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Study identifier: NCT04665206 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Evaluate VT3989 in Patients With Metastatic Solid Tumors

Condition: Solid Tumor, Adult · Mesothelioma · NSCLC  ·  Sponsor: Vivace Therapeutics, Inc

PhasePhase 1/Phase 2
Planned participants434
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is an open-label, dose escalation and expansion study to evaluate the safety, tolerability, PK, and biological activity of VT3989 administered, alone or in combination, once daily in patients with mesothelioma and/or metastatic solid tumors that are resistant to standard therapy or for which no effective standard therapy is available.

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

Talk to the study team

Heather Fritz  ·  650-627-7437  ·  hfritz@inclin.com

Neelesh Sharma, MD  ·  732-476-4978  ·  nsharma@vivacetherapeutics.com

Always discuss trial participation with your own doctor first.

Locations (12)

UCSF Helen Diller Family Comprehensive Cancer CenterSan Francisco, California, United StatesRecruiting
University of Chicago Medical CenterChicago, Illinois, United StatesRecruiting
Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Dana-Farber Cancer InstituteBoston, Massachusetts, United StatesRecruiting
M Health Fairview University of Minnesota Medical CenterMinneapolis, Minnesota, United StatesRecruiting
Memorial Sloan Kettering Cancer CenterNew York, New York, United StatesRecruiting
MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
NEXT OncologySan Antonio, Texas, United StatesRecruiting
Virginia Cancer Specialists, PCArlington, Virginia, United StatesRecruiting
Monash HealthClayton, Victoria, AustraliaRecruiting
Peter MacCullum Cancer CentreMelbourne, Victoria, AustraliaRecruiting
Linear Clinical ResearchNedlands, Western Australia, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT04665206