试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-06
Evaluation of K9 in Subjects With Diabetic Macular Edema (DME)
编号:NCT06781255登记状态:提前终止企业 / 申办者:Michelle Abou-Jaoude
药物 / 成分:Kamuvudine-9
登记的停止原因(原文):Low recruitment outcome
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-06
A Study to Investigate Efficacy, Safety, Tolerability, and Pharmacokinetics of JZP441 Compared With Placebo in Participants With Narcolepsy Type 1
编号:NCT06961266登记状态:提前终止企业 / 申办者:Jazz Pharmaceuticals
药物 / 成分:JZP441、Matching Placebo
登记的停止原因(原文):The study was terminated based on a business decision by the Sponsor.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
Study of Growth-promoting and Metabolic Effects of Growth Hormone (rhGH)
编号:NCT00597480登记状态:提前终止企业 / 申办者:Assistance Publique - Hôpitaux de Paris
药物 / 成分:rhGH (Norditropine SimpleXx®)、rhGH norditropine simple Xx
登记的停止原因(原文):no more inclusions
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
Lenalidomide in Kaposi Disease Associated With HIV Infection
编号:NCT01282047登记状态:提前终止企业 / 申办者:French National Agency for Research on AIDS and Viral Hepatitis
药物 / 成分:Lenalidomide
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
Fludarabine and Busulfan vs. Fludarabine, Busulfan and Total Body Irradiation
编号:NCT01366612登记状态:提前终止企业 / 申办者:Hackensack Meridian Health
药物 / 成分:Fludarabine and Busulfan plus/minus Total Body Irradiation (low dose)、Fludarabine and Busulfan + Low Dose Total Body Irradiation (LD TBI)
登记的停止原因(原文):Lack of Accrual
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
Check Point Inhibition After Autologous Stem Cell Transplantation in Patients at High Risk of Post Transplant Recurrence
编号:NCT02681302登记状态:提前终止企业 / 申办者:Hackensack Meridian Health
药物 / 成分:Ipilimumab、Nivolumab
登记的停止原因(原文):Lack of Accrual
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
Safety, Efficacy, PK and PD of CTAP101 (Calcifediol) ER Capsules for SHPT in HD Patients VDI
编号:NCT03602261登记状态:提前终止企业 / 申办者:OPKO Health, Inc.
药物 / 成分:Calcifediol Oral Capsule、Placebo oral capsule
登记的停止原因(原文):Cohort 1 completed and cohort 2 terminated prior to initiation per company decision
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
An Open-Label Study of Golodirsen in Non-Ambulant Patients With Duchenne Muscular Dystrophy
编号:NCT04708314登记状态:提前终止企业 / 申办者:Rare Disease Research, LLC
药物 / 成分:Golodirsen 50 MG/1 ML Intravenous Solution [VYONDYS 53]
登记的停止原因(原文):The Sponsor has decided to focus their resources on other areas of therapy.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
Dose Escalation and Dose Expansion Study of CPO-100 in Patients With Advanced Solid Tumors
编号:NCT04931823登记状态:提前终止企业 / 申办者:Conjupro Biotherapeutics, Inc.
药物 / 成分:CPO-100
登记的停止原因(原文):Business Decision
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
A Trial of SHR3680 in Prostate Cancer Patients Who Are Candidates for Radical Prostatectomy
编号:NCT05009290登记状态:提前终止企业 / 申办者:Jiangsu HengRui Medicine Co., Ltd.
药物 / 成分:SHR3680、Placebo
登记的停止原因(原文):Due to the adjustment of the sponsor's development plan, after discussion with leading PI, sponsor has decided to terminate this study.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-03
PRV-3279-2a Trial in Systemic Lupus
编号:NCT05087628登记状态:提前终止企业 / 申办者:Provention Bio, a Sanofi Company
药物 / 成分:PRV-3279、Placebo
登记的停止原因(原文):Termination for Strategic Reasons
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Evaluation of Raltegravir Plus Maraviroc Therapy in Controlled HIV Patients Presenting With Lipohypertrophy
编号:NCT01420523登记状态:提前终止企业 / 申办者:ANRS, Emerging Infectious Diseases
药物 / 成分:Raltegravir-Maraviroc
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Study of TelmisartanFor the Prevention of Acute GVHD Post Allogeneic Hematopoietic Stem Cell Transplantation
编号:NCT02338232登记状态:提前终止企业 / 申办者:Hackensack Meridian Health
药物 / 成分:Telmisartan
登记的停止原因(原文):Lack of Accrual
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Giant Cell Arteritis and Anakinra Trial
编号:NCT02902731登记状态:提前终止企业 / 申办者:University Hospital, Caen
药物 / 成分:PLACEBO、ANAKINRA
登记的停止原因(原文):experimental treatment no longer available
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Stereotactic Body Radiation Therapy Followed by Surgery in Treating Patients With Stage I-IIIA Non-small Cell Lung Cancer
编号:NCT03348748登记状态:提前终止企业 / 申办者:Roswell Park Cancer Institute
药物 / 成分:Laboratory Biomarker Analysis、Quality-of-Life Assessment、Stereotactic Body Radiation Therapy、Stereotactic Body Radiation Therapy
登记的停止原因(原文):low accrual
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Study of Efficacy, Safety, and Tolerability of LNA043 in Patients With Knee Osteoarthritis
编号:NCT04864392登记状态:提前终止企业 / 申办者:Novartis Pharmaceuticals
药物 / 成分:LNA043、Placebo
登记的停止原因(原文):Study early terminated due to lack of effect (did not meet primary/ secondary endpoints). This decision was not linked to safety concerns
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
An Extension Study to Evaluate the Long-Term Efficacy, Safety and Tolerability of Minzasolmin (UCB0599) in Study Participants With Parkinson's Disease
编号:NCT05543252登记状态:提前终止企业 / 申办者:UCB Biopharma SRL
药物 / 成分:Minzasolmin (UCB0599)
登记的停止原因(原文):Based on available data, the decision was made to stop development of UCB0599/minzasolmin as treatment of Parkinson's Disease.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Tazemetostat and Venetoclax in Relapsed/Refractory Non-Hodgkin Lymphoma
编号:NCT05618366登记状态:提前终止企业 / 申办者:Weill Medical College of Cornell University
药物 / 成分:Venetoclax、Tazemetostat
登记的停止原因(原文):Low accrual
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
Trastuzumab Deruxtecan in First-line HER2-positive Locally Advanced/MBC Patients Resistant to Trastuzumab+Pertuzumab
编号:NCT05744375登记状态:提前终止企业 / 申办者:Spanish Breast Cancer Research Group
药物 / 成分:Trastuzumab deruxtecan
登记的停止原因(原文):The study stopped due to insufficient accrual (only two patients were included), and the sponsor has decided on its premature termination.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-04-02
A Study of TAS3351 in NSCLC Patients With EGFRmt
编号:NCT05765734登记状态:提前终止企业 / 申办者:Taiho Oncology, Inc.
药物 / 成分:TAS3351
登记的停止原因(原文):Sponsor's decision, not based on safety concerns
查看官方原始记录 ↗