Phase I Study of Hemay102 in Patients With Advanced Solid Tumors

NCT ID: NCT03982303

Last Updated: 2021-10-01

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 39 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-01-03
• Study Completion Date: 2021-12-31

Brief Summary

This trial was a single-center, open-label, dose-increasing Phase I clinical study with subjects enrolled in patients with advanced solid tumors who failed standard treatment or who were unable to receive effective treatment. The trial is divided into two stages: dose escalation and dose extension.

Detailed Description

Dose escalation:

A total of 7 dosage groups were set at this stage, which were 5 mg/m2, 10 mg/m2, 20 mg/m2, 40 mg/m2, 60 mg/m2, 90 mg/m2, and 120 mg/m2, respectively. Accelerated dosage titration was performed in the first 3 dose groups, 1 subject was enrolled in each group; the last 4 dose groups were perfromed into dosage groups by the principle of "3+3" dose increment rule, and the number of subjects enrolled in each group is 3 to 6 cases.

Dose extension:

According to the test results of the dose escalation phase, two extensions of MTD (tentative 60 mg/m2, 90 mg/m2) were selected for the expansion trial. Each dose level was planned to enroll 6 subjects (12 in total), subjects were administered once every 3 weeks (1 treatment cycle every 3 weeks), and received 4 treatment cycles in a row for Hemay102. Safety, tolerability, pharmacokinetic characteristics, and initial anti-tumor efficacy were evaluated.

Conditions

Patients With Advanced Stage Solid Tumors

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Hemay102 at the dosage of 5mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 5mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Hemay102 at the dosage of 10mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 10mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Hemay102 at the dosage of 20mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 20mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Hemay102 at the dosage of 40mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 40mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Hemay102 at the dosage of 60mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 60mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Hemay102 at the dosage of 90mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 90mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Hemay102 at the dosage of 120mg/m2

Hemay102 will be administered to patients through i.v. drip for 4hrs at the dosage of 120mg/m2.

Group Type: EXPERIMENTAL

Hemay102

Intervention Type: DRUG

Hemay102 was administered through i.v. infusion for 4hrs.

Interventions

Hemay102

Hemay102 was administered through i.v. infusion for 4hrs.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Age ≥18 years old and ≤70 years old, male or female;
• A patient who has been confirmed by histology or cytology to have advanced or metastatic solid tumors (in the patients with locally advanced hepatocellular carcinoma or metastatic liver cancer, patients can be recruited by clinical diagnosis) and who have failed standard treatment or who are unable to receive/do not have effective treatment;
• At least one evaluable tumor lesion (spiral CT scan with a long diameter ≥ 10 mm, in accordance with RECIST version 1.1);
• ECOG PS score 0~1 within 1 week before enrollment;
• Estimated survival time of more than 3 months;
• Appropriate hematopoietic function: white blood cell count ≥ 3 × 10^9 / L; absolute neutrophil count ≥ 1.5 × 10^9 / L; platelet count ≥ 100 × 10^9 / L; hemoglobin ≥ 90 g / L;
• Appropriate liver function: total bilirubin ≤ 1.5 × upper limit of normal (ULN); aspartate transferase (AST) ≤ 2.5 × ULN; alanine aminotransferase (ALT) ≤ 2.5 × ULN;
• Proper renal function: serum creatinine ≤ 1.5 × ULN or creatinine clearance ≥ 50 mL / min according to the Cockcroft-Gault formula;
• For clinically confirmed unresectable locally advanced hepatocellular carcinoma or metastatic liver cancer, the patient's liver function must meet the criteria below: ALT≤2.5×ULN, AST≤2.5×ULN, TBIL≤1.5×ULN, Child-Pugh score A or B Grade (≤7 points), blood ammonia ≤100μmol/L (only for patients with hepatocellular carcinoma);
• A qualified male or female patient with fertility must agree to use a reliable method of contraception (hormone or barrier method) after signing the informed consent until at least 12 weeks after the last dose;
• Subjects must give informed consent to the study prior to the trial and voluntarily sign a written informed consent form;
• Subjects are able to communicate well with the investigator and are able to complete the study in accordance with the trial regulations.

• Uncontrolled or important cardiovascular disease, which included a) New York Heart Association (NYHA) grade II or higher congestive heart failure, unstable angina, myocardial infarction, or arrhythmia requiring treatment (including atrial fibrillation, at screening) within 6 months prior to the first study drug administration Supraventricular tachycardia, ventricular tachycardia or ventricular fibrillation, or left ventricular ejection fraction (LVEF) < 50%; b) Primary cardiomyopathy (eg dilated cardiomyopathy, hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, restrictive cardiomyopathy, undetermined cardiomyopathy); c) Clinically significant QTc interval prolongation history, or screening period QTc interval (corrected by Bazette) ≥ 450ms (male) or ≥ 470ms (female); d) Coronary heart disease with symptoms requiring medication; e) Uncontrollable hypertension (refers to post-treatment systolic blood pressure > 160 mmHg and / or diastolic blood pressure > 100 mmHg);
• A history of hemorrhagic or thromboembolic events in the past 6 months, such as cerebrovascular accidents (including transient ischemic attacks), pulmonary embolism, and spontaneous bleeding of the tumor;
• Medical treatment for other clinical trials within 4 weeks prior to enrollment;
• <4 weeks after major surgery or trauma after enrollment;
• Must take other treatments during the trial, such as other chemotherapy, targeted therapy, hormone therapy, immunotherapy, radiotherapy (except for local symptomatic radiotherapy) or Chinese medicine;
• Concomitant mental illness;
• The investigator believes that the subject is not suitable for this clinical study.

Exclusion Criteria

• Subjects known to have or suspected to have brain metastases;
• Have received radiation therapy within 4 weeks before enrollment;
• Drugs that may affect the metabolism of this product, such as CYP3A4 strong inducer (rifampicin, carbamazepine, phenytoin, etc.) or strong inhibitors (clarithromycin, protease, triazole antifungals, etc.), should be combined within 2 weeks before the study or during the study period;
• Patients who have previously received anthracycline treatment; or who are known to have a history of allergies to anthracyclines (eg, doxorubicin, epirubicin);
• Have active infection or HIV-positive infection or other serious illness;

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tianjin Hemay Oncology Pharmaceutical Co., Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ti Zhang, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Tianjing medical university cancer hospital

Locations

Tianjin medical university cancer hoapital

Tianjin, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Yueying Zhen, Ph.D.

Role: CONTACT

zhenyueying@hemay.com.cn

86-22-2492-9366

Facility Contacts

Ti Zhang, Ph.D.

Role: primary

zhangti@tjmuch.com

86-22-23340123 ext. 3094

Other Identifiers

HM102ST1S01

Identifier Type: -

Identifier Source: org_study_id