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Spots Global Cancer Trial Database for A Dose-escalation Study of ARX788, IV Administered in Subjects With Advanced Cancers With HER2 Expression

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Trial Identification

Brief Title: A Dose-escalation Study of ARX788, IV Administered in Subjects With Advanced Cancers With HER2 Expression

Official Title: A Phase 1, Multicenter, Open-label, Multiple Dose-escalation Study of ARX788, Intravenously Administered as a Single Agent in Subjects With Advanced Cancers With HER2 Expression

Study ID: NCT02512237

Interventions

ARX788

Study Description

Brief Summary: This is a 2-part, Phase 1 FIH study with Phase 1a designed to determine the maximum tolerated dose (MTD)/recommended Phase 2 dose (RP2D) in subjects with metastatic cancers with a human epidermal growth factor receptor 2 (HER2) test result that is in situ hybridization (ISH) positive (+) or immunohistochemistry (IHC) 3+ or 2+, and Phase 1b designed to assess anticancer activity and safety in three expansion cohorts: two different advanced breast cancer expansion cohorts (namely, for tumors that test as HER2 ISH positive or IHC3+ and for tumors that test as HER2 ISH negative with IHC 2+), and one advanced gastric cancer expansion cohort (for tumors that test as HER2 ISH positive or IHC3+).

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mater Adult Hospital, South Brisbane, Queensland, Australia

Princess Alexandra Hospital, Woolloongabba, Queensland, Australia

Monash Medical Centre, Clayton, Victoria, Australia

Epworth Healthcare, Richmond, Victoria, Australia

Auckland City Hospital, Grafton, Auckland, New Zealand

Wellington Hospital, Newtown, Wellington, New Zealand

Christchurch Hospital, Christchurch, , New Zealand

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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