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NCT06701656 · ClinicalTrials.gov registry record · Phase 2

JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS- Cohort C: Bevacizumab

A Phase 2 study of Acute Respiratory Distress Syndrome and ARDS, sponsored by PPD Development.

Recruiting
Registry status
Phase 2
Development phase
200
Enrollment target
20
Study locations

NCT06701656: Recruiting Phase 2 study of Acute Respiratory Distress Syndrome and ARDS, sponsored by PPD Development.

NCT06701656 is a Phase 2 study of Acute Respiratory Distress Syndrome and ARDS that is actively recruiting participants, run by PPD Development. The registered enrollment target is 200 participants, below the 361-participant average among 31 other Acute Respiratory Distress Syndrome trials with a reported enrollment target (45% lower). The trial reports 20 study locations across 13 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06701656, a Phase 2 study of Acute Respiratory Distress Syndrome and ARDS, is actively recruiting participants, sponsored by PPD Development.

RECRUITING
Registry status
Phase 2
Development phase
200 participants
Enrollment target
20
Study locations

Study Summary

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 C: Participants will be randomized to receive either a placebo or bevacizumab. This record describes the default procedures and analyses for Cohort C. Please see NCT06703073 for information on the BP-ARDS-P2-001 Master Protocol.

Interventions

  • DRUG Cohort C: bevacizumab
  • DRUG Cohort C: placebo

Study Locations (20)

California

  • 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

Florida

  • Nova Clinical Research - Bradenton
  • North Florida / South Georgia Veterans Health System - Gainesville
  • Sarasota Memorial Hospital - Sarasota

Massachusetts

  • Tufts Medical Center - Boston
  • Lahey Hospital and Medical Center - Burlington

Michigan

  • University of Michigan Hospital - Ann Arbor
  • Henry Ford Health Hospital - Detroit

Alabama

  • University of Alabama Hospital - Birmingham

Colorado

  • Denver Health Hospital and Authority - Denver

District of Columbia

  • MedStar Washington Hospital Center - Washington D.C.

Idaho

  • St. Luke's Boise Medical Center - Boise

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2025-10-28
Est. Completion 2028-09
Phase Phase 2
PPD Development

4 total trials

What NCT06701656 shows while recruiting

NCT06701656 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 361-participant average among 31 other Acute Respiratory Distress Syndrome trials with a reported enrollment target (45% lower).

The record links to 4 conditions, with Acute Respiratory Distress Syndrome appearing as the primary indexed condition, and to 2 interventions - of which Cohort C: bevacizumab is the first listed.

NCT06701656 names 20 study sites across 13 states, led by California, Florida, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT06701656 about?

NCT06701656 is a clinical study titled "JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS- Cohort C: Bevacizumab". 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 C: Participants wil...

What is the current status of trial NCT06701656?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2025-10-28. Estimated completion is 2028-09.

What conditions does trial NCT06701656 study?

This clinical trial studies the following conditions: Acute Respiratory Distress Syndrome, ARDS, Acute Respiratory Distress Syndrome (ARDS), ARDS (Acute Respiratory Distress Syndrome).

What interventions are being tested in trial NCT06701656?

The interventions under investigation include: Cohort C: bevacizumab (DRUG), Cohort C: placebo (DRUG).

Who is sponsoring clinical trial NCT06701656?

This trial is sponsored by PPD Development, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06701656 being conducted?

This trial has 20 study locations across Alabama, California, Colorado, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Acute Respiratory Distress Syndrome

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06701656's enrollment target sits among peer trials

200 10th of 31 higher than 20 of 31 other Acute Respiratory Distress Syndrome trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Acute Respiratory Distress Syndrome trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06701656, the US trial registry maintained by the National Library of Medicine. NCT06701656 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.