Clinical Trials Sponsored by Medingo Ltd

Total 17235 results

EndoCross Ltd.

Withdrawn

Accessing Peripheral Occluded LesiOns II (APOLO-II) (APOLO-II)

Femoropopliteal Occlusive Disease
Xention Ltd

Completed

ADME Study in Healthy Male Subjects With TA-8995

Dyslipidemia

United Kingdom
Egalet Ltd

Completed

Efficacy and Safety of Intranasal Ketorolac for the Acute Treatment of Migraine

Migraine

Germany
Calcivis Ltd

Completed

Post-Approval Clinical Study to Evaluate the Calcivis Caries Activity Imaging System

Dental Caries

United Kingdom
Optimata Ltd.

Unknown

Multi-Centre, Retrospective, Open Label Study, to Validate ML-PrediCare by Patients With Melanoma Under 1st and 2nd Lines of Immunotherapy

Melanoma

Israel
Novaremed Ltd.

Completed

Effect of NRD135S.E1 in Peripheral Neuropathic Pain in Diabetic Patients

Diabetic Peripheral Neuropathic Pain

Israel
NovoCure Ltd.

Unknown

Safety, Feasibility and Effect of TTFields (200 kHz) Concomitant With Weekly Paclitaxel in Recurrent Ovarian Carcinoma (INNOVATE)

Ovarian Carcinoma

Switzerland, Belgium, Germany, Spain
Nitiloop Ltd.

Completed

A Prospective, Non-randomized Study to Evaluate the Safety and Performance of the NovaCross™ Microcatheter in Femoropopliteal Chronic Total Occlusion (CTO).

Chronic Total Occlusion

Poland
Egalet Ltd

Completed

Effects of a Single Dose of Egalet® Morphine Combined With a Single Dose of Alcohol in Healthy Moderate Drinkers

Pain
Lonza Ltd.

Completed

Effects of Carnipure® Tartrate on Postprandial Endothelial Function and Recovery

Healthy Volunteers | Recovery | Endothelial Function

Germany
Sinocelltech Ltd.

Unknown

Pharmacokinetic Study of SCT800 in Previously Treated Patients With Hemophilia A

Hemophilia A

China
Egalet Ltd

Terminated

A Study of Controlled-Release Carvedilol Compared to Immediate-Release Carvedilol in Patients With Primary Hypertension

Hypertension

Denmark
Egalet Ltd

Completed

A Efficacy and Safety Trial of Controlled Release (CR) Morphine in Cancer Patients

Pain | Cancer

Lithuania, Poland
Amorphical Ltd.

Terminated

A Study Comparing the Effect of Amorphous Calcium Carbonate (ACC) on Healing Time of Distal Radius Fractures

Distal Radius Fractures

Israel
Efranat Ltd.

Unknown

Safety Study of EF-022 in Adults With Recurrent Respiratory Papillomatosis (RRP)

Recurrent Respiratory Papillomatosis
EarlySense Ltd.

Withdrawn

Evaluation of EverOn™ System in Medical / Surgical Ward

Post Operative Patient | Patients Requiring PCA | Respiratory Patients | Patients in Risk of Fall

United States
Alcobra Ltd.

Completed

A 6-week, Study of MG01CI Low Dose and High Dose Compared With Placebo in Adults and Adolescents With Fragile X Syndrome

Fragile X Syndrome

United States, Israel
BioLineRx, Ltd.

Completed

Phase IIa Study Evaluating Safety and Efficacy of BL-8040 in Relapsed/Refractory AML Patients

Acute Myeloid Leukemia

United States, Israel
Kamada, Ltd.

Completed

Phase II Study of the Safety and Efficacy of Inhaled Alpha-1 Antitrypsin (AAT ) in Cystic Fibrosis Patients

Cystic Fibrosis

Israel
PainReform LTD

Unknown

A Study to Evaluate the Safety, Pharmacokinetics and Preliminary Efficacy of PRF110 in Bunionectomy Surgery

Post Operative Pain

Israel
Firstkind Ltd

Completed

Firefly ANKLE Sprain Study

Grade I/II Ankle Sprain

United Kingdom
Polyphor Ltd.

Completed

Safety and Efficacy of POL6326 for Mobilization/Transplant of Sibling Donor in Patients With Hematologic Malignancies

Myeloproliferative Disorders | Adult Acute Lymphoblastic Leukemia in Remission | Chronic Lymphocytic Leukemia (CLL) | Myelodysplastic Syndrome (MDS) | Acute Myeloid Leukemia in Remission | Chronic Myelogenous Leukemia (CML) | Multiple Myeloma (MM) | Non-Hodgkin's Lymphoma (NHL) or Hodgkin's Disease...

United States
CorAlert Ltd.

Completed

Correlation of Non-invasive Assessment, Using C.A 2.0 Device, Versus Invasive Assessment of LVEDP

Heart Failure

Israel
LunGuard Ltd.

Unknown

Safety & Initial Efficacy of the LunGuard PFT Sys. on Enteral-Fed, Sedated and Mechanically Ventilated Patients Peristaltic Feeding Tube (PFT)

Gastro-esophageal Reflux
Echosense Ltd.

Withdrawn

Evaluation of Pulmonary Doppler Signals in Patients With Systemic Sclerosis(SSc)

Systemic Sclerosis | Pulmonary Hypertension

Israel
Echosense Ltd.

Completed

Changes in Doppler Signals From the Lung Due to Cardiac Resynchronization in Heart Failure Patients

Change in LDS Signals Due to Cardiac Synchronization Therapy

United States
Echosense Ltd.

Completed

The Use of a Ultra-sound of the Lung to Diagnose Lung Diseases

Pulmonary Pathologies | Cardio-pulmonary Diseases

Israel
BioLineRx, Ltd.

Completed

A Phase I Study Evaluating Safety, Tolerability, PK and PD of BL-8040 for Stem Cell Mobilization in Healthy Volunteers

Mobilization of Hematopoietic Stem Cells (HSC) to Peripheral Blood (PB)

Israel
BioGaming Ltd.

Completed

Performance of the BioGaming Device (YuGo) in the Support of Physical Rehabilitation

Physical Rehabilitation

Israel
Nexstim Ltd

Terminated

Navigated Transcranial Magnetic Stimulation in Monitoring Stroke Recovery

Ischemic Stroke

United States
Lupin Ltd.

Completed

A Study to Test the Safety/Tolerability of Increasing Doses of LNP1892 Versus Placebo in Healthy Male/Female Subjects

Healthy

United Kingdom
ElMindA Ltd

Completed

Normative Data of Brain Network Activation in Adolescents and Young Adults

Healthy Controls

United States
ElMindA Ltd

Completed

A Prospective Study of Brain Network Activation (BNA) Changes in High School Athletes Following Concussion

Mild Traumatic Brain Injury

United States
IonMed Ltd

Withdrawn

Evaluation of the BioWeld1 System as a Method for Surgical Incision Closure

Child Delivery Using an Elective C- Section

Israel
Xention Ltd

Completed

Fed-Fasted, Single and Multiple Ascending Dose Trial of XEN-D0103

Atrial Fibrillation

United Kingdom
OrthoSpace Ltd.

Completed

Prospective Study for Safety and Efficacy of InSpace™ in Rotator Cuff Tear Subjects

Rotator Cuff Tear

Israel
Alcobra Ltd.

Completed

Safety and Tolerability Study of Metadoxine Extended Release (MDX) (Previously Known as MG01CI) in PI-ADHD Adolescent Subjects

ADHD, Predominantly Inattentive Type

Israel
Xention Ltd

Completed

Study of the Electrocardiographic Effects of TA-8995

Dyslipidaemia

United Kingdom
Respivert Ltd

Completed

Safety, Tolerability and Pharmacokinetics (PK) of RV1162 in Healthy Subjects and COPD Patients

Healthy Volunteers | Chronic Obstructive Pulmonary Disease (COPD)

United Kingdom
BioLineRx, Ltd.

Terminated

Phase IIb-III Study of BL-1020 Small Molecule for Schizophrenia (CLARITY)

Schizophrenia | Cognitive Effect on Schizophrenic Patients

India, Moldova, Republic of, Romania
Vantia Ltd

Completed

Dose Range Finding Study of Fedovapagon in Men With Nocturia

Nocturia

United States
Sealantis Ltd.

Completed

Seal-V Safety and Performance Study

C.Surgical Procedure; Vascular (Peripheral)

Israel
Vantia Ltd

Completed

VA111913 Dysmenorrhoea Efficacy and Safety Proof of Concept

Primary Dysmenorrhea

United States, United Kingdom
Kamedis Ltd.

Unknown

Efficacy of KAM2904 Face Cream and KAM3008 Body Lotion Treatment in Children With Atopic Dermatitis (AD)

Atopic Dermatitis

Spain
Alcobra Ltd.

Completed

Study Comparing Two Doses of MG01CI and Placebo in Adults With Predominantly Inattentive Attention Deficit Hyperactivity Disorder

ADHD Predominantly Inattentive Type

Israel
AOTI Ltd.

Terminated

Evaluation of Topical Wound Oxygen (two2) Therapy

Diabetic Ulcer

United States, Canada
RegeneCure, Ltd.

Unknown

Guided Bone Regeneration Using Synthetic Membrane

Jaw, Edentulous, Partially | Jaw, Edentulous

Israel
Echosense Ltd.

Terminated

Measuring Blood Pressure in the Lung Circulation With Sonar Technology (Echo-Doppler)

Pulmonary Arterial Hypertension

Israel
OrSense, Ltd.

Unknown

Evaluate the Accuracy of the NBM200 for Noninvasive Hemoglobin Measurements on Obstetric/Gynecological Patients

Anemia
Respivert Ltd

Completed

A Study to Investigate the Safety and Tolerability of a New Inhaled Formulation of RV568 in Healthy Volunteers

Healthy Volunteers | COPD

United Kingdom

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