Phase I, double-blind, randomized, placebo-controlled, dose-escalation study of NI-0401 (a fully human anti-CD3 monoclonal antibody) in patients with moderate to severe active Crohn's disease
✍ Scribed by C. Janneke van der Woude; Pieter Stokkers; Ad A. van Bodegraven; Gert Van Assche; Zbigniew Hebzda; Leszek Paradowski; Geert D'Haens; Subrata Ghosh; Brian Feagan; Paul Rutgeerts; Gerard Dijkstra; Dirk J. de Jong; Bas Oldenburg; Mahdi Farhan; Tristan Richard; Yann Dean; Daniel W. Hommes
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 274 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1078-0998
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✦ Synopsis
Background: NI-0401 is a fully human monoclonal antibody, which binds to the CD3 subunit of the T-cell receptor, causing modulation of T-cell activity. We investigated the safety and the ability to modulate the TCR-CD3 complex of NI-0401 in patients with active Crohn's disease (CD).
Methods: A double-blind, placebo-controlled, randomized, multicenter, dose-escalating trial was conducted in CD patients age 18-70 years, a Crohn's Disease Activity Index (CDAI) of 220-450, and detectable levels of C-reactive protein. The primary outcome was safety and the ability of NI-0401 to modulate the TCR-CD3 complex on T cells. Efficacy parameters included the proportion of patients achieving remission (CDAI <150), clinical response (CDAI fall !100), and change from baseline in the CD Endoscopy Index of Severity (CDEIS).
Results: Forty patients received placebo (n ¼ 7) or NI-0401 (n ¼ 33) 0.05-10 mg daily for 5 days. NI-0401 doses 1 mg were well tolerated. Infusion reactions occurred at doses !2 mg. The extent and duration of TCR-CD3 modulation increased with dose. No differences between groups were observed in the proportions of patients achieving clinical remission or response. The mean CDEIS at week 6 differed significantly between the 1-mg and placebo group.
Conclusions: NI-0401 was tolerated at doses 1 mg with manageable side effects. NI-0401 induced a dose-dependent modulation of the TCR-CD3 complex. No significant improvement of CDAI was observed but 1 mg NI-0401 demonstrated an improvement in CDEIS.
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