试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-12
Anti-tumor Effect of Ixabepilone in Metastatic Breast Cancer (mBC) Selected by the Ixabepilone DRP.
编号:NCT04796324登记状态:提前终止企业 / 申办者:Allarity Therapeutics
药物 / 成分:Ixabepilone Injection
登记的停止原因(原文):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:2026-03-12
A Study to Test Whether Spesolimab Helps People With a Skin Disease Called Netherton Syndrome
编号:NCT05856526登记状态:提前终止企业 / 申办者:Boehringer Ingelheim
药物 / 成分:Spesolimab - solution for infusion、Placebo matching to spesolimab - solution for infusion、Spesolimab - solution for injection、Placebo matching to spesolimab - solution for injection
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-12
Phase 1, Open-label, Dose-escalation Trial With CD38-SADA:177 Lu-DOTA Drug Complex in Subjects With Relapsed or Refractory Non-Hodgkin Lymphoma
编号:NCT05994157登记状态:提前终止企业 / 申办者:Y-mAbs Therapeutics
药物 / 成分:CD38-SADA:177Lu-DOTA Complex
登记的停止原因(原文):Study is terminated by Sponsor decision due to recruitment challenges.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-12
A Dose Escalation Study of TCD601 Compared to ATG in de Novo Renal Transplantation
编号:NCT06365437登记状态:提前终止企业 / 申办者:ITB-Med LLC
药物 / 成分:TCD601、Tacrolimus (TAC)、Corticosteroids (CS)、Mycophenolate Mofetil (MMF)
登记的停止原因(原文):After enrolment was complete, and sufficient data was collected to fully characterize the highest dose cohort, study follow up was terminated by the sponsor for non-safety related 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:2026-03-11
The Role of Secondary Bile Acids in Intestinal Inflammation
编号:NCT03724175登记状态:提前终止企业 / 申办者:Stanford University
药物 / 成分:ursodiol (ursodeoxycholic acid, UDCA)
登记的停止原因(原文):Lack of recruitment and funding.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-11
Durvalumab Plus Tremelimumab for the Treatment of Patients With Progressive, Refractory Advanced Thyroid Carcinoma -The DUTHY Trial
编号:NCT03753919登记状态:提前终止企业 / 申办者:Grupo Espanol de Tumores Neuroendocrinos
药物 / 成分:Durvalumab、Tremelimumab
登记的停止原因(原文):In compliance with current legislation applicable to Clinical Trials, following the instructions of the Spanish Agency for Medicines and Health Products.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-11
Comparing Mortality for Low vs High Peripheral Oxygen Saturation in COPD-patients With Acute Exacerbation
编号:NCT04223050登记状态:提前终止企业 / 申办者:Esbjerg Hospital - University Hospital of Southern Denmark
药物 / 成分:Oxygen gas
登记的停止原因(原文):Not possible to include patients at the required speed
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-11
A Study Evaluating the Safety and Efficacy of Neoadjuvant and Adjuvant Tiragolumab Plus Atezolizumab, With or Without Platinum-Based Chemotherapy, in Participants With Previously Untreated Locally Advanced Resectable Stage II, IIIA, or Select IIIB Non-Small Cell Lung Cancer
编号:NCT04832854登记状态:提前终止企业 / 申办者:Hoffmann-La Roche
药物 / 成分:Atezolizumab、Tiragolumab、Carboplatin、Cisplatin
登记的停止原因(原文):Study was terminated as data became available from Phase 3 trials of perioperative regimens combining chemotherapy with immunotherapy showing improved efficacy outcomes versus chemotherapy alone.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-11
A Trial of the Safety, Tolerability, and Pharmacodynamics of CVL-871 in Subjects With Dementia-Related Apathy
编号:NCT04958031登记状态:提前终止企业 / 申办者:AbbVie
药物 / 成分:CVL-871 1.0 mg、CVL-871 3.0 mg、Placebo
登记的停止原因(原文):Sponsor Decision - Not Safety Related
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-11
Personalized Infliximab Induction Strategy With Model-informed Dosing in Patients With Crohn's Disease
编号:NCT04974099登记状态:提前终止企业 / 申办者:Children's Hospital Medical Center, Cincinnati
药物 / 成分:RoadMAB precision dashboard、Infliximab precision dosing
登记的停止原因(原文):This was the Pilot study. The larger, confirmatory study has started
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-11
A Study to Evaluate the Safety and Preliminary Efficacy of ATA3219 in Participants With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma
编号:NCT06256484登记状态:提前终止企业 / 申办者:Atara Biotherapeutics
药物 / 成分:ATA3219
登记的停止原因(原文):Financial 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:2026-03-11
Efficacy and Tolerability of Deucravacitinib in the Management of Palmoplantar Pustulosis
编号:NCT07000630登记状态:提前终止企业 / 申办者:Peking University First Hospital
药物 / 成分:Deucravacitinib
登记的停止原因(原文):Terminated early due to lack of expected efficacy. Three participants were enrolled but none completed the 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:2026-03-10
Next Generation Personalized Neuroblastoma Therapy
编号:NCT02780128登记状态:提前终止企业 / 申办者:Yael P Mosse
药物 / 成分:Biopsy、Next Generation Sequencing、Tumor Scans、Bone marrow Tests
登记的停止原因(原文):The goals of Part 1 (molecular screening) were met, but lack of therapies to match molecular aberrations made Part 2 (treatment) no longer feasible.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-10
Venetoclax and Decitabine in Treating Participants With Relapsed/Refractory Acute Myeloid Leukemia or Relapsed High-Risk Myelodysplastic Syndrome
编号:NCT03404193登记状态:提前终止企业 / 申办者:M.D. Anderson Cancer Center
药物 / 成分:Decitabine、Laboratory Biomarker Analysis、Venetoclax
登记的停止原因(原文):\<75% participation
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-10
VB-111 in Combination With Nivolumab in People With Metastatic Colorectal Cancer (mCRC)
编号:NCT04166383登记状态:提前终止企业 / 申办者:National Cancer Institute (NCI)
药物 / 成分:Vascular Biogenics (VB)-111、Nivolumab
登记的停止原因(原文):Interim analysis indicated limited efficacy
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-10
A Study of Tazemetostat With Enzalutamide or Abiraterone/Prednisone in Participants With Advanced Prostate Cancer
编号:NCT04179864登记状态:提前终止企业 / 申办者:Epizyme, Inc.
药物 / 成分:Tazemetostat、Abiraterone/prednisone、Enzalutamide
登记的停止原因(原文):The study was terminated early as Sponsor decided to discontinue the development of tazemetostat in metastatic castration resistant prostate cancer and the primary endpoint was not met for this study. There were no 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:2026-03-10
Study to Evaluate the Effect of GBT440 on TCD in Pediatrics With Sickle Cell Disease
编号:NCT04218084登记状态:提前终止企业 / 申办者:Pfizer
药物 / 成分:Voxelotor、Placebo
登记的停止原因(原文):Emerging clinical data evaluated by Pfizer and shared with regulatory authorities indicates that the risk profile of voxelotor in people with SCD exceeds the benefits observed in previously generated global research and requires further assessment.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-10
Crofelemer for Functional Diarrhea
编号:NCT04486326登记状态:提前终止企业 / 申办者:Beth Israel Deaconess Medical Center
药物 / 成分:Crofelemer、Placebo
登记的停止原因(原文):low enrollment
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-10
Anti-PD-1 Antibody Combined With Histone Deacetylase Inhibitor in Patients With Advanced Cervical Cancer
编号:NCT04651127登记状态:提前终止企业 / 申办者:Sun Yat-sen University
药物 / 成分:Toripalimab + Chidamide
登记的停止原因(原文):Five patients were enrolled in the study, but no treatment response was observed and all the patients had the best of response of prgressive disease. Given the lack of efficacy, the trial was terminated.
查看官方原始记录 ↗试验终止ClinicalTrials.gov(美国登记平台)来源日期:2026-03-10
Study of Brexucabtagene Autoleucel in Adults With Rare B-cell Malignancies
编号:NCT05537766登记状态:提前终止企业 / 申办者:Kite, A Gilead Company
药物 / 成分:Brexucabtagene Autoleucel、Cyclophosphamide、Fludarabine
登记的停止原因(原文):Sponsor decision to terminate study.
查看官方原始记录 ↗