scholarly journals Randomized, Ascending Dose, Phase 2 Study of KHK4083, an Anti-OX40 Monoclonal Antibody, in Moderately Active Ulcerative Colitis

2020 ◽  
Vol 2 (3) ◽  
Author(s):  
Jaroslaw Kierkus ◽  
Marina Pesegova ◽  
Maria Klopocka ◽  
Marija Brankovic ◽  
Noriyuki Kasai ◽  
...  

Abstract Background OX40 (CD134) plays a role in the maintenance of late T-cell proliferation and survival. KHK4083 is a monoclonal antibody directed against OX40. We aimed to assess the safety and preliminary efficacy of KHK4083 in patients with moderately active ulcerative colitis (UC). Methods In this multicenter, double-blind, parallel-group, phase 2 study, patients with moderately active UC patients were randomized to ascending doses of intravenous KHK4083 (1, 3, or 10 mg/kg) or placebo every 2 weeks for 12 weeks. The primary endpoint was safety. The primary efficacy end point was the change from baseline in mean modified Mayo endoscopy subscore at week 12. Treatment with KHK4083 or placebo was continued every 4 weeks for up to 52 weeks in responders. Results Long-term treatment with KHK4083 was well tolerated, with treatment-related adverse events being predominantly transient mild-to-moderate infusion-related reactions. Exploratory analysis of biopsy samples showed the virtually complete elimination of OX40+ cells in colon mucosa after 12 weeks of KHK4083 treatment. There were no significant differences between any of the randomized KHK4083 dose groups and placebo for the mean change in Mayo endoscopy subscore from baseline to week 12. Conclusions KHK4083 can be safely administered intravenously at doses up to 10 mg/kg every 2 or 4 weeks for up to 52 weeks. Proof of pharmacodynamic action was confirmed by depletion of the elevated levels of the OX40+ cells associated with UC at all tested doses. Clinical response and mucosal healing (endoscopic improvement) in this population was not correlated with ablation of OX40+ T cells.

2020 ◽  
Vol 2 (4) ◽  
Author(s):  
Jaroslaw Kierkus ◽  
Marina Pesegova ◽  
Maria Klopocka ◽  
Marija Brankovic ◽  
Noriyuki Kasai ◽  
...  

2019 ◽  
Vol 156 (6) ◽  
pp. S-217 ◽  
Author(s):  
Laurent Peyrin-Biroulet ◽  
Julian Panés ◽  
Michael V. Chiorean ◽  
Jinkun Zhang ◽  
Severine Vermeire ◽  
...  

2020 ◽  
Vol 158 (6) ◽  
pp. S-1187 ◽  
Author(s):  
Rish Pai ◽  
James Canavan ◽  
Jay Tuttle ◽  
Michael Durante ◽  
Vipin Arora ◽  
...  

2005 ◽  
Vol 20 (2) ◽  
pp. 92-95 ◽  
Author(s):  
JR Calabrese ◽  
DJ Rapport ◽  
EA Youngstrom ◽  
K. Jackson ◽  
S. Bilali ◽  
...  

AbstractThe rapid cycling variant of bipolar disorder is defined as the occurrence of four periods of either manic or depressive illness within 12 months. Patients suffering from this variant of bipolar disorder have an unmet need for effective treatment. This review examines two major studies in an attempt to update understanding of the current therapies available to treat rapid cycling patients. The first trial compares lamotrigine versus placebo in 182 patients studied for 6 months. The second is a recently completed, 20-month trial comparing divalproate and lithium in 60 patients. Both trials had a double-blind, randomized parallel-group design. The data from the latter study indicate that there are no large differences in efficacy between lithium and divalproate in the long-term treatment of rapid cycling bipolar disorder. In addition, lamotrigine has the potential to complement the spectrum of lithium and divalproate through its greater efficacy for depressive symptoms.


2011 ◽  
Vol 140 (5) ◽  
pp. S-110 ◽  
Author(s):  
William J. Sandborn ◽  
Subrata Ghosh ◽  
Julian Panes ◽  
Ivana Vranic ◽  
Chinyu Su ◽  
...  

2014 ◽  
Vol 146 (5) ◽  
pp. S-240
Author(s):  
Caroline Looney ◽  
Franklin Fuh ◽  
Meina T. Tang ◽  
Xiaohui Wei ◽  
Mary E. Keir ◽  
...  

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