# Once-Daily Oral Ozanimod for Japanese Patients With Ulcerative Colitis: Results From the Phase 2/3 J-True North Study

**Authors:** Hiroshi Nakase, Toshimitsu Fujii, Tadakazu Hisamatsu, Yasuo Suzuki, Mamoru Watanabe, Sakuma Takahashi, Makoto Ooi, Ken Takeuchi, Tsuguhiro Kimura, Ken Furuya, Nobuo Aoyama, Kenkei Hasatani, Noriyuki Horiki, Kazunari Kanke, Satoki Tokito, Souken Sai, Yoko Uchikawa, Shoichiro Goto, Go Fujimoto, Changliang Zhang, AnnKatrin Petersen, Toshifumi Hibi

PMC · DOI: 10.1016/j.gastha.2025.100812 · 2025-09-16

## TL;DR

A clinical trial showed that once-daily ozanimod is effective and safe for Japanese patients with moderate to severe ulcerative colitis.

## Contribution

First large-scale verification of ozanimod's efficacy and safety in Asian patients with ulcerative colitis.

## Key findings

- Ozanimod significantly improved clinical response compared to placebo at week 12.
- Efficacy was maintained over 52 weeks with no unexpected safety issues.
- Higher rates of remission and mucosal healing were observed in ozanimod-treated patients.

## Abstract

Ozanimod is a once-daily, oral, selective sphingosine 1-phosphate receptor 1 and 5 modulator. The objective of the randomized, phase 2/3 J-True North study (NCT03915769) was to assess the efficacy and safety of ozanimod in Japanese patients with moderately to severely active ulcerative colitis.

In the 12-week induction period (IP), patients were randomized 1:1:1 to receive placebo, ozanimod 0.46 mg, or ozanimod 0.92 mg. Patients who completed the IP with a clinical response at week (w) 12 were eligible to enter a 40-week maintenance period where they received the same treatment as they did in the IP. The primary endpoint was clinical response (complete Mayo score) at w12; clinical and mucosal secondary endpoints were assessed at w12 and w52.

Of 198 patients randomized, 176 completed the IP. Of these patients, 97 entered and 77 completed the maintenance period. A significantly higher proportion of patients receiving ozanimod achieved clinical response at w12 versus placebo (ozanimod 0.46 mg: 52.9%, P = .0158; ozanimod 0.92 mg: 61.5%, P = .0006; vs placebo: 32.3%). Similar results were observed in the secondary endpoints where patients receiving ozanimod achieved higher rates of clinical remission, endoscopic improvement, and mucosal healing at w12 than those receiving placebo. Efficacy was maintained at w52 for all endpoints. Both doses of ozanimod were well tolerated, with no unexpected safety signals.

This large-scale clinical trial demonstrated the efficacy and safety of once-daily oral ozanimod in Japanese patients with moderately to severely active ulcerative colitis. This is the first time that the efficacy and safety of ozanimod were verified in a large number of patients in Asia.

## Linked entities

- **Chemicals:** ozanimod (PubChem CID 52938427)
- **Diseases:** ulcerative colitis (MONDO:0005101)

## Full-text entities

- **Diseases:** Ulcerative Colitis (MESH:D003093)
- **Chemicals:** Ozanimod (MESH:C000607776)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12630022/full.md

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Source: https://tomesphere.com/paper/PMC12630022