A Trial of C-met Kinase Inhibitor HS-10241 in Subjects With Advanced Solid Tumours

Solid Tumor, Adult Clinical Trial

Official title:

Phase I Trial to Investigate Safety and Tolerability Profile and Pharmacokinetics of C-met Kinase Inhibitor HS-10241 in Subjects With Advanced Solid Tumours

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02977364
• Other study ID #: HS-10241-101
• Status: Recruiting
• Phase: Phase 1
• First received: November 11, 2016
• Last updated: November 27, 2016
• Start date: November 2016
• Est. completion date: November 2021

Study information

• Verified date: November 2016
• Source: Jiangsu Hansoh Pharmaceutical Co., Ltd.
• Contact: Yuankai Shi, MD
• Phone: 86(10)87788293
• Email: syuankaipumc[@]126.com
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

To investigate safety, tolerability and pharmacokinetics of C-met Kinase Inhibitor HS-10241 in Subjects With Advanced Solid Tumours that are not eligible for conventional or intensive treatment. The dose of HS-10241 will be escalated to determine the dose limiting toxicity (DLT) and the maximum tolerated dose (MTD) of HS-10241 in advanced cancer patients. At the same time, pharmacokinetic characteristics and preliminary efficacy of HS-10241 will be observed in advanced cancer patients. To determine the recommended dosage regimen for phase II.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: November 2021
• Est. primary completion date: November 2018
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Histologically confirmed advanced or metastatic solid tumor for which standard therapy does not exist, has failed, or has been refused.

2. c-MET positive patients preferred in dose escalation phase; c-MET of patients must fulfill ICH++~+++ or FISH=4 times in dose expansion phase.

3. Confirmed that there are at least 1 can be measured in accordance with the standard RECIST1.1 by CT or MRI.

4. 18 ~65 years of age.

5. ECOG performance status of 0~1.

6. Life expectancy of at least 3 months.

7. Recovered from toxicities of prior anti-cancer treatment to Grade 1 or less (except alopecia).

8. Acceptable hematologic status (without hematologic supports including hematopoietic factor, blood transfusion) defined below:

• Absolute neutrophil count (ANC) = 1500/µL

• Platelet count = 100000/µL

• Hemoglobin = 9.0 g/dL

9. Acceptable liver function defined below:

• Total bilirubin = 2 times upper limit of normal range (ULN)

• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 3 times ULN; however, = 5 times ULN in a subject who has liver metastases

10. Acceptable renal function defined below:

• Serum creatinine = 1.5 times ULN or calculated creatinine clearance (by the Cockcroft-Gault formula) = 60 mL/minutes

11. Acceptable coagulation status defined below:

• Prothrombin time < 1.5 times ULN

• Partial thrombin time < 1.5 times UL

12. HIV Ag/Ab(-).

13. HCV Ab(-);or HCV Ab(+) but HCV RNA(-).

14. HBsAg(-)and HBcAb(-)in dose escalation phase;HBV DNA<1×103copies/ml if HBsAg(+)or HBcAb(+)in dose expansion phase.

15. Ability to understand the purposes and risks of the trial and his/her informed consent using the human research ethics committee (HREC) approved informed consent form was obtained before the entering the trial.

Exclusion Criteria:

1. Treatment with other c-MET TKI( specific target or multi-target);

2. Anti-cancer treatment with radiation therapy(not including non target lesions receiving palliative radiotherapy), chemotherapy,hormonotherapy or surgery(small surgery, including the implantation of external equipment or fine needle aspiration, at least 7 days; diagnostic or palliative surgery, at least 14 days) within 4 weeks (6 weeks for nitrosoureas or Mitomycin C)prior to trial entry.

3. Medical history of difficulty swallowing, malabsorption or other chronic gastrointestinal disease, or conditions that may hamper compliance and/or absorption of the tested product

4. Cardiac disease with New York Heart Association (NYHA) Class III or IV, including congestive heart failure, myocardial infarction within 6 months prior to the trial entry, unstable arrhythmia, or symptomatic peripheral arterial vascular disease.

5. Symptomatic brain metastases or unstable brain metastases (notes: Patients with asymptomatic brain metastases previously treated for the study, but must be kept stable for at least 4 weeks and receive a stable dose of the drug)

6. Obvious neurological and mental disorder.

7. Other previous or concomitant tumors (except for the effective treatment of melanoma, cervical carcinoma in situ, ductal carcinoma in situ or malignant tumor after effective treatment, remission 3 years and considered to have been cured).

8. Active, uncontrolled bacterial, fungal infections, requiring systemic therapy.

9. Recent venous thrombosis (including deep vein thrombosis or pulmonary embolism within 0.5 year of trial entry)

10. History of organ allograft, autologous stem cell transplantation, or allogeneic stem cell transplantation.

11. Participation in an investigational drug or device trial within 4 weeks prior to the trial entry.

12. Anti-cancer treatment with radiation therapy, chemotherapy or immunotherapy within 4 weeks (6 weeks for nitrosoureas or Mitomycin C) prior to trial entry.

13. Major surgery, other than diagnostic surgery, within 4 weeks prior to the trial entry, without complete recovery

14. Taking a medication that is a moderate or strong inhibitor or inducer of CYP2C9; taking a medication that prolongs QT interval and has a risk of Torsades de Pointes .

15. Pregnant (positive serum beta human chorionic gonadotropin [ß-HCG] test at Screening) or is currently breast-feeding, their partner anticipates becoming pregnant/impregnating during the trial or within 6 months after receiving the last dose of trial treatment.

16. Known drug abuse or alcohol abuse.

17. Concomitant disease or condition that could interfere with the conduct of the trial, or that would, in the opinion of the Investigator, pose an unacceptable risk to the subject in this trial.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma
• Solid Tumor, Adult

Intervention

Drug:
• HS-10241

Locations

Country	Name	City	State
China	Cancer Hospital Chinese Academy of Medical Sciences	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Jiangsu Hansoh Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	MTD of HS-10241 based on the incidence of dose limiting toxicities		4 weeks	Yes
Secondary	Progression-free survival (PFS)		12 months	No
Secondary	Max concentration (Cmax) of HS-10241		4 weeks	No
Secondary	Objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumours (RECIST) v1.1		8 weeks	No
Secondary	Incidence and intensity of Adverse Events according to Common Toxicity Criteria for AEs (CTCAE version 4.0)		8 weeks	Yes
Secondary	Area under the plasma concentration versus time curve (AUC) of HS-10241		4 weeks	No
Secondary	Elimination half-life(T1/2) of HS-10241		4 weeks	No