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Study identifier: NCT06665100 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

PUL-042 Treatment in Patients With Parainfluenza Virus (PIV), Human Metapneumovirus (hMPV) or Respiratory Syncytial Virus (RSV)

Condition: Hematologic Malignancies · Hematopoietic Stem Cell Transplant (HSCT)  ·  Sponsor: Pulmotect, Inc.

PhasePhase 2
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

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

Talk to the study team

Colin Broom, MD  ·  484 354 0615  ·  cbroom@pulmotect.com

Brenton Scott, Ph D  ·  713 579 9226  ·  bscott@pulmotect.com

Always discuss trial participation with your own doctor first.

Locations (11)

City of Hope National Medical CenterDuarte, California, United StatesRecruiting
Northside HospitalAtlanta, Georgia, United StatesRecruiting
Johns Hopkins HospitalBaltimore, Maryland, United StatesRecruiting
Brigham and Women's HospitalBoston, Massachusetts, United StatesRecruiting
Barbara Ann Karmanos Cancer InstituteDetroit, Michigan, United StatesRecruiting
University of MinnesotaMinneapolis, Minnesota, United StatesRecruiting
John Theurer Cancer CenterHackensack, New Jersey, United StatesRecruiting
Lineberger CancerChapel Hill, North Carolina, United StatesRecruiting
OU Health Physicians - Infectious Disease ClinicOklahoma City, Oklahoma, United StatesRecruiting
University of Texas MD Anderson MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Fred Hutchinson Cancer CenterSeattle, Washington, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06665100