FDA Accepts Integral Molecular's Membrane Proteome Arraytm Qualification Plan, Advancing The Platform For Approval As A Drug Development Tool

(MENAFN- PR Newswire)

PHILADELPHIA, Feb. 5, 2025 /PRNewswire/ -- Integral Molecular, a leader in antibody discovery technologies, is proud to announce that the FDA has accepted their Membrane Proteome ArrayTM (MPA) Qualification Plan for advancement as a Drug Development Tool (DDT) to assess antibody binding specificity. Antibody drug developers already routinely include MPA data in regulatory packages, and qualification as a DDT will allow them to further rely on the MPA in the approval process. Integral Molecular's MPA is the industry-leading technology for antibody specificity testing and is the only specificity platform under FDA consideration as a DDT.

Learn more about the Membrane Proteome ArrayTM , and how it enables the precise identification of off-target binding interactions

Non-specific drug binding is a significant cause of adverse events in patients that can lead to severe complications or even death, and early specificity testing can de-risk drug development and enhance patient safety. Recent research has demonstrated that up to one-third of antibody drugs exhibit non-specific binding to unintended targets.

The MPA assesses binding across ~6,000 structurally intact membrane proteins and is the only platform of its kind that screens membrane proteins in their native conformation. The MPA has been used to screen over 2,000 preclinical antibody therapeutics for customers worldwide, and MPA specificity data has been accepted by regulatory bodies globally, including the FDA, EMA, and NMPA.

"This milestone towards MPA qualification reflects the continued dedication of our team to set a new standard in testing antibody drug specificity. Our continued improvements to the MPA-including statistical analyses, bioinformatic comparisons, and enhanced quality systems-have been critical to our qualification plan and have supported ISO 9001 certification of our processes. We thank the FDA for their confidence in our approach and commitment to advancing the safety of biologics."
-Benjamin Doranz, CEO, Integral Molecular

The MPA is progressing toward DDT qualification under the FDA's ISTAND Pilot Program, which promotes Innovative Science and Technology Approaches for New Drugs. As part of this process, Integral Molecular has been invited to submit a Full Qualification Plan (FQP) for the MPA, which is the final step in achieving DDT status.

About Integral Molecular

Integral Molecular (integralmolecular ) is the industry leader in creating transformative technologies that advance the discovery of therapeutics against difficult protein targets. With 20+ years of experience focused on membrane proteins, viruses, and antibodies, Integral Molecular's technologies have been integrated into the drug discovery pipelines of over 600 biotech and pharmaceutical companies to help discover new therapies for cancer, diabetes, autoimmune disorders, and viral threats such as SARS-CoV-2, Ebola, Zika, and dengue viruses.

Follow Integral Molecular on LinkedI

Press Contact
Integral Molecular
Soma Banik, PhD, Director of Public Relations
215-966-6061

SOURCE Integral Molecular

WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE? 440k+
Newsrooms &
Influencers 9k+
Digital Media
Outlets 270k+
Journalists
Opted In GET STARTED

MENAFN05022025003732001241ID1109171808