A Multi-Center, Open-Label, Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumor Activity of Pan-RAS Inhibitor YL-17231 in Patients With Advanced Solid Tumors Harboring Mutations in KRAS, HRAS, or NRAS
Overview
- Phase
- Phase 1
- Intervention
- YL-17231
- Conditions
- Advanced Solid Tumors
- Sponsor
- Shanghai YingLi Pharmaceutical Co. Ltd.
- Enrollment
- 60
- Locations
- 3
- Primary Endpoint
- TEAEs
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
This study will evaluate the safety, tolerability, drug levels, pharmacodynamic effects, and clinical activity of YL 17231 in patients with advanced solid tumors harboring mutations in KRAS, HRAS, or NRAS.
Detailed Description
The study is a Phase 1, multi-center, open label study in 2 parts. Part 1 (Phase Ia): This is a 3 + 3 design dose escalation study, to evaluate the safety and tolerability, and to determine the MTD and/or RP2D of YL-17231 treatment when administered orally QD in patients with advanced solid tumors harboring mutations in KRAS, HRAS or NRAS. Up to 9 doses cohorts are planned for the dose escalation part of the study, with the starting dose of 0.25mg QD. The actual number of dose cohorts to be explored in this study will be determined by the non-tolerable dose based on dose limiting toxicities (DLTs) in conjunction with the PK and preliminary efficacy signal data. If suggested by safety and PK findings from planned dose treatment cohorts, additional dose levels may be evaluated and dosing interval may be modified under the Safety Monitoring Committee (SMC) guidance. In Part 1, the 3+3 trial design for the dose escalation will be used and a total of 9 dose levels starting dose of 0.25 mg OD is planned. One cycle is 21 days. DLT observation period is one cycle. The maximum tolerated dose (MTD) is the highest dose at which ≤1 of 6 patients experiences a DLT during the DLT observation period. The study will identify a maximum tolerated dose (MTD) if possible, with safety and tolerability data. All available data, including safety, tolerability, PK, PD and preliminary anti-tumor activity from each cohort will be reviewed by the SMC to determine the RP2D. Patients may be permitted an intra-patient dose-escalation of YL-17231 to a higher dose level that has been cleared and deemed safe by the SMC if they have completed Cycle 2 at their initial enrolled dose level and continued on-study with no treatment related ≥ Grade 2 AEs. The Investigator must consult with the Medical Monitor to confirm if the patient is permitted be dose-escalated to a dose-level already cleared by the SMC. Backfilling Additional patients (up to total of 12) may be enrolled in the dose levels which have been cleared and deemed safe by SMC to further evaluate the safety, tolerability and PK. This is referred to as backfilling. Part 2 (Phase Ib): This is a dose expansion phase to further evaluate the safety, tolerability and preliminary anti-tumor activity of YL 17231 at the RP2D selected by SMC. The number of patients to be enrolled for the expansion cohorts, the RP2D and the desired patient population will be determined by the emerging data from part 1 of the study, including safety, tolerability, PK, PD and preliminary anti-tumor efficacy, as well as any other relevant evolving clinical data, and will be clarified through a protocol amendment.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Unresectable or metastatic advanced solid tumors with no standard therapies, or having progressed on or intolerable to standard therapies.
- •Advanced solid tumors harboring mutations in KRAS, HRAS or NRAS as determined by laboratory testing, including local laboratory testing.
- •Measurable disease with at least one lesion amenable to response assessment per RECIST 1.
- •Demonstrate adequate organ function as defined below. All screening laboratories should be performed within 7 days of study treatment initiation.
- •1）Absolute neutrophil count (ANC) ≥1.2 × 10\^9/L；2）Platelets ≥100 × 10\^9/L Hemoglobin ≥9 g/dL or ≥5.6 mmol/L；3）Measured or calculated creatinine clearance (CrCl)(Cockcroft-Gault) ≥60 mL/min；4）Total bilirubin ≤1.5 × ULN (patients with Gilbert's syndrome, total bilirubin ≤3.0 × ULN) ；5）Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × ULN or ≤5 × ULN for patients with liver metastases
- •Has an ECOG performance status of 0-
- •Life expectancy ≥12 weeks at baseline.
- •Women of childbearing potential must have negative serum or urine pregnancy test within 72 hours prior to receiving the first study drug administration. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
- •For women of childbearing potential, must be willing to use an adequate method of contraception from 30 days prior to the first study drug administration and at least 3 months following last day study drug administration.
- •Male patients of childbearing potential must be surgically sterile, or must agree to use adequate method of contraception during the study and at least 3 months following the last day of study drug administration.
Exclusion Criteria
- •Known symptomatic brain metastases requiring dexamethasone ≥4mg (or equivalent) or requiring steroid dose increase within 14 days prior to the first dose of YL-
- •Any concurrent chemotherapy, immunotherapy, or biologic or hormonal therapy for cancer treatment.
- •Unresolved toxicities from prior therapy, defined as having not resolved to NCI CTCAE v.5.0 Grade ≤1 1 or baseline, with exception of endocrinopathies from prior therapy and successfully treated (such as hypothyroidism), alopecia, vitiligo, and ≤ grade 2 peripheral neuropathy.
- •Human immunodeficiency virus (HIV) infection with a current or a known history of AIDS-defining illness or HIV infection with a CD4+ T cell count \<350 cells/µL and an HIV viral load more than 400 copies/µL.
- •Patients with active viral (any etiology) hepatitis are excluded. However, patients with serologic evidence of chronic hepatitis B virus (HBV) infection (defined by a positive hepatitis B surface antigen test and a positive anti-hepatitis core antigen antibody test) who have a viral load below the limit quantification (HBV DNA titer \<1000 cps/mL or 200 IU/mL), and are not currently on viral suppressive therapy may be eligible and should be discussed with the Medical Monitor. Patients with a history of hepatitis C virus (HCV) infection who have completed curative antiviral treatment and have a viral load below the limit of quantitation may be eligible and should be discussed with the Medical Monitor.
- •Any of the following cardiac criteria experienced currently or within the last 6 months:
- •Congestive heart failure (New York Heart Association ≥ Class 2).
- •Any clinically significant abnormalities (as assessed by the Investigator) in rhythm, conduction, or morphology of resting electrocardiograms (ECGs), e.g., complete left bundle branch block or third-degree heart block.
- •Acute coronary syndrome within 6 months.
- •Clinically significant cardiac arrhythmia.
Arms & Interventions
Dose Escalation and Expansion
Dose escalation of YL-17231 to determine maximum tolerated dose.Expansion cohort to ensure sufficient safety experience, pharmacokinetic information, and early evidence of clinical activity of YL-17231 to recommend Phase 2 regimens
Intervention: YL-17231
Outcomes
Primary Outcomes
TEAEs
Time Frame: Through study completion, an average of 1 year
AEs will be coded using Medical Dictionary for Regulatory Activities current version. AEs will be regarded as treatment-emergent AEs (TEAEs) if they occur after first treatment. The frequencies will be presented including number and percentages of patients having experienced an event and the total number of events.
SAEs
Time Frame: Through study completion, an average of 1 year
Serious AEs
Occurrence of dose limiting toxicities (DLTs)
Time Frame: The first cycle (21 days)
A toxicity will be considered dose-limiting if it occurs during the first cycle (21 days) of treatment with YL-17231.
Secondary Outcomes
- Overall Response Rate (ORR)(From first dose of study treatment to the first documented disease progression or death due to any cause, whichever occurs first， assessed up to 30 months.)
- Progression Free Survival (PFS)(From first dose of study treatment to the first documented disease progression or death due to any cause, whichever occurs first, assessed up to 30 months.)
- Disease Control Rate (DCR)(From first dose of study treatment to the first documented disease progression or death due to any cause, whichever occurs first, assessed up to 30 months.)
- Duration of Response (DOR)(From first documentation of a response (PR or CR) to the first documented disease progression or death due to any cause, whichever occurs first， assessed up to 30 months.)
- AUC(0-T)(During Cycles 1 and 2 (each cycle is 21 days))
- T1/2(During Cycles 1 and 2 (each cycle is 21 days))
- Tmax(During Cycles 1 and 2 (each cycle is 21 days))
- Cmax(During Cycles 1 and 2 (each cycle is 21 days))