JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS (Master Record)

Official title

Phase 2 Clinical Platform Trial Investigating Multiple Therapeutic Options for the Treatment of Hospitalized Patients With Acute Respiratory Distress Syndrome (ARDS)

Overview

This is a Phase 2 multicenter, randomized, double-blinded, placebo-controlled study that will evaluate the safety and efficacy of host-directed therapeutics in hospitalized adults diagnosed with Acute Respiratory Distress Syndrome (ARDS) utilizing a platform trial design. Participants will be randomized to receive either a placebo or one of the active treatments. This record describes the default procedures and analyses for all cohorts. Each specific cohort may have additional eligibility requirements, safety and efficacy procedures, or endpoints, which will be described in the corresponding intervention-specific records on clinicaltrials.gov listed below in the detailed description.

Detailed description

This is a master protocol for a Phase 2 platform clinical trial to evaluate host-directed therapeutic candidates (i.e., investigational product, IP) for the treatment of hospitalized participants diagnosed with ARDS. The safety and efficacy of each IP will be studied within its own cohort (IP versus Placebo). All patients will continue to receive standard treatments for ARDS as per the investigator. An individual participant will complete the study in approximately 90 days. The study will include a screening period (\<24 hours from providing informed consent to treatment), in-hospital treatment period with IP/placebo starting on Day 1 through discharge from the hospital, and a follow-up period after discharge from the hospital through the end of study (Day 90 + 2 weeks).

Outcome data will be assembled for each patient over time (such as ventilatory status, oxygenation, and survival). Functional status using the WHO Ordinal scale and Karnofsky scale will be collected. Resource utilization will be calculated (length of stay in a critical care setting, days intubated, and survival).

All participants will undergo a series of physical exams, laboratory assessments/biomarker collections, ECG, Chest X-ray or CT scan, and questionnaires through Day 90. Exploratory biomarkers will be evaluated over time to facilitate clinical learning.

For information specific to each intervention included in this platform trial, please refer to the below corresponding, separate, clinicaltrials.gov records:

Vilobelimab NCT06701682 ; Paridiprubart NCT06701669 ; Bevacizumab NCT06701656

Interventions

• Drug Cohort A: vilobelimab
  Administered as an IV formulation of 800 mg per dose and up to 6 doses (planned for Days 1, 2, 4, 8, 15, and 22, if participant is in hospital setting and deemed appropriate by the investigator)
• Drug Cohort A: placebo
  Administered as an IV formulation of placebo of up to 6 doses (planned for Days 1, 2, 4, 8, 15, and 22, if participant is in hospital setting and deemed appropriate by the investigator)
• Drug Cohort B: paridiprubart
  Administered as a single IV dose of 15 mg/kg up to maximum of 1440 mg on Day 1
• Drug Cohort B: placebo
  Administered as a single IV dose of placebo on Day 1
• Drug Cohort C: bevacizumab
  Administered as a single IV dose of 500 mg on Day 1
• Drug Cohort C: placebo
  Administered as a single IV dose of placebo on Day 1

Primary outcome measures

• All-cause mortality (ACM) rate at Day 28 [Time frame: Day 28]

Secondary outcome measures (12)

• ACM at Day 60 and Day 90 [Time frame: Day 60 and Day 90]
• ACM+ at Day 28, Day 60, and Day 90 [Time frame: Day 28, Day 60, and Day 90]
• Improvements in oxygenation measured as change from baseline in PaO2/FiO2 ratio up to and including Day 28 (or discharge, whichever is earlier) [Time frame: Up to and including Day 28 or until Discharge (whichever is earlier)]
• Incidence of new invasive mechanical ventilation use during the study up to and including Day 28 [Time frame: Up to and including Day 28]
• Ventilator-free days up to and including Day 28 [Time frame: Up to and including Day 28]
• Proportion of participants alive and free of mechanical ventilation at Days 28, 60, and 90 [Time frame: Days 28, 60, and 90]
• Time to recover gas exchange to a PaO2/FiO2 ≥ 300 measured on 2 consecutive days during the first 28 days after informed consent [Time frame: Up to and including Day 28]
• Extracorporeal Membrane Oxygenation (ECMO) free days up to and including Day 28 [Time frame: up to and including Day 28]
• Incidence of participants with new ECMO use during the study up to and including Day 28. [Time frame: up to and including Day 28]
• Proportion of participants alive and free of ECMO at Days 28, 60, and 90 [Time frame: Days 28, 60, and 90.]
• Proportion of participants achieving a ≥2-point improvement from baseline in the World Health Organization (WHO) 8-levels ordinal scale (from 0-8) [Time frame: While Hospitalized (up to 90 days)]
• Time to an improvement of one category and two categories from baseline using the WHO 8-levels ordinal scale (from 0-8) at Days 28, 60, and 90 (while hospitalized) [Time frame: While Hospitalized (up to 90 days)]

Eligibility criteria

Inclusion criteria

Each participant must meet all of the following criteria to be enrolled in this study:

• Participant (or their Legally Authorized Representative (LAR)) provides informed consent and agrees to comply with protocol requirements
• Participant is at least 18 years of age or older at the time of consent.
• Participant with signs and symptoms of ARDS according to the Berlin definition of ARDS.

Note that participants on noninvasive ventilation may be screened.

• Participant of childbearing potential must agree to either abstinence or use at least one primary form of contraception, not including hormonal contraception, from the time of screening through Day 28. Additional cohort-specific requirements may apply
• Participant agrees to not participate in another investigational interventional study while participating in this study (i.e., through Day 90).

Exclusion criteria

Participants will be excluded from the study if any of the following apply:

• Participant with ARDS or at risk of developing ARDS due to the following reasons: trauma, large volume aspiration, or transfusion.
• Participant with pulmonary edema due to cardiogenic pulmonary edema/fluid overload or hypoxemia primarily attributable atelectasis, in the absence of a predisposing risk factor for ARDS.
• Participant who demonstrates an improvement in oxygenation and ventilatory support 24 hours prior to or during screening up to randomization, such that per investigator clinical judgement, the participant is expected to have significant improvement in lung function over subsequent 24 hours regardless of additional interventions.
• Participant is known to be pregnant, nursing, or with a positive (urine and/or serum test) pregnancy test.
• Participant is anticipated to be transferred to another hospital which is not a study site within 72 hours.
• Participant is not expected to survive for 72 hours.
• Participant has been on invasive mechanical ventilation or ECMO for ARDS for more than 48 hours for ARDS at the time of consent.
• Participant has an underlying clinical condition where, in the opinion of the Investigator and based on their clinical judgement, it would be extremely unlikely that the participant would come off ventilation
• Participant has severe COPD requiring continuous long-term home oxygen therapy or mechanical ventilation (noninvasive ventilation or via tracheotomy) except for CPAP or bi-level positive airway pressure used solely for sleep-disordered breathing.
• Participant has interstitial lung disease or idiopathic pulmonary fibrosis requiring continuous chronic home oxygen therapy.
• Participant has NY Heart Association Class IV congestive heart failure.
• Participant has a known allergy to any study medication or any of its excipients.
• Participant is receiving systemic immunosuppressive therapy for solid organ or hematopoietic cancer or transplant anti-rejection medication therapy OR systemic immunosuppressive corticosteroids (prednisone ≥20 mg daily or equivalent). NOTE: Patients onreceiving chronic low dose immunosuppressive therapy may be enrolled(e.g., prednisone <20 mg/day or equivalent) and patients on stable, long-term maintenance immunosuppression (e.g., tacrolimus, mycophenolate, orsirolimus) and patients receiving physiologic replacement and hormonal therapies for breast cancer (e.g., tamoxifen, letrozole) or prostate cancer (leuprolide, bicalutamide) for >60 days may be eligible at the investigator's discretion of the investigator in consultation with the medical monitor.
• Participant is receiving ongoing cytotoxic chemotherapy (IV or oral), OR combination targeted/immunotherapy regimens for cancer within the past 60 days. Note: Participants receiving non-myelosuppressive cancer therapy (e.g., hormonal therapy or selected targeted / immunotherapy regimens) may be eligible if therapy has been stable ≥60 days; The use of hydroxyurea to manage patients with chronic myeloid leukemia, polycythemia vera, essential thrombocythemia or sickle cell disease is permitted.
• Participant received treatment with an investigational immunomodulator or immunosuppressant drugs within 5 half-lives or 30 days (whichever is longer) before randomization.
• Participant with concurrent infections or history of the following:

• Known active tuberculosis,
• Known active Hepatitis B, or
• HIV and a CD4 count less than 50 or a detectable viral load of >200 copies/mL HIV RNA.
• Participant received treatment with any other investigational drugs within 30 days prior to consent.
• Participant had a history of abdominal fistula, gastrointestinal perforation, intra-abdominal abscess within 28 days of screening or inadequate wound healing secondary to major thoracoabdominal surgery at the time of screening.
• Participant is considered by the investigator, for any reason, to be an unsuitable candidate for the study.

Participant may have additional cohort-specific requirements.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Triple blind

Primary purpose

Treatment

Study locations

United States · 41 centers

• University of Alabama Hospital — Birmingham
• Community Regional Medical Center — Fresno
• Long Beach Memorial Medical Center — Long Beach
• University of California Irvine Medical Center — Orange
• University of California Davis Medical Center - Pulmonary Medicine — Sacramento
• Stanford Medical Center — Stanford
• Denver Health Hospital and Authority — Denver
• MedStar Washington Hospital Center — Washington D.C.
• … and 33 more centers

Publications

• Truwit JD, Fleming K, Nanchal RS. Empowering Respiratory Therapists to Restrict Nebulized 3% Saline and N-Acetylcysteine During Mechanical Ventilation. Respir Care. 2025 Aug;70(8):937-945. doi: 10.1089/respcare.12586. Epub 2025 Feb 24. PMID 40028879

Identifiers

NCT: NCT06703073 · BP-ARDS-P2-001 (Master Record) · 75A50124C00001

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗