Clinical Study of SPH3348 Tablets, a C-Met Inhibitor, in Patients with Advanced Solid Tumors

Shanghai Pharmaceuticals

Status and phase

Completed

Phase 1

Conditions

Solid Tumor

Treatments

Drug: SPH 3348

Study type

Interventional

Funder types

Industry

Identifiers

NCT05088070

SPH3348-101

Details and patient eligibility

About

This is a phase 1 clinical trial of SPH3348 tablets, a c-Met inhibitor, in patients with advanced solid tumors with c-Met abnormalities. A modified 3 + 3 design was adopted in patients with advanced solid tumors with c-Met abnormalities, with a total of 6 dose groups, in which accelerated dose escalation was adopted for the lowest dose group, and 3 + 3 dose escalation was adopted from the second dose group. The primary objective was to evaluate the safety and tolerability of SPH3348 tablets in patients with advanced solid tumors with c-Met abnormalities.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with advanced solid tumors with c-Met abnormalities who have failed standard of care or are not eligible for standard therapy currently
ECOG score of 0 or 1.
Patients must have measurable lesion that can be assessed by imaging per RECIST 1.1 criteria.
Expected survival > 12 weeks.
Patients must have adequate organ function
Patients must give informed consent to the study and sign the informed consent form prior to the trial.

Exclusion criteria

Received anti-tumor therapies, including but not limited to chemotherapy, biotherapy, radiotherapy, targeted therapy, etc., within 4 weeks prior to the first dose of study drug; received nitrosoureas or mitomycin C within 6 weeks prior to the start of study drug.
Received small molecule tyrosine kinase inhibitors within 2 weeks prior to the first dose.
Received strong CYP3A4 inducers or inhibitors or CYP3A4 substrates with narrow therapeutic windows within 2 weeks prior to the start of study drug.
Patients with active hepatitis B (hepatitis B surface antigen (HBsAg) positive) or hepatitis C (HCV).
Toxicities caused by prior treatments have not recovered to CTCAE Grade ≤ 1 or having ≥Grade 2 peripheral neuropathy, except for alopecia and other events judged as tolerable by the investigator.
Known allergy to any component of the reference drug.
Known drug or alcohol dependence.
Received surgical treatment including surgical and interventional procedures within 4 weeks prior to the start of study drug.
Patients with brain metastases.
Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or evidence of any clinically active interstitial lung disease.
Acute bacterial, viral, or fungal infection requiring systemic therapy or unexplained fever (temperature > 38.5 °C) during screening, prior to the first dose.
Neurological and psychiatric patients with obvious poor compliance.
Any of the following within 6 months prior to signing of informed consent form: uncontrolled congestive cardiac failure, severe or unstable angina pectoris, myocardial infarction, stroke, coronary/peripheral artery bypass surgery, pulmonary embolism.
Arrhythmia uncontrolled by medication or sustained QTcB prolongation.
Hypertension uncontrolled by medication
Participated in other drug clinical studies within 28 days prior to the first dose of study drug.
Women who are pregnant or in lactation period or women/men with childbearing plans.
Patients who cannot take oral medication, or have previous surgical history or serious gastrointestinal diseases such as dysphagia, active gastric ulcer, which may impair the absorption of the study drug in the investigator's opinion.
Other prior or current concomitant malignancies.
Patients who are ineligible to participate in this trial for any reason judged by the investigator.