Inclusion Criteria:
1. Understand and sign the informed consent form voluntarily.
2. ≥18 years old when signing the informed consent, regardless of sex.
3. Have histologically or cytologically confirmed unresectable advanced, recurrent, or
metastatic solid tumors (including but not limited to small cell lung cancer,
glioblastoma, urothelial carcinoma, endometrial cancer, cervical cancer, ovarian
cancer, breast cancer, and liver cancer) for which standard therapy has failed or
was intolerable, and currently no standard treatment is available.
- - Radiological or histopathological evidence indicating disease progression
should be documented.
- - Intolerance is defined as discontinuation of treatment due to adverse events
during therapy.
- - Recurrence is based on radiological or histopathological results.
4. For glioblastoma: at least one measurable intracranial tumor lesion according to the
RANO 2.0 criteria. For other solid tumors: at least one measurable lesion according
to RECIST v1.1 criteria. Note: Target lesions can be located in previously
irradiated areas, but must be confirmed by imaging to show disease progression after
radiation.
5. For glioblastoma: KPS score ≥60. For other solid tumors: ECOG performance status of
0 or 1.
6. Meet the following laboratory criteria (without receiving any blood products,
hematopoietic growth factors, albumin, or other treatments within 14 days prior to
testing, except iron supplements):
- - Hematology: Hemoglobin (Hb) ≥100 g/L, absolute neutrophil count (ANC)
≥1.5×10^9/L, platelet (PLT) count ≥100×10^9/L.
- - Biochemistry: 1) Dose escalation phase: Serum creatinine (Cr) ≤ upper limit of
normal (ULN); total bilirubin (TBIL) ≤1.25×ULN; alanine aminotransferase (ALT),
aspartate aminotransferase (AST) ≤1.5×ULN (for subjects with liver metastases
or hepatocellular carcinoma: ≤3×ULN).
2) Cohort expansion phase: Cr ≤1.5×ULN;
TBIL ≤1.5×ULN; ALT, AST ≤2.5×ULN (for subjects with liver metastases or
hepatocellular carcinoma: ≤5×ULN).
- - Coagulation: International normalized ratio (INR) ≤1.5×ULN; prothrombin time
(PT) and activated partial thromboplastin time (APTT) ≤1.5×ULN (for
participants receiving prophylactic anticoagulation, the INR and APTT should be
within a safe and effective therapeutic range as judged by the investigator).
- - Urinalysis: Urine protein <2+; if ≥2+, a 24-hour urine protein quantification
should be performed.
<1 g/24 h can be enrolled but ≥1 g/24 h is prohibited.
without quantification when urine protein ≥2+ is not allowed.
7. Expected survival ≥12 weeks.
8. Cohort Expansion Phase: 1) Cohort 1: Histologically or cytologically confirmed small
cell lung cancer (SCLC) that has progressed or recurred after at least two lines of
systemic chemotherapy (including a platinum-based regimen). Note: A new line of
treatment is defined as a change in treatment due to disease progression, not due to
toxicity or other reasons. Re-initiation of the same treatment regimen after initial
progression is considered a new line of treatment. 2) Cohort 2: Recurrent or
progressive glioblastoma confirmed by histopathology or imaging, which has
progressed or recurred after at least one prior treatment with temozolomide.
Exclusion Criteria:
1. Received any form of intracranial radiotherapy within 3 months prior to the first
dose.
2. Received any anti-tumor treatment (including but not limited to chemotherapy,
targeted therapy, immunotherapy, cellular therapy, radiation therapy [see exclusion
criterion #1 for head], endocrine anti-tumor therapy, tumor embolization) or
unapproved investigational drugs or devices within 28 days prior to the first dose.
Also, received Traditional Chinese Medicine (TCM) approved by the National Medical
Products Administration (NMPA) for treating malignant tumors within 14 days prior to
the first dose.
3. Previously received Aurora kinase inhibitors.
4. Used strong inducers or inhibitors of cytochrome P450 3A (CYP3A) enzymes within 14
days prior to the first dose or are still within 7 half-lives of such drugs
(whichever is longer).
5. For glioblastoma only: >5 mg/day dexamethasone or equivalent doses of other
glucocorticoids for systemic treatment related to glioblastoma within 1 week prior
to the first dose.
6. Underwent major surgery (cranial, thoracic, or abdominal) within 28 days prior to
the first dose or have unresolved wounds, ulcers, or fractures as judged by the
investigator at screening.
7. Have unresolved toxicities from previous treatments that have not recovered to CTCAE
v5.0 grade ≤1, except for alopecia or laboratory abnormalities deemed no clinical
significant by the investigator.
8. History of other primary malignancies within 5 years prior to the first dose, except
for adequately treated in situ carcinoma, non-melanoma skin cancer, or malignant
melanosis.
9. For solid tumors other than glioblastoma: Unstable brain metastases. Stable brain
metastases are allowed if:
- - No immediate or planned local treatment for brain metastases during the study.
- - No neurological symptoms or signs (e.g., increased intracranial pressure,
seizures, cognitive impairment) at screening.
- - Brain lesions stable for ≥2 weeks prior to the first dose without
corticosteroid or anticonvulsant treatment.
10. Leptomeningeal metastasis (except glioblastoma).
11. Severe brain herniation or risk thereof.
12. For glioblastoma only: who had wafer(s) implantation during surgery.
13. Received drainage of pleural effusion, ascites, or pericardial effusion within 1
month prior to the first dose or have significant clinical symptoms (e.g., chest
tightness, shortness of breath, dyspnea).
14. Uncontrolled or significant cardiovascular disease, including:
- - NYHA Class II or higher congestive heart failure, unstable angina, myocardial
infarction within 6 months prior to the first dose, or arrhythmias requiring
treatment, left ventricular ejection fraction (LVEF) <50% at screening.
- - Primary cardiomyopathy (e.g., dilated, hypertrophic, arrhythmogenic right
ventricular, restrictive, or unclassified cardiomyopathy).
- - Symptomatic coronary artery disease requiring medication at screening.
- - Clinically significant QTcF prolongation history or QTcF >470 ms (females) and
>450 ms (males) at screening.
- - Significant cerebrovascular accident (including cerebral hemorrhage, transient
ischemic attack) within 6 months prior to the first dose.
- - Use of ≥3 antihypertensive drug components within 14 days prior to the first
dose or inadequately controlled blood pressure (systolic BP ≥140 mmHg or
diastolic BP ≥90 mmHg) at screening.
- - Other cardiovascular conditions deemed unsuitable by the investigator.
15. Poorly controlled diabetes (fasting glucose >10 mmol/L).
16. Significant gastrointestinal abnormalities at screening that may affect drug intake,
transport, or absorption (e.g., inability to swallow, chronic diarrhea, bowel
obstruction, small bowel resection, or total gastrectomy).
17. Clinically significant hemoptysis or tumor bleeding within 14 days prior to the
first dose; significant active bleeding within 2 months prior to the first dose
(e.g., gastrointestinal bleeding); currently on anticoagulants (e.g., warfarin,
phenprocoumon, but low-dose aspirin and heparin for prophylaxis allowed); high-risk
bleeding tendency at screening (e.g., esophageal varices, active ulcerative lesions,
positive occult blood in stool, imaging evidence of tumor invasion into large
vessels).
18. Serious thromboembolic events within 6 months prior to the first dose (e.g.,
arterial thrombosis, pulmonary embolism, deep vein thrombosis). Implanted venous
port or catheter-related thrombi, superficial vein thrombi, or those deemed stable
and not requiring emergency medical intervention are not considered "serious."
19. Active infection requiring intravenous treatment at screening. Severe infections
(e.g., hospitalization due to infection, bacteremia, severe pneumonia complications)
within 28 days prior to the first dose. Patients receiving prophylactic antibiotics
(e.g., for urinary tract infections or COPD exacerbations) can be enrolled.
20. Known active tuberculosis, currently receiving anti-tuberculosis treatment, or
received anti-tuberculosis treatment within 1 year prior to the first dose.
21. Active hepatitis B (HBsAg or HBcAb positive with viral replication) or hepatitis C
(HCV antibody positive with viral replication) at screening.
22. Human immunodeficiency virus (HIV) infection or syphilis infection (positive
specific antibody test followed by positive non-specific antibody test) at
screening.
23. Allergy or hypersensitivity to any component of the trial drug or known excipients,
or history of severe allergic diseases.
24. History of organ transplantation or allogeneic hematopoietic stem cell
transplantation.
25. History of alcohol abuse or drug abuse.
26. Any psychiatric or cognitive disorder that may limit understanding of informed
consent, compliance with the protocol, or participation in the trial.
27. Unwilling or unable to use effective contraception methods during the entire
treatment period and up to 3 months after the last dose for women of childbearing
potential (defined as having experienced menarche and not undergone successful
artificial sterilization [hysterectomy, bilateral tubal ligation, or bilateral
oophorectomy] or not postmenopausal) or male patients whose partners are women of
childbearing potential; pregnant or breastfeeding women.
28. Other conditions deemed unsuitable for participation in this trial by the
investigator.
