A First-in-Human, Phase 1 Study of SY-4798 in Patients With Advanced Solid Tumor

Shouyao Holdings

Status and phase: Enrolling; Phase 1

Conditions: Advanced Solid Tumor

Treatments: Drug: SY-4798

Study type: Interventional

Funder types: Other

Identifiers

NCT05498519

SY-4798-I-01

Details and patient eligibility

About

This is a Phase 1, open-label and multicenter study of SY-4798, a highly specific and potent inhibitor of FGFR4, in patients with advanced solid tumor. This study has two phases: dose-escalation phase and dose-expansion phase.

Full description

Dose-escalation phase is designed to determine the DLTs (Dose-limiting toxicity) and recommended phase II dose (RP2D) and characterize the safety, tolerability, pharmacokinetics (PK) and Pharmacodynamics (PD) of SY-4798. Other dose regimens may be explored based on the analysis of emerging PK and safety data. At this study phase, SY-4798 will be administered orally once daily (QD) in 28-day treatment cycles to adult patients with advanced solid tumor.

Dose-expansion phase is designed to evaluate the anti-tumor activity (ORR and DOR) of SY-4798 in patients with FGF19+ advanced tumor.

Enrollment: 80 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female, age ≥ 18 years at the time of screening.

2. Eastern Collaboration Oncology Group (ECOG) performance status (PS) scored of 0-1.

3. Escalation Part: Patients must have histological or cytological confirmed advanced solid tumor, which is refractory or inappropriate at this stage to standard therapies or for which no standard therapy exists. In this part, patients with hepatocellular carcinoma (HCC) and Child-Pugh scores of ≤7 are preferred.

4. Expansion Part: Patients must have histological or cytological confirmed and FGF19 IHC+ advanced solid tumor (patients with HCC should have Child-Pugh scores of ≤7), which is refractory to or inappropriate at this stage to standard therapies or for which no standard therapy exists.

5. Estimated Life expectancy ≥ 12 weeks.

6. Must have at least one assessable lesion in dose-escalation part and one measurable lesion in dose-expansion part per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1;

7. Adequate organ function as defined in the below:

   Hepatic function

   Total serum bilirubin (TBIL) ≤ 1.5 times upper limit of normal (ULN); Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 3 times ULN if no demonstrable liver metastases, or ≤ 5 times ULN in the presence of liver metastases/ in HCC patients.

   Bone marrow function (no blood transfusion or hematopoietic stimulator treatment within 14 days)

   Absolute neutrophil count (ANC) ≥ 1.5 x 109/L; Platelets (PLT) count ≥ 75×109/L; Hemoglobin (Hb) ≥ 85 g/L

   Renal function

   Creatinine clearance ≥ 45 mL/min.

   Coagulation function

   International standardized ratio (INR) or prothrombin time (PT) ≤ 1.5 times ULN.

8. Female patients with reproductive potential must have a negative serum pregnancy test within 7 days prior to starting trial treatment, male and female patients of childbearing potential must be willing to completely abstain or agree to use an appropriate method of contraception during the entire study duration and for at least 3 months after the last dose of study medication.

9. Willingness and ability to give informed consent and follow protocol procedures, and comply with follow-up visit requirements.

Exclusion criteria

Patients with any of the following are excluded:

1. Patients who received chemotherapy, radiotherapy, biological therapy, endocrine therapy, immunotherapy, and other anti-tumor treatment within 4 weeks before the first administration, except for the following: Nitrosourea or mitomycin C was received within 6 weeks before the first administration; Oral fluoropyrimidines and small molecule targeted drugs within 2 weeks or 5 half-lives of the drug (whichever is longer) prior to the first administration; Chinese proprietary medicines with anti-tumor indications were received within 2 weeks before the first administration.
2. Received other unmarketed investigational drugs or treatments within 4 weeks prior to the first administration.
3. Have undergone major organ surgery (excluding needle biopsy) or had significant trauma within 4 weeks prior to the first administration.
4. Have received the treatment of FGFR4 selective or pan-FGFR inhibitors.
5. Adverse effects of previous antitumor therapy have not recovered to CTCAE 5.0 grade ≤1 (except toxicities that the investigator judged to be of no safety risk, such as alopecia, grade 2 peripheral neurotoxicity, and stable hypothyroidism with hormone replacement therapy).
6. Patients with central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence indicates that the patient's central nervous system metastasis or meningeal metastasis has not been controlled, and those who are judged by the investigators to be unsuitable for inclusion.
7. Patients with active infection who need systematic anti-infective therapy.
8. History of immunodeficiency, including positive HIV antibody test.
9. Active hepatitis B (HBV-DNA > 103 copies/mL or 200 IU/ mL; HBV-DNA> 104 copies/mL or 2000 IU/ mL for patients with HCC), antiviral therapies except interferon are allowed. Hepatitis C virus infection (HCV-RNA >ULN).
10. A history of serious cardiovascular and cerebrovascular disease, including but not limited to: Severe cardiac rhythm and conduction abnormalities, such as ventricular arrhythmias and degree II-III atrioventricular block requiring clinical intervention; Longer QT interval at rest (QTc > 480 msec) obtained from 3 electrocardiograms (ECGs); Acute coronary syndrome, congestive heart failure, aortic dissection, stroke, or other grade 3 or higher cardiovascular and cerebrovascular events occurred within 6 months prior to first administration; Heart failure with the New York Heart Association (NYHA) Heart function rating ≥ II or left ventricular ejection fraction (LVEF) < 50%; Clinically uncontrolled hypertension.
11. Uncontrolled effusion in the third space, not suitable for entry as determined by the investigator.
12. Patient used CYP3A4 potent inhibitors or potent inducers within 7 days before enrollment.
13. Unable to swallow or conditions that seriously affects gastrointestinal absorption as judged by the investigator.
14. Known alcohol or drug dependence.
15. Patients with mental disorders or poor compliance.
16. Pregnant and/or lactating individuals.
17. The investigator considered that the subjects had a history of other serious systemic diseases or other reasons that made them unsuitable for the study.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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80 participants in 1 patient group

Dose-escalation and Dose-expansion

Experimental group

Description:

SY-4798 will be given orally in ascending doses (escalation cohort) until the DLT or RP2D is reached. In dose-expansion phase, preliminary anti-tumor activity will be assessed in FGF19+ advanced tumor.

Treatment:

Drug: SY-4798