scholarly journals One-year investigator-blind randomized multicenter trial comparing asacol 2.4 g once daily with 800 mg three times daily for maintenance of remission in ulcerative colitis

2012 ◽  
Vol 18 (10) ◽  
pp. 1885-1893 ◽  
Author(s):  
Barney A. Hawthorne ◽  
Rachel Stenson ◽  
David Gillespie ◽  
Edwin T. Swarbrick ◽  
Anjan Dhar ◽  
...  
2009 ◽  
Vol 104 ◽  
pp. S459-S460
Author(s):  
Gary Lichtenstein ◽  
Glenn Gordon ◽  
Salam Zakko ◽  
Uma Murthy ◽  
Shahriar Sedghi ◽  
...  

2014 ◽  
Vol 20 (8) ◽  
pp. 1399-1406 ◽  
Author(s):  
Gary R. Lichtenstein ◽  
Andrew C. Barrett ◽  
Enoch Bortey ◽  
Craig Paterson ◽  
William P. Forbes

2017 ◽  
Vol 23 (5) ◽  
pp. 822-832 ◽  
Author(s):  
Yasuo Suzuki ◽  
Mitsuo Iida ◽  
Hiroaki Ito ◽  
Haruo Nishino ◽  
Toshihide Ohmori ◽  
...  

2020 ◽  
Author(s):  
Shizuma Omote ◽  
Tatsuya Toyokawa ◽  
Ryohei Sumii ◽  
Akira Nakanishi ◽  
Yuka Kadowaki ◽  
...  

Abstract Background Tacrolimus is a calcineurin inhibitor used for the treatment of 5-Amino-salicylic acid (5-ASA) and systematic corticosteroid refractory ulcerative colitis. However, systemic administration of tacrolimus could lead to many adverse events. Therefore, we used tacrolimus suppositories as a local therapeutic agent and examined its efficacy and safety with strict blood concentration monitoring. Methods Sixteen patients with ulcerative colitis were administered a 0.5-mg tacrolimus suppository once daily. In cases with an insufficient clinical effect, additional amounts, at an increment of 0.5 mg of tacrolimus, were administered. The blood concentration was measured two weeks after the start of treatment or any dose change and every four weeks thereafter. Results The partial Mayo score was 5.31 before the start of treatment, and it decreased significantly after 2 (2.56, P = 0.001), 4 (1.53, P < 0.001), and 8 (1.47, P = < 0.001) weeks of treatment. The median duration of tacrolimus treatment was 24 (range 2–96) weeks, and 6 patients were treated continuously for more than one year after the pMayo score improved. No exacerbation of adverse events during the treatment regimen was observed. The effects and safety of tacrolimus suppositories were verified with strict blood concentration monitoring. Conclusions Our findings suggest that the application of tacrolimus suppositories is safe and effective in the treatment of patients with ulcerative colitis.


2009 ◽  
Vol 1 ◽  
pp. CMT.S38
Author(s):  
A Barney Hawthorne

MMX™ mesalazine is a novel delayed release mesalazine formulation with a high-strength 1.2 g tablet for the treatment of active mild to moderate colitis and maintenance of remission. In vitro and in vivo studies show initiation of drug release in the terminal ileum and caecum with gradual release of 5-ASA as the tablet passes through the colon. Pharmacokinetic data are comparable to other 5-ASA formulations with low systemic absorption and high levels in feces and in mucosal biopsies in the left colon. Clinical trials have shown high rates of clinical and endoscopic remission in active mild to moderate colitis over 8 weeks with a 2.4 g once daily dose. There do not appear to be higher remission rates with the 4.8 g dose. Prolongation of treatment with a further 8 weeks of 2.4 g twice daily can induce remission in those failing the initial 8 weeks of therapy. A maintenance study enrolling patients who achieved remission in the acute studies showed high rates of remission maintained at one year with 1.2 g twice daily (68.5%) and 2.4 g once daily (64.4%) using the strict definition of remission (including mucosal healing) that was used in the active treatment trials. The drug is safe and effective in colitis. The high tablet strength, and once-daily dosage make this formulation a welcome addition to therapy options for patients with colitis.


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