RecruitingPhase 4NCT06935890

Jack Jumper Ant Venom Immunotherapy Long-term Effectiveness Investigation


Sponsor

Murdoch Childrens Research Institute

Enrollment

100 participants

Start Date

Nov 25, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Jack Jumper ant (JJA) venom allergy is a uniquely Australian medical condition. It is the leading cause of venom allergy and affects up to three per cent of the population. 70 percent of people with JJA allergy will have another reaction on a repeat sting and this sensitivity appears to persist for many years. Venom immunotherapy (VIT) has been shown to be a safe and effective treatment in the prevention of severe systemic allergic reactions (anaphylaxis) to future stings. It is currently offered to patients as standard care in Tasmania, South Australia and Victoria. However, whilst JJA VIT has been used for many years, there is a lack of evidence on the long-term benefit of the treatment and how it impacts patient quality of life. This trial will offer patients who have completed a JJA VIT program (between 3 and \< 6-years duration) and have been off-treatment for at least 18-months and \< 5 years, to have a supervised JJA sting challenge and blood test to assess their JJA venom tolerance level. It will also ask them to complete a set of questionnaires at different timepoints to obtain a history of their exposure and reactions to JJA stings outside of the hospital setting (field stings), and to measure the impact of the completed VIT and knowledge of their sting challenge outcome on their quality of life and their behaviours around auto-injectors. These measures will be used to explore the long-term effectiveness of JJA VIT and the impact of a sting challenge post VIT on a patient's quality of life.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • Eligibility criteria
  • \- Any adult (≥ 18 years) who has completed a JJA VIT program at one of the three participating sites.
  • Completed a continuous program of JJA VIT of between 3 and \< 6 years duration.
  • Have ceased JJA VIT for ≥ 18 months but \< 5 years.
  • Have the ability to provide informed consent.

Exclusion Criteria5

  • Any person \< 18 years.
  • Any adult (≥ 18 years) who has not completed a continuous JJA VIT program of duration between 3 and \< 6 years.
  • Any adult (≥ 18 years) who has completed a continuous JJA VIT program of duration between 3 and \< 6 years but ceased JJA VIT \< 18 months or \> 5 years ago.
  • Any person who has a medical condition, that in the opinion of the investigator, may place them at increased risk if they were to have a sting challenge.
  • Unable to understand study requirements and provide informed consent.

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Interventions

OTHERJack Jumper Ant Venom Immunotherapy

Jack Jumper Ant Venom Immunotherapy involves injections, under the skin, of gradually increasing doses of insect venom. The treatment is usually between 3-\<6 years duration. Participants will have completed this treatment at least 18 months prior to their enrolment in this trial.


Locations(3)

Royal Adelaide Hospital

Adelaide, South Australia, Australia

Royal Hobart Hospital

Hobart, Tasmania, Australia

Monash Medical Centre

Clayton, Victoria, Australia

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NCT06935890


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