Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia

Community-acquired pneumonia (CAP) that is of sufficient severity to require admission to an intensive care unit (ICU) is associated with substantial mortality.

Patients with pneumonia who are being treated in an ICU will receive therapy that consists of many different treatments, as many as 20 or 30. These treatments act together to treat both the infection and its effects on the body. When treating a patient, doctors choose from many different treatments, most of which are known or believed to be safe and effective. However, doctors don't always know which treatment option is the better one, as individuals or groups of individuals may respond differently. This study aims to help doctors understand which treatments work best.

This clinical study has been designed in a way that allows the information from patients already in the study to help new patients joining the study. Most studies aren't able to do that. REMAP-CAP has been designed to:

* Evaluate multiple treatment strategies, at the same time, in the same patient.

* Reach platform conclusions when sufficient data is accrued, rather than when a pre-specified sample size is reached

* Utilise data that is already accrued to increase the likelihood that patients within the trial are randomised to treatments that are more likely to be beneficial

* New questions can be substituted into the trial as initial questions are answered, meaning that the trial can be perpetual or open-ended

* Interactions between interventions in different domains can be evaluated

It is reasonable to presume that any pandemic respiratory infection of major significance to public health will manifest as life-threatening respiratory infection including Severe Acute Respiratory illness and severe Community Acquired Pneumonia (CAP) with concomitant admission to hospital, and for some patients, admission to an Intensive Care Unit (ICU). Previous pandemics and more localized outbreaks of respiratory emerging infections have resulted in severe CAP and ICU admission.

Previous pandemics and outbreaks of emerging infectious diseases have outlined the urgent need for evidence, preferably from Randomized Controlled Trials (RCTs), to guide best treatment. However, there are substantial challenges associated with being able to organize such trials when the time of onset of a pandemic and its exact nature are unpredictable. As an adaptive platform trial that enrolls patients during the interpandemic period, REMAP-CAP is ideally positioned to adapt, in the event of a respiratory pandemic, to evaluate existing treatments as well as novel approaches.

Primary Outcome Measures

1. All-cause mortality
2. Days alive and not receiving organ support in ICU
   Primary end-point for patients with suspected or proven COVID-19 pandemic infection

Secondary Outcome Measures

1. ICU Mortality
2. ICU length of stay
3. Hospital length of stay
4. Ventilator free days
5. Organ failure free days
6. All-cause mortality
7. Health-related Quality of life assessment
   EQ5D-5L and WHODAS 2.0 (not completed in all regions)
8. Proportion of intubated patients who receive a tracheostomy
9. Destination at time of hospital discharge
   Characterised as home, rehabilitation hospital, nursing home or long-term care facility, or another acute hospital
10. Readmission to the index ICU during the index hospitalization
11. World Health Organisation 8-point ordinal scale outcome