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A Study of Ramucirumab in Participants With Metastatic Renal Cell Carcinoma

2014년 5월 16일 업데이트: Eli Lilly and Company

Phase II Single Arm Study of IMC-1121B in Patients With Metastatic Renal Cell Carcinoma With Disease Progression on or Intolerance to Tyrosine Kinase Inhibitor Therapy

The purpose of this study is to determine whether ramucirumab is effective treatment in participants with metastatic renal cell carcinoma who have developed progressive disease or become intolerant to tyrosine kinase inhibitor therapy.

연구 개요

상태

완전한

상세 설명

The Primary objective is to determine the best objective response rate (ORR) of ramucirumab when administered to participants with metastatic renal cell carcinoma (RCC) whose disease has progressed during therapy with a tyrosine kinase inhibitor (TKI, sunitinib and/or sorafenib) or who have developed intolerance to these agents.

연구 유형

중재적

등록 (실제)

39

단계

  • 2 단계

연락처 및 위치

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

연구 장소

    • California
      • San Francisco, California, 미국, 94115
        • ImClone Investigational Site
    • Illinois
      • Chicago, Illinois, 미국, 60637
        • ImClone Investigational Site
    • Louisiana
      • Metairie, Louisiana, 미국, 70006
        • ImClone Investigational Site
    • Massachusetts
      • Boston, Massachusetts, 미국, 02115
        • ImClone Investigational Site
    • New Jersey
      • Flemington, New Jersey, 미국, 08822
        • ImClone Investigational Site
    • New York
      • Buffalo, New York, 미국, 14263
        • ImClone Investigational Site
    • Ohio
      • Cleveland, Ohio, 미국, 44195
        • ImClone Investigational Site
    • Pennsylvania
      • Drexel Hill, Pennsylvania, 미국, 19026
        • ImClone Investigational Site
      • Philadelphia, Pennsylvania, 미국, 19111
        • ImClone Investigational Site
    • Texas
      • Arlington, Texas, 미국, 76012
        • ImClone Investigational Site
    • Washington
      • Seattle, Washington, 미국, 98109
        • ImClone 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

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • The participant has histologically or cytologically confirmed clear cell RCC
  • The participant is ≥ 18 years of age
  • The participant has an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-1 or Karnofsky Performance Status (KPS) ≥ 80%
  • The participant has had a prior nephrectomy (as therapy for RCC)
  • The participant has metastatic RCC
  • The participant has a life expectancy of > 3 months
  • The participant has measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST)
  • The participant has received prior therapy with a TKI (sunitinib and/or sorafenib) with either disease progression on TKI therapy (progression within 60 days of the last dose of TKI) or intolerance to TKI (unable to continue therapy because of side-effects). A participant with progression during a protracted treatment break is not eligible unless the participant has had progression or intolerance as defined above
  • The participant has resolution of all clinically significant toxic effects of prior cancer therapy to grade ≤ 1 by the National Cancer Institute Common Terminology Criteria for Adverse Events, version 3.0 (NCI-CTCAE)
  • The participant has adequate hematological functions [absolute neutrophil count (ANC) ≥ 1500 cells per milliliter (cells/mL), hemoglobin ≥ 9 grams per deciliter (g/dL) and platelets ≥ 100,000 cells/mL]
  • The participant has adequate hepatic function [bilirubin within normal limits (WNL), aspartate transaminase (AST) and/or alanine transaminase (ALT) ≤ 2.5 times the upper limit of normal (ULN), or ≤ 5.0 times the ULN if the transaminase elevation is due to liver metastases]
  • The participant has normal renal function or mild renal dysfunction [creatinine ≤ 2.2 milligrams per deciliter (mg/dL)]
  • The participant's urinary protein ≤ 1+ on dipstick or routine urinalysis [(UA); if urine dipstick or routine analysis is ≥ 2+, a 24-hour urine for protein must demonstrate < 1000 (milligrams) mg of protein in 24 hours to allow participation in the study]
  • The participant must have adequate coagulation function as defined by International Normalized Ratio (INR) ≤ 1.8 and a partial thromboplastin time (PTT) ≤ 1.5 X ULN. Participants on full-dose anticoagulation must be on a stable dose of oral anticoagulant or low molecular weight (LMW) heparin and if on warfarin must have a INR between 2 and 3 and have no active bleeding or pathological condition that carries a high risk of bleeding (for example, tumor involving major vessels or known varices)
  • The participant is able to provide informed written consent
  • The participant , if sexually active, is postmenopausal (last menstrual period > 2 years prior to study), surgically sterile, or is using effective method of contraception in the opinion of the investigator
  • The participant , if female, must have a negative serum pregnancy test upon entry into this study
  • The participant has a normal thyroid stimulating hormone (TSH) value. Participants with an abnormal TSH may be eligible provided they meet all other eligibility criteria and have ECOG performance status 0-1. Participants with an abnormal TSH value require a full thyroid evaluation prior to enrollment. Endocrinology consultation may be performed at the discretion of the investigator
  • The participant has serum calcium within normal limits

Exclusion Criteria:

  • The participant has received prior treatment with bevacizumab
  • The participant has known brain or leptomeningeal metastases
  • The participant has received >2 prior cytotoxic chemotherapy regimens for RCC
  • The participant has received antitumor therapy (biologic agents, major surgery, or investigational agent) within 28 days prior to enrollment on study. The participant has received radiation therapy within 14 days prior to enrollment on study. Participants with metastasis in weight bearing bones at high risk for pathologic fracture may participate provided that appropriate surgical intervention and/or radiation therapy is undertaken and completed at least 28 days prior to enrollment
  • The participant has received > 1 prior bio-immunotherapy regimens (defined as either interleukin-2 or interferon alpha given as monotherapy, concurrently, or sequentially as planned)
  • The participant has a concurrent active malignancy other than adequately treated non-melanomatous skin cancer or other non-invasive carcinoma or in situ neoplasm. A participant with previous history of malignancy is eligible, provided that he/she has been disease free for > 3 years
  • The participant has a nonhealing wound or ulcer
  • The participant has a known alcohol or drug dependency
  • The participant is pregnant or breastfeeding
  • The participant has a coexisting medical or psychiatric problem of sufficient severity to limit compliance with the study and/or increase the risks associated with study participation or study drug administration or interfere with the interpretation of study results
  • The participant has an ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, symptomatic or poorly controlled cardiac arrhythmia, psychiatric illness/social situations, or any other serious uncontrolled medical disorders in the opinion of the investigator
  • The participant has known human immunodeficiency virus infection or acquired immunodeficiency syndrome-related illness

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: Ramucirumab
Intravenous infusion at 8 milligrams per kilogram (mg/kg) on day 1 of every 14-day cycle.
Ramucirumab is an injectable solution administered as an intravenous infusion over 1 hour at a dose of 8 mg/kg day 1 of every 14-day cycle.
다른 이름들:
  • LY3009806
  • IMC-1121B

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Percentage of Participants With Objective Response (Objective Response Rate)
기간: First dose to date of objective progressive disease or death due to any cause (up to 34 months)
The percentage of participants with a best overall response of confirmed complete response (CR) or partial response (PR) as classified according to Response Evaluation Criteria In Solid Tumors (RECIST, version 1.0) criteria. CR is the disappearance of all target and non-target lesions and normalization of tumor marker levels. PR is having at least a 30% decrease in the sum of the longest diameter of target lesions without new lesions and progression of non-target lesions. The percentage of participants with objective response=(number of participants whose best overall response during therapy is CR or PR/number of participants treated)*100.
First dose to date of objective progressive disease or death due to any cause (up to 34 months)

2차 결과 측정

결과 측정
측정값 설명
기간
Progression-Free Survival
기간: First dose to measured progressive disease or death due to any cause (up to 34 months)
Progression-free survival (PFS) is measured from the date of the first dose to the first documented date of disease progression as classified according to Response Evaluation Criteria In Solid Tumors (RECIST, version 1.0) criteria or death from any cause. Disease progression is having at least a 20% increase in the sum of the longest diameter of target lesions and/or unequivocal progression of a non-target lesion and/or detection of a new lesion. Data for participants whose disease does not progress or for whom no post-baseline assessment is made are censored at the day of their last tumor assessment. Data for participants whose disease does not progress who are subsequently lost to follow-up are also censored at the day of their last tumor assessment.
First dose to measured progressive disease or death due to any cause (up to 34 months)
Percentage of Participants Showing Disease Control at Week 12
기간: Week 12 [Cycle 6 (1 cycle=14 days)]
Participants who were alive and did not experience disease progression were considered to have disease control at 12 weeks. Disease control was based on lack of disease progression using Response Evaluation Criteria In Solid Tumors (RECIST, version 1.0) criteria. According to RECIST criteria, disease progression was having at least a 20% increase in the sum of the longest diameter of target lesions and/or unequivocal progression of non-target lesion and/or detection of new lesion. Participants whose disease progression was symptomatic were not considered to have disease control. The percentage of participants showing disease control=(number of participants who did not have disease or symptomatic progression at Week 12/number of participants treated)*100.
Week 12 [Cycle 6 (1 cycle=14 days)]
Percentage of Participants With Objective Response (Objective Response Rate) at 12 Weeks
기간: Week 12 [Cycle 6 (1 cycle=14 days)]
The percentage of participants with a confirmed best overall response of complete response (CR) or partial response (PR) at Week 12, as classified according to Response Evaluation Criteria In Solid Tumors (RECIST, version 1.0) criteria. CR is the disappearance of all target and non-target lesions and the normalization of tumor marker levels. PR is having at least a 30% decrease in the sum of the longest diameter of target lesions without new lesions and progression of non-target lesions. The percentage of participants with objective response=(number of participants whose best overall response achieved at 12 weeks was CR or PR/number of participants treated)*100.
Week 12 [Cycle 6 (1 cycle=14 days)]
Median Duration of Overall Response
기간: Time of first response (CR or PR) to disease progression, initiation of other (or additional) antitumor therapy, or death due to any cause (up to 34 months)
Duration of response is the interval from the date of initial documented response [confirmed complete response (CR) or partial response (PR)] to the first documented date of disease progression as classified according to Response Evaluation Criteria In Solid Tumors (RECIST version 1.0) criteria, or initiation of other (or additional) antitumor therapy is first reported, or death due to any cause. CR is the disappearance of all target and non-target lesions and the normalization of tumor marker levels. PR is having at least a 30% decrease in the sum of the longest diameter of target lesions without new lesions and progression of non-target lesions. Disease progression is having at least a 20% increase in the sum of the longest diameter of target lesions and/or unequivocal progression of a non-target lesion and/or detection of a new lesion. Data from participants who did not relapse were censored on the day of their last tumor assessment.
Time of first response (CR or PR) to disease progression, initiation of other (or additional) antitumor therapy, or death due to any cause (up to 34 months)
Minimum Concentration (Cmin) of Ramucirumab
기간: Immediately prior to the Week 32 infusion treatment [Cycle 16 (1 cycle=14 days)]
Immediately prior to the Week 32 infusion treatment [Cycle 16 (1 cycle=14 days)]
Maximum Concentration (Cmax) of Ramucirumab
기간: 1 hour after the end of the Week 32 infusion treatment [Cycle 16 (1 cycle=14 days)]
1 hour after the end of the Week 32 infusion treatment [Cycle 16 (1 cycle=14 days)]
Summary Listing of Participants Reporting Drug-Related Treatment-Emergent Adverse Events
기간: First dose to study completion (up to 34 months) plus 30-day safety follow-up
Data presented are the number of participants who experienced treatment-emergent adverse events (TEAE), serious adverse events (SAE), Grade 3 or 4 TEAE, or adverse events (AE) leading to discontinuation of treatment that were considered to be related to ramucirumab. A summary of SAEs and other nonserious AEs, regardless of causality, is located in the Reported Adverse Events section.
First dose to study completion (up to 34 months) plus 30-day safety follow-up

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

2007년 11월 1일

기본 완료 (실제)

2011년 5월 1일

연구 완료 (실제)

2011년 5월 1일

연구 등록 날짜

최초 제출

2007년 8월 13일

QC 기준을 충족하는 최초 제출

2007년 8월 13일

처음 게시됨 (추정)

2007년 8월 14일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2014년 6월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2014년 5월 16일

마지막으로 확인됨

2014년 5월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 13921
  • I4T-IE-JVBP (기타 식별자: Eli Lilly and Company)
  • CP12-0605 (기타 식별자: ImClone Systems)

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. .

전이성 신장 세포 암종에 대한 임상 시험

Ramucirumab에 대한 임상 시험

구독하다