Donskey, Curtis J.
    Dubberke, Erik R.
    Klein, Nicola P.
    Liles, Elizabeth G.
    Szymkowiak, Katarzyna
    Wilcox, Mark H.
    Lawrence, Jody
    Bouguermouh, Salim
    Zhang, Haiying
    Koury, Kenneth
    Bailey, Ruth
    Smith, Helen M.
    Lockhart, Stephen
    Lamberth, Erik
    Kalina, Warren, V
    Pride, Michael W.
    Webber, Chris
    Anderson, Annaliesa S.
    Jansen, Kathrin U.
    Gruber, William C.
    Kitchin, Nicholas
    CLINICAL INFECTIOUS DISEASES, 2024, 79 (06) : 1503 - 1511
  • [29] A phase 3, randomized, double-blind, clinical study to evaluate the long-term safety and efficacy of gefapixant in Japanese adult participants with refractory or unexplained chronic cough
    Niimi, Akio
    Sagara, Hironori
    Kikuchi, Masashi
    Arano, Ichiro
    Sato, Asako
    Shirakawa, Masayoshi
    La Rosa, Carmen
    Muccino, David
    ALLERGOLOGY INTERNATIONAL, 2022, 71 (04) : 498 - 504
  • [30] Safety and efficacy of fruquintinib in patients with previously treated metastatic colorectal cancer: a phase Ib study and a randomized double-blind phase II study
    Xu, Rui-Hua
    Li, Jin
    Bai, Yuxian
    Xu, Jianming
    Liu, Tianshu
    Shen, Lin
    Wang, Liwei
    Pan, Hongming
    Cao, Junning
    Zhang, Dongsheng
    Fan, Songhua
    Hua, Ye
    Su, Weiguo
    JOURNAL OF HEMATOLOGY & ONCOLOGY, 2017, 10 : 1 - 8