Randomized Adaptive Platform Trial of Pathogen-Directed Anti-inflammatory Therapy in Severe Community-Acquired Pneumonia(Core Protocal)

Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorQingyuan Zhan

About this trial

Severe community-acquired pneumonia (sCAP) has a high mortality rate of 25-50%. Excessive host inflammatory responses contribute to poor outcomes. Corticosteroid therapy may provide benefit; however, the optimal dosage remains unclear, and it is uncertain whether all etiologies (e.g., Pneumocystis jirovecii, adenovirus, influenza) of sCAP can benefit equally.

This study will first establish a comprehensive trial platform based on a prospective sCAP cohort, embedding a randomized, multifactorial, adaptive platform trial (APT). The response-adaptive design will increase the likelihood of patients being assigned to more effective treatment arms, while Bayesian statistical modeling will dynamically assess the efficacy of interventions, allowing early achievement of study endpoints.

At the starting stage, two pathogen-specific APTs will be conducted, focusing on adenovirus- and pneumocystis Jirovecii-induced sCAP. Patients admitted to the ICU with confirmed diagnoses of adenovirus or pneumocystis Jirovecii-associated sCAP will be randomized into a control group or one of two corticosteroid dosage groups. The primary endpoint will be 28-day all-cause mortality. Completion of these APTs will provide a theoretical basis for novel anti-inflammatory strategies in sCAP.

Moreover, this platform will serve as an essential research infrastructure for the efficient evaluation of new therapeutic options in the event of emerging or re-emerging respiratory pathogens causing sCAP in the future.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Admission to ICU;

Age ≥ 18 years;

ICU length of stay ≤ 48 hours; ④ Meeting the IDSA/ATS diagnostic criteria for SCAP.

Disqualifiers

Confirmed diagnosis of hospital-acquired pneumonia (HAP) or ventilator-associated pneumonia (VAP);

Expected death within 24 hours;

Presence of septic shock prior to randomization; ④ History of allergy or contraindications to corticosteroids (e.g., active gastrointestinal bleeding, severe osteoporosis, uncontrolled hyperglycemia, bone marrow suppression);

Active fungal (except Pneumocystis jirovecii), tuberculosis, or hepatitis infection;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Low dose steroids

    Drug

    Receive 0.5mg/kg Methylprednisolone

  • Moderate dose steroids

    Drug

    Receive 1.0mg/kg Methylprednisolone

  • Saline (0.9% NaCl)

    Drug

    Saline 100ml

Treatment groups

1,500 Participants
are divided into 3 treatment groups
Group A: Standard of CarePlacebo comparator 1 intervention
Group B: Low dose steroidsExperimental treatment 1 intervention
Group C: Moderate dose steroidsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

28-day all cause mortality

death at 28th day after inclusion

Time frame
28 days from inclusion

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Qingyuan Zhan

Lead sponsor

China-Japan Friendship Hospital

Sponsor institution

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