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A Phase I of FXS0260 in Advanced Solid Tumor

This Study is a Phase I, Single-arm, Open-label, Dose-escalation and Dose-expansion Clinical Study Designed to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Preliminary Efficacy of FXS0260 in Participants With Advanced Solid Tumors.

This study is a Phase I, single-arm, open-label, dose-escalation and dose-expansion clinical study designed to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of FXS0260 in participants with advanced solid tumors.

A tanulmány áttekintése

Állapot

Még nincs toborzás

Beavatkozás / kezelés

Részletes leírás

The study consists of two parts: Phase Ia dose escalation and Phase Ib dose expansion.

Phase Ia is an open-label, dose-escalation study designed to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of FXS0260 in participants with advanced solid tumors. Approximately 20 participants are expected to be enrolled.

Dose escalation will be conducted using an accelerated titration design combined with the Bayesian Optimal Interval (BOIN) design. The prespecified dose levels are 5 mg BID, 20 mg BID, 60 mg BID, 120 mg BID, and 180 mg BID.

The accelerated titration design will be applied to the 5 mg BID and 20 mg BID dose cohorts, while the BOIN design will be implemented starting from the 60 mg BID dose cohort.Only one participant will initially be enrolled in each of the 5 mg BID and 20 mg BID dose cohorts. If a dose-limiting toxicity (DLT) or a Grade ≥2 study drug-related adverse event (AE) occurs during the DLT observation period, the current dose cohort will transition to the BOIN design, with enrollment expanded to a total of 3 participants.

Participants will receive a single oral dose of FXS0260 under fasting conditions during the single-dose administration period. The DLT observation period will be 24 days following the first dose (including the single-dose administration period and Cycle 1). Participants will subsequently enter Cycle 2 and subsequent cycles for multiple-dose treatment.Study treatment will continue until disease progression, death, unacceptable toxicity, withdrawal of informed consent, or other reasons requiring discontinuation of study treatment, whichever occurs first.

Phase Ib is an open-label, dose-expansion study that will enroll eligible participants with advanced solid tumors. The sample size will be determined based on the results of the Phase Ia dose-escalation study.This phase aims to further evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of FXS0260 at the recommended dose level(s) for expansion (1-2 dose cohorts).

Tanulmány típusa

Beavatkozó

Beiratkozás (Becsült)

20

Fázis

  • 1. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi kapcsolat

Tanulmányozza a kapcsolattartók biztonsági mentését

Tanulmányi helyek

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kína, 200000
        • Fudan University Shanghai Cancer Center
        • Kapcsolatba lépni:
        • Kapcsolatba lépni:

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

18 év és régebbi (Felnőtt, Idősebb felnőtt)

Egészséges önkénteseket fogad

Nem

Tanulmányozható nemek

Összes

Leírás

Inclusion Criteria:

  1. Male or female participants aged ≥18 years;

  2. Fully understand the requirements of this study and voluntarily sign the written informed consent form;

  3. Participants with histologically/cytologically diagnosed advanced solid tumors who have received standard treatment before participating in this study and for whom standard treatment has failed or no standard treatment is available; priority will be given to participants with advanced endometrial cancer, advanced ovarian cancer, advanced colorectal cancer, advanced gastric cancer, and advanced breast cancer;

  4. At least one measurable lesion according to the Response Evaluation Criteria in Solid Tumours (RECIST) v1.1 (lesions previously treated with radiotherapy cannot be considered target lesions unless obvious progression has occurred);

  5. Eastern Cooperative Oncology Group performance status score of 0-1;

  6. Life expectancy ≥12 weeks;

  7. Adequate organ and bone marrow function:

    Hematology (no red blood cell or platelet transfusion or growth factor infusion within 7 days before the first administration of FXS0260):

    • Hemoglobin ≥95 g/L;
    • ANC ≥1.5 × 10⁹/L (≥1500 cells/mm³);
    • Platelet count ≥100 × 10⁹/L (≥100,000 cells/mm³);

    Coagulation:

    • Prothrombin time and APTT ≤1.5 × ULN;
    • INR ≤1.5 × ULN.

    Liver:

    • Total bilirubin ≤1.5 × ULN (if the participant is diagnosed with Gilbert's syndrome, total bilirubin ≤3 × ULN and direct bilirubin ≤1.5 × ULN are allowed);
    • ALT/AST ≤3 × ULN (≤5 × ULN in the presence of liver metastases).

    Kidney:

    • Creatinine clearance ≥60 mL/min. Creatinine clearance will be calculated using the Cockcroft-Gault formula.
  8. Female participants of childbearing potential must have a negative serum pregnancy test within 7 days before the first administration of the study drug; eligible participants of reproductive potential (male and female) must agree to use reliable contraceptive methods (hormonal or barrier methods or abstinence, etc.) together with their partners during the study and for at least 6 months after the last dose.

Exclusion Criteria:

  1. Participants who are still within the washout period of previous antitumor treatment drugs before the first administration of FXS0260 (4 weeks or 5 half-lives after the last dose, whichever is shorter);

  2. Participants who have previously received PKMYT1 inhibitors;

  3. Participants who have participated in a clinical study within 4 weeks before the first administration of FXS0260;

  4. Participants with a history of allergy to any known component or analogue of FXS0260;

  5. Participants who require strong CYP3A inhibitors and/or inducers and P-gp inhibitors and/or inducers within 14 days (or 5 half-lives, whichever is longer) before the first administration and during the study;

  6. Participants with active infections requiring systemic anti-infective treatment within 1 week before the first administration;

  7. Participants who have received systemic glucocorticoids or other immunosuppressants, such as cyclophosphamide, azathioprine, methotrexate, and anti-tumor necrosis factor α agents, within 14 days before the first administration;

  8. Participants with other malignancies within 3 years before the first administration (except adequately treated basal cell/squamous cell carcinoma of the skin and carcinoma in situ of the cervix/breast);

  9. Participants who have not recovered from adverse events caused by previous antitumor treatment (recovered to Grade 1 or baseline level), except for alopecia, pigmentation of any grade, peripheral sensory neuropathy of Grade ≤2, and items already explicitly specified in the inclusion criteria, as well as other abnormalities that are clinically insignificant or considered to pose no risk by the investigator;

  10. Participants with a significant risk of thrombosis, such as deep vein thrombosis or pulmonary embolism within 3 months before screening, excluding venous thrombosis related to indwelling catheters or other procedures, superficial venous thrombosis, or thrombosis effectively treated with conventional anticoagulant therapy;

  11. Participants with refractory nausea, vomiting, chronic gastrointestinal diseases including but not limited to active diverticulitis and symptomatic peptic ulcers, inability to swallow oral medications, or conditions such as previous extensive small bowel resection that, in the investigator's judgment, seriously affect gastrointestinal absorption;

  12. Participants with a history of or current retinal vein stenosis or occlusion (RVO), retinal pigment epithelial detachment (RPED), central retinal vein occlusion, glaucoma, or other ocular diseases that affect the assessment of ocular toxicity after administration of the investigational product;

  13. Participants who have undergone major surgery within 4 weeks before the first administration or have not recovered from surgical complications;

  14. Participants who have received radiotherapy within 14 days before the first administration;

  15. Participants with symptomatic or unstable brain metastases. Participants with previously treated brain metastases may participate in the study, provided that the following conditions are met: the metastatic lesions are stable (no evidence of progression on imaging examinations within 4 weeks before the first administration of study treatment, and any neurological symptoms are controlled and stable), there is no evidence of new or enlarging brain metastases, the investigator assesses the clinical condition as stable, and steroids have been discontinued for at least 14 days before the first administration of study treatment;

  16. Participants with any of the following cardiovascular diseases:

    • Symptomatic heart failure (New York Heart Association [NYHA] functional classification ≥ Class II);
    • Left ventricular ejection fraction <50% by echocardiography (ECHO) or multiple-gated acquisition (MUGA) scan;
    • Poorly controlled hypertension repeatedly observed despite standard of care (SOC) treatment (systolic blood pressure >150 mmHg or diastolic blood pressure >100 mmHg);
    • Prolonged QT/QTc interval on electrocardiogram during screening (QTcF >470 ms);
    • Acute coronary syndrome/acute myocardial infarction, unstable angina, percutaneous coronary intervention or coronary artery bypass grafting within 6 months before screening;
    • Cardiomyopathy of any etiology or clinically significant valvular heart disease;
    • Transient ischemic attack or stroke within 6 months before screening that, in the investigator's judgment, may affect this study;
    • Severe arrhythmias requiring clinical intervention;
    • Any other cardiovascular disease that, in the investigator's opinion, makes the participant unsuitable for participation in the study.
  17. Participants with uncontrolled pleural effusion, pericardial effusion, or ascites, or pleural effusion, pericardial effusion, or ascites requiring repeated drainage and medical intervention;

  18. Participants with any of the following viral infections at screening:

    • Active hepatitis B: HBV-DNA >500 IU/mL or 2000 copies/mL;
    • Active hepatitis C: positive HCV antibody and positive HCV-RNA;
    • Human immunodeficiency virus (HIV) infection: positive antibody test;
    • Active syphilis: positive Treponema pallidum antibody (such as TPHA or FTA-ABS) and positive titer test (such as RPR or VDRL).
  19. Participants with a history of interstitial lung disease, drug-induced interstitial lung disease or radiation pneumonitis requiring steroid treatment, or clinically active interstitial lung disease;

  20. Participants with known drug abuse or psychiatric disorders that would interfere with compliance with study requirements;

  21. Participants who are pregnant or breastfeeding or intend to become pregnant during the study;

  22. Participants who, in the investigator's opinion, have other factors that may affect the study results or interfere with their participation throughout the study, including previous or existing physical conditions, treatments, or laboratory abnormalities, unwillingness to comply with the study procedures, restrictions, and requirements, or other circumstances that make them unsuitable for enrollment.

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Kezelés
  • Kiosztás: N/A
  • Beavatkozó modell: Egyetlen csoportos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: FXS0260

Participants will receive FXS0260, an oral small-molecule PKMYT1 inhibitor, at prespecified dose levels of 5, 20, 60, 120, or 180 mg twice daily (BID) during the dose-escalation phase (Phase Ia). Participants will receive a single oral dose during the single-dose administration period, followed by repeated dosing in subsequent treatment cycles.

During the dose-expansion phase (Phase Ib), participants will receive FXS0260 at one or two recommended dose levels selected based on the results of Phase Ia.

Treatment will continue until disease progression, unacceptable toxicity, death, withdrawal of informed consent, or other protocol-defined reasons for treatment discontinuation, whichever occurs first.

FXS0260 is an orally administered, selective small-molecule inhibitor of PKMYT1

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Incidence of DLTs
Időkeret: From the first dose through Day 24 (Phase Ia only)

DLTs will be assessed during the DLT observation period in Phase Ia. DLT-evaluable participants are defined as those who experience a DLT during the DLT observation period or receive at least 70% of the planned doses and complete the safety assessments.

From the first dose through Day 24 (Phase Ia only)
Determination of MTD or MAD
Időkeret: Up to 12 Months

The MTD will be inferre based on DLT data and all safety data observed at all dose levels. The MTD is defined as the highest dose level at which no more than 30% of participants experience a DLT during the DLT observation period in the dose-escalation phase.If the MTD is not reached, the highest safe dose level will be defined as the MAD.

Up to 12 Months
Incidence, Severity, and Relationship to Study Drug of Adverse Events (AEs)
Időkeret: From the first dose of FXS0260 through 28 days after the last dose.

The incidence, severity, and relationship to FXS0260 of adverse events will be assessed. The severity of adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 6.0.

From the first dose of FXS0260 through 28 days after the last dose.
Determination of RP2D
Időkeret: Through completion of the dose-escalation and dose-expansion assessments

The RP2D of FXS0260 will be determined based on an integrated assessment of safety, tolerability, pharmacokinetic (PK), pharmacodynamic (PD), and efficacy data.

Through completion of the dose-escalation and dose-expansion assessments

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Peak Plasma Concentration (Cmax) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
The area under the plasma concentration-time curve from time 0 to the last measurable ocncentration (AUC0-t)of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Time to reach maximum plasma concentration (Tmax) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Elimination Half-life (T1/2) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Apparent Clearance (CL/F) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Apparent volume of distribution (Vz/F) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Average concentration at steady state(Cavg,ss) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Minimum observed concentration at steady state(Cmin,ss) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Maximum observed concentration at steady state(Cmax,ss)of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Elimination rate constant (λz) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Apparent volume of distribution at steady state(Vss/F) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Area under the plasma concentration time curve from time 0 to infinity(AUC0-∞)of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Area under the plasma concentration-time curve over the dosing interval at steady state (AUCtau,ss) of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Accumulation ratio(AR) based on Cmax of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Accumulation ratio(AR) based on AUCtau, ss of FXS0260
Időkeret: From prodose on Day1 to 7 days after last dose of FXS0260

Pharmacokinetic parameter

From prodose on Day1 to 7 days after last dose of FXS0260
Objective response rate, ORR
Időkeret: From first dose of study drug until disease progression as defined by RECIST v1.1 , initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.

Antitumor activity by evaluation of tumor response assessments based on RECIST 1.1

From first dose of study drug until disease progression as defined by RECIST v1.1 , initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.
Progression Free Survival
Időkeret: From first dose of study drug until disease progression as defined by RECIST v1.1 , initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.

Antitumor activity by evaluation of tumor response assessments based on RECIST 1.1

From first dose of study drug until disease progression as defined by RECIST v1.1 , initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.
Duration of Response (DoR)
Időkeret: From first dose of study drug until disease progression as defined by RECIST v1.1, initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.

Antitumor activity by evaluation of tumor response assessments based on RECIST 1.1

From first dose of study drug until disease progression as defined by RECIST v1.1, initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.
Disease Control Rate (DCR)
Időkeret: From first dose of study drug until disease progression as defined by RECIST v1.1, initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.

Antitumor activity by evaluation of tumor response assessments based on RECIST 1.1

From first dose of study drug until disease progression as defined by RECIST v1.1, initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.
Overall Suivaval (OS)
Időkeret: From first dose of study drug until disease progression as defined by RECIST v1.1 , initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.

Antitumor activity by evaluation of tumor response assessments based on RECIST 1.2

From first dose of study drug until disease progression as defined by RECIST v1.1 , initiation of new anticancer therapy, death, withdrawal of informed consent, loss to follow-up, or the end of the study, whichever occurs first, assessed up to 24 months.

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete (Becsült)

2026. december 15.

Elsődleges befejezés (Becsült)

2028. december 15.

A tanulmány befejezése (Becsült)

2029. december 15.

Tanulmányi regisztráció dátumai

Először benyújtva

2026. október 25.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2026. november 10.

Első közzététel (Tényleges)

2026. november 12.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Tényleges)

2026. november 12.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2026. november 10.

Utolsó ellenőrzés

2026. október 1.

Több információ

A tanulmányhoz kapcsolódó kifejezések

Egyéb vizsgálati azonosító számok

  • FXS0260-I101

Gyógyszer- és eszközinformációk, tanulmányi dokumentumok

Egy amerikai FDA által szabályozott gyógyszerkészítményt tanulmányoz

Nem

Egy amerikai FDA által szabályozott eszközterméket tanulmányoz

Nem

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