- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07924930
A Study of Tersolisib (LY4064809) in Participants With Kidney Impairment Compared With Participants With Normal Kidney Function
A Phase 1, Multicenter, Parallel-Design, Single-Dose, Open-Label Study to Investigate the Pharmacokinetics and Safety of Tersolisib in Participants With Renal Impairment Compared With Participants With Normal Renal Function
The main purpose of this study is to measure how much tersolisib gets into the bloodstream and how long it takes the body to eliminate it in participants with kidney impairment compared to those with normal kidney function. The safety of tersolisib will also be evaluated.
For each participant, the study will last about 7 weeks including a 14-night stay in the clinical research unit (CRU) and one follow-up telephone call.
연구 개요
연구 유형
등록 (추정된)
단계
- 1단계
연락처 및 위치
연구 연락처
- 이름: Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
- 전화번호: 1-317-615-4559
- 이메일: LillyTrials@Lilly.com
연구 연락처 백업
- 이름: Physicians interested in becoming principal investigators please contact
- 이메일: clinical_inquiry_hub@lilly.com
연구 장소
-
-
Florida
-
Altamonte Springs, Florida, 미국, 32714
- Omega Research Orlando
-
Miami Lakes, Florida, 미국, 33016
- Floridian Clinical Research
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Have a body mass index (BMI) within the range 19 to 42 kilograms per square meter (kg/m²), inclusive
- Participants assigned male at birth (AMAB) who agree to follow contraception guidance or participants assigned female at birth (AFAB) who are individuals not of childbearing potential (INOCBP)
Participants with Normal Renal Function:
- Are healthy with normal renal function, defined as estimated glomerular filtration rate (eGFR) greater than or equal to 90 milliliters per minute (mL/min) at screening
Participants with Renal Impairment:
- Have moderate renal impairment, defined as eGFR greater than or equal to 30 and less than 60 mL/min, or severe renal impairment, defined as eGFR less than 30 mL/min and not requiring dialysis
- Are on stable doses of prescription or over-the-counter medications for the management of chronic kidney disease
- Have acceptable blood pressure as defined by systolic blood pressure less than 160 millimeters of mercury (mmHg) and diastolic blood pressure less than 95 mmHg, as well as acceptable pulse rate, defined as no less than 50 beats per minute (bpm) and no greater than 100 bpm.
Exclusion Criteria:
-
Have history of chronic liver disease, or any evidence for hepatic impairments, or
- alanine aminotransferase (ALT) or aspartate aminotransferase (AST) greater than 1.5 times (x) upper limit normal (ULN) or
- total bilirubin (TBL) greater than 1.5 x ULN
-
Have a current, functional renal transplant
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Have a history or presence of any of the following clinically significant conditions: metabolic, biliary, gastrointestinal, hematological, neurological diseases, active cardiovascular (CV) disease or history of myocardial infarction within 3 months of planned dose of tersolisib, or 12-lead electrocardiogram (ECG) abnormalities that are clinically significant at screening, admission or predose.
-
Have a clinically significant history of multiple or severe drug hypersensitivity reactions, or drug allergies, such as anaphylaxis, hepatotoxicity, or treatment with steroids or epinephrine.
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Have a history of a major surgical procedure within 30 days prior to screening.
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Have been diagnosed with, or treated for, malignancy within 5 years prior to screening with the exception of curatively treated basal cell carcinoma of the skin, squamous cell carcinoma of the skin, and curatively resected in situ carcinoma of the cervix.
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Have evidence of Human Immunodeficiency Virus (HIV) infection or positive HIV-1 and HIV-2 antibodies.
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Have a current infection with Hepatitis C Virus (HCV), that is, positive for HCV Ribonucleic Acid (RNA).
-
Have a current infection with Hepatitis B Virus (HBV), that is, positive test for Hepatitis B Surface Antigen (HBsAg) or polymerase chain reaction positive for HBV DNA
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 기초 과학
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Tersolisib Group 1 (Normal Renal Function)
Tersolisib administered orally to participants with normal renal function |
Administered orally
다른 이름들:
|
|
실험적: Tersolisib Group 2 (Severe Renal Impairment)
Tersolisib administered orally to participants with severe renal impairment |
Administered orally
다른 이름들:
|
|
실험적: Tersolisib Group 3 (Moderate Renal Impairment, Optional)
Tersolisib administered orally to participants with moderate renal impairment |
Administered orally
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Pharmacokinetics (PK): Maximum Concentration (Cmax) of Tersolisib
기간: Predose on Day 1 through Day 14
|
Predose on Day 1 through Day 14
|
|
PK: Area Under the Concentration Versus Time Curve (AUC) of Tersolisib
기간: Predose on Day 1 through Day 14
|
Predose on Day 1 through Day 14
|
공동 작업자 및 조사자
수사관
- 연구 책임자: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST), Eli Lilly and Company
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
- 27965
- J6M-MC-JSGK (기타 식별자: Scorpion Therapeutics, a wholly owned subsidiary of Eli Lilly and Company)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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