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A Study of KX2-391 With Paclitaxel in Patients With Solid Tumors

2015년 5월 15일 업데이트: Hanmi Pharmaceutical Company Limited

An Open-label Phase I/II Study of KX2-391 in Combination With Paclitaxel in Patients With Advanced Solid Tumors

The primary objective of this study is to determine the maximum tolerated dose (MTD) of KX2-391 in Combination with paclitaxel in Phase I, and to evaluate the efficacy of KX2-391 in combination with paclitaxel in patients who are diagnosed as gastric and breast cancer, respectively in Phase II.

연구 개요

연구 유형

중재적

등록 (예상)

60

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • Seoul, 대한민국, 110-744
        • 모병
        • Seoul National University Hospital
        • 연락하다:
          • Eunkyung Kim
          • 전화번호: +82-2-2072-7616
    • Gyeonggi-Do
      • Seongnam, Gyeonggi-Do, 대한민국, 463-707
        • 모병
        • Seoul National University Bundang Hospital
        • 연락하다:
          • Yun Jin Kim
          • 전화번호: +82-31-787-1421

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:

Phase I Portion:

- Diagnosis of solid tumors on histopathological examination or cytological examination for which no standard of care is available or conventional treatment modalities have no therapeutic effect at the time of entering into the study

Phase II Portion:

  • Diagnosis of advanced/metastatic/recurrent stomach cancer or breast cancer on histopathological examination or cytological examination for which no standard of care is available or conventional treatment modalities have no therapeutic effect at the time of entering into the study
  • Subjects with stomach cancer without prior taxane therapy
  • Subjects with breast cancer with prior taxane therapy
  • (Optional) Providing exploratory biomarker informed consent form to obtain archival tumor tissue and/or new tumor biopsy sample

Common:

  1. Based on clinical screening,

    ① If radiotherapy was given, at least 4 weeks should have passed from the last treatment date and the patient should have recovered from the toxicity (However, for limited regional radiotherapy, at least 2 weeks from the last treatment date)

    ② If hormonal therapy was given, at least 2 weeks should have passed from the last treatment date and the patient should have recovered from the toxicity.

    ③ If chemotherapy was given, at least 3 weeks should have passed from the last treatment date and the patient should have recovered from the toxicity (However, for nitrosourea or mitomycin, at least 6 weeks)

  2. Aged ≥ 20 years
  3. ECOG (Eastern Cooperative Oncology Group) ≤ 2
  4. Life expectancy ≥ 12 weeks
  5. Should meet the followings,

    ① Bone marrow function ANC (Absolute Neutrophil Count) ≥ 1.5 X 109/L, PLT (Platelet Count) ≥ 100 X 109/L, Hemoglobin ≥ 9.0 g/dl (In the case of hemoglobin of < 9.0 g/dl, the patient can be enrolled if the value is reversed to ≥ 9.0 g/dl.)

    ② Kidney function Creatinine Clearance > 50 ml/min or Serum Clearance ≤ 1.5 mg/dl

    ③ Liver function AST (Aspartate Aminotransferase)/ALT (Alanine Aminotransferase)/ALP (Alkaline Phosphatase) ≤ 3.0 X UNL and Total bilirubin ≤ 2.0 mg/dl (With bone metastasis, ALP ≤ 5.0 X UNL)

  6. At least one measurable lesions with the length of the longest diameter of ≥ 10 mm on spiral CT or multidetector CT or ≥ 20 mm on conventional CT
  7. Subjects who voluntarily consent to participate in this study and sign the written informed consent form

Exclusion Criteria:

  1. Uncontrolled central nervous system metastasis
  2. Malignant ascites requiring surgical treatment
  3. Subjects who have blood malignancies including leukemia; or who have received or will receive bone marrow transplantation
  4. Severe concurrent diseases as follows,

    ① History of unstable angina, heart failure, atrial or ventricular arrhythmia requiring pharmacological treatment, or having received treatment for myocardial infarction within 6 months (however, may be included under the judgment of the investigator if medically controlled), heart failure of Class III or IV by New York Heart Association Classes, or left ventricular ejection fraction of < 40%

    ② Receiving therapeutic dose administration of coumarin-type anticoagulants (however, up to 2 mg daily is permitted for line opening)

    ③ Uncontrolled diabetes (fasting plasma glucose > 2.0 X UNL), severe hypertension, thyroid disorder and active infectious disease

    ④ Psychiatric or neurological history including dementia or epilepsy which may threaten the compliance with this protocol

    ⑤ A condition not allowing oral application of tablet formulation, and any clinically significant gastrointestinal abnormalities which may interfere with taking, passing or absorption of the study drug

  5. Using disallowed concomitant medications (strong CYP3A4 (Cytochrome P450 3A4) inhibitors or inducers) (When a patient is using any of the disallowed concomitant medications below, wash-out of 1 week from the medication date is required)
  6. Received other investigational product within 4 weeks prior to the administration of this study drug
  7. Pregnant or breast-feeding women (however, women with 12 months of natural (spontaneous) amenorrhea or surgical bilateral oophorectomy (alone or with hysterectomy) at least 6 weeks ago, with appropriate clinical profile (e.g., appropriate age, history of vasomotor symptoms), will be considered women postmenopausal and of non-childbearing potential. In the case of oophorectomy alone, a woman will be considered to be of non-childbearing potential only if her reproductive condition is confirmed by follow-up hormone level assessment)
  8. History of hypersensitivity to paclitaxel, compounds with similar chemical structure, or cremophor (polyoxyethylated castor oil) ingredient
  9. Neuropathy of grade ≥ 3 based on clinical screening
  10. Known history of hepatitis B or C and known history of HIV serum positive
  11. Others unable to participate in the study under the judgment of the investigator

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: KX2-391 and Paclitaxel

The phase I portion is a standard, three-patient per cohort, dose escalation schedule will be used. 3 or 6 subjects with solid tumor per dose group will likely be necessary to determine the MTD of KX2-391 in combination with weekly paclitaxel. With paclitaxel dose fixed at 80 mg/m2/weekly, KX2-391 treatment will be started at 20 mg dose once daily (QD)

The phase II portion of this trial has a design to determine the efficacy of KX2-391 when administered in combination with paclitaxel in 20 subjects with stomach cancer and 20 subjects with breast cancer

A treatment cycle in phase I will consist of 28 days, according to the following schedule:

KX2-391 20 mg PO once daily, Weekly paclitaxel 80 mg/m2 given intravenously over 1 hour on day 1, 8, and 15 of a 28 day cycle.

The trial will initially test the combination of weekly paclitaxel and KX2-391 given PO, once daily , continuously. In case of 2 dose-limiting toxicities (DLT) in the first cohort, this intervention will be terminated

A treatment cycle in phase II will consist of 28 days, according to the following schedule:

KX2-391 MTD PO once daily, Weekly paclitaxel 80 mg/m2 given intravenously over 1 hour on day 1, 8, and 15 of a 28 day cycle.

다른 이름들:
  • 탁솔
  • KX01

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Dose-limiting Toxicities (DLTs) in Phase I Portion
기간: From start of the treatment to end of cycle 1, which are 4 weeks
Maximum tolerated dose (MTD) of KX2-391 in combination with weekly paclitaxel as determined by number of participants With DLTs related to KX2-391 in combination with weekly paclitaxel
From start of the treatment to end of cycle 1, which are 4 weeks
Tumor Overall Response Rates (ORRs) in Phase II Portion
기간: In every 2 cycles up to end of the treatment, an expected average of 16 weeks
The efficacy (overall response rate; ORR; complete response (CR) + partial response (PR)) of KX2-391 in combination with weekly paclitaxel at the MTD established during the phase I portion of this trial based on Response Evaluation Criteria in Solid Tumor (RECIST) 1.1
In every 2 cycles up to end of the treatment, an expected average of 16 weeks

2차 결과 측정

결과 측정
측정값 설명
기간
Pharmacokinetic (PK) Evaluation in Phase I Portion
기간: Time points at day 0, 1 and 8 in cycle 1
PK parameters, including but not limited to, plasma concentration, AUC (Area Under Curve) 0-t, Cmax, Tmax, and T1/2 of KX2-391 alone and in combination with weekly paclitaxel
Time points at day 0, 1 and 8 in cycle 1
The Preliminary Efficacy Data in Phase I Portion
기간: In every 2 cycles up to end of the treatment, an expected average of 8 weeks
The preliminary efficacy of KX2-391 in combination with weekly paclitaxel as determined by ORRs based on RECIST 1.1
In every 2 cycles up to end of the treatment, an expected average of 8 weeks
Safety in Phase II Portion
기간: From start of the treatment to end of the treatment, an expected average of 16 weeks
Adverse events and their frequency, duration and severity, physical examination, laboratory parameters, vital signs and ECG change monitoring as determined based on CTCAE (Common Toxicity Criteria for Adverse Effects) 4.03
From start of the treatment to end of the treatment, an expected average of 16 weeks
The Efficacy Data in Phase II Portion
기간: Up to die, an expected average of 24 weeks
Overall survival (OS), progression free survival (PFS), time to tumor progression (TTP) and duration of response
Up to die, an expected average of 24 weeks
Pharmacokinetic (PK) Evaluation in Phase II Portion
기간: Time points at day 1 and 8 in cycle 1
PK parameters, including but not limited to, plasma concentration, AUC0-t, Cmax, Tmax, and T1/2 of KX2-391 alone and in combination with weekly paclitaxel
Time points at day 1 and 8 in cycle 1

기타 결과 측정

결과 측정
측정값 설명
기간
Pharmacodynamic (PD) Evaluation in Phase I Portion
기간: Time points at day 0 and 1 in cycle 1
Pre-dose and post-dose tubulin inhibition in peripheral blood monocytes extracted from blood samples, as measured by immunofluorescence staining
Time points at day 0 and 1 in cycle 1
Exploratory Biomarker Evaluation in Phase II Portion
기간: Time points at day -6 and day 0
Pre-dose and post-dose Src signaling inhibition (p-Src and Ki-67) in archival tumor tissue and new biopsy sample, as measured by immunohistochemistry
Time points at day -6 and day 0

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Seock-Ah Im, M.D., Ph.D., Seoul National University Hospital

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

2012년 12월 1일

기본 완료 (예상)

2015년 12월 1일

연구 완료 (예상)

2016년 5월 1일

연구 등록 날짜

최초 제출

2013년 1월 2일

QC 기준을 충족하는 최초 제출

2013년 1월 7일

처음 게시됨 (추정)

2013년 1월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2015년 5월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2015년 5월 15일

마지막으로 확인됨

2014년 3월 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. .

유방암에 대한 임상 시험

KX2-391 and Paclitaxel에 대한 임상 시험

구독하다