A Natural History Study in Participants With Congenital Myasthenic Syndromes (CMS) Due to Mutations in DOK7, MUSK, AGRN, or LRP4
Recruiting
Participants will attend up to 4 study visits to collect clinical assessments. The assessments will evaluate participants' symptoms and quality of life to understand disease activity in patients with CMS due to mutations in DOK7, MUSK, AGRN, or LRP4.
Gender:
ALL
Ages:
2 years and above
Trial Updated:
05/07/2025
Locations: UC Davis Health - UC Davis Health Midtown Ambulatory Care Center, Sacramento, California +9 locations
Conditions: Congenital Myasthenic Syndrome
Study to Evaluate CCS1477 (Inobrodib) in Haematological Malignancies
Recruiting
A Phase 1/2a study to assess the safety, tolerability, PK and biological activity of CCS1477 (inobrodib) in patients with Non-Hodgkin Lymphoma, Multiple Myeloma, Acute Myeloid Leukaemia or High Risk Myelodysplastic syndrome.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
05/07/2025
Locations: Community Health Network, Indianapolis, Indiana +21 locations
Conditions: Haematological Malignancy, Acute Myeloid Leukemia, Non Hodgkin Lymphoma, Multiple Myeloma, Higher-risk Myelodysplastic Syndrome, Peripheral T Cell Lymphoma
Hemithyroidectomy or Total-Thyroidectomy in 'Low-risk' Thyroid Cancers
Recruiting
This is a multi-centre, randomised, non-inferiority, phase III study in patients with low risk differentiated thyroid cancer. Patients will be identified via oncology multidisciplinary team meetings. There will be two sources of patients in the trial, with the same histological diagnoses and prognosis (i.e. recurrence risk): * Group 1: Patients who have already had a HT for thyroid problems and are then subsequently diagnosed with low risk DTC will be randomised 1:1 to undergo surveillance onl... Read More
Gender:
ALL
Ages:
16 years and above
Trial Updated:
05/06/2025
Locations: Leighton Hospital, Crewe, Cheshire +34 locations
Conditions: Differentiated Thyroid Cancer
Assessing the Impact of a Leucine Enriched Whey Protein vs Isonitrogenous Whey on Muscle Protein Synthetic Responses in the Rested and Acute Post Exercise States in Older Adults
Recruiting
Occupying \~45-55% of body mass, skeletal muscle is the largest organ of the body and plays a pivotal role in locomotion, structural support and whole-body metabolic health. Additionally, skeletal muscle serves as the largest reservoir of amino acids (AA), which negatively adapts in states of disease and fasting to provide energy and AAs for vital organs, but also positively adapts to nutrition (i.e. protein consumption) and exercise (i.e. resistance exercise (RE)). With the current global agein... Read More
Gender:
MALE
Ages:
65 years and above
Trial Updated:
05/06/2025
Locations: Royal Derby Hospital Medical School, Derby, Derbyshire
Conditions: Healthy Male Volunteers Over 65
Safety and Efficacy of TSHA-102 in Pediatric Females With Rett Syndrome (REVEAL Pediatric Study)
Recruiting
The REVEAL Pediatric Study is a multi-center, Phase 1/2 open-label, dose-escalation and dose-expansion study of TSHA-102, an investigational gene therapy, in pediatric females with Rett Syndrome. The safety, tolerability, and preliminary efficacy of two dose levels will be evaluated. The study duration is up to 6 years.
Gender:
FEMALE
Ages:
Between 5 years and 8 years
Trial Updated:
05/06/2025
Locations: University of California San Diego (UCSD), La Jolla, California +9 locations
Conditions: Rett Syndrome
Optical Coherence Tomography And NEphropathy: The OCTANE Study
Recruiting
Patients with high blood pressure (hypertension) and chronic kidney disease are at an increased risk of developing heart disease and strokes. Part of this risk is due to changes in the structure and function of the blood vessels throughout the body. It is thought that reducing high blood pressure and treating chronic kidney disease improves the structure and function of blood vessels but information on this is limited. Optical coherence tomography (OCT) is a method of looking at the blood vessel... Read More
Gender:
ALL
Ages:
Between 18 years and 80 years
Trial Updated:
05/06/2025
Locations: University of Edinburgh, Edinburgh, Midlothian
Conditions: Health, Hypertension, Chronic Kidney Disease
Coronary Bifurcations With Ischaemia and Flow Assessment
Recruiting
The coronary arteries are blood vessels that provide oxygen rich blood to the muscle of the heart. If these vessels become narrowed or blocked, this can lead to chest pain (called angina) or heart attacks. Narrowings are usually treated using metal scaffolds called drug eluting stents. However, in one in five cases where the narrowing occurs at a branching point, treating it with stents is more challenging and can cause complications. A possible alternative treatment is using a special type of b... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
05/06/2025
Locations: Norwich Medical School, University of East Anglia, Norwich, Norfolk
Conditions: Coronary Bifurcation Lesions
Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears
Recruiting
The purpose of the study is to assess whether the REGENETEN™ Bioinductive Implant allows patients to get back to their everyday activities quicker than if the tendon is repaired by the standard repair technique 'Completion and Repair' for surgically treating partial-thickness rotator cuff tears.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
05/06/2025
Locations: Harbin Clinic, Rome, Georgia +19 locations
Conditions: Rotator Cuff Injuries
Visual Frailty in Ageing
Recruiting
The goal of this observational study is to define visual frailty and refine monitoring for an ageing population. It involves piloting a visual frailty assessment tool in a cohort of patients aged 60 and above with a known diagnosis of Age-related Macular Degeneration (AMD) in Princess Alexandra Eye Pavilion (PAEP), Anne Rowling Clinic which is hosting the NHS Low Visual Aid Clinic, or any other NHS Lothian facility treating patients with Age-related Macular Degeneration (AMD). The main questions... Read More
Gender:
ALL
Ages:
60 years and above
Trial Updated:
05/06/2025
Locations: The Princess Alexandra Eye Pavilion, Edinburgh, Scotland +1 locations
Conditions: Frailty, Age-Related Macular Degeneration, Functional Status, Mental Health, Depression, Anxiety, Cognitive Impairment, Visual Impairment
A Two-Part First-In-Human Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GUB014295
Recruiting
This is a two-part, single centre, double-blind (within cohorts), randomised, placebo-controlled, single (Part 1) and multiple (Part 2) ascending subcutaneous dose study in lean to overweight or obese but otherwise healthy men (Part 1) and men and non-pregnant, non-lactating women (Part 2). The primary objective is to assess the safety and tolerability. Secondary objectives are to characterize the pharmacokinetics (PK) and to investigate pharmacodynamic effects.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
05/06/2025
Locations: Quotient Sciences, Nottingham, Not set
Conditions: Healthy Volunteers, Overweight
The Poor Responders Study
Recruiting
Obesity and type 2 diabetes are major causes of illness and premature death worldwide and their incidence is increasing rapidly. Bariatric surgery is considered as the "gold-standard" surgical treatment for both conditions. However, not all patients do equally well after surgery and indeed the weight loss experienced by patients undergoing bariatric surgery can vary. As such when patients are seen after bariatric surgery in clinic they fall in one of the following two categories: 1. Good respo... Read More
Gender:
ALL
Ages:
Between 18 years and 70 years
Trial Updated:
05/06/2025
Locations: Imperial College London, London, Not set
Conditions: Bariatric Surgery Candidate, Obesity, Morbid, Diabetes Mellitus, Type 2
A Study to Investigate APL-4098 Alone and/or in Combination With Azacitidine in R/R AML and High-Risk MDS
Recruiting
This is an open-label, Phase 1/2 study to determine the safety, tolerability, and efficacy of APL-4098 alone and/or in combination with azacitidine for the treatment of relapsed or refractory (R/R) acute myeloid leukemia (AML), myelodysplastic syndrome (MDS)/AML and MDS-excess blasts (EB). Participants with the MDS-EB subtype will be eligible for the Phase 1 part of the study only.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
05/06/2025
Locations: Monash Health, Clayton, Victoria +5 locations
Conditions: Acute Myeloid Leukemia Refractory, Myelodysplastic Syndrome Acute Myeloid Leukemia, Myelodysplastic Syndrome With Excess Blasts, Acute Myeloid Leukemia, in Relapse