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Study identifier: NCT04421820 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

BOLD-100 in Combination With FOLFOX for the Treatment of Advanced Solid Tumours

Condition: Colorectal Cancer · Pancreatic Cancer · Gastric Cancers  ·  Sponsor: Bold Therapeutics, Inc.

PhasePhase 1/Phase 2
Planned participants220
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

BOLD-100 is an intravenously administered sterile solution containing the ruthenium-based small molecule. BOLD-100 has been shown to preferentially decrease the expression of GRP78 in tumour cells and ER stressed cells when compared to normal cells. BOLD-100 will be combined with cytotoxic FOLFOX chemotherapy in this study, with a dose escalation cohort to ensure tolerability and safety, followed by a cohort expansion phase.

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

Talk to the study team

Michelle Jones  ·  604-262-9899  ·  clinical@bold-therapeutics.com

Jim Pankovich  ·  604-262-9934  ·  jp@bold-therapeutics.com

Always discuss trial participation with your own doctor first.

Locations (24)

University of California, Los AngelesSanta Monica, California, United StatesCompleted
Moffitt Cancer CenterTampa, Florida, United StatesCompleted
Cross Cancer InstitueEdmonton, Alberta, CanadaRecruiting
Juravinski Cancer CentreHamilton, Ontario, CanadaRecruiting
The Ottawa Hospital Cancer CentreOttawa, Ontario, CanadaRecruiting
Princess Margaret Cancer CentreToronto, Ontario, CanadaRecruiting
Jewish General HospitalMontreal, Quebec, CanadaRecruiting
McGill University Health Centre Glen SiteMontreal, Quebec, CanadaRecruiting
Universitatsklinikum BonnBonn, GermanyRecruiting
University Hospital of UlmUlm, GermanyRecruiting
Mater Miserecordiae University HospitalDublin, IrelandRecruiting
St. James HospitalDublin, IrelandRecruiting

+ 12 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT04421820