EUCTR2019-003597-10-IT进行中（未招募）1 期
A Phase 2 Clinical Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Doravirine/Islatravir in Adolescents with HIV-1 Infection who are Virologically Suppressed, are >=12 to <18 Years of Age, and Weigh >=35 kg - DOR/ISL in Adolescents with HIV-1, >=12 to <18 years of Age and >=35 kg
MERCK SHARP & DOHME CORP. UNA SUSSIDIARIA DI MERCK & CO. INC.0 个研究点目标入组 30 人开始时间: 2020年10月7日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Is HIV-1 positive with plasma HIV-1 RNA <50 copies/mL at screening
- •2. Has been receiving continuous, stable oral 2-drug or 3-drug cART (± PK booster) with documented viral suppression (HIV-1 RNA <50 copies/mL) for >=3 months prior to signing informed consent/assent
- •3. Is male or female, >=12 to <18 years of age and weighing >=35 kg at the time of signing the informed consent/assent
- •4. A female participant is eligible to participate if she is not pregnant or breastfeeding, and at least one of the following conditions applies:
- •- Is not a WOCBP
- •- Is a WOCBP and using an acceptable contraceptive method, or be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis), during the intervention period and for at least 6 weeks, corresponding to the time needed to eliminate any study intervention(s) (eg, 5 terminal half-lives)] after the last dose of study intervention. The investigator should evaluate the potential for contraceptive method failure (ie, noncompliance, recently initiated) in relationship to the first dose of study intervention
- •- A WOCBP must have a negative highly sensitive pregnancy test ([urine or serum] as required by local regulations) within 24 hours before the first dose of study intervention
- •- If a urine test cannot be confirmed as negative (eg, an ambiguous result), a serum pregnancy test is required. In such cases, the participant must be excluded from participation if the serum pregnancy result is positive
- •- The investigator is responsible for review of medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a woman with an early undetected pregnancy
- •5. The participant and legally acceptable representative if applicable provides written informed consent/assent for the study. The participant may also provide consent/assent for future biomedical research. However, the participant may participate in the main study without participating in future biomedical research
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Has HIV-2 infection
- •2. Has hypersensitivity or other contraindication to any of the components of the study drugs as determined by the investigator
- •3. Has an active diagnosis of hepatitis due to any cause, including active HBV infection (defined as HBsAg-positive or HBV DNA positive)
- •4. Has a history of malignancy <=5 years prior to signing informed consent except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or cutaneous Kaposi’s sarcoma
- •5. Has a history or current evidence of any condition (including active tuberculosis infection), therapy, laboratory abnormality or other circumstance (including drug or alcohol use or dependence) that might, in the opinion of the investigator, confound the results of the study or interfere with the participant’s participation for the full duration of the study, such that it is not in the best interest of the participant to participate
- •6. Is taking or is anticipated to require systemic immunosuppressive therapy, immune modulators, or any prohibited therapies from 45 days prior to Day 1 through the study treatment period
- •7. Is currently taking long-acting cabotegravir-rilpivirine
- •8. Is currently participating in or has participated in an interventional clinical study with an investigational compound or device from 45 days prior to Day 1 through the study treatment period
- •9. Has a documented or known virologic resistance to DOR, as demonstrated by any of the following DOR resistance substitutions in reverse transcriptase: V106A/M, V108I, Y188L, H221Y, P225H, F227C/L, M230I/L, L234I, P236L, or Y318F
- •10. Has exclusionary laboratory values (completed by the central laboratory) within 45 days prior to Day 1
- •11. Is female and expecting to conceive or donate eggs at any time during the study
研究者
相似试验
进行中（未招募）
1 期
DOR/ISL in Adolescents with HIV-1, =12 to <18 years of Age and =35 kgHIV-1 InfectionMedDRA version: 20.1Level: LLTClassification code 10068341Term: HIV-1 infectionSystem Organ Class: 10021881 - Infections and infestationsEUCTR2019-003597-10-Outside-EU/EEAMerck Sharp & Dohme Corp., a subsidiary of Merck & Co.,Inc40
进行中（未招募）
1 期
The Combination Regimen of Elbasvir (EBR)/Grazoprevir (GZR) in Pediatric Participants with Chronic Hepatitis C InfectioEUCTR2015-003006-16-SEMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.57
进行中（未招募）
1 期
The Combination Regimen of Elbasvir (EBR)/Grazoprevir (GZR) in Pediatric Participants with Chronic Hepatitis C InfectioEUCTR2015-003006-16-DEMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.57
进行中（未招募）
1 期
The Combination Regimen of Elbasvir (EBR)/Grazoprevir (GZR) in Pediatric Participants with Chronic Hepatitis C InfectioChronic genotype 1 or genotype 4 Hepatitis C Virus infectionMedDRA version: 20.1Level: LLTClassification code 10047457Term: Viral hepatitis CSystem Organ Class: 100000004862EUCTR2015-003006-16-PLMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.57
已完成
2 期
A Phase II Study of MR19A13A.JPRN-jRCT2051220112obuyo Oya12