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Study of Lenvatinib in Combination With Everolimus in Participants With Unresectable Advanced or Metastatic Renal Cell Carcinoma (RCC)

2019년 3월 7일 업데이트: Eisai Co., Ltd.

Phase 1 Study of Lenvatinib in Combination With Everolimus in Subjects With Unresectable Advanced or Metastatic RCC

Phase 1 study to investigate the tolerability and safety of lenvatinib in combination with Everolimus in participants with unresectable advanced or metastatic RCC.

연구 개요

연구 유형

중재적

등록 (실제)

7

단계

  • 1단계

연락처 및 위치

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

연구 장소

      • Chiba, 일본
        • Eisai Trial Site #1
      • Tokyo, 일본
        • Eisai Trial Site #2
      • Tokyo, 일본
        • Eisai Trial Site #1

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:

  1. Voluntary agreement to provide written informed consent of this study.
  2. Willing and able to comply with all aspects of the protocol after being fully informed of the content.
  3. Males or females aged greater than or equal to 20 years at the time of informed consent.
  4. Histological or cytological confirmation of RCC.
  5. Participants must have confirmed diagnosis of unresectable advanced and/or metastatic RCC.
  6. Disease progression following vascular endothelial growth factor (VEGF) targeted therapy.
  7. Eastern Cooperative Oncology Group Performance Status (ECOG-PS) of 0 to 1.
  8. Adequately controlled blood pressure with or without the use of antihypertensive agents.
  9. Participants with adequate function of major organs.
  10. Adequate blood coagulation function, defined as international normalized ratio (INR) less than or equal to 1.5.
  11. Survival expectation of 3 months or longer after study enrollment.
  12. Participants with adequate washout period from the end of prior treatment to the start of study drug administration.
  13. Females of childbearing potential must not have had unprotected sexual intercourse within 28 days before participant registration and must agree to use a highly effective method of contraception throughout the entire study period and for 30 days after final administration of investigational drug. If currently abstinent, the participant must agree to use a double-barrier method as described above if she becomes sexually active during this study period or for 30 days after investigational drug discontinuation. Females who are using hormonal contraceptives must have been on a stable dose of the same hormonal contraceptive product for at least 4 weeks before administration and must continue to use the same contraceptive during this study and for 30 days after investigational drug discontinuation.
  14. Male participants and their female partners must meet the criteria above.

Exclusion Criteria:

  1. Participants with central nervous system (CNS) metastases are not eligible, unless they have completed local therapy and have discontinued the use of corticosteroids for this indication for at least 4 weeks before starting treatment in this study. Any signs (example, radiologic) or symptoms of brain metastases must be stable for at least 4 weeks before starting study treatment.
  2. Prior exposure to lenvatinib.
  3. Participants who have not recovered from toxicities to less than or equal to Grade 1 as a result of prior anticancer therapy, except alopecia.
  4. Major surgery within 3 weeks prior to the first dose of lenvatinib.
  5. Participants with a urine protein greater than or equal to 1 gram per 24 hours (g/24 hours).
  6. Uncontrollable diabetes as defined by fasting glucose greater than 1.5* upper limit of normal (ULN).
  7. Fasting total cholesterol greater than 7.75 millimole per liter (mmol/L) (greater than 300 milligram per decilitre [mg/dL]).
  8. Fasting triglycerides greater than 2.5 * ULN.
  9. Any condition that might affect the absorption of lenvatinib and/or everolimus.
  10. Significant cardiovascular impairment.
  11. Bleeding or thrombotic disorders or use of anticoagulants requiring therapeutic INR monitoring.
  12. Active hemoptysis.
  13. Active infections that require systemic treatment.
  14. Human immunodeficiency virus (HIV) positive.
  15. Hepatitis B virus (HBV).
  16. A history of interstitial pneumonia with clinical manifestation or as confirmed by means of diagnostic imaging.
  17. Medical need for the continued use of potent or moderate inhibitors of cytochrome P450 3A (CYP3A) or P-gp, or potent or moderate inducer of CYP3A.
  18. Known intolerance to lenvatinib (or any of the excipients) or known hypersensitivity to everolimus (or any of the excipients) or rapmycins (sirolimus, temsirolimus and so on).
  19. Alcohol or drug dependency or abuse, inability to comply with every aspects of the study protocol, or any physical or mental conditions that in the opinion of the investigators would preclude the participant's participation in the study.
  20. Females who are pregnant or breastfeeding (not eligible even she discontinues breastfeeding).
  21. Any medical or other condition which, in the opinion of the investigator, would preclude participation in a clinical trial.

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: Lenvatinib plus Everolimus
다른 이름들:
  • 렌바티닙과 에베로리무스를 1일 1회 경구 투여

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Number of Participants Who Experienced Any Dose Limiting Toxicity (DLT)
기간: From first dose of study drug up to Cycle 1 Day 28 (Cycle length=28 days)
DLT was defined as toxicity related to the combination therapy and was graded according to Common Terminology Criteria for Adverse Events version 4.03 (CTCAE v4.03).
From first dose of study drug up to Cycle 1 Day 28 (Cycle length=28 days)
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
기간: Baseline up to 30 days after the last dose of study drug (up to approximately 21.5 months)
Baseline up to 30 days after the last dose of study drug (up to approximately 21.5 months)

2차 결과 측정

결과 측정
측정값 설명
기간
Cmax: Maximum Observed Plasma Concentration for Levatinib and Everolimus
기간: Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Css,Max: Maximum Observed Plasma Concentration at Steady State for Levatinib and Everolimus
기간: Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Levatinib and Everolimus
기간: Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Tss,Max: Time to Reach the Maximum Plasma Concentration (Cmax) at Steady State for Levatinib and Everolimus
기간: Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
AUC 0-t: Area Under the Concentration-time Curve From Zero (Pre-dose) to Time of Last Quantifiable Concentration for Levatinib and Everolimus
기간: Cycle 1 Day 1 and Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 1 and Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Number of Participants With Best Overall Response (BOR)
기간: From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
BOR included complete response (CR), partial response (PR), stable disease (SD), and PD (progressive disease). BOR was assessed using Response Evaluation Criteria in Solid Tumor (RECIST) 1.1
From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
Objective Response Rate (ORR)
기간: From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
ORR was defined as the percentage of participants who achieved BOR of CR or PR. ORR was assessed using RECIST 1.1.
From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
Disease Control Rate (DCR)
기간: From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
DCR was defined as the percentage of participants who achieved BOR of CR, PR, or SD. DCR was assessed based on RECIST 1.1.
From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
Number of Participants With the Minimum Percent Change From Baseline in the Sum of Diameters of Target Lesions
기간: Baseline up to first tumor assessment at which diameter of target lesions were available (up to approximately 23 months)
Baseline up to first tumor assessment at which diameter of target lesions were available (up to approximately 23 months)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

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 7월 1일

기본 완료 (실제)

2017년 5월 29일

연구 완료 (실제)

2017년 5월 29일

연구 등록 날짜

최초 제출

2015년 5월 22일

QC 기준을 충족하는 최초 제출

2015년 5월 22일

처음 게시됨 (추정)

2015년 5월 27일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2019년 3월 19일

QC 기준을 충족하는 마지막 업데이트 제출

2019년 3월 7일

마지막으로 확인됨

2018년 9월 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. .

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