- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03792958
Study of Challenge Meditech 082 (CM082) Tablets in Patients With Advanced Malignant Solid Tumors
Phase I Study of CM082 Tablets in the Treatment of Advanced Malignant Solid Tumors: Safety, Tolerance and Pharmacokinetics
연구 개요
상세 설명
연구 유형
등록 (실제)
단계
- 1단계
연락처 및 위치
연구 장소
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Shanghai
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Shanghai, Shanghai, 중국, 200120
- Shanghai East Hospital
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Age:≥18 years.
- BMI generally ranges from 18-28 (BMI=Weight (Kg)/Height (m)2)
- Patients with advanced malignant solid tumors confirmed by histological or cytological examination.
- According to Recist1.1 criteria, patients have measurable or assessable tumors, and patients with advanced malignant solid tumors who have failed to respond to previous standard treatment regimens, are unable to tolerate previous treatment regimens or lack effective treatment regimens.
Organ function level must meet the following requirements (7 days before treatment):
- Bone marrow: absolute neutrophil count (ANC)≥1.5^109/L, platelet (PLT)≥100^109/L, hemoglobin (HB)≥9g/dL (no blood transfusion or component blood received within 14 days before detection).
- Liver: Serum bilirubin (TBIL) ≤1.5 * upper limit of normal (ULN) , aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 * ULN (If the patient's liver metastases, AST and ALT are allowed to be ≤ 5 * ULN) ).
- Serum creatinine≤1.5 * ULN and endogenous creatinine clearance rate≥50mL/min. According to Cockcroft-Gault formula, Please refer to attachment 7 for details.
- International normalized ratio (INR) and activated partial thromboplastin time (APTT)≤1.5 * ULN (This provision applies only to patients who do not receive anticoagulant treatment; for patients receiving anticoagulant treatment, anticoagulants should be used within the treatment requirements).
- Urine protein (UP)≤1+. If UP>1+, 24-hour UP should be collected for determination, and the total amount of UP should be ≤1g.
- FT3、FT4 and thyroid-stimulating hormone (TSH) are normal or abnormal without clinical significance(Except for advanced thyroid cancer).
- No immunodeficiency.
- The damage causes by other treatments is restored to 1 grade (CTCAE version 4.03), except for hair loss and pigmentation; If the nutritional status is stable, the long-term toxicity that cannot be recovered is allowed to exist by the investigator'judgement.
- Expected survival time≥ 3 months.
- Eastern Cooperative Group (ECOG) Performance Status score of ≤1.
- The results of serum pregnancy test for women of childbearing age should be negative within 7 days before treatment.
- Men who are fertile or women who are likely to become pregnant must use highly effective contraceptive methods (e.g., oral contraceptives, intrauterine contraceptives, sex control or barrier contraceptives combined with spermicides ) throughout the trial and continue to use contraception for 12 months after the end of treatment.
- Patients can voluntarily sign written informed consent.
Exclusion Criteria:
-Within 4 weeks before the first use of the study drug, the patient received anti- tumor drug therapy such as chemotherapy, targeted therapy, radiotherapy, biological therapy or endocrine therapy, except for the following: Nitrous urea or mitomycin C were used within 6 weeks before the first use of the study drug; Oral fluorouracil and small molecular targeted drugs were used within 2 weeks before the first use of the study drug or within 5 half-lives (whichever is the longer); Chinese medicine with anti-cancer indications was used within 1 week before the first use of the study drug.
- Surgical treatment (except biopsy) was performed within 4 weeks before the first use of study drug.
- Patients who have participated in or are participating in any other drug/therapy clinical trial (including but not limited to the anti-tumor clinical trial) within 4 weeks before treatment, counting from the time of last administration of the last clinical trial.
- Patients who received hematopoietic stimulating factors (e.g., granulocyte colony stimulating factor (G-CSF), erythropoietin, etc.) within one week before treatment.
- Pleural or ascites with clinical symptoms and requiring symptomatic treatment.
- Patients with active pulmonary disease, interstitial pneumonia or pulmonary fibrosis.
Having any uncontrollable clinical problems or associated risk factors, including but not limited to:
- Poorly controlled hypertension (blood pressure persistently greater than 150/90 mmHg).
- Left ventricular ejection fraction (LVEF)≤50%.
- The QT interval of heart rate correction (QTc) > 450 msec (males) or 460 msec (females) ( Bazett's correction (QTcB)=QT/(RR^0.5)).
- Patients have a clinically significant history of arrhythmia or current evidence of arrhythmia, but control of atrial fibrillation for more than 30 days before administration does not affect inclusion.
- Patients implanted with cardiac defibrillator.
- Poorly controlled diabetes [(fasting blood glucose should not be greater than 8.9 mmol/L after drug control) refer to CTCAE version 4.03-grade 1 of hyperglycemia].
- Heart disease (Class III/IV congestive heart failure or cardiac block defined by the New York Heart Association).
- Decompensated cirrhosis.
The following conditions occur within 6 months before treatment:
- Deep venous thrombosis or pulmonary embolism.
- Myocardial infarction.
- Severe or unstable arrhythmia or angina pectoris.
- Percutaneous Coronary Intervention, Acute Coronary Syndrome, Coronary Artery Bypass Transplantation.
- Cerebrovascular accident, transient ischemic attack or resting limping of lower limbs.
- Patients have not yet fully recovered from previous operations.
- Patients who have taken strong inhibitors and inducers of CYP3A hepatic metabolic enzymes within 2 weeks before treatment.
- Patients also take drugs that are at risk of prolonging QTc and/or Tdp.
- Patients with a history of allergy to CM082 similar drugs (e.g., sunitinib, sorafenib, pazopanib, etc.).
- Pregnant or lactating women.
- Women/men with fertility who refuse to use contraception during the trial.
- Any uncontrollable clinical problem (such as serious mental, neurological, cardiovascular, respiratory and other system diseases) or active infection that significantly affects clinical trials.
- The patient has clinical symptoms or uncontrolled central nervous system metastasis or meningeal metastasis, which is judged by the investigator to be unsuitable for admission;
- Patients with active upper gastrointestinal ulcer or other diseases known to affect drug absorption, distribution, metabolism or clearance.
- Patients with obvious abnormal gastrointestinal function such as vomiting、 diarrhea, etc..
- Positive results of HIV or Treponema pallidum antibodies (Acceptance of Treponema pallidum antibody titer test results in a Class III Grade I hospital including research centers).
Patients with active hepatitis B or C:
- HBsAg or HBcAb are positive, and hepatitis B virus (HBV) DNA is detected (the results are higher than the upper limit of the normal range of the research center).
- Hepatitis C virus (HCV) antibody test results are positive, and HCV RNA is detected (the results are higher than the upper limit of the normal range of the research center).
- Patients who have progressed after using a receptor tyrosine kinase inhibitor that targets VEGFR.
- Investigators consider that it is not appropriate for subjects to participate in this study from the perspective of clinical treatment.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 순차적 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: CM082
CM082 태블릿
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CM082 tablets taken orally 200、400、600 and 800 mg (QD or BID)
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Maximum tolerable dose (MTD) or dose to absorb saturation
기간: From the first dose to the 28th day of administration
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From the first dose to the 28th day of administration
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Dose-Limiting Toxicity
기간: From the first dose to the 28th day of administration
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Characteristics of dose-limiting toxicity (DLT), evaluation criteria: National Cancer Institute (NCI) CTC classification (version 4.03)
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From the first dose to the 28th day of administration
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Pharmacokinetic parameters
기간: From the first dose to the 28th day of administration
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Peak concentration
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From the first dose to the 28th day of administration
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Pharmacokinetic parameters
기간: From the first dose to the 28th day of administration
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Area under the time curve of blood concentration from 0 h to the last time of blood collection
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From the first dose to the 28th day of administration
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Pharmacokinetic parameters
기간: From the first dose to the 28th day of administration
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0 to Infinite Area under Blood Drug Concentration Curve
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From the first dose to the 28th day of administration
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Pharmacokinetic parameters
기간: From the first dose to the 28th day of administration
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Peak time
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From the first dose to the 28th day of administration
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Pharmacokinetic parameters
기간: From the first dose to the 28th day of administration
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Apparent terminal elimination half-life
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From the first dose to the 28th day of administration
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Pharmacokinetic parameters
기간: From the first dose to the 28th day of administration
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Terminal elimination rate constant
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From the first dose to the 28th day of administration
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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무진행 생존
기간: 12 개월
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12 개월
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전반적인 생존
기간: 36개월
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36개월
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객관적 응답률
기간: 12 개월
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12 개월
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방역률
기간: 12 개월
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12 개월
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- CM082-CA-I-105
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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