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Long-term efficacy and safety of biosimilar infliximab (CT-P13) after switching from originator infliximab: open-label extension of the NOR-SWITCH trial.


ABSTRACT:

Background and objectives

The 52-week, randomized, double-blind, noninferiority, government-funded NOR-SWITCH trial demonstrated that switching from infliximab originator to less expensive biosimilar CT-P13 was not inferior to continued treatment with infliximab originator. The NOR-SWITCH extension trial aimed to assess efficacy, safety and immunogenicity in patients on CT-P13 throughout the 78-week study period (maintenance group) versus patients switched to CT-P13 at week 52 (switch group). The primary outcome was disease worsening during follow-up based on disease-specific composite measures.

Methods

Patients were recruited from 24 Norwegian hospitals, 380 of 438 patients who completed the main study: 197 in the maintenance group and 183 in the switch group. In the full analysis set, 127 (33%) had Crohn's disease, 80 (21%) ulcerative colitis, 67 (18%) spondyloarthritis, 55 (15%) rheumatoid arthritis, 20 (5%) psoriatic arthritis and 31 (8%) chronic plaque psoriasis.

Results

Baseline characteristics were similar in the two groups at the time of switching (week 52). Disease worsening occurred in 32 (16.8%) patients in the maintenance group vs. 20 (11.6%) in the switch group (per-protocol set). Adjusted risk difference was 5.9% (95% CI -1.1 to 12.9). Frequency of adverse events, anti-drug antibodies, changes in generic disease variables and disease-specific composite measures were comparable between arms. The study was inadequately powered to detect noninferiority within individual diseases.

Conclusion

The NOR-SWITCH extension showed no difference in safety and efficacy between patients who maintained CT-P13 and patients who switched from originator infliximab to CT-P13, supporting that switching from originator infliximab to CT-P13 is safe and efficacious.

SUBMITTER: Goll GL 

PROVIDER: S-EPMC6850326 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Long-term efficacy and safety of biosimilar infliximab (CT-P13) after switching from originator infliximab: open-label extension of the NOR-SWITCH trial.

Goll G L GL   Jørgensen K K KK   Sexton J J   Olsen I C IC   Bolstad N N   Haavardsholm E A EA   Lundin K E A KEA   Tveit K S KS   Lorentzen M M   Berset I P IP   Fevang B T S BTS   Kalstad S S   Ryggen K K   Warren D J DJ   Klaasen R A RA   Asak Ø Ø   Baigh S S   Blomgren I M IM   Brenna Ø Ø   Bruun T J TJ   Dvergsnes K K   Frigstad S O SO   Hansen I M IM   Hatten I S H ISH   Huppertz-Hauss G G   Henriksen M M   Hoie S S SS   Krogh J J   Midtgard I P IP   Mielnik P P   Moum B B   Noraberg G G   Poyan A A   Prestegård U U   Rashid H U HU   Strand E K EK   Skjetne K K   Seeberg K A KA   Torp R R   Ystrøm C M CM   Vold C C   Zettel C C CC   Waksvik K K   Gulbrandsen B B   Hagfors J J   Mørk C C   Jahnsen J J   Kvien T K TK  

Journal of internal medicine 20190412 6


<h4>Background and objectives</h4>The 52-week, randomized, double-blind, noninferiority, government-funded NOR-SWITCH trial demonstrated that switching from infliximab originator to less expensive biosimilar CT-P13 was not inferior to continued treatment with infliximab originator. The NOR-SWITCH extension trial aimed to assess efficacy, safety and immunogenicity in patients on CT-P13 throughout the 78-week study period (maintenance group) versus patients switched to CT-P13 at week 52 (switch gr  ...[more]

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