A First-in-human Study of HRS2398 Tablets in Subjects With Advanced Malignant Tumors

Advanced Malignant Tumor Clinical Trial

Official title:

A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK) of HRS2398 in Subjects With Advanced Malignant Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05144061
• Other study ID #: HRS2398-I-101
• Status: Recruiting
• Phase: Phase 1
• Start date: December 20, 2021
• Est. completion date: November 30, 2023

Study information

• Verified date: November 2022
• Source: Shanghai Hengrui Pharmaceutical Co., Ltd.
• Contact: Li Xiang
• Phone: 18661801805
• Email: li.xiang[@]hengrui.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is being conducted to determine the dose limited toxicity(DLT) and maximum tolerated dose(MTD) and recommended Phase 2 dose(RP2D) of HRS2398 in subjects with advanced malignant tumor ; The second objectives is to evaluate safety and preliminary efficacy and PK profile of HRS2398 in subjects with advanced malignant tumor ; Exploratory cohort is to explore the relationship between gene mutation and efficacy and resistance mechanisms.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 122
• Est. completion date: November 30, 2023
• Est. primary completion date: May 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Subjects are able to give voluntary informed consent, understand the study and are willing to follow and complete all the test procedures.

2. subjects =18 years and =70 years.

3. Patients with Histologically or cytologically confirmed advanced Malignant tumors who had failed standard treatment or had not been treated with standard therapy.

4. ECOG =1.

5. Subjects with life expectancy of = 3 months.

6. At least one measurable lesion ( RECIST version 1.1).

7. Subjects must have adequate organ function (whole blood or component transfusion or

BFGF within 2 weeks before 1st dose of study drug is prohibited):

1. Absolute neutrophil count (ANC) =1.5 x10^9/L;

2. Platelet count = 100 x 10^9/L;

3. Hemoglobin = 90 g / L;

4. Total bilirubin (TBil) =1.5 x ULN;

5. Liver function tests alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =3 x ULN, for patients with known liver cancer or liver metastases, AST and ALT = 5 x ULN;

6. Gr = 1.5x ULN or an estimated glomerular filtration rate (eGFR) > 50 mL/min;

7. INR =1.5 x ULN and APTT = 1.5 x ULN;

8. LVEF=50%,QTc Male: <450ms; Female: <470ms.

8. Subjects (males and females) of childbearing potential should be willing to use reliable contraception methods that are deemed effective by the investigator from visit 1 through 180 days following the last dose of study drug.

9. Archived wax lump tumor tissue samples or biopsy and blood sample collection during screening period.

10. As judged by the investigator, can follow protocol.

Exclusion Criteria:

1. Untreated and/or uncontrolled brain metastases.

2. Patients with clinical symptoms of cancer ascites, pleural effusion, who need to drainage, or who have undergone ascites drainage within 2 weeks prior to the first administration.

3. Failure to recover from adverse events from the most recent anti-tumor treatment to CTCAE = grade2.

4. Inability to swallow tablets or gastrointestinal disease, possible impairment of adequate absorption of study drugs.

5. Have severe cardiac disease:NYHA class =grade II heart failure; unstable angina pectoris;myocardial infarction within 12 months; clinically significant supraventricular or ventricular arrhythmias require treatment or intervention; Hypertension that cannot be well controlled by antihypertensive medication (systolic blood pressure =150 mmHg or diastolic blood pressure =100 mmHg).

6. Known active hepatitis C virus, or known active hepatitis B virus.

7. Allergic to the HRS2398 or the similar drug.

8. Concurrent anticancer treatment or use of other investigational product within 4 weeks before start of trial treatment; major surgery, radiotherapy, chemotherapy within 4 weeks before 1st dose of trial treatment.

9. The patient is currently using a drug known to be a strong inhibitor of CYP3A4 within 2 weeks before 1st dose of study drug ,or strong inducer of CYP3A4 within 4 weeks before 1st dose of study drug .

10. The investigator determined that the patient should not participate in the study.

Related Conditions & MeSH terms

• Advanced Malignant Tumor
• Neoplasms

Intervention

Drug:
• HRS2398 Tablets
Take 5mg to 320mg once or twice a day ; Oral administration , 21 days as a cycle.

Locations

Country	Name	City	State
China	Affiliated Cancer Hospital of Zhengzhou University/Henan Cancer Hospital	Zhengzhou	Henan

Sponsors (1)

Lead Sponsor	Collaborator
Shanghai Hengrui Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose-limiting toxicity(DLT)		up to 21 days
Primary	Maximum tolerated dose(MTD)		up to 6 months
Primary	Recommended Phase II Dose (RP2D)		up to 21 days
Secondary	Number of subjects with adverse events and the severity of adverse events		from the first drug administration to within 30 days for the last treatment dose
Secondary	Cmax of HRS2398 of Single administration		Single administration : 30min before administration of Day1, 5min, 0.25 hour, 0.5 hour, 0.75 hour, 1 hour , 2hours, 4hours, 6hours, 8hours, 10hours, 24hours, 48hours, 72hours after administration of Day1
Secondary	Tmax of HRS2398 of Single administration		Single administration : 30min before administration of Day1, 5min, 0.25 hour, 0.5 hour, 0.75 hour, 1 hour , 2hours, 4hours, 6hours, 8hours, 10hours, 24hours, 48hours, 72hours after administration of Day1
Secondary	AUC0-t of HRS2398 of Single administration		ingle administration : 30min before administration of Day1, 5min, 0.25 hour, 0.5 hour, 0.75 hour, 1 hour , 2hours, 4hours, 6hours, 8hours, 10hours, 24hours, 48hours, 72hours after administration of Day1
Secondary	AUC0-12 of HRS2398 of Single administration		Single administration : 30min before administration of Day1, 5min, 0.25 hour, 0.5 hour, 0.75 hour, 1 hour , 2hours, 4hours, 6hours, 8hours, 10hours after administration of Day1
Secondary	T1/2 of HRS2398 of Single administration		Single administration : 30min before administration of Day1, 5min, 0.25 hour, 0.5 hour, 0.75 hour, 1 hour , 2hours, 4hours, 6hours, 8hours, 10hours, 24hours, 48hours, 72hours after administration of Day1
Secondary	Cmax of HRS2398 of Multiple doses		Multiple administration: Day8, Day15, Day17 of Cycle1, Day1 of Cycle2-4 (each cycle is 21 days)
Secondary	Tmax of HRS2398 of Multiple administration		Multiple administration: Day8, Day15, Day17 of Cycle1, Day1 of Cycle2-4 (each cycle is 21 days)
Secondary	AUC0-t of HRS2398 of Multiple administration		Multiple administration: Day8, Day15, Day17 of Cycle1, Day1 of Cycle2-4 (each cycle is 21 days)
Secondary	AUC0-12 of HRS2398 of Multiple administration		Multiple administration: Day8, Day15, Day17 of Cycle1, Day1 of Cycle2-4 (each cycle is 21 days)
Secondary	T1/2 of HRS2398 of Multiple administration		Multiple administration: Day8, Day15, Day17 of Cycle1, Day1 of Cycle2-4 (each cycle is 21 days)
Secondary	Bioavailability of fasting state	PK blood samples from subjects were collected for bioavailability ,Postprandial AUC divided by fasting AUC	up to 4 months
Secondary	Objective Response Rate(ORR)	Radiological scans performed at baseline then every 6 weeks until objective radiological disease progression	up to 4 months
Secondary	Disease Control Rate(DCR)	Complete response + Partial response + Stable disease (CR+PR+SD) based on RECIST 1.1	up to 4 months
Secondary	Duration of response (DoR)	Time from documentation of tumor response to disease progression assessed among patients who had an objective response	up to 4 months
Secondary	Progression free survival(PFS)	Defined as Progression free survival per RECIST 1.1 criteria according to Investigator's assessment	up to 4 months