- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT02442531
A Study of CriPec® Docetaxel Given to Patients With Solid Tumours (NAPOLY)
2018년 9월 21일 업데이트: Cristal Therapeutics
A Phase I Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of CriPec® Docetaxel in Patients With Solid Tumours
The goal of this Phase1 clinical research study is to find the highest safe dose of CriPec® docetaxel that can be given in the treatment of patients with solid tumours.
연구 개요
상세 설명
The study is designed to explore the safety, tolerability, pharmacokinetics and pharmacodynamics of CriPec® docetaxel and to identify the Maximum Tolerated Dose (MTD).
연구 유형
중재적
등록 (실제)
33
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
18년 이상 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
- At least 18 years old
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1
- Estimated life expectancy of at least 12 weeks
Ability and willingness to give written informed consent and to comply with the requirements of the study
For Part 1:
Patients with pathologically confirmed diagnosis of advanced, recurrent and progressive solid tumours that are refractory to standard therapy or for whom no standard therapy exists and with measurable or evaluable disease according to RECIST 1.1.
For Part 2:
- Patients with pathologically confirmed diagnosis of advanced, recurrent and progressive cancer with measurable disease according to RECIST 1.1 of a histological type that are refractory to standard therapy or for whom no standard therapy exists and where treatment with a taxane is an appropriate treatment option.
Exclusion Criteria:
- Less than 4 weeks since the last treatment of chemotherapy, biological therapy, immunotherapy or systemic radiotherapy (except palliative radiation delivered to <20% of bone marrow), and less than 6 weeks for nitrosoureas and mitomycin C prior to Cycle 1 Day 1.
- Current or recent (within 4 weeks prior to Cycle 1 Day 1) treatment with another Investigational Product or participation in another investigational interventional study.
- Symptomatic brain metastases.
- Toxicities incurred as a result of previous anticancer therapy (radiation therapy, chemotherapy, or surgery) that have not resolved to ≤ grade 2 (as defined by CTCAE version 4.03).
Inadequate bone marrow function at screening as evidenced by any of the following:
- Absolute Neutrophil Count (ANC) < 1.5 x 109/L.
- Platelet count < 100 x 109/L.
- Haemoglobin < 6.0 mmol/L (< 9.6 g/dL). The patient should not have received a transfusion or growth factors for these abnormalities in the 7 days prior to Cycle 1 Day 1.
- Serum (total) bilirubin > 1.5 x the Upper Limit of Normal (ULN) for the institution if no liver metastases (> 2 x ULN in patients with liver metastases).
- AST or ALT > 2.5 x ULN if no liver metastases (> 5x ULN in patients with liver metastases).
- Alkaline phosphatase levels > 2.5 x ULN if no liver metastases (> 5 x ULN in patients with liver metastases, or > 10 x ULN in patients with bone metastases).
- Increased plasma prothrombin time or International Normalized Ratio (INR), consequence of reduced hepatic production of Vitamin K.
- Hepatitis B surface antigen or hepatitis C positivity with abnormal liver function tests.
Medical history of:
- Nonalcoholic steatohepatitis (NASH).
- History of human immunodeficiency virus (HIV) antibody positive or use of antiretroviral therapy.
- Alcoholic and autoimmune hepatitis.
- Ischemic hepatitis, Cardiovascular dysfunction or impaired liver oxygenation, including hypotension or right heart failure.
- Serum creatinine > 1.5 x ULN.
- Estimated Glomerular Filtration Rate of < 50 mL/min/1.73m2 calculated by Modification of Diet in Renal Disease (MDRD) formula or creatinine clearance of < 50 mL/min calculated by Cockcroft-Gault.
- Stroke within 6 months prior to Cycle 1 Day 1.
- Transient Ischemic Attack (TIA) within 6 months prior to Cycle 1 Day 1.
- Myocardial infarction within 6 months prior to Cycle 1 Day 1.
- Unstable angina.
- New York Heart Association (NYHA) Grade II or greater Congestive Heart Failure at screening.
- Serious cardiac arrhythmia requiring medication.
- Patients who are pregnant or breastfeeding.
- Absence of effective means of contraception in female patients of childbearing potential (defined as <2 years after last menstruation and not surgically sterile) or in male patients who are not surgically sterile and who have female partners of childbearing potential.
- Major surgical procedure (including open biopsy and excluding central line intravenous catheter) within 28 days prior to the first study treatment, or anticipation of the need for major surgery during the course of the study treatment.
- Grade ≥2 motor or sensory neuropathy symptoms (as defined by CTCAE version 4.03).
- Known hypersensitivity to any of the Investigational Product's excipients or taxanes.
- History of drug or alcohol abuse in the opinion of the investigator within 3 years before screening.
- Evidence of any other medical conditions (such as psychiatric illness, infectious diseases, physical examination or laboratory findings) that may interfere with the planned treatment, affect patient compliance or place the patient at high risk for treatment-related complications.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: CriPec® docetaxel
Docetaxel containing nanoparticle
|
-3 weekly IV dose.
Dose escalation; start dose 15 mg/m2.
Number of cycles: 6 or until progression or unacceptable toxicity develops
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Part 1: Incidence of grade 3 or 4 adverse events (AEs) as a measure of safety and tolerability.
기간: 9 months
|
Part 1: Incidence of grade 3 or 4 adverse events (AEs) will be determined after escalating doses of CriPec® docetaxel once every three weeks.
|
9 months
|
|
Part 1: Incidence of clinical laboratory abnormalities as a measure of safety and tolerability.
기간: 9 months
|
Part 1: Incidence of laboratory abnormalities will be determined after escalating doses of CriPec® docetaxel once every three weeks.
|
9 months
|
|
Part 1: Incidence of electrocardiogram (ECG) abnormalities as a measure of safety and tolerability.
기간: 9 months
|
Part 1: Incidence of electrocardiogram (ECG) abnormalities will be determined after escalating doses of CriPec® docetaxel once every three weeks.
|
9 months
|
|
Part 2: Incidence of grade 3 or 4 adverse events (AEs) at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1.
기간: 9 months
|
Part 2: Incidence of grade 3 or 4 adverse events (AEs) at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
|
9 months
|
|
Part 2: Incidence of clinical laboratory abnormalities at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1
기간: 9 months
|
Part 2: Incidence of clinical laboratory abnormalities at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
|
9 months
|
|
Part 2: Incidence of electrocardiogram (ECG) abnormalities at the Maximum Tolerated Dose (MTD) of CriPec® docetaxel as defined in Part 1
기간: 9 months
|
Part 2: Incidence of electrocardiogram (ECG) abnormalities at the Maximum Tolerated Dose will be determined after CriPec® docetaxel dosing once every three weeks.
|
9 months
|
|
Part 1 and 2: Pharmacokinetic profile of CriPec® docetaxel following IV infusion
기간: First two cycles of CriPec® docetaxel (each cycle is 3 weeks)
|
Pharmacokinetic parameters such as time to peak concentration (Tmax), peak concentration (Cmax), volume of distribution (Vd), half life (t1/2), total body clearance (CL) and area under the concentration-time curve (AUC) will be determined using plasma concentration data.
|
First two cycles of CriPec® docetaxel (each cycle is 3 weeks)
|
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
Early signs of anti-tumor efficacy (overall response rate [ORR]) of CriPec® docetaxel
기간: 18 months in total for part 1 and 2
|
18 months in total for part 1 and 2
|
|
Early signs of anti-tumor efficacy (duration of response) of CriPec® docetaxel
기간: 18 months in total for part 1 and 2
|
18 months in total for part 1 and 2
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2015년 8월 1일
기본 완료 (실제)
2018년 7월 1일
연구 완료 (실제)
2018년 7월 1일
연구 등록 날짜
최초 제출
2015년 5월 1일
QC 기준을 충족하는 최초 제출
2015년 5월 8일
처음 게시됨 (추정)
2015년 5월 13일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2018년 9월 24일
QC 기준을 충족하는 마지막 업데이트 제출
2018년 9월 21일
마지막으로 확인됨
2018년 7월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .