Terminated • Phase I • Stage III, IV • ER negative • PR negative • HER2 negative • Medical Oncology • Post-Menopausal • Interventional
The following is imported from ClinicalTrials.gov:
This is an open-label, multicenter, First-In-Human (FIH), Phase 1a/1b study of PY159 in subjects with locally advanced (unresectable) and/or metastatic solid tumors that are refractory or relapsed to Standard Of Care (including Checkpoint Inhibitors, if approved for that indication).
Part A: Dose escalation of PY159 alone and in combination with pembrolizumab in a standard 3+3 design Part B: Dose expansion of one or more dose levels of PY159 administered alone and in combination with pembrolizumab for predefined tumor histology
Breast Cancer
Interventional
127 participant
November 10, 2020
18 - 999
both
PY159 Single agent dose level 1
PY159 Single agent dose level 2
PY159 Single agent dose level 3
PY159 Single agent dose level 4
PY159 Single agent dose level 5
PY159 Single agent dose level 6
PY159 Single agent dose level 7
PY159/Pembrolizumab Combination dose level 1
PY159/Pembrolizumab Combination dose level 2
PY159/Pembrolizumab Combination dose level 3
PY159/Pembrolizumab Combination dose level 4
PY159 Single agent dose expansion cohort
PY159/Pembrolizumab Combination dose expansion cohort 1
PY159/Pembrolizumab Combination dose expansion cohort 2
PY159/Pembrolizumab Combination dose expansion cohort 3
PY159/Pembrolizumab Combination dose expansion cohort 4
PY159/Pembrolizumab Combination dose expansion cohort 5
PY159/Pembrolizumab Combination dose expansion cohort 6
Terminated
127
03/24/2024
Len Reyno, MD
Ikena Oncology
Philadelphia, Pennsylvania, United States
The University of Texas MD Anderson Cancer Center
Houston, Texas, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
Detroit, Michigan, United States
Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, United States
Case Western Reserve University
Cleveland, Ohio, United States
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