Phase I Study of HRS-7053 Injection in the Treatment of Patients With Advanced Malignancies

Trial Title: Phase I Study of HRS-7053 Injection in the Treatment of Patients With Advanced Malignancies

NCT ID: NCT05983146

Condition: Advanced Malignant Cancer

Conditions: Official terms:
Neoplasms

Study type: Interventional

Study phase: Phase 1

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: HRS-7053 Injection
Description: HRS-7053 is administered by intravenous (IV) infusion once a week (QW) for one treatment cycle every 4 weeks
Arm group label: HRS-7053 Injection

Summary: To evaluate the safety and tolerability of multiple administration of HRS-7053 in patients with advanced malignancies Determine the maximum tolerated dose (MTD, if possible) and the recommended dose for Phase II clinical studies (RP2D)

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Voluntary participation in this study, signed informed consent, compliance is good, can cooperate with follow-up 2. Age ≥18 years, both male and female 3. Histologically or cytologically confirmed patients with advanced hematologic malignancies that have not responded to standard antitumor therapy and currently indicate treatment 4. Have measurable lesions 5. ECOG PS score: 0-1 6. Have a life expectancy of at least 3 months 7. The functional level of the major organs must meet the requirements 8. Fertile female patients must have a serum pregnancy test within 7 days before the first medication and the result is negative; And must be non-lactating Exclusion Criteria: 1. The tumor infiltrates the central nervous system 2. Received autologous stem cell transplantation within 12 weeks prior to administration of the first study; Patients who have previously received allogeneic bone marrow transplantation or solid organ transplantation; In the first study, Car T cell therapy was administered within 12 weeks prior to drug administration 3. Had major surgery or severe trauma 4 weeks prior to the first study; Or plan to undergo major surgery during the study 4. Received antitumor therapy within 2 weeks prior to administration of the first study drug; Received Chinese herbal therapy within 2 weeks before the first dose of study drug administration; Receiving steroid hormones for antitumor purposes within 7 days before the first dose of the investigational drug administration 5. Use of live attenuated vaccine within 28 days prior to signing the informed consent, or expected to require live attenuated vaccine during the study period to 5 months after the final dose 6. Use of any potent drug that inhibits the liver drug metabolizing enzyme CYP3A for 14 days prior to first administration; Any potent drug that induces the liver drug metabolizing enzyme CYP3A has been used for 28 days prior to first administration 7. Previous treatment-induced adverse events did not recover to ≤CTCAE grade 1 8. Participating in other clinical studies or signing informed consent less than 1 month after the last medication in the previous clinical study 9. The active phase of HBV or HCV infection is known 10. A history of immunodeficiency, including HIV seropositive, or other acquired, congenital immunodeficiency disorders 11. Active infection or unexplained fever > 38.5 ° c 12. A history of clinically severe cardiovascular disease; A history of myocarditis within one year prior to drug administration was first studied 13. The abnormality of electrocardiogram (ECG) was clinically significant 14. In the first study, cerebrovascular accident, transient ischemic attack occurred within 6 months prior to drug administration 15. History of other malignancies within 5 years prior to drug administration was first studied 16. Known allergy to any component of the HRS-7053 product 17. The presence of other serious physical or mental illnesses, abnormal laboratory tests, and other factors that may increase the risk of participating in the study or interfere with the study results; And any other conditions that the investigator deems inappropriate for participation in this study 18. Female subjects are pregnant or breastfeeding

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Start date: September 1, 2023

Completion date: June 30, 2027

Lead sponsor:
Agency: Jiangsu HengRui Medicine Co., Ltd.
Agency class: Industry

Source: Jiangsu HengRui Medicine Co., Ltd.

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05983146