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Study identifier: NCT06938867 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Phase 1b/2a Randomized Double-blind Study to Investigate Safety Tolerability PK PD Preliminary Efficacy of Oral Administration of SNIPR001 in Patients With Hematologic Malignancy Scheduled for Allogeneic Hematopoietic Stem-Cell Transplant Receiving FQ Prophylaxis & Harboring FQR Ecoli Pre-Transplant

Condition: E Coli Infections · Allogenic Transplant Patients  ·  Sponsor: SNIPR Biome Aps.

PhasePhase 1/Phase 2
Planned participants24
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a Phase 1b/2a study in allogenic hematopoietic stem cell transplant patients to investigate the safety, PK, PD and preliminary efficacy of multiple oral administrations of SNIPR001 when given concomitantly with SoC levofloxacin.

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

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (8)

City of HopeDuarte, California, United StatesRecruiting
University of California, San FranciscoSan Francisco, California, United StatesRecruiting
John Hopkins UniversityBaltimore, Maryland, United StatesRecruiting
University of MinnesotaMinneapolis, Minnesota, United StatesRecruiting
Weill Cornell MedicineNew York, New York, United StatesRecruiting
UPMCPittsburgh, Pennsylvania, United StatesRecruiting
University of Texas MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Fred Hutchinson Cancer CenterSeattle, Washington, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06938867