Could toothpaste featuring peanut proteins help reduce allergic reactions in children? Intrommune plans to run a Phase II trial testing its medical toothpaste INT301 in 80–100 children with peanut allergies to find out, CEO Michael Nelson says.

New York-based Intrommune is looking to start the multi-center, North America-based Phase II trial in late 2022 or early 2023, Nelson says. The exact timeline will depend on an ongoing $40-45 million Series B fundraise, which will fund the planned Phase II study and preparation for a potential future Phase III trial and commercialisation, he adds.

As a primary endpoint, patients will undergo a food challenge before and after treatment, Nelson says. A food challenge entails gradually giving patients allergens until they demonstrate early signs of an allergic reaction.

Nelson says food challenges are the FDA’s “gold-standard” for clinical trials, but Intrommune is also exploring ways to assess its treatment without a food challenge. As an exploratory endpoint, an ongoing Phase I trial (NCT04603300) of INT301 is assessing level changes in the antibodies IgG4 and IgE, which are though to be associated with peanut allergies.

INT301 is an oral mucosal immunotherapy, delivering small amounts of allergens via toothpaste that cause patients to build up a tolerance toward peanut proteins. “The biggest advantage is toothbrushing is already built into most Americans’ daily routines,” Nelson explains.

Ongoing Phase I could see switch-up

Intrommune is running the ongoing Phase I OMEGA trial testing the safety of INT301 in adults with peanuts allergies. OMEGA has moved to the third cohort after meeting safety goals across 11 doses. Now, the biotech is asking the FDA if the ongoing trial can begin collecting long-term safety data, continuing patients on maintenance, and administering a food challenge at the end of the study, Nelson adds.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

As a primary endpoint, the Phase I study is investigating the percentage of patients that can tolerate escalating doses of INT301 by comparing the rate of adverse reactions between INT301 and placebo. The Phase I trial’s listing does not include a food challenge as an endpoint.

Peanut allergy clinical trials driven by institutions

Despite the high global prevalence of peanut allergies, the pharma industry has lagged behind institutions in initiating peanut allergy studies. According to GlobalData’s Clinical Trials Database, institutions are sponsoring 25 of the 31 ongoing Phase I-III studies. Most ongoing peanut allergy studies are at the Phase II stage.

Globally, over 200 million people have food allergies, including an estimated 32 million in the US. People with peanut allergies who are inadvertently exposed to peanuts can face serious and potentially fatal side effects, including anaphylaxis.