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Study identifier: NCT06926075 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Early Phase Study of KESONOTIDE™in Participants With Solid Tumours

Condition: Prostate Cancers · Breast Cancer · Lung Cancers  ·  Sponsor: Filamon LTD

PhasePhase 1/Phase 2
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This clinical trial is an adaptive study of a novel vimentin inhibitor in cancers. It is an open label, multicentre, single ascending dose level in phase I and cohort exploration in phase II. Primary objective is to evaluate safety and tolerability of KESONOTIDE™ as a monotherapy in participants with advanced/metastatic solid cancers. Secondary objective is to characterise the pharmacokinetics of KESONOTIDE™. Phase I study will enrol 20-32 participants and Phase II approximately 80 participants.

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

Talk to the study team

Admir Huseincehajic  ·  +61467451064  ·  admir.huseincehajic@filamon.com

Graham Kelly  ·  +61 429 854 390  ·  graham.kelly@filamon.com

Always discuss trial participation with your own doctor first.

Locations (3)

St George Private HospitalKogarah, New South Wales, AustraliaRecruiting
South Western Sydney Local Health DistrictLiverpool, New South Wales, AustraliaRecruiting
Southside Cancer CentreMiranda, New South Wales, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT06926075