The purpose of this study is to establish the safety and preliminary antitumor activity of ORIC-944 as a single agent and in combinations with ARPIs in patients with metastatic prostate cancer.
ORIC-944 is a potent, highly selective, allosteric, orally bioavailable, small molecule inhibitor of PRC2 via binding the embryonic ectoderm development (EED) subunit. This is a first-in-human, open-label, multicenter, dose escalation study of ORIC-944 as a single agent (Part I) or in combination with an Androgen Receptor Pathway Inhibitor (ARPI) (Part II) to establish the safety and preliminary antitumor activity of ORIC-944 as a single agent and in combination with ARPIs in patients with metastatic prostate cancer. Part III of the protocol (dose optimization) will explore two potential dose levels of ORIC-944 selected from Part II in combination with ARPIs to select the final RP2D for each combination across two separate patient populations.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
275
Oral, once daily, continuous
Oral, 1000 mg once daily, continuous
Oral, 240 mg once daily, continuous
Recommended Phase 2 Dose (RP2D)
RP2D as determined by interval 3+3 dose escalation design
Time frame: 12 months
Maximum plasma concentration (Cmax)
PK of ORIC-944 single agent and in combination with an ARPI
Time frame: 28 Days
Time to maximum observed concentration (Tmax)
PK of ORIC-944 single agent and in combination with an ARPI
Time frame: 28 Days
Area under the curve (AUC)
PK of ORIC-944 single agent and in combination with an ARPI
Time frame: 28 Days
Apparent plasma terminal elimination half-life (t1/2)
PK of ORIC-944 single agent and in combination with an ARPI
Time frame: 28 Days
Clinical benefit rate (CBR)
Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: 36 months
Objective response rate (ORR)
Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: 36 months
Duration of response (DOR)
Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: 36 months
Progression-free survival (PFS)
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Oral, 600 mg twice daily, continuous
Oral, 160 mg once daily, continuous
Rocky Mountain Cancer Center
Colorado Springs, Colorado, United States
RECRUITINGSouth Florida Oncology and Hematology
Plantation, Florida, United States
RECRUITINGIllinois Cancer Specialists
Arlington Heights, Illinois, United States
RECRUITINGComprehensive Urologic Care
Lake Barrington, Illinois, United States
RECRUITINGFirst Urology
Jeffersonville, Indiana, United States
RECRUITINGMarlene & Stewart Greenebaum Comprehensive Cancer Center, University of Maryland
Baltimore, Maryland, United States
RECRUITINGMaryland Oncology Hematology
Silver Spring, Maryland, United States
RECRUITINGKarmanos
Detroit, Michigan, United States
RECRUITINGMinnesota Oncology Hematology
Minneapolis, Minnesota, United States
RECRUITINGMemorial Sloane Kettering Cancer Center
New York, New York, United States
RECRUITING...and 17 more locations
Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: 36 months
On-treatment PSA levels and change from baseline
Prostate cancer working group 3 criteria (PCWG3)
Time frame: 36 months