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  • Jefferson Adams
    Jefferson Adams

    Celiac Disease Drug KAN-101 Gets FDA Fast Track

    Reviewed and edited by a celiac disease expert.

    A new drug designed to treat celiac disease has received fast track status from the FDA ahead of Phase 2 Trials slated for the second half 2022.

    Celiac Disease Drug KAN-101 Gets FDA Fast Track - Fast. Image: CC BY 2.0--fhir.photograph
    Caption: Fast. Image: CC BY 2.0--fhir.photograph

    Celiac.com 07/26/2022 - Previous drugs designed to induce tolerance to gliadin have met with failure. Will the latest effort fare any better? 

    In people with celiac disease, gliadin-specific T cells drive an adverse immune response to gluten peptides, which can cause symptoms, long-term gut damage, and other related conditions. Currently,  the only treatment for celiac disease is a gluten-free diet.

    Celiac.com Sponsor (A12):
    A new drug, KAN-101, designed to treat celiac disease by inhibiting a key celiac disease biomarker, has received fast track status from the FDA ahead of Phase 2 Trials slated for the second half 2022. Designed by Anokion SA, a clinical-stage biotechnology company focused on treating autoimmune disease by restoring normal immune tolerance, KAN-101 has been found to be safe, well-tolerated, and to provide the proper immune responses.

    KAN-101 is designed to induce tolerance to gliadin, a core component of gluten, through natural pathways in the liver. 

    The Phase 1, randomized, double-blind, placebo-controlled trial enrolled a total of 41 individuals with celiac disease on a gluten-free diet in both single-ascending dose (SAD) and multi-ascending dose (MAD) cohorts. Findings from the Phase 1 trial showed that treatment with KAN-101 was safe and tolerated, and successfully reduced T cell responses following gluten challenge.

    The primary endpoint of the Phase 1 trial is to assess the safety and tolerability of KAN-101, with secondary endpoints to assess KAN-101 serum concentrations and pharmacokinetics. Additional end points include the assessment of cytokines critical to both innate and adaptive immunity, T cell responses, and other serum cytokines and celiac disease symptoms.

    Patients who recieved KAN-101 experienced dose-dependent reductions of gluten-induced plasma IL-2, a cytokine that is elevated in celiac patients after gluten ingestion, and which reflects severity of acute symptoms. Patients who received the 0.6mg/kg dose experienced statistically significant reductions of IL-2, compared to other groups

    Administration of KAN-101 did not increase gut-homing CD8 T cell responses after gluten challenge, an indicator of immune response to gluten exposure in patients with celiac disease.

    Stories about new drugs designed to induce tolerance to gluten always cause great excitement within the celiac disease community. However, previous drugs designed to induce tolerance to gliadin have met with failure. 

    Will the latest effort fare any better? Stay tuned for more as KAN-101 moves into its Phase 2 trial later this year.

    Read more at Businesswire.com



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    Guest Question

    Posted

    Is this drug classified as an immunosuppressant?

     Karen

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    trents
    1 hour ago, Guest Question said:

    Is this drug classified as an immunosuppressant?

     Karen

    "KAN-101 is an investigational drug that aims to re-educate the immune cells that drive celiac disease, so they do not respond to gluten antigens, while leaving the healthy components of the immune system intact." (From: Open Original Shared Link)

    Doesn't sound like it is an immunosuppressant. Sounds like it reprograms the particular spectrum of the immune response system that reacts to gluten in celiacs without suppressing the entire immune system.

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    RMJ

    I found this on the Anokion website:

    Quote

    KAN-101 is an investigational treatment for Celiac Disease (CeD). It encompasses a well-described gluten antigen that is implicated in driving the onset of Celiac Disease. We deliver the antigen to the liver and immune system with our liver targeting glycosylation signature.

     

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    RMJ

    One of the exclusion criteria for the clinical trial was being positive for HLA-DQ8 (DQA1*03, DQB1*0302)  Does that mean the drug isn’t expected to work in these patients? Interesting.

    Open Original Shared Link

    More information:

    Open Original Shared Link

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    trents
    57 minutes ago, RMJ said:

    One of the exclusion criteria for the clinical trial was being positive for HLA-DQ8 (DQA1*03, DQB1*0302)  Does that mean the drug isn’t expected to work in these patients? Interesting.

    Open Original Shared Link

    More information:

    Open Original Shared Link

    And also a history DH.

    I emailed the following inquiry to Celiac.org:

    A couple of us moderators at Celiac.com noticed from Open Original Shared Link that the exclusionary criteria for participating in the KAN-101 study included having the DQ8 gene and a history of DH.

    Do you have any knowledge of why these two classes of celiac disease sufferers were excluded? They comprise a large slice of the celiac disease community.

    Thank you,

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  • About Me

    Jefferson Adams

    Jefferson Adams is Celiac.com's senior writer and Digital Content Director. He earned his B.A. and M.F.A. at Arizona State University. His articles, essays, poems, stories and book reviews have appeared in numerous magazines, journals, and websites, including North American Project, Antioch Review, Caliban, Mississippi Review, Slate, and more. He is the author of more than 2,500 articles on celiac disease. His university coursework includes studies in science, scientific methodology, biology, anatomy, physiology, medicine, logic, and advanced research. He previously devised health and medical content for Colgate, Dove, Pfizer, Sharecare, Walgreens, and more. Jefferson has spoken about celiac disease to the media, including an appearance on the KQED radio show Forum, and is the editor of numerous books, including "Cereal Killers" by Scott Adams and Ron Hoggan, Ed.D.

    >VIEW ALL ARTICLES BY JEFFERSON ADAMS

     


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