Integrated safety analysis of filgotinib for ulcerative colitis : Results from SELECTION and SELECTIONLTE
© 2023 Galapagos NV. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd..
BACKGROUND: Filgotinib 200 mg (FIL200) is an approved treatment for adults with moderately to severely active ulcerative colitis (UC).
AIM: To report integrated safety data from the phase 2b/3 SELECTION study (NCT02914522) and its ongoing long-term extension study SELECTIONLTE (NCT02914535).
METHODS: Safety outcomes were analysed in adults with moderately to severely active UC who received FIL200, filgotinib 100 mg (FIL100) or placebo once daily throughout the 11-week SELECTION induction study, the 47-week SELECTION maintenance study (if applicable) and SELECTIONLTE (if applicable). Exposure-adjusted incidence rates (EAIRs) per 100 censored patient-years of exposure with 95% confidence intervals were reported for treatment-emergent adverse events (AEs). Certain AE data were presented in subgroups, including age and prior biologic exposure status.
RESULTS: This interim analysis included 1348 patients representing 3326.2 patient-years of exposure. Baseline characteristics of patients entering SELECTION were similar across treatment groups. EAIRs for serious infection, thromboembolic events and major adverse cardiovascular events (MACE) were consistently low across treatment groups. Most patients with MACE had cardiovascular risk factors. The EAIR for herpes zoster was numerically higher for FIL200 than for placebo. Infection incidences were numerically higher in biologic-experienced than biologic-naive patients. Higher incidences of certain AEs in patients 65 years of age or older were as expected. Four deaths occurred, including three cardiovascular deaths, none of which was considered related to filgotinib.
CONCLUSION: FIL200 and FIL100 were well tolerated with no unexpected safety signals in patients with moderately to severely active UC, regardless of previous biologic exposure or age.
CLINICALTRIALS:.
GOV IDENTIFIERS (NCT NUMBERS): NCT02914522, NCT02914535.
Errataetall: |
ErratumIn: Aliment Pharmacol Ther. 2023 Dec 3;:. - PMID 38044590 |
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Medienart: |
E-Artikel |
Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:58 |
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Enthalten in: |
Alimentary pharmacology & therapeutics - 58(2023), 9 vom: 15. Nov., Seite 874-887 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Schreiber, Stefan [VerfasserIn] |
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Links: |
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Biological Products |
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Anmerkungen: |
Date Completed 15.12.2023 Date Revised 15.12.2023 published: Print-Electronic ClinicalTrials.gov: NCT02914535, NCT02914522, NCT02914522 ErratumIn: Aliment Pharmacol Ther. 2023 Dec 3;:. - PMID 38044590 Citation Status MEDLINE |
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doi: |
10.1111/apt.17674 |
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500 | |a ErratumIn: Aliment Pharmacol Ther. 2023 Dec 3;:. - PMID 38044590 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023 Galapagos NV. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd. | ||
520 | |a BACKGROUND: Filgotinib 200 mg (FIL200) is an approved treatment for adults with moderately to severely active ulcerative colitis (UC) | ||
520 | |a AIM: To report integrated safety data from the phase 2b/3 SELECTION study (NCT02914522) and its ongoing long-term extension study SELECTIONLTE (NCT02914535) | ||
520 | |a METHODS: Safety outcomes were analysed in adults with moderately to severely active UC who received FIL200, filgotinib 100 mg (FIL100) or placebo once daily throughout the 11-week SELECTION induction study, the 47-week SELECTION maintenance study (if applicable) and SELECTIONLTE (if applicable). Exposure-adjusted incidence rates (EAIRs) per 100 censored patient-years of exposure with 95% confidence intervals were reported for treatment-emergent adverse events (AEs). Certain AE data were presented in subgroups, including age and prior biologic exposure status | ||
520 | |a RESULTS: This interim analysis included 1348 patients representing 3326.2 patient-years of exposure. Baseline characteristics of patients entering SELECTION were similar across treatment groups. EAIRs for serious infection, thromboembolic events and major adverse cardiovascular events (MACE) were consistently low across treatment groups. Most patients with MACE had cardiovascular risk factors. The EAIR for herpes zoster was numerically higher for FIL200 than for placebo. Infection incidences were numerically higher in biologic-experienced than biologic-naive patients. Higher incidences of certain AEs in patients 65 years of age or older were as expected. Four deaths occurred, including three cardiovascular deaths, none of which was considered related to filgotinib | ||
520 | |a CONCLUSION: FIL200 and FIL100 were well tolerated with no unexpected safety signals in patients with moderately to severely active UC, regardless of previous biologic exposure or age | ||
520 | |a CLINICALTRIALS: | ||
520 | |a GOV IDENTIFIERS (NCT NUMBERS): NCT02914522, NCT02914535 | ||
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