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PUFFIN Peanut Allergy Study

Auckland

We are looking for people aged 18-55 years with a physician-diagnosed peanut allergy to participate in the Puffin study, which is investigating a potential new trial medication designed to reduce allergic reactions while promoting protective immune responses.

Description

What to expect

Study details

Ages

Adults aged 18-55 years old

Duration

10-12 clinic visits over 5-9 months

Compensation

Up to $5,937 (pre-tax)

Eligibility Criteria

  • Adults aged 18-55 years old
  • Doctor-diagnosed peanut allergy
  • In otherwise good general health (apart from peanut allergy)
  • Non-smoker or occasional smoker
  • Willing to avoid peanuts during study

Locations

Auckland

Description

About the investigational medication
The study drug is a new investigational medication being developed for people with peanut allergy.
It’s an mRNA-based therapy similar in technology to some COVID-19 vaccines; however, instead of protecting against a virus, it’s designed to help your immune system react differently to peanut proteins.

People with peanut allergies have immune systems that overreact to certain peanut proteins (called Ara h1 and Ara h2). This overreaction causes the release of chemicals like histamine, which lead to allergic symptoms from hives to serious reactions like anaphylaxis.

The study drug contains messenger RNA (mRNA) that instructs the body’s cells to make modified, “safer” versions of the same peanut proteins. These modified proteins:

  • Do not cause an allergic reaction like real peanut exposure would
  • Help the immune system learn to tolerate peanut proteins gradually
  • May shift the immune response away from allergy-triggering IgE antibodies toward more protective IgG antibodies

You can think of it like “immune training”. Instead of avoiding peanuts completely, this approach carefully “teaches” the immune system to stop overreacting. 

What to expect

Study Aim 
The main purpose of this study is to learn about the study medication and to assess its safety and tolerability at different dosages. We would also like to assess the efficacy of the study medications in reducing allergic reactions.

Reason to participate
Your involvement in this study may help advance scientific knowledge that could contribute to the development of a new medication and better treatment for people with peanut allergies in the future. Other reasons to participate may include:

  • Help advance research towards the first mRNA-based trial medication for peanut allergy
  • Receive study-related medical care and monitoring at no cost
  • Contribute to a trial medication that could improve the quality of life for people living with food allergies
What does taking part involve? 
Taking part in the study involves firstly meeting with the research Doctor to find out more about your health and to see if the study is right for you.  If you wish to take part and you are eligible, we would like to see you for 10-12 clinic visits over a period of around 5-9 months, depending on the cohort you are assigned to.

Participants will attend around 10–12 visits over 5–9 months, including:

  • 1–3 screening visits
  • 3 trial medication treatment visits
  • Food challenges before and after trial medication administration
  • Several follow-up and monitoring visits

During visits, we conduct health checks that may include physical examinations and blood tests. We would like to ask you questions about your peanut allergy and your general health. Other procedures throughout the study include:

  • Medical history review
  • Vital signs and health checks
  • Review of peanut allergy history and prior reactions
  • Skin prick test (SPT) to confirm peanut allergy
  • Routine safety bloodwork (haematology, chemistry, urinalysis)
  • ECGs (electrocardiogram)
  • Pregnancy test (if applicable)
  • Screening food challenge
  • 3 intramuscular injections of study medication

All participants will receive the active study drug; placebo is used only in the food challenge meals, not as a trial medication treatment arm.
The study medication is administered 3 times throughout the study as an intramuscular (IM) injection in the upper arm. The medication is administered at the clinic by trained clinical staff. There is one overnight stay after the first injection for safety monitoring.

The study aims to investigate the study medication at different dosages and intervals to evaluate its safety, tolerability and efficacy in reducing peanut allergy reactions.

Apply now

Fill out your details, and our team will be in touch to discuss your potential involvement in this study and answer any questions you may have.

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