A paper published in Pharmaceutics describes development and validation of a production process for 5 mg tablets of infliximab, using biosimilar CT-P13 (Remsima, Inflectra), for the treatment of inflammatory bowel disease.
The oral delivery of biologic drugs represents an as-yet unattained goal. However, the potential benefits of oral administration of these therapies in terms of compliance, comfort, and drug storage are many, and several drug makers are pursuing the possibility: Last year, Amgen and Entera Bio announced a research collaboration into oral administration of biologics, and Protalix BioTherapeutics announced positive results from a study on oral administration of anti—tumor necrosis factor (anti-TNF) therapies.
Now, a paper published in Pharmaceutics describes development and validation of a production process for 5 mg tablets of infliximab, using biosimilar CT-P13 (Remsima, Inflectra), for the treatment of inflammatory bowel disease (IBD).
The authors of the paper hypothesized that, in IBD, targeting infliximab administration to the ileo-colonic region could be efficacious in treating local IBD inflammation.
The researchers used the biosimilar infliximab and reconstituted it into a sugar solution that, when lyophilized, yielded powder that could be further compounded and treated with a coating.
The coating technology (called ColoPulse) used on the tablets has a pH sensitive polymer; the intraluminal pH of the gastrointestinal tract rises during transit from the jejunum to the ileum, then drops in the colon, and the tablet’s coating uses this period of pH increase to disintegrate in the terminal ileum.
According to the researchers, the in vitro stability of infliximab in simulated gastrointestinal systems is “encouraging,” and analyses of infliximab content, tertiary protein structure, aggregates, and potency showed that the infliximab present in the coated tablet was stable during compounding and could bind to TNF.
Stability data showed that the preparation was stable for up to 6 months at 25°C.
The authors note that a clinical trial will be necessary to determine the such factors as the pharmacokinetics of the proposed coated tablet, as well as the potential for development of anti-drug antibodies.
Reference
Gareb B, Posthumus S, Beugeling M, et al. Towards the oral treatment of ileo-colonic inflammatory bowel disease with infliximab tablets: development and validation of the production process. Pharmaceutics. 2019;11(9):428. doi: 10.3390/pharmaceutics11090428.
Senators Introduce Bipartisan Legislation to Protect Skinny Labeling
January 2nd 2025To close out the year, 4 senators came together to introduce a new bipartisan bill to protect biosimilar and generic drug manufacturers from patent litigation when obtaining “skinny label” approvals for their products.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
The Top 5 Most-Read Gastroenterology Articles of 2024
December 21st 2024The top gastroenterology biosimilar news from 2024 highlight fluctuations in the adalimumab biosimilar market throughout the year, while FDA and European approvals for ustekinumab biosimilars are set to improve access and reduce costs for patients with Crohn disease and ulcerative colitis.
Biosimilars Gastroenterology Roundup for May 2024—Podcast Edition
June 2nd 2024On this episode of Not So Different, we review the biggest gastroenterology biosimilar stories from May 2024, covering new data from conferences and journals on infliximab and adalimumab products that demonstrate positive clinical results and confirm the safety of these biosimilars, as well as the feasibility of switching to them.
Stable Patient Satisfaction Found After Switching From the Humira or Biosimilar CT-P17
December 14th 2024A real-world study in France found patient satisfaction was stable after switching from either the reference product or a low-concentration adalimumab biosimilar to the adalimumab biosimilar CT-P17, a high-concentration, citrate-free formulation.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.