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Study identifier: NCT06022029 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Dose Escalation and Dose Expansion Study of Intratumoral ONM-501 Alone and in Combination With Cemiplimab in Patients With Advanced Solid Tumors and Lymphomas.

Condition: Triple Negative Breast Cancer · Diffuse Large B Cell Lymphoma · Follicular Lymphoma  ·  Sponsor: OncoNano Medicine, Inc.

PhasePhase 1
Planned participants168
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A phase 1, multicenter, open label, non-randomized dose escalation and dose expansion study to examine the maximum tolerated dose, (MTD), minimum effective dose (MED) and/or recommended dose for expansion (RDE) of intratumoral ONM-501 as monotherapy and in combination with a PD-1 checkpoint inhibitor in patients with advanced solid tumors and lymphomas.

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

Talk to the study team

Trials@OncoNanoMed.com  ·  (682) 285-1411  ·  trials@onconanomed.com

Always discuss trial participation with your own doctor first.

Locations (16)

California Research InstituteLos Angeles, California, United StatesActive Not Recruiting
BRCR GlobalTamarac, Florida, United StatesWithdrawn
Gabrail Cancer Center ResearchCanton, Ohio, United StatesCompleted
Ohio State UniversityColumbus, Ohio, United StatesCompleted
Allegheny Health NetworkPittsburgh, Pennsylvania, United StatesCompleted
UPMC Hillman Cancer CenterPittsburgh, Pennsylvania, United StatesCompleted
University of Texas Southwestern Medical CenterDallas, Texas, United StatesCompleted
MD Anderson Cancer CenterHouston, Texas, United StatesActive Not Recruiting
Virginia Cancer Specialists, PCFairfax, Virginia, United StatesCompleted
St Vincent's HospitalDarlinghurst, New South Wales, AustraliaRecruiting
Cancer Care WollongongWollongong, New South Wales, AustraliaRecruiting
University of the Sunshine Coast Clinical TrialsBuderim, Queensland, AustraliaRecruiting

+ 4 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06022029