This is an open-label, Phase 1b dose escalation and expansion study to determine the maximum tolerated dose (MTD) of OP-1250 in combination with palbociclib (Ibrance®️, Pfizer Inc.). Purpose of study is to evaluate the safety and pharmacokinetic (PK) profile, and estimate the preliminary anti-tumor activity of the combination in adult subjects with hormone receptor-positive (ER+ / HER2-) advanced or metastatic breast cancer (MBC).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Complete Estrogen Receptor Antagonist
Palbociclib is an approved CDK 4/6 Inhibitor drug
Clinical Trial Site
Waratah, New South Wales, Australia
Clinical Trial Site
Westmead, New South Wales, Australia
Clinical Trial Site
South Brisbane, Queensland, Australia
Clinical Trial Site
Southport, Queensland, Australia
Incidence of Dose Limiting Toxicities
Time frame: From Cycle 1 Day 1 through C1 Day 28
Characterization and Incidence in Adverse Events and Serious Adverse Events
Time frame: From initial inform consent date through 30 days post last dose
Plasma levels of OP-1250 and Palbociclib
Time frame: Up to 9 months
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Clinical Trial Site
Clayton, Victoria, Australia
Clinical Trial Site
Frankston, Victoria, Australia
Clinical Trial Site
Geelong, Victoria, Australia
Clinical Trial Site
Nedlands, Western Australia, Australia