Status:
UNKNOWN
Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK) and Anti-tumor Activity of SYHA1801 Monotherapy in Patients With Advanced Solid Tumors
Lead Sponsor:
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Conditions:
Advanced Solid Tumors
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
Brief Summary
This is a safety, pharmacokinetic and pharmacodynamic study designed to estimate the maximum tolerated dose (MTD), and determine the Recommended Phase 2 Dose (RP2D) of SYHA1801, a BRD4 inhibitor in pa...
Detailed Description
This study will be performed in two parts. Part 1 will enroll patients with advanced solid tumors. Patients will receive SYHA1801 orally on Days 1 and 4-31 in the first cycle. Enrollment will follow a...
Eligibility Criteria
Inclusion
- Age ≥18, ≤75 years, no gender limitation.
- Histologically or cytologically confirmed diagnosis of advanced or metastatic solid tumors, for which standard therapy either does not exist or has proven ineffective, intolerable or inacceptable for the patient.
- At least one measurable lesion as per RECIST version 1.1.
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) ≤1.
- Life expectancy ≥3 months.
- Adequate bone marrow reserve, renal and liver function.
- Women of childbearing potential should agree to use contraceptive measures (such as IUD, contraceptive or condom) during the study and within 6 months after the end of the study; the serum pregnancy test should be negative within 7 days before enrollment, and must be non-lactating subjects; men should agree to use contraceptive measures during the study and within 6 months after the end of the study.
- Signed informed consent form.
Exclusion
- Administration of chemotherapy, radiotherapy, biotherapy, endocrine therapy, targeted therapy, immunotherapy and other anti-tumor treatment within 4 weeks before the first dose of the study drug, except the following: using nitrosourea and mitomycin C within 6 weeks, using fluorouracil and small molecule targeted drugs within 2 weeks (or within 5 half time period), using traditional Chinese medicine with anti-tumor indications within 2 weeks.
- Administration of other unlisted clinical research drugs within 4 weeks before the first dose of SYHA1801.
- Major organ surgery (excluding biopsy) or significant trauma within 4 weeks before the first dose of SYHA1801.
- Administration of glucocorticoids or other immunosuppressants within 14 days prior to the first dose of SYHA1801, except the following: local, ocular, intraarticular, intranasal and inhaled glucocorticoids; short-term use of glucocorticoids for preventive treatment.
- Concomitant therapy with strong CYP3A4 inhibitors or inducers within 14 days.
- Prior treatment with BET inhibitors.
- Persistent grade \>1 clinically significant toxicity related to prior antineoplastic therapies (except alopecia).
- Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence that the patient's central nervous system metastasis or meningeal metastasis has not been controlled, that is not suitable for the group according to the judgment of the investigator.
- Uncontrollable active infection.
- History of autoimmune diseases, immunodeficiency, including HIV positive, or other acquired, congenital immunodeficiency, or organ transplant history.
- Active hepatitis B; positive for hepatitis C antibody.
- History of serious cardiovascular disease.
- Inability to swallow oral medications or presence of a gastrointestinal disorder deemed to jeopardize intestinal absorption of SYHA1801.
- Other serious illness or medical conditions.
- Alcohol or drug dependence.
- A clear history of neurological or psychiatric disorders.
- Pregnant or breast-feeding female.
- In the opinion of the investigator, not suitable for enrollment due to other reasons.
Key Trial Info
Start Date :
April 7 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2023
Estimated Enrollment :
186 Patients enrolled
Trial Details
Trial ID
NCT04309968
Start Date
April 7 2020
End Date
June 30 2023
Last Update
June 9 2020
Active Locations (1)
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1
Tianjin Cancer Hospital
Tianjin, Tianjin Municipality, China, 022