PUL-042 Treatment in Patients With Parainfluenza Virus (PIV), Human Metapneumovirus (hMPV) or Respiratory Syncytial Virus (RSV)
Efficacy and Safety of PUL-042 Inhalation Solution in Reducing Lower Respiratory Tract Complications in Patients With Hematologic Malignancies and Recipients of Hematopoietic Stem Cell Transplantation (HSCT) With Documented Viral Infections With PIV, hMPV or RSV
Pulmotect, Inc.
100 participants
Jun 27, 2025
INTERVENTIONAL
Conditions
Summary
The purpose of this research study is to try to see whether an experimental drug, PUL 042 Inhalation Solution (PUL 042), is effective in reducing the severity of lung infections in patients with hematologic malignancies and recipients of hematopoietic stem cell transplantation with documented viral infections due to PIV, hMPV, or RSV. PUL-042 or a placebo will be administered 3 times over a 6-day period. The total duration of the study will be approximately 30 days.
Eligibility
Plain Language Summary
Simplified for easier understanding
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Interventions
Pam2 : ODN (PUL-042) PUL-042 Inhalation Solution
Sterile Saline for Inhalation
Locations(11)
View Full Details on ClinicalTrials.gov
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NCT06665100