Publication: Randomized, Double-Blind, Placebo-Controlled Study of Anti-Mycobacterial Therapy (RHB-104) in Active Crohn’s Disease
| dc.contributor.author | Graham, David Y. (57217496412) | |
| dc.contributor.author | Naser, Saleh A. (6603966766) | |
| dc.contributor.author | Borody, Thomas (24529556700) | |
| dc.contributor.author | Hebzda, Zbigniew (6507862074) | |
| dc.contributor.author | Sarles, Harry (59269185600) | |
| dc.contributor.author | Levenson, Scott (57206433917) | |
| dc.contributor.author | Hardi, Robert (16444323900) | |
| dc.contributor.author | Arłukowicz, Tomasz (55490521100) | |
| dc.contributor.author | Svorcan, Petar (8950517800) | |
| dc.contributor.author | Fathi, Reza (57215317321) | |
| dc.contributor.author | Bibliowicz, Aida (57278312000) | |
| dc.contributor.author | Anderson, Patricia (57277982300) | |
| dc.contributor.author | McLean, Patrick (59303344900) | |
| dc.contributor.author | Fehrmann, Clara (57793731200) | |
| dc.contributor.author | Harris, M. Scott (55449174300) | |
| dc.contributor.author | Zhao, Shuhong (59303109700) | |
| dc.contributor.author | Kalfus, Ira N. (35620327600) | |
| dc.date.accessioned | 2025-06-12T11:41:38Z | |
| dc.date.available | 2025-06-12T11:41:38Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | This study, conducted between 4 October 2013, and 30 November 2018, tested the hypothesis that triple antimicrobial therapy, targeting Mycobacterium avium subspecies paratuberculosis (MAP), long considered a putative cause, would favorably affect Crohn’s disease. A double-blind multicenter study of adults with active Crohn’s disease, (i.e., Crohn’s Disease Activity Index [CDAI] 220–450 plus C-reactive protein ≥ 1.0 mg/dL, fecal calprotectin (FCP) >162.9 µg/g stool, or recent endoscopic or radiographic confirmation of active disease) receiving concomitant standard-of-care Crohn’s disease treatment (Clinicaltrials.gov: NCT01951326) were stratified by anti-tumor necrosis factor use and randomized (1:1) to anti-MAP RHB-104 (clarithromycin 95 mg, rifabutin 45 mg, and clofazimine 10 mg per capsule) (n = 166), resulting in clarithromycin 950 mg/day, rifabutin 450 mg/day, and clofazimine 100 mg/day, or placebo (n = 165) for up to 52 weeks. A greater proportion of RHB-104 versus placebo-treated patients met the primary endpoint—remission (i.e., CDAI < 150)—at week 26 (36.7% [61/166] vs. 22.4% [37/165], respectively; 95% CI for difference: 4.6, 24.0, p = 0.0048; chi-square test). Clinical response (reduction of CDAI by ≥100 points from baseline) at week 26 (first secondary endpoint) was also higher among the patients treated with RHB-104 (73/166 [44.0%]) compared with placebo (50/165 [30.3%]; 95% CI for difference: 3.4, 24.0, p = 0.0116), and it remained higher at week 52 among the patients treated with RHB-104 (59/166 [35.5%] vs. (35/165 [21.2%] for placebo; 95% CI for difference: 4.7, 23.9, p = 0.0042). A statistically significantly greater decline in FCP (another prospective efficacy endpoint) was also observed in RHB-104-treated patients, compared with placebo, at weeks 12, 26, and 52. The rates of serious adverse events were similar between groups (RHB-104: 18.7%; placebo: 18.8%). No patient died during the study. Antimicrobial therapy directed against MAP resulted in significantly greater improvement in clinical and laboratory (FCP) measures of active Crohn’s disease. © 2024 by the authors. | |
| dc.identifier.uri | https://doi.org/10.3390/antibiotics13080694 | |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85202468043&doi=10.3390%2fantibiotics13080694&partnerID=40&md5=8e23c6e1ea1effa916f173875bce20ef | |
| dc.identifier.uri | https://remedy.med.bg.ac.rs/handle/123456789/970 | |
| dc.subject | clarithromycin | |
| dc.subject | clinical trial | |
| dc.subject | clofazimine | |
| dc.subject | Crohn’s disease | |
| dc.subject | Mycobacterium avium subspecies paratuberculosis | |
| dc.subject | RHB-104 | |
| dc.subject | rifabutin | |
| dc.title | Randomized, Double-Blind, Placebo-Controlled Study of Anti-Mycobacterial Therapy (RHB-104) in Active Crohn’s Disease | |
| dspace.entity.type | Publication |
