OKI-219-101 is a Phase 1a/1b, open-label, multicenter, dose-escalation study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and efficacy of OKI-219 as monotherapy and in combination with other anti-cancer drugs. Phase 1a (Part A) will investigate escalating doses of OKI-219 monotherapy, and Phase 1b will investigate OKI-219 (at a tolerated dose determined in Part A) in combination with fulvestrant (Part B), trastuzumab and tucatinib (Part C), atirmociclib (Part D), and ribociclib and fulvestrant (Part E). Participants will continue to receive study treatment until disease progression, intolerable toxicity, or other study treatment withdrawal criteria are met.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
200
Oral twice daily
Intramuscular injection
Intravenous (IV)
Oral twice daily
Oral twice daily
Oral once daily continuous for 21-days followed by 7 days off
California Cancer Associates for Research and Excellence
Encinitas, California, United States
RECRUITINGUniversity of California San Diego UCSD
La Jolla, California, United States
RECRUITINGUCLA Jonsson Comprehensive Cancer Center
Los Angeles, California, United States
RECRUITINGHoag - Huntington Beach
Newport Beach, California, United States
Identify maximum tolerated dose (MTD) of OKI-219 in monotherapy
Frequency of participants experiencing dose-limiting toxicities during the first 28-day cycle
Time frame: Cycle 1 (First 28 days on treatment)
Assess safety of OKI-219 as monotherapy or in combination with other anti-cancer therapies: incidence of SAEs
Number and type of SAEs experienced by participants during treatment and follow-up
Time frame: Through 30 days after last dose, an average of 1 year
Assess safety of OKI-219 as monotherapy or in combination with other anti-cancer therapies: incidence of Grade 2 or greater treatment emergent adverse events
Number of treatment-emergent adverse events (TEAEs) equal or greater than Grade 2 experienced during treatment and follow-up
Time frame: Through 30 days after last dose, an average of 1 year
Assess rate of dose modifications during treatment with OKI-219 as monotherapy or in combination with other anti-cancer therapies
rate of dose modifications
Time frame: Through last study dose, an average of 1 year
Assess the plasma PK of OKI-219 following single and multiple doses as monotherapy or in combination with other anti-cancer therapies: maximum plasma concentration (Cmax)
PK of OKI-219: Cmax
Time frame: Through cycle 6 of treatment (up to 28 weeks)
Assess the plasma PK of OKI-219 following single and multiple doses as monotherapy or in combination with other anti-cancer therapies: time of maximum plasma concentration (Tmax)
PK of OKI-219: Tmax
Time frame: Through cycle 6 of treatment (up to 28 weeks)
Assess the plasma PK of OKI-219 following single and multiple doses as monotherapy or in combination with other anti-cancer therapies: area under the plasma concentration-time curve (AUC)
PK of OKI-219: AUC
Time frame: Through cycle 6 of treatment (up to 28 weeks)
Assess the plasma PK of OKI-219 following single and multiple doses as monotherapy or in combination with other anti-cancer therapies: terminal elimination half-life time (t1/2)
PK of OKI-219: t1/2
Time frame: Through cycle 6 of treatment (up to 28 weeks)
To estimate the preliminary antitumor activity of OKI-219 as monotherapy and in combination with other anti-cancer therapies: objective response rate (ORR)
ORR per investigator assessed Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1)
Time frame: Up to approximately 36 months
To estimate the preliminary antitumor activity of OKI-219 as monotherapy and in combination with other anti-cancer therapies: clinical benefit rate (CBR)
CBR per investigator assessed Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1)
Time frame: Up to approximately 36 months
Dose optimization only: to estimate the preliminary antitumor activity of OKI-219 as monotherapy and in combination with other anti-cancer therapies: progression free survival (PFS)
PFS per investigator assessed Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1)
Time frame: Up to approximately 36 months
To assess the dose-response impact of OKI-219 as monotherapy and in combination with other anti-cancer therapies on PI3KαH1047R ctDNA levels
Changes in PI3KαH1047R ctDNA on treatment and end of treatment (EOT) compared to baseline.
Time frame: Through last study dose, an average of 1 year
To determine the impact of OKI-219 dosing as monotherapy and in combination with other anti-cancer therapies on blood glucose and insulin
Changes in plasma glucose, serum insulin, serum c-peptide levels, and hemoglobin A1c (HbA1c) will be evaluated on treatment compared to baseline.
Time frame: Through last study dose, an average of 1 year
To assess the PDx activity of OKI-219 as monotherapy and in combination with other anti-cancer therapies
PDx activity will be evaluated with serial tumor biopsy samples assessed for PI3K/AKT/mTOR downstream pathway changes.
Time frame: Through last study dose, an average of 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Regents of the University of Colorado
Aurora, Colorado, United States
RECRUITINGSarah Cannon Research Institute at HealthONE
Denver, Colorado, United States
RECRUITINGMassachusetts General Hospital
Boston, Massachusetts, United States
RECRUITINGKarmanos Cancer Insitute
Detroit, Michigan, United States
WITHDRAWNComprehensive Cancer Centers of Nevada
Las Vegas, Nevada, United States
RECRUITINGStony Brook University
Stony Brook, New York, United States
RECRUITING...and 24 more locations