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

C.J. van der Woude, P Stokkers, AA van Bodegraven, G van Assche, Z Hebzda, L Paradowski, G D'Haens, S Ghosh, B Feagan, P Rutgeerts, GJJ (Gerard) Dijkstra, DJ de Jong, B Oldenburg, M Farhan, T Richard, Y Dean, DW (Daan) Hommes

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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 220450, 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 = 7) or NI-0401 (n 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.
Original languageUndefined/Unknown
Pages (from-to)1708-1716
Number of pages9
JournalInflammatory Bowel Diseases
Issue number10
Publication statusPublished - 2010

Research programs

  • EMC MM-04-20-01

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