JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS- Cohort B: Paridiprubart
Eligible age
18+ yrs
Accepts
All genders
Locations
23 states
Healthy volunteers
No
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About this study
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. Cohort B: Participants will be randomized to receive either a placebo or paridiprubart. This record describes the default procedures and analyses for Cohort B. Please see NCT06703073 for information on the BP-ARDS-P2-001 Master Protocol.
Sponsor: PPD Development, LP
You may qualify if…
- ✓ The following inclusion criteria are in addition to the exclusion criteria specified in the Master Protocol NCT06703073:
- ✓ ARDS Severity of moderate or severe based on PaO2/FiO2 or SpO2/FiO2 assessment at the time of randomization.
You may not qualify if…
- ✕ The following exclusion criteria are in addition to the exclusion criteria specified in the Master Protocol NCT06703073.
- ✕ Participant has a known allergy or known hypersensitivity to paridiprubart or its excipients, including polysorbate 80
- ✕ Participant with established cirrhosis and a modified Child-Pugh Score of 12 or greater
Where it's recruiting
Birmingham
Fresno · Long Beach · Orange · Sacramento …
Denver
Washington D.C.
Bradenton · Gainesville · Sarasota
Boise
Evanston · Peoria
Boston · Burlington
Ann Arbor · Detroit
Rochester
Reno
New Brunswick
Source: ClinicalTrials.gov · NCT06701669 · last updated 2026-07-31