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Switching standard dosed intravenous to subcutaneous infliximab leads to similar drug exposure in inflammatory bowel disease patients independent of concomitant immunosuppressants (SHUFFLE study).
British journal of clinical pharmacology

Cure8 research brief

Switching standard dosed intravenous to subcutaneous infliximab leads to similar drug exposure in inflammatory bowel disease patients independent of concomitant immunosuppressants (SHUFFLE study).

2 min read
Medications Infliximab Biosimilars Anti-TNF Clinical study Adult patients Patients On Biologics Clinicians

Why This Matters

The findings suggest people with IBD on IV infliximab could switch to fixed-dose SC infliximab without losing drug exposure, and many may gain convenience and higher trough drug levels regardless of concomitant immunosuppressant use.

Who Should Pay Attention

Adults with IBD receiving intravenous infliximab, patients considering switching to subcutaneous biologic formulations, clinicians who manage biologic dosing and monitoring, and researchers studying biologic delivery methods.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

This single-centre prospective study followed 35 adults with IBD who were in clinical remission on IV infliximab and switched to biweekly SC infliximab for 24 weeks. The primary outcome—area under the concentration–time curve (AUC)—was comparable between IV and SC dosing.

Trough infliximab concentrations were higher after switching to SC dosing, and this increase persisted at ≥12 months across patients on monotherapy, combination therapy, or after stopping immunosuppressants.

Patients reported a substantial decrease in time burden (median reduction ~9.3 hours per 6 months) and a small improvement in IBD-specific quality of life (IBDQ-NL). Nearly all participants (97%) remained on SC infliximab at 24 weeks, and no disease exacerbations were reported during follow-up.

The study addresses a practical question for people receiving infliximab: SC dosing may keep exposure at least equivalent while raising trough levels and reducing infusion-related time demands.

Keep In Mind

This report is a single-centre prospective pharmacokinetic study with 35 patients and an abstract-level source. The structured content is grounded in the article abstract; it does not replace individualized medical advice. Details on clinical efficacy beyond remission maintenance, long-term safety, and broader generalizability may require larger multicentre studies.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Research paper Evidence type derived from source or registry metadata.
PublicationBritish journal of clinical pharmacology
AuthorsLieke M J van de Ven-van Dinter, Mariëlle J L Romberg-Camps, Dennis R Wong +2 more
InstitutionDepartment of Clinical Pharmacy, Pharmacology and Toxicology, Zuyderland Medical Centre, Heerlen, The Netherlands.
Study typeJournal article
Indexed viaPubMed
Source typeResearch paper
PublishedSep 18, 2026, 12:00 AM
Content availableJournal abstract

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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