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Study identifier: NCT07558538 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Single Dose, Dose Escalation Clinical Trial on the Safety, Tolerability and Efficacy of Lyophilized Powder for Inhalation of Recombinant Human Keratinocyte Growth Factor-2 (Rh-KGF-2) in The Treatment of Patients With Acute Respiratory Distress Syndrome

Condition: ARDS (Moderate or Severe) · ARDS (Acute Respiratory Distress Syndrome)  ·  Sponsor: Shanghai Zhongshan Hospital

PhaseEARLY_Phase 1
Planned participants24
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

This study is a randomized, blank-controlled, open-label, single-dose, dose-escalation clinical study of rhKGF-2 in patients with ARDS. The trial is designed with three dose groups (5 mg, 10 mg, and 15 mg), which will be escalated sequentially from the lowest dose group to the highest dose group. Each dose group will enroll 8 subjects, randomized in a 6:2 ratio according to the order of enrollment, to receive either the corresponding dose of rhKGF-2 (6 subjects) or serve as a blank control (2 subjects). Each subject will receive a single dose, administered once via a disposable bronchoscopic catheter. All subjects will receive the trial intervention on top of standard ARDS treatment (see Concomitant Medications for details). Following the completion of drug administration, subjects will enter a 28-day follow-up period. Outcome measures include adverse events (AE), vital signs, laboratory parameters, oxygenation index (PFR), chest imaging changes, etc., to evaluate the safety, tolerability, and efficacy of the treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Yi Wei  ·  +86 18872984075  ·  yiwei4075@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

ShanghaiZhongshanShanghai, Shanghai Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07558538