• Friday, May 10, 2024 @ 12:00 am

In collaboration with Pfizer Ignite, Mabylon nominates its anti-allergen multispecific antibody product that is undergoing Investigative New Drug (IND)-enabling studies and subsequent clinical development for the treatment of peanut allergy.

Mabylon AG, a leader in the high-throughput discovery, characterization, and development of human-derived antibodies, today announced the nomination of an anti-allergen multispecific antibody that is undergoing Investigative New Drug (IND)-enabling studies and subsequent clinical development for the treatment of peanut allergy.

For the latest development phases of its allergy program, Mabylon has entered into a collaboration agreement with Pfizer through its Pfizer Ignite program.  Pfizer Ignite is an end-to-end R&D service that connects innovative companies to Pfizer’s suite of research, development, and manufacturing services alongside input from an expert advisory network. This collaboration allows Mabylon to ensure the highest industry-standards, thus validating each step of the chemistry/manufacturing/controls (CMC), and clinical development processes of its multispecific antibody product. Mabylon, however, retains all rights to its product and maintains independence in the decision process.

Allergies, which are caused by a malfunctioning immune system, are a rapidly expanding social and economic burden, which lately attracted the interest of pharma companies and investors. Some allergies, such as peanut allergy, can be deadly through anaphylactic shock, while many others have a deleterious effect on long term conditions such as asthma and can significantly impact quality of life.

In addressing this huge, yet unmet medical need, Mabylon has taken an allergen-neutralizing approach by developing allergen-specific antibody products. “Based on an extensive preclinical analysis, we anticipate that Mabylon’s development candidate product for peanut allergy will be safe, will offer rapid protection, higher compliance because of low frequency of administration, and will be efficacious also in patients less responsive or not eligible for the only two approved peanut allergy treatments”, said Alcide Barberis, Ph.D., Chief Executive Officer of Mabylon.

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