Long-term Safety and Efficacy of the Anti-MAdCAM-1 Monoclonal Antibody Ontamalimab [SHP647] for the Treatment of Ulcerative Colitis: The Open-label Study TURANDOT II
Language English Country Great Britain, England Media print
Document type Clinical Trial, Phase II, Journal Article, Multicenter Study, Randomized Controlled Trial
PubMed
33599720
PubMed Central
PMC8218706
DOI
10.1093/ecco-jcc/jjab023
PII: 6144575
Knihovny.cz E-resources
- Keywords
- MAdCAM-1, Ulcerative colitis, phase 2,
- MeSH
- C-Reactive Protein analysis MeSH
- Adult MeSH
- Endoscopy, Gastrointestinal methods statistics & numerical data MeSH
- Gastrointestinal Agents administration & dosage adverse effects MeSH
- Antibodies, Monoclonal, Humanized * administration & dosage adverse effects MeSH
- Dose-Response Relationship, Immunologic MeSH
- Leukocyte L1 Antigen Complex analysis MeSH
- Humans MeSH
- Cell Adhesion Molecules antagonists & inhibitors MeSH
- Drug Monitoring * methods statistics & numerical data MeSH
- Mucoproteins antagonists & inhibitors MeSH
- Colitis, Ulcerative * diagnosis drug therapy immunology MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase II MeSH
- Multicenter Study MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- C-Reactive Protein MeSH
- Gastrointestinal Agents MeSH
- Antibodies, Monoclonal, Humanized * MeSH
- Leukocyte L1 Antigen Complex MeSH
- MADCAM1 protein, human MeSH Browser
- Cell Adhesion Molecules MeSH
- Mucoproteins MeSH
- ontamalimab MeSH Browser
BACKGROUND AND AIMS: Ontamalimab, a fully-human monoclonal antibody targeting MAdCAM-1, induced remission in patients with moderate-to-severe ulcerative colitis [UC] in the TURANDOT study. We aimed to assess long-term safety, tolerability, and efficacy of ontamalimab in TURANDOT II. METHODS: TURANDOT II was a phase 2, multicentre, open-label [OL] study in patients with moderate-to-severe UC who completed TURANDOT on placebo or ontamalimab (NCT01771809). Patients were randomised to 75 mg or 225 mg ontamalimab every 4 weeks for 72 weeks [OL1]. The dosage could be increased to 225 mg from Week 8 at the investigator's discretion. All patients then received 75 mg every 4 weeks for 72 weeks [OL2], followed by 6-month safety follow-up. The primary objective was safety, measured by adverse events [AEs], serious AEs [SAEs], and AEs leading to withdrawal. Mucosal healing [MH; centrally read endoscopy] was assessed. RESULTS: Of 330 patients, 180 completed OL1; 94 escalated to 225 mg; 127 completed OL2. Overall, 36.1% experienced drug-related AEs. The most common SAE [10.0%] was worsening/ongoing UC; 5.5% of patients had serious infections, the most common being gastroenteritis [0.9%]. One death and four cancers [all unrelated to ontamalimab] occurred. No PML [progressive multifocal leukoencephalopathy]/lymphoproliferative disorders occurred. Geometric mean high-sensitivity C-reactive protein [hsCRP] and faecal calprotectin decreased across OL1 in both dose groups. The proportion of patients assigned to placebo in TURANDOT achieving MH increased from 8.8% [6/68] at baseline to 35.3% at Week 16 [24/68; non-responder imputation]. The corresponding increase in the ontamalimab group was from 23.3% [61/262] to 26.7% [70/262]. CONCLUSIONS: Ontamalimab was well tolerated up to 144 weeks in patients with moderate-to-severe UC, with good safety and efficacy.
Clinic of Gastroenterology and Hepatology Military Medical Academy Belgrade Serbia
Department of Gastroenterology University Hospitals Leuven Leuven Belgium
Department of Internal Medicine Medical University of Vienna Vienna Austria
Department of Medicine University of California San Diego La Jolla CA USA
Faculty of Medicine Charles University Hospital Hradec Králové Czech Republic
Gastroenterology Centre Nitra Slovakia
Gastroenterology Nature Coast Clinical Research Inverness FL USA
Inflammatory Bowel Disease Clinic Alfred Hospital Melbourne VIC Australia
Inflammatory Bowel Diseases Center Humanitas University Milan Italy
Nicolaus Copernicus University Collegium Medicum in Bydgoszcz Bydgoszcz Poland
Seoul National University College of Medicine Seoul South Korea
Shire a Takeda company Lexington MA USA
Shire a Takeda company Zug Switzerland
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