Adaptive Platform Trial of Treatments for Respiratory Infections in Community Settings (TreatResp) (NCT07314905) | Clinical Trial Compass
Not Yet RecruitingPhase 3
Adaptive Platform Trial of Treatments for Respiratory Infections in Community Settings (TreatResp)
Canada264 participantsStarted 2026-01-02
Plain-language summary
TreatResp is a double-blind, individually randomized, multi-centre adaptive platform trial. TreatResp aims to establish an adaptive platform trial aimed at evaluating the clinical- and cost-effectiveness, practical challenges, and outcomes of therapeutics for respiratory pathogens in non-hospitalized patients. Participants will be randomized to receive usual care (i.e., supportive care and symptom relief) or a study therapeutic, which will be determined by the TreatResp Therapeutics Committee. The primary outcomes being evaluated is time to recovery.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* 18 years or older
* A positive test (PCR or RAT) for one of the pathogens included in the trial's domains (influenza A/B, or other future specified respiratory pathogens),
* Enrolled within 5 days of symptoms onset. However, this window may vary depending on the domain or specific interventions within each domain (for example 72 hours for Baloxavir).
* At least two symptoms commonly associated with respiratory infections, including:
* rhinitis
* cough
* wheezing
* sore throat
* nasal congestion
* shortness of breath
* fatigue
* rapid breathing
* excessive mucus production
* loss of smell or taste
* hemoptysis
* trouble sleeping or insomnia due to breathing difficulties
* fever (defined for purposes of this study as \>37.5°C/ 41).
Exclusion Criteria:
* Admitted to hospital or in an ED for more than 24 hours
* Previously randomized to TreatResp within the past 12 months
* Currently participating in a clinical trial of a therapeutic agent for acute respiratory pathogen infection that is not/suspected not compatible with the study therapeutics
* Already taking a study therapeutic or contraindication to a study therapeutic
* Inability for participant or caregiver to provide informed consent.
Additional eligibility criteria will be applied based on the intervention assigned. For instance, if a participant is randomized to an antiviral treatment, they must not have contraindications specific to that antiviral. This ensures that ea…
What they're measuring
1
time to recovery (defined as the first instance that a participant report feeling fully recovered)