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Study of YL-17231 for Advanced Solid Tumors with RAS Mutations

This study is testing a new drug called YL-17231 for people with advanced solid tumors that have specific changes (mutations) in their KRAS, HRAS, or NRAS genes. These are tumors that have either not responded to standard treatments or for which standard treatments are not available or tolerated. The main goals are to see how safe YL-17231 is, what side effects it causes, and how well the body handles it. Researchers will also look for early signs of the drug's effectiveness. To join, you must have advanced solid tumors with these specific gene mutations and measurable disease. The study is currently unclear on its recruitment status.

Study design
This is a Phase 1, multi-center, open-label study with two parts, aiming to enroll 60 participants. It uses a 3+3 dose escalation design to find the safest and most effective dose.
What's involved
Participants will take YL-17231 by mouth once daily. The first cycle of treatment is 21 days, and safety will be monitored throughout the study, which is expected to last about one year.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for side effects (TEAEs and SAEs) through study completion, which is an average of one year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06096974

Pan-RAS Inhibitor YL-17231 in Patients With Advanced Solid Tumors Harboring Mutations in KRAS, HRAS, or NRAS

Recruiting
PHASE1Ages 18+InterventionalTreatment
Shanghai YingLi Pharmaceutical Co. Ltd.
~60 participants
Updated 2025-04-09 on ClinicalTrials.gov
What's tested:YL-17231

At a glance

Recruiting sites
3 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Occurrence of dose limiting toxicities (DLTs)
Measured over The first cycle (21 days)
+2 more outcomes measured

Conditions

Advanced Solid Tumors

Explore related trials

Solid NeoplasmGTPase KRasHRAS GeneNRAS Gene

NCT06096974

Where you'd take part

This study runs at 3 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Huntsman Cancer Institute and Hospital, University of Utah

    Salt Lake City, Utahstudy coordinator listed

    Recruiting

  • MD Anderson Cancer Center

    Houston, Texasstudy coordinator listed

    Recruiting

  • The Lindner Center for Research & Education at The Christ Hospital

    Cincinnati, Ohiostudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Who to contact

David S. Hong, MD
[email protected]
(713) 563-1930
Email the study team

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Eligibility criteria

Inclusion

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 1.1.
Demonstrate adequate organ function as defined below. All screening laboratories should be performed within 7 days of study treatment initiation.
Has an ECOG performance status of 0-1.
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.
Age ≥18 years at screening.
Able and willing to provide written informed consent and to follow study instructions.
Washout from prior anti-tumor therapy:1）Cytotoxic therapies ≥ 3 weeks Mitomycin C or nitrosoureas ≥ 6 weeks；2）Small molecule agents ≥2 weeks or 5x T1/2, whichever is longer；3）Biologic agents (e.g., antibodies) ≥ 4weeks Immunotherapy (e.g., CTLA4, PD-1, PD-L1 inhibitors) ≥ 4 weeks；4）Radiotherapy ≥ 4 weeks；5）Limited field radiotherapy or palliative radiotherapy ≥ 2 weeks ；6）Major surgery, excluding biopsy ≥ 4 weeks (exception: patients may enroll if fully recovered or without intolerable or clinically significant adverse effects, but at least 14 days must have elapsed between major surgery and first study drug administration)；7）Study drug with an investigational product, or non-approved use of a drug or device ≥ 4 weeks (≥2 weeks or 5x T1/2, whichever is longer for small molecule agents

Exclusion

Known symptomatic brain metastases requiring dexamethasone ≥4mg (or equivalent) or requiring steroid dose increase within 14 days prior to the first dose of YL-17231.
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:
Mean QTC interval corrected (Frederica) for heart rate \>450 ms.
Left ventricular ejection fraction (LVEF) \<50% or the lower limit of normal (per institutional standard).
Evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension, uncontrolled diabetes mellitus, active bleeding diatheses, or active infection, as determined by the investigator.
Any condition that impairs a patient's ability to swallow whole pills. Presence of an active gastrointestinal disease or other condition that will interfere significantly with the absorption, distribution, metabolism, or excretion of YL-17231, as determined by the investigator.
History noninfectious pneumonitis required steroids treatment or concurrent pneumonitis or interstitial lung diseases.
An active additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer.
Known allergy to any component of YL-17231.
Patient has known psychiatric, substance abuse or other disorders that would interfere with cooperation with the requirements of the trial, in the opinion of the investigator.
Patients who are pregnant or breastfeeding or expecting to conceive within the projected duration of the trial, starting with the screening visit through 3 months after the last dose of trial treatment.

What this trial measures

  • Occurrence of dose limiting toxicities (DLTs)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.

  • TEAEsThrough 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.

  • SAEsThrough study completion, an average of 1 year

    Serious AEs