RecruitingPhase 3ACTRN12624001107516

PROlonged versus Single dose in PEnicillin oral Challenge Testing-2

PROlonged versus Single dose in PEnicillin oral Challenge Testing double-blind parallel randomized placebo cOntrolled tRial – PROSPECTOR-2 Study: Evaluating the efficacy of prolonged oral penicillin challenge over single dose oral penicillin challenge to ascertain true penicillin allergy


Sponsor

Austin Health

Enrollment

712 participants

Start Date

Mar 26, 2025

Study Type

Interventional

Conditions

Summary

Penicillin allergies are highly prevalent in the healthcare setting and are associated with second-line inferior antibiotics being prescribed. An incorrect penicillin allergy label leads to increased risk of resistant organisms, side effects from second-line antibiotics as well as increased medical costs. The gold standard for penicillin allergy testing is an oral challenge – either direct or following skin testing. What remains unknown is if a single dose is sufficient to determine if the patient has a delayed or unknown timing immune mediated penicillin allergy or if a prolonged oral challenge (5 days or more) is required. The PROSPECTOR pilot trial demonstrated the feasibility and safety of a placebo-controlled trial of single dose penicillin challenge versus prolonged challenge (5-day). PROSPECTOR2 continues from the PROSECTOR pilot trial (ACTRN12623001242617) to assess the superiority of prolonged oral challenge versus single dose challenge for identifying immune-mediated penicillin allergy. The current Drug Allergy Practice Parameters recommend “against the routine use of multiple-day challenges in the evaluation of penicillin allergy”, providing a “strong recommendation” but with “low certainty of evidence”. The European guidelines reviewed the literature of over 6484 patients, demonstrating a 2.3% positive rate following the initial challenge and 5.5% during the varied prolonged challenges. They concluded there is no consensus on a preferred procedure and could not provide a recommendation for or against prolonged challenge. In Europe, a mixture of observational and retrospective studies has suggested that extended challenges ranging from 3 to 10 days may be superior to single dose challenges at excluding delayed immune reactions, however the reported prevalence of delayed reactions is highly variable (5-12% of patients) and many were reliant on patient self-reporting. In a recent retrospective single centre Danish experience of 3,179 low-risk patients, 2.6% were positive on day 1 of challenge and 7.2% on days 3-10. This is in contrast to the North American experience, where delayed prolonged challenges have been associated with low rates of delayed reactions (0-1.8%). Whilst a study of children demonstrated that delayed reactions may occur less than 7 days following a single challenge. Therefore, whilst oral challenge is the well-defined gold standard for penicillin allergo-immunological investigation, limited controlled evidence is available regarding the efficacy of single dose versus prolonged oral challenge.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria2

  • Adult patients referred to the inpatient or outpatient allergy services for a suspected penicillin allergy with an immune-related allergy history of delayed (> 6 hours after first dose of drug administration) or unknown timing, who tolerate first single-dose of an oral amoxicillin challenge.
  • Willing and able to give consent and undergo telehealth/telephone review

Exclusion Criteria5

  • Patient age is < 18 years;
  • Any other illness that, in the investigator’s judgement, will substantially increase the risk associated with subject’s participation in this study;
  • Stevens-Johnson Syndrome or Toxic Epidermal Necrolysis to beta-lactam
  • Inpatients concurrently receiving or likely to receive a beta-lactam antibiotic therapy during the 14-day study period.
  • Concurrent use of antihistamines and systemic steroid therapy (i.e. > 10mg daily)

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Interventions

Amoxicillin 500mg (oral capsule) twice daily for 5 days. Participants will complete study dosing log and return study bottle to trial pharmacy to monitor adherence to protocol

Amoxicillin 500mg (oral capsule) twice daily for 5 days. Participants will complete study dosing log and return study bottle to trial pharmacy to monitor adherence to protocol


Locations(9)

Austin Health - Austin Hospital - Heidelberg

NSW,QLD,VIC, Australia

Peter MacCallum Cancer Centre - Melbourne

NSW,QLD,VIC, Australia

Royal Melbourne Hospital - Royal Park campus - Parkville

NSW,QLD,VIC, Australia

St George Private Hospital - Kogarah

NSW,QLD,VIC, Australia

Royal North Shore Hospital - St Leonards

NSW,QLD,VIC, Australia

Royal Brisbane & Womens Hospital - Herston

NSW,QLD,VIC, Australia

Canada

South Africa

Denmark

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ACTRN12624001107516