이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

An Absorption, Distribution, Metabolism and Excretion (ADME) Study of Single Oral Dose [14C] GSK2118436 in Subjects With BRAF Mutant Solid Tumors

2017년 11월 8일 업데이트: GlaxoSmithKline

An Open-Label Study to Characterize the Absorption, Distribution, Metabolism and Elimination of a Single Oral 14C Labeled Dose of GSK2118436 in Subjects With BRAF Mutant Solid Tumors

The study is a Phase 1, open-label study designed to characterize the absorption, distribution, metabolism and excretion of GSK2118436 following administration of a single oral 14C labeled dose of GSK2118436 as a suspension in subjects with BRAF mutation positive tumors.

연구 개요

상태

완전한

정황

개입 / 치료

상세 설명

GSK2118436 is an orally administered, potent and selective small molecule BRAF inhibitor that is being developed for the treatment of BRAF mutation-positive tumors. The study is a Phase 1, open-label study designed to characterize the absorption, distribution, metabolism and excretion of GSK2118436 following administration of a single oral 14C labeled dose of GSK2118436 as a suspension in subjects with BRAF mutation positive tumors. A sufficient number of subjects will be enrolled to complete approximately four subjects. Following completion of the study, subjects may continue dosing with GSK2118436 in the rollover study, BRF114144.

연구 유형

중재적

등록 (실제)

4

단계

  • 1단계

연락처 및 위치

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

연구 장소

    • Washington
      • Tacoma, Washington, 미국, 98418
        • GSK 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:

  • Male or female at least 18 years of age at the time of signing the informed consent form;
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form;
  • Body weight >= 45 kg and a body mass index (BMI) >/= 19 kg/m2 and </= 35 kg/m2 (inclusive);
  • Able to swallow and retain oral medication;
  • BRAF mutation-positive tumor (V600 E/K mutation) as determined via relevant genetic testing;
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 [Oken, 1982]; NOTE: Subjects with an ECOG performance status of 2 may be eligible with the approval of the GSK Medical Monitor
  • Women of child-bearing potential and men with reproductive potential must be willing to practice acceptable methods of birth control. Additionally, women of childbearing potential must have a negative serum pregnancy test within 14 days prior to the first dose of study treatment;
  • Must have adequate organ function as defined by the following values:
  • Absolute neutrophil count (ANC) >/=1.2 x 10^9/L
  • Hemoglobin >/=9 g/dL
  • Platelets >/=100 x 10^9/L
  • Serum bilirubin </=1.5 x upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) </= 2.5 x ULN; <5 x ULN if liver metastases are present (with approval of GSK medical monitor)
  • Serum creatinine </= ULN or calculated creatinine clearance >/= 60 mL/min
  • Prothrombin time (PT)/International normalized ratio (INR) and partial thromboplastin time (PTT) </=1.3 x ULN
  • Left ventricular ejection fraction </= institutional lower limit of normal by ECHO

Exclusion Criteria:

  • Currently receiving cancer therapy (e.g., chemotherapy with delayed toxicity, extensive radiation therapy, immunotherapy, biologic therapy, or major surgery) within the last three weeks; chemotherapy regimens without delayed toxicity within the last two weeks; or use of an investigational anti-cancer drug within four weeks preceding the first dose of GSK2118436;
  • Current use of a prohibited medication or requires any of these medications during the study;
  • Consumption of red wine, Seville oranges, grapefruit or grapefruit juice from seven days prior to the first dose of study medication;
  • Current use of therapeutic warfarin (note: low molecular weight heparin and prophylactic low-dose warfarin are permitted);
  • History of sensitivity to heparin or heparin-induced thrombocytopenia;
  • The radiation exposure from the previous three year period is over 10 millisieverts (mSv) for subjects who have been exposed to ionizing radiation above background as a result of their work with radiation as Category A (classified) workers or as a result of research studies they may have been involved in. Subjects will be excluded if exposure levels cannot be verified. Clinical (therapeutic or diagnostic) exposure will not be included;
  • An occupation which requires monitoring for radiation exposure, nuclear medicine procedures or excessive x-rays within the past 12 months;
  • Any major surgery within the last four weeks;
  • Unresolved toxicity equal to or greater than National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0 (NCI CTCAE v4.0) [NCI, 2009] Grade 2 from previous anti-cancer therapy except alopecia;
  • Presence of active gastrointestinal disease or other condition (e.g., gastrectomy, bariatric surgery, small bowel or large bowel resection) that may interfere significantly with the absorption of drugs. If clarification is needed as to whether a condition will significantly affect absorption of drugs, contact the GSK medical monitor for permission to enroll the subject;
  • A history of known Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV) infection (subjects with laboratory evidence HBV clearance may be enrolled with permission of the GSK medical monitor);
  • Patients with a history of malignancy that have been definitively treated can be enrolled with approval of the GSK medical monitor;
  • Subjects with brain metastases are excluded if their brain metastases are either:

Symptomatic Treated (surgery, radiation therapy) but not clinically and radiographically stable one month after local therapy, or Asymptomatic and untreated but > 1 cm in the longest dimension Patients with small (</= 1 cm in the longest dimension), asymptomatic brain metastases that do not need immediate local therapy can be enrolled with the approval of the GSK medical monitor. Subjects on a stable dose of corticosteroids for more than one month, or those who have been off corticosteroids for at least two weeks can be enrolled with approval of the GSK medical monitor. Subjects must also be off of enzyme-inducing anticonvulsants for more than four weeks;

  • History of alcohol or drug abuse within six months prior to screening;
  • Corrected QT (QTc) interval >/= 480 msecs;
  • History of acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting within the past 24 weeks;
  • Class II, III, or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system; abnormal cardiac valve morphology documented by echocardiogram (subjects with minimal abnormalities [ie, mild regurgitation/stenosis] can be entered on study with approval from the GSK medical monitor); or history of known cardiac arrhythmias (except sinus arrhythmias) within the past 24 weeks;
  • Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study drugs, or excipients (note: to date there are no known drugs chemically related to GSK2118436 which are approved by the Food and Drug Administration);
  • Uncontrolled medical conditions (e.g., diabetes mellitus, hypertension), psychological, familial, sociological, or geographical conditions that do not permit compliance with the protocol; or unwillingness or inability to follow the procedures required in the protocol;
  • Subjects with known glucose 6 phosphate dehydrogenase (G6PD) deficiency;
  • The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, five half-lives or twice the duration of the biological effect of the investigational product (whichever is longer);
  • Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period;
  • Pregnant females as determined by positive pregnancy test at screening or prior to dosing;
  • Lactating females who are actively breast feeding;
  • Subject is mentally or legally incapacitated;

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: Study Medication
GSK2118436 suspension
A single oral dose of 95 mg of GSK2118436 containing approximately 80 µCi of radioactivity

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
• Excretion of radioactivity in urine following oral administration of [14C]GSK2118436
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Excretion of radioactivity in feces following oral administration of [14C]GSK2118436
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.

2차 결과 측정

결과 측정
기간
• Quantity of GSK2118436 metabolites in plasma
기간: Pre-dose, and up to 48 hours post dose.
Pre-dose, and up to 48 hours post dose.
• Potential covalent binding of drug-related material to plasma proteins
기간: Pre-dose, and up to 48 hours post dose.
Pre-dose, and up to 48 hours post dose.
• Blood total radioactivity
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Blood:plasma ratio of total drug-related material (radioactivity)
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Area under the plasma-concentration time curve (AUC) of plasma GSK2118436 and metabolites
기간: Pre-dose, and up to 48 hours post dose.
Pre-dose, and up to 48 hours post dose.
• Number of subjects with adverse events as a measure of safety and tolerability
기간: From date of dosing until transition to rollover protocol BRF114144 (approximately 4 - 11 days) or study follow up visit if subject does not transition to BRF114144 (approximately 14 - 21 days)
From date of dosing until transition to rollover protocol BRF114144 (approximately 4 - 11 days) or study follow up visit if subject does not transition to BRF114144 (approximately 14 - 21 days)
• Quantity of GSK2118436 metabolites in feces
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Quantity of GSK2118436 metabolites in urine
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Character of GSK2118436 metabolites in plasma
기간: Pre-dose, and up to 48 hours post dose.
Pre-dose, and up to 48 hours post dose.
• Character of GSK2118436 metabolites in feces
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Character of GSK2118436 metabolites in urine
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Plasma total radioactivity
기간: Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
Pre-dose, and post-dose for a minimum of 96 hours, and a maximum of 240 hours after dosing.
• Maximum plasma concentration (Cmax) of plasma GSK2118436 and metabolites
기간: Pre-dose, and up to 48 hours post dose
Pre-dose, and up to 48 hours post dose
• Time to Cmax (Tmax) of plasma GSK2118436 and metabolites
기간: Pre-dose, and up to 48 hours post dose
Pre-dose, and up to 48 hours post dose
• Terminal half-life (t1/2) of plasma GSK2118436 and metabolites
기간: Pre-dose, and up to 48 hours post dose.
Pre-dose, and up to 48 hours post dose.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 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)

2011년 1월 26일

기본 완료 (실제)

2011년 4월 8일

연구 완료 (실제)

2011년 4월 8일

연구 등록 날짜

최초 제출

2010년 12월 2일

QC 기준을 충족하는 최초 제출

2010년 12월 16일

처음 게시됨 (추정)

2010년 12월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 11월 13일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 11월 8일

마지막으로 확인됨

2017년 11월 1일

추가 정보

이 연구와 관련된 용어

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. .

암에 대한 임상 시험

GSK2118436에 대한 임상 시험

구독하다