- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03294603
Radiolabeled Study of CC-220 in Healthy Male Subjects
2017년 10월 24일 업데이트: Celgene
A Phase 1, Single-center, Open-label Study to Evaluate the Metabolism and Excretion of (14C)-CC-220 in Healthy Male Subjects
This is a single-center, open-label study to characterize the biotransformation and excretion of [14C]-CC-220 in healthy male subjects.
Each subject will participate in screening, a treatment phase (including baseline), and a follow-up phone call.
Subjects will be screened for eligibility.
Subjects who have met all inclusion criteria and none of the exclusion criteria at screening will return to the study site on Day -1, and will be domiciled at the study site from Day -1 to Day 10.
On Day 1, subjects will receive a single oral dose of 1 mg [14C]-CC-220 under fasted conditions.
Blood, urine, and fecal samples will be collected throughout the study for pharmacokinetic (PK; inclusive of metabolite profiling / characterization), mass balance, and/or clinical laboratory assessments.
Safety will be monitored throughout the study.
Subjects will be discharged from the study site on Day 10 following completion of the scheduled study procedures and satisfactory safety review.
Subjects will participate in a follow-up phone call within 5 to 7 days following discharge.
연구 개요
연구 유형
중재적
등록 (실제)
6
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
-
-
Wisconsin
-
Madison, Wisconsin, 미국, 53704
- Covance Clinical Research Unit
-
-
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 (성인)
건강한 자원 봉사자를 받아들입니다
예
연구 대상 성별
남성
설명
Inclusion Criteria:
- Subject is ≥ 18 and ≤ 55 years of age at the time of signing the informed consent form (ICF).
- Subject is male.
- Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted.
- Subject is willing and able to adhere to the study visit schedule and other protocol requirements.
- Subject is in good health, as determined by the Investigator based on a physical examination at screening.
- Subject agrees to abide by the requirements and restrictions outlined in the CC-220 Pregnancy Prevention Plan for Subjects in Clinical Trials.
- Subject must agree to use a barrier method of birth control (condoms not made out of natural [animal] membrane [latex condoms are recommended]) during sexual contact with a pregnant female or a female of childbearing potential (FCBP)1 while participating in the study and for at least 90 days following administration of CC-220, even if he has undergone a successful vasectomy.
- Subject has a body mass index (BMI) ≥ 18 and ≤ 33 kg/m2 at screening.
- Subject has clinical laboratory safety test results that are within normal limits or considered not clinically significant by the Investigator. Platelet count, absolute neutrophil count (ANC), and absolute lymphocyte count (ALC) must be above the lower limit of normal at screening.
- Subject is afebrile, with supine systolic blood pressure (BP) ≥ 90 and ≤ 140 mmHg, supine diastolic BP ≥ 50 and ≤ 90 mmHg, and pulse rate ≥ 40 and ≤ 110 bpm at screening.
- Subject has a normal or clinically acceptable 12-lead electrocardiogram (ECG), with a QTcF value ≤ 430 msec, at screening.
Exclusion Criteria:
- Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study.
- Subject has any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he were to participate in the study.
- Subject has any condition that confounds the ability to interpret data from the study.
- Subject was exposed to an investigational drug (new chemical entity) within 30 days prior to dosing, or 5 half-lives of that investigational drug, if known (whichever is longer).
- Subject has used any prescribed systemic or topical medication (including but not limited to analgesics, anesthetics, etc) within 14 days or 5 half-lives of that medication, whichever is longer, prior to dosing.
- Subject has used any non-prescribed systemic or topical medication (including vitamin/mineral supplements and herbal medicines) within 7 days prior to dosing.
- Subject has used CYP3A inducers and/or inhibitors (including St. John's Wort) within 30 days prior to dosing. The Indiana University "Cytochrome P450 Drug Interaction Table" should be utilized to determine inducers and/or inhibitors of CYP3A.
Subject has any surgical or medical conditions possibly affecting drug absorption, distribution, metabolism, and excretion, eg, bariatric procedure.
Note: prior appendectomy is acceptable, but prior cholecystectomy would result in exclusion from the study.
- Subject donated blood or plasma within 8 weeks prior to dosing to a blood bank or blood donation center.
- Subject has a history of drug abuse (as defined by the current version of the Diagnostic and Statistical Manual [DSM]) within 2 years prior to dosing, or positive drug test reflecting consumption of illicit drugs.
- Subject has a history of alcohol abuse (as defined by the current version of the DSM) within 2 years prior to dosing, or positive alcohol test.
- Subject is known to have serum hepatitis or known to be a carrier of hepatitis B surface antigen (HBsAg) or hepatitis C antibody (HCV Ab), or have a positive result to the test for human immunodeficiency virus (HIV) antibodies at screening.
- Subject smokes > 10 cigarettes per day, or equivalent in other tobacco products (self-reported).
- Subject has received immunization with a live or live attenuated vaccine within 2 months prior to dosing or is planning to receive immunization with a live or live attenuated vaccine for 2 months following dosing.
- Subject participated in a radiolabeled drug study, where exposures are known to the Investigator, within the previous 4 months prior to check-in (Day -1); or participated in a radiolabeled drug study, where exposures are not known to the Investigator, within the previous 6 months prior to check-in (Day -1). The total 12-month exposure from this study and a maximum of 2 other previous studies within 4 to 12 months of this study will be within the CFR recommended levels considered safe, per US Title 21 CFR 361.1: less than 5,000 mrem whole body annual exposure, with consideration given to the half-lives of the previous radiolabeled study drugs received.
- Subject was exposed to significant radiation (eg, serial X-ray or computed tomography scans, barium meal, current employment in a job requiring radiation exposure monitoring) within 12 months prior to check-in (Day -1).
- History of less than 1 to 2 bowel movements per day.
- Subject is part of the study site personnel or a family member of the study site staff.
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: [14C]-CC-220 solution
A single oral dose of 1 mg [14C]-CC-220 solution, containing approximately 1.4 μCi of radioactivity, will be administered on Day 1 under fasted conditions.
|
1mg [14C]-CC-220 will be administered as a single dose
Single dose of [14C]-CC-220 will contain approximately 1.4 μCi of radioactivity
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Pharmacokinetics -Total [14C]-Radioactivity (RA)
기간: Up to approximately Day 10
|
Total [14C]-RA in whole blood, plasma, urine, and feces (and vomit, if applicable) will be measured via AMS.
|
Up to approximately Day 10
|
|
Pharmacokinetics - Cumulative excretion of total [14C]-RA
기간: Up to approximately Day 10
|
Total RA recovery will be computed as the sum of the cumulative excretion (as % dose) in urine and feces (and vomit, if applicable).
|
Up to approximately Day 10
|
|
Pharmacokinetics - Total [14C]-RA whole blood-to-plasma
기간: Up to approximately Day 10
|
Total [14C]-RA in whole blood and plasma will be converted to ngEq/mL concentration of [14C]-CC-220 based on specific activity of the dose.
|
Up to approximately Day 10
|
|
Pharmacokinetics - metabolite profiling/characterization
기간: Up to approximately Day 10
|
Percentage of the administered dose attributed to CC-220 and metabolite(s), and the RA of [14C]-CC-220 and metabolite(s), as appropriate, will be estimated.
|
Up to approximately Day 10
|
|
Pharmacokinetics -Cmax
기간: Up to approximately Day 10
|
Observed maximum plasma concentration, provided sufficient data available
|
Up to approximately Day 10
|
|
Pharmacokinetics -AUC
기간: Up to approximately Day 10
|
Area under the concentration-time curve, provided sufficient data available
|
Up to approximately Day 10
|
|
Pharmacokinetics -Tmax
기간: Up to approximately Day 10
|
Time to Cmax, provided sufficient data available
|
Up to approximately Day 10
|
|
Pharmacokinetics -t1/2
기간: Up to approximately Day 10
|
Terminal elimination half-life, provided sufficient data available
|
Up to approximately Day 10
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
부작용(AE)
기간: 등록부터 연구 치료 완료 후 최소 28일까지
|
부작용이 있는 참가자 수
|
등록부터 연구 치료 완료 후 최소 28일까지
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
스폰서
수사관
- 연구 책임자: Maria Palmisano, MD, Celgene
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)
2017년 9월 11일
기본 완료 (실제)
2017년 10월 16일
연구 완료 (실제)
2017년 10월 16일
연구 등록 날짜
최초 제출
2017년 9월 22일
QC 기준을 충족하는 최초 제출
2017년 9월 22일
처음 게시됨 (실제)
2017년 9월 27일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2017년 10월 25일
QC 기준을 충족하는 마지막 업데이트 제출
2017년 10월 24일
마지막으로 확인됨
2017년 10월 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. .
CC-220에 대한 임상 시험
-
Celgene완전한전신성 홍반성 루푸스미국, 벨기에, 독일, 스페인, 캐나다, 세르비아, 콜롬비아, 폴란드, 아르헨티나, 브라질, 멕시코, 헝가리, 프랑스, 러시아 연방, 이탈리아
-
Celgene Corporation완전한
-
Bristol-Myers SquibbCelgene완전한
-
Juno Therapeutics, Inc., a Bristol-Myers Squibb...모병