Aller au contenu principal
xMedica

Rechercher

164 études correspondent à ces filtres. Affichage de 76 à 100 sur 164 études

Résultats de la recherche
Numéro d'enregistrementÉtudeStatutPhaseRecrutementSites / paysAnnée de débutDernière mise à jourActions
NCT06297291Global Paradise System US Post Approval Study

The objective of the Global Paradise® System US Post Approval Study (US GPS) is to evaluate the real-world use of the Paradise Ultrasound Renal Denervation System indicated for patients who are unable to lower their blood pressure with lifestyle changes and medication. This system is comprised of a…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 43 centres au total · contact indiqué

En recrutement1 000objectif43 / 1202412 août 2026
NCT05485961Combined Dose-Finding and CV Outcomes Study With CSL300 (Clazakizumab) in Adult Subjects With ESKD Undergoing Dialysis (POSIBIL6ESKD)

This is a two-part, phase 2b and phase 3 combined prospective, interventional, multicenter, randomized, double-blind, placebo-controlled study. Part 1: Phase 2b is a dose-finding study for CSL300 vs placebo. Part 2: Phase 3 aims to assess the efficacy of CSL300 vs placebo on cardiovascular (CV) out…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 557 centres au total · contact indiqué

En recrutementPhase 2 / Phase 33 110objectif557 / 35202211 août 2026
NCT06215716A Study Evaluating Efruxifermin in Subjects With Non-Cirrhotic Nonalcoholic Steatohepatitis (NASH)/Metabolic Dysfunction-Associated Steatohepatitis (MASH) and Fibrosis

This is a multi-center evaluation of efruxifermin (EFX) in a randomized, double-blind, placebo-controlled study in subjects with non-cirrhotic NASH/MASH and fibrosis stage 2 or 3 (F2 or F3). The study will enroll subjects in two cohorts for a total samples size of 1650 subjects.

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 356 centres au total

En recrutementPhase 31 650objectif356 / 1820237 août 2026
NCT06880055Shield Post-Approval Study Protocol

The Shield post-approval study (PAS) is a prospective, longitudinal study supplemented with Real World Evidence (RWE) to evaluate the longitudinal performance of Shield in an average risk population at a second round of testing for individuals between the ages of 45 and 81 at average risk of CRC usi…

Contact Revendiqué

Centre le plus proche : Hutchinson, Kansas, United States — à 36 km · 69 centres au total

En recrutement3 375objectif69 / 120257 août 2026
NCT06571669BOOM-IBD2 Pivotal Clinical Trial

Ulcerative colitis is a long-lasting condition that causes swelling and sores in the large intestine. This study tests whether a small device placed under the skin can help reduce bowel urgency in people with ulcerative colitis. The investigational device sends mild signals to a nerve near the tailb…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 19 centres au total · contact indiqué

En recrutementSans objet137objectif19 / 120256 août 2026
NCT05812807Pembrolizumab vs. Observation in People With Triple-negative Breast Cancer Who Had a Pathologic Complete Response After Chemotherapy Plus Pembrolizumab

This phase III trial compares the effect of continuation of treatment with pembrolizumab (usual approach) to observation only at preventing cancer from coming back in patients with early-stage triple-negative breast cancer (TNBC) who achieved a pathologic complete response after preoperative chemoth…

Contact Revendiqué

Centre le plus proche : Kingman, Kansas, United States — à 28 km · 846 centres au total · contact indiqué

En recrutementPhase 31 295objectif846 / 320235 août 2026
NCT06588855A Study to Assess the Efficacy and Safety of Induction Therapy With Afimkibart (Also Known as RO7790121) in Participants With Moderately to Severely Active Ulcerative Colitis

This Phase III, multicenter, double-blind, placebo-controlled study will evaluate the efficacy and safety of induction therapy with Afimkibart (RO7790121) compared with placebo in participants with moderately to severely active ulcerative colitis (UC).

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 200 centres au total

En recrutementPhase 3350objectif200 / 3020245 août 2026
NCT04267848Testing the Addition of a Type of Drug Called Immunotherapy to the Usual Chemotherapy Treatment for Non-small Cell Lung Cancer, an ALCHEMIST Treatment Trial (Chemo-IO [ACCIO])

This phase III ALCHEMIST treatment trial tests the addition of pembrolizumab to usual chemotherapy for the treatment of stage IIA, IIB, IIIA or IIIB non-small cell lung cancer that has been removed by surgery. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immun…

Contact Revendiqué

Centre le plus proche : Kingman, Kansas, United States — à 28 km · 1 151 centres au total

En recrutementPhase 31 210objectif1 151 / 220208 sept. 2026
NCT06982521Phase 3 Study of RLY-2608 + Fulvestrant vs Capivasertib + Fulvestrant as Treatment for Locally Advanced or Metastatic PIK3CA-mutant HR+/HER2- Breast Cancer

This is a global, multicenter, open-label, randomized Phase 3 study comparing the efficacy and safety of RLY-2608 (zovegalisib) + fulvestrant to capivasertib + fulvestrant for the treatment of patients with HR+/HER2- ABC with PIK3CA mutation following recurrence or progression on or after treatment…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 231 centres au total

En recrutementPhase 3540objectif231 / 2420253 sept. 2026
NCT06547489Zelquistinel or Placebo for the Reduction of Symptoms of Major Depressive Disorder

The goal of this clinical trial is to learn if zelquistinel works to treat depression in adults. It will also learn about the safety of zelquistinel. The main questions it aims to answer are: Does zelquistinel reduce depression scores in participants compared to participants who take a placebo (a l…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 34 centres au total

En recrutementPhase 2164objectif34 / 120253 août 2026
NCT07610278A Study to Evaluate the Pharmacodynamics of a Combination of QCZ484 and Inclisiran in Participants With Hypertension and Concomitant Hypercholesterolemia

This is a multicenter, randomized, double-blind, factorial design Phase 2 study to evaluate the pharmacodynamics, safety and tolerability of a combination of QCZ484 and inclisiran compared to QCZ484, inclisiran, and placebo in participants with hypertension and concomitant hypercholesterolemia.

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 29 centres au total · contact indiqué

En recrutementPhase 2120objectif29 / 1202630 juil. 2026
NCT07543120An Open-label Extension Safety and Efficacy Study of QCZ484 in Hypertensive Patients.

The purpose of this extension study is to collect additional safety and efficacy on QCZ484 for hypertensive patients who successfully completed the parent study, CQCZ484A12201 or additional QCZ484 studies as specified in the respective parent study protocols.

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 25 centres au total · contact indiqué

En recrutementPhase 2323objectif25 / 3202630 juil. 2026
NCT05268289Study of Efficacy and Safety of LNP023 in Participants With Active Lupus Nephritis Class III-IV, +/- V

The overall purpose of this two-part study is to evaluate the efficacy, safety and tolerability of iptacopan (LNP023) in addition to standard of care treatment.

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 103 centres au total · contact indiqué

En recrutementPhase 2240objectif103 / 20202230 juil. 2026
NCT05655182A Study of BLB-201 RSV Vaccine in Infants and Children

This Phase 1/2a trial is a randomized, placebo-controlled trial to evaluate the safety, tolerability and immunogenicity of two ascending doses (10\^6 PFU and 10\^7 PFU) of intranasal BLB-201 (a recombinant parainfluenza virus type 5) administered in infants (8-24 months of age) and children (18-59 m…

Contact Revendiqué

Centre le plus proche : Newton, Kansas, United States — à 53 km · 16 centres au total · contact indiqué

En recrutementPhase 1 / Phase 2137objectif16 / 1202329 juil. 2026
NCT03899155Pan Tumor Rollover Study

Main Objective of this study is to examine long-term safety of nivolumab monotherapy including combinations and other cancer therapies in various tumor types.

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 399 centres au total

En recrutementPhase 21 500objectif399 / 38201929 juil. 2026
NCT07045194Virtue® SAB in the Treatment of Coronary ISR Trial

A prospective, multi-center, single-blind, randomized (1:1), non-inferiority study comparing clinical outcomes of the Virtue® Sirolimus AngioInfusion™ Balloon (SAB) to the AGENT™ Paclitaxel Drug-Coated Balloon (DCB) in the treatment of coronary artery in-stent restenosis (ISR).

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 15 centres au total · contact indiqué

En recrutementSans objet740objectif15 / 1202523 juil. 2026
NCT06915233A Study of MACI in Patients Aged 17 to 65 Years With Symptomatic Chondral or Osteochondral Defects of the Ankle

The objective of this study is to demonstrate the superiority of MACI (autologous cultured chondrocytes on porcine collagen membrane) versus Bone Marrow Stimulation in the treatment of patients aged 17 to 65 years with symptomatic articular chondral or osteochondral defects of the talus.

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 7 centres au total · contact indiqué

En recrutementPhase 3309objectif7 / 1202623 juil. 2026
NCT06932263Dose Range Finding Study to Assess Efficacy and Safety of Tozorakimab in Adults With Uncontrolled Asthma on Medium-to-High Dose Inhaled Corticosteroids

This is a dose-range finding, double-blind, placebo-controlled, phase IIb study designed to assess efficacy and safety of tozorakimab administered subcutaneously in adult participants with uncontrolled asthma receiving medium-to-high dose inhaled corticosteroids.

Contact Revendiqué

Centre le plus proche : Hutchinson, Kansas, United States — à 36 km · 221 centres au total

En recrutementPhase 2540objectif221 / 21202520 juil. 2026
NCT05946629SELUTION 4 De Novo Small Vessel IDE Trial

Prospective, randomized controlled, single-blind, multicenter, clinical trial to demonstrate the safety and efficacy of the SELUTION SLR 014 PTCA DEB for treatment of de novo lesions in small coronary vessels, defined as reference vessel diameter (RVD) of 2.00 mm to 2.75 mm, in support of a pre-mark…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 70 centres au total · contact indiqué

En recrutementSans objet960objectif70 / 2202316 juil. 2026
NCT06937177Safely Optimizing Body Weight With Mifomelatide (TCMCB07) in Patients With Newly Diagnosed Colorectal Cancer (CRC) or Pancreatic Ductal Adenocarcinoma (PDAC) Undergoing Chemotherapy

This is a randomized, double-blind, placebo-controlled basket trial evaluating mifomelatide (TCMCB07) administered daily by subcutaneous (SC) injection in up to 120 patients. Patients will be enrolled into two cohorts 1) patients with newly diagnosed, advanced, unresectable colorectal cancer (CRC) o…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 26 centres au total · contact indiqué

En recrutementPhase 2120objectif26 / 2202515 juil. 2026
NCT05712200Study to evaLuate the effIcacy and Safety of abeLacimab in High-risk Patients With Atrial Fibrillation Who Have Been Deemed Unsuitable for Oral antiCoagulation (LILAC-TIMI 76)

A study to evaluate the effect of abelacimab relative to placebo on the rate of ischemic stroke or systemic embolism (SE) in patients with Atrial Fibrillation (AF) who have been deemed by their responsible physicians or by their own decision to be unsuitable for oral anticoagulation therapy.

Contact Revendiqué

Centre le plus proche : Hutchinson, Kansas, United States — à 36 km · 789 centres au total · contact indiqué

En recrutementPhase 32 500objectif789 / 35202213 juil. 2026
NCT06582810Lidocaine Infusion Treatment for Subarachnoid Hemorrhage Headaches

The goal of this observational study is to evaluate intravenous lidocaine efficacy and safety in treating headache following non-traumatic subarachnoid hemorrhage. Through this prospective analysis, the investigators hope to: 1. show that intravenous lidocaine infusion causes a clinically significa…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · contact indiqué

En recrutement20objectif1 / 1202510 juil. 2026
NCT04142437Study to Learn More About the Safety and Effectiveness of the Drug VITRAKVI During Routine Use in Patients With TRK Fusion Cancer Which is Locally Advanced or Spread From the Place Where it Started to Other Places in the Body

In this observational study researcher want to learn more about the effectiveness of drug VITRAKVI (generic name: larotrectinib) and how well the drug is tolerated during routine use in patients with TRK fusion cancer which is locally advanced or spread from the place where it started to other place…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 76 centres au total

En recrutement150objectif76 / 2620207 juil. 2026
NCT05378347Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial

The purpose of this trial is to generate clinical evidence related to key performance outcomes of Endurant II/IIs Stent Graft Systems verses Gore Excluder / Excluder Conformable AAA Endoprosthesis in subjects with Abdominal Aortic Aneurysms. Subjects are randomized and imaging collected at all follo…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 68 centres au total · contact indiqué

En recrutementSans objet600objectif68 / 1220236 juil. 2026
NCT06847321Study of LHP588 in Subjects With P. Gingivalis-Positive Alzheimer's Disease

This study is to test LHP588 in persons who have mild to moderate Alzheimer's disease (AD) who have shown progressive mental decline in the last year and who have P. gingivalis (Pg) infection. P. gingivalis infection has been linked to the development of dementia. LHP588 is designed to target the P.…

Contact Revendiqué

Centre le plus proche : Wichita, Kansas, United States — à 43 km · 38 centres au total · contact indiqué

En recrutementPhase 2300objectif38 / 1202515 sept. 2026

Filtres

Effacer tous les filtres