Safety and Efficacy of EXO-CD24 in Preventing Clinical Deterioration in Patients With Mild-Moderate ARDS

Phase 2

Recruiting

• Conditions: ARDS
• Interventions: Drug: EXO-CD24; Other: Placebo

• Registration Number: NCT05947747
• Lead Sponsor: Nano24med

Brief Summary

This is phase IIb, Randomized, Double-blinded, Placebo-controlled Study to Evaluate the Safety and Efficacy of Exosomes Overexpressing CD24 of one dose 10\^10 exosome particles, to Prevent Clinical Deterioration in Patients with Mild-Moderate ARDS

Detailed Description

The study population will include patients with mild-moderate ARDS and laboratory markers predictive of the cytokine storm, who have provided an informed consent.

90 patients will be initially screened, randomized and stratified by center in a 2:1 ratio to receive either 1010 exosome particles (60 patients) or placebo (30 patients).

Study drug will be delivered using standard jet nebulizer that produce aerosol particles size of 0.4-4.4 µm.

The exosomes will be diluted in 1.5 ml normal saline for inhalation, administered twice a day (bid) for 5 days

Study treatments will be given as an add-on to the standard of care. Following the 5 days of treatment, patients will remain in follow-up for 23 additional days. In case of hospital discharge before the full follow-up planned, the patient will be required to return to the site for completion of all study assessments.

Study Timeline

• Study First Submitted: 2023-05-31
• Status Verified: 2023-07
• Study Start: 2023-07-04
• Study First Submitted QC: 2023-07-07
• Study First Posted: 2023-07-17
• Last Update Submitted: 2023-07-24
• Last Update Posted: 2023-07-27
• Primary Completion: 2025-12-20
• Study Completion: 2025-12-20

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

1. Direct and indirect lung injury etiology
2. Age ≥18 years
3. Patients with Early Acute Lung Injury (EALI) > 2 ,or patient on HFNC/NIPPV [(1 point for an oxygen requirement > 2 to 6 liters/min or 2 points for > 6 liters/min; 1 point each for a respiratory rate ≥ 30 breaths/min and baseline immune suppression) (immune system compromised by exogenous drug etc.)] (For saturation goal >90%) [1], or ARDS diagnosis (mild/moderate)
4. Willing and able to sign an informed consent, or has a legal guardian who is able to sign

Exclusion Criteria

1. Any concomitant illness that, based on the judgment of the investigator might affect the interpretation or the results of the study (immunodeficiency, primary immune deficiency due to virus, hematological malignancy etc.)
2. Patients with SaO2/FiO2<150
3. Patients with mechanical ventilation (ECMO).
4. Pregnancy [positive urine pregnancy test (women of childbearing potential only)] or breastfeeding
5. Participation in any other interventional study in the last 30 days or within 5 half-lives of receiving an investigational agent.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group 1: investigational drug EXO-CD24 at a dose of 10^10	EXO-CD24	60 patients who will receive a 5-day treatment with the investigational drug EXO-CD24 at a dose of 10\^10
Group 2: treatment in a clean sterile saline solution (placebo)	Placebo	30 patients who will receive a 5-day treatment in a clean sterile saline solution (placebo)

Primary Outcome Measures

Name	Time	Method
Safety: Number of participants with treatment-related adverse events as assessed by CTCAE v.5 during the 28 days of the study.	28 days
Efficacy: the rate of hypoxemic respiratory failure (reported as S/F<150) at day 28	28 days
Efficacy: the rate of hypoxemic respiratory failure (reported as S/F<150) at day 7	7 days

Trial Locations

Locations (1)

Tel-Aviv Sourasky Medical Center; 🇮🇱 Tel-Aviv, Israel