- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00768469
Study Evaluating Safety And Tolerability, Solid Tumor
2018년 4월 24일 업데이트: Puma Biotechnology, Inc.
A Phase 1 Study Of Neratinib (HKI-272) In Combination With Paclitaxel In Subjects With Solid Tumors
This is an open-label, phase 1 study of ascending multiple oral doses of HKI-272 in combination with paclitaxel.
연구 개요
연구 유형
중재적
등록 (실제)
10
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
-
-
-
Shizuoka, 일본
- Investigational Site
-
Tokyo, 일본
- Investigational Site
-
-
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
20년 이상 (성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
- Subjects must have confirmed pathologic diagnosis of a solid tumor that is not curable with available therapy for which HKI-272 plus paclitaxel is a reasonable treatment option.
- At least 1 measurable lesion as defined by RECIST criteria.
- Eastern Cooperative Oncology Group (ECOG) 0 to 1
- LVEF within institutional limits of normal (by MUGA or ECHO).
Screening laboratory values within the following parameters:
- ANC: greater than or equal to 1.5 x 10E9 /L (1,500 /mm3)
- Platelet count: 10 x 10E10 /L (100,000 /mm3)
- Hemoglobin: greater than or equal to 9.0 g/dL
- Serum creatinine: less than or equal to 1.5 x upper limit of normal (ULN)
- Total bilirubin: less than or equal to 1.5 xULN · AST and ALT: less than or equal to 2.5 xULN (less than or equal to 5 x ULN if liver metastases are present)
- For women of child bearing potential, a negative urine or serum pregnancy test result before study entry. A woman of childbearing potential is one who is biologically capable of becoming pregnant. This includes women who are using contraceptives or other means of birth control or whose sexual partners are either sterile or using contraceptives.
- All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 28 days after the last dose of test article.
Exclusion Criteria:
- Prior treatment with anthracyclines with a cumulative dose of doxorubicin of greater than 400 mg/m^2, epirubicin dose of greater than 800 mg/m^2, or the equivalent dose for other anthracyclines or derivatives.
- Major surgery, chemotherapy, radical (curative intent) radiotherapy, investigational agents, or other cancer therapy within 2 weeks of treatment day 1 or non-recovery from all clinically significant acute adverse effects of prior therapies (excluding alopecia).
- Subjects with bone or skin as the only site of disease.
- Active central nervous system (CNS) metastases, as indicated by clinical symptoms, cerebral edema, and/or progressive growth (subjects with a history of CNS metastases or cord compression are allowable if they have been definitively treated and have been clinically stable for at least three months, and off steroids or anticonvulsants, before first dose of test article).
- QTc interval greater than 0.47 second or known history of QTc prolongation or Torsade de Pointes (TdP).
- Known hypersensitivity to paclitaxel or Cremophor EL (polyoxyethylated castor oil).
- Pregnant or breast feeding women.
- Significant chronic or recent acute gastrointestinal disorder with diarrhea as a major symptom (e.g., Crohn's disease, malabsorption, or Grade greater than or equal to 2 diarrhea of any etiology at baseline).
- Inability or unwillingness to swallow the HKI-272.
- Treatment with a taxane within 3 months of treatment day 1.
- Pre-existing grade 2 or greater motor or sensory neuropathy.
- Any other cancer within 5 years prior to screening with the exception of contralateral breast carcinoma, adequately treated cervical carcinoma in situ, or adequately treated basal or squamous cell carcinoma of the skin.
- Presence of clinically significant or uncontrolled cardiac disease, including congestive heart failure (New York Heart Association [NYHA] functional classification of greater than or equal to 2), angina requiring treatment, myocardial infarction within the past 12 months, or any clinically significant supraventricular arrhythmia or ventricular arrhythmia requiring treatment or intervention.
- Evidence of significant medical illness or abnormal laboratory finding that would, in the investigator's judgment, make the subject inappropriate for this study. Examples include, but are not limited to, serious active infection (ie, requiring intravenous antibiotic or antiviral agent), uncontrolled major seizure disorder, or significant pulmonary disorder (e.g. interstitial pneumonitis, pulmonary hypertension).
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: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Nera 160 + Pac
Neratinib 160 mg + Paclitaxel 80 mg/m^2
|
Administered orally, continuous, once daily.
다른 이름들:
Administered IV, on days 1, 8, 15 of 28 day cycle.
|
|
실험적: Nera 240 + Pac
Neratinib 240 mg + Paclitaxel 80 mg/m^2
|
Administered orally, continuous, once daily.
다른 이름들:
Administered IV, on days 1, 8, 15 of 28 day cycle.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Dose Limiting Toxicity (DLT) - Percentage of Participants With DLT Events
기간: From first dose day through day 28.
|
The incidence of DLTs in subjects with advanced solid tumors, treated with neratinib in combination with paclitaxel 80 mg/m^2.
DLT was defined as any neratinib plus paclitaxel related Grade 3 or 4 nonhematologic toxicity or Grade 4 hematologic toxicity with few exceptions.
|
From first dose day through day 28.
|
|
Maximum Tolerated Dose
기간: From first dose day through day 28.
|
The maximum tolerated dose of neratinib, as determined by the incidence of DLTs, in combination with paclitaxel 80 mg/m^2, in subjects with advanced solid tumors.
|
From first dose day through day 28.
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Objective Response Rate
기간: From first dose date to progression/death or last tumor assessment, up to 78 weeks.
|
Percentage of participants with partial response (PR) or complete response (CR) per Response Evaluation Criteria In Solid Tumors Criteria (RECIST) v.1.0:
Complete Response (CR), disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; and Non-PD for non-target lesions, and no new lesions.
|
From first dose date to progression/death or last tumor assessment, up to 78 weeks.
|
|
Progression Free Survival
기간: From first dose date to progression/death, up to 78 weeks.
|
Number of weeks between the date of the first dose of test article and the first date of disease recurrence or progression, or death due to any cause, was documented, censored at the last evaluation, investigator assessment.
Progression is defined using Response Evaluation Criteria in Solid Tumors Criteria (v1.0), as at least a 20% increase in the sum of the longest diameters (LD) of target lesions, taking as reference the nadir LD, meaning the smallest sum of the LDs recorded since the treatment started; or unequivocal progression of existing nontarget lesions; or the appearance of any new lesions.
|
From first dose date to progression/death, up to 78 weeks.
|
|
Duration of Response
기간: From start date of response to first disease progression, up to 71 weeks.
|
Number of weeks from the time at which measurement criteria are met for Complete Response (CR) or Partial Response (PR) (whichever status is recorded first) until the first date on which recurrence or progressive disease (PD) is objectively documented, taking as reference for PD the smallest measurements recorded since the treatment started, for responders only, per Response Evaluation Criteria In Solid Tumors Criteria (RECIST) v.1.0:
CR, disappearance of all target lesions; PR, >=30% decrease in the sum of the longest diameter of target lesions; and Non-PD for non-target lesions, and no new lesions.
|
From start date of response to first disease progression, up to 71 weeks.
|
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)
2008년 10월 1일
기본 완료 (실제)
2011년 1월 1일
연구 완료 (실제)
2011년 1월 1일
연구 등록 날짜
최초 제출
2008년 10월 7일
QC 기준을 충족하는 최초 제출
2008년 10월 7일
처음 게시됨 (추정)
2008년 10월 8일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2018년 11월 19일
QC 기준을 충족하는 마지막 업데이트 제출
2018년 4월 24일
마지막으로 확인됨
2018년 4월 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. .