Clinical Trials Sponsored by Kamada, Ltd.

Total 19395 results

Spircare Ltd.

Unknown

Accuracy of Spircare Device as Compared to the Conventional Plethysmograph

Pulmonary Fibrosis | COPD Asthma

Israel
Brainmarc Ltd.

Completed

Evaluation of Use of Brain Activity Monitoring for Evaluation of Depression Treatment

Depression

Israel
LifeBond Ltd.

Unknown

SEAL Registry - European Registry for the Effectiveness of LifeSeal® Kit

Anastomotic Leakage

Belgium, Netherlands
Neurolief Ltd.

Terminated

A Randomized, Double-blind Clinical Investigation to Evaluate the Use of the Relievion™ Device in Treating Migraine.

Migraine

Israel
Medinol Ltd.

Completed

PIONIR Study (Presillion™ and Presillion™ Plus Stent Systems)

Ischemic Heart Disease

Israel, Sweden, Belgium, Germany
Egalet Ltd

Completed

Study of the Tolerability of Ketorolac Tromethamine Following Intranasal Administration in Healthy Volunteers

Healthy Volunteers

United Kingdom
Egalet Ltd

Completed

Study to Assess the Absorption and Tolerability of Intranasal Ketorolac Tromethamine and to Assess the Effects of Oxymetazoline Hydrochloride and Fluticasone Propionate on the Absorption and Tolerability of Intranasal Ketorolac Tromethamine in Participants With Allergic Rhinitis

Allergic Rhinitis

Australia
Egalet Ltd

Completed

Safety and Tolerability of Egalet-002 in Patients With Moderate-to-Severe Chronic Noncancer Pain

Moderate-to-severe Chronic Noncancer Pain

United States
AOTI Ltd.

Unknown

Efficacy, Safety and Economic Benefits of Topical Wound Oxygen Therapy in the Treatment of Chronic Diabetic Foot Ulcers (TWO2DFU)

Diabetic Foot Ulcer

United Kingdom, United States, Germany, France, Luxembourg
Firstkind Ltd

Withdrawn

Intermittent Pneumatic Compression of the Foot vs Geko Plus R-2 Neuromuscular Electrostimulation Device in Venous Leg Ulcer Patients

Venous Leg Ulcer
Vibrant Ltd.

Unknown

A Study to Assess the Efficacy and Safety of the Vibrant Capsule Administered 5 Times Per Week

Constipation

United States
Actegy Ltd.

Completed

Aerosure and Six Minute Walk Distance in Severe COPD (ACCORD)

COPD

United Kingdom
Colospan Ltd.

Completed

Safety, Tolerability and Performance Profile of the Colospan Device CG-100 in Patients Undergoing Colorectal Surgery

Gastrointestinal Anastomosis

Belgium, Israel, Croatia, Hungary
Vibrant Ltd.

Completed

Performance, Efficacy and Safety of Vibrating Capsule in Aiding Constipated Individuals

Chronic Idiopathic Constipation

United States, Israel
Ocuwize LTD

Completed

To Evaluate the Efficacy and Safety of LO2A Eye Drops in Patients With Conjunctivochalasis

Conjunctivochalasis

Israel
Healthy.io Ltd.

Completed

Healthy.io Method Comparison & User Performance Study

Diabetes | Urinary Tract Infection | Kidney Failure

United States
Scancell Ltd

Terminated

Study of a DNA Immunotherapy to Treat Melanoma

Malignant Melanoma

United Kingdom
EarlySense Ltd.

Completed

Evaluation of EarlySense Home Care Tele-monitoring Device -For Early Detection of Deterioration For Cardiac Patients at Home

Post Cardiac Surgery

Israel
Brainmarc Ltd.

Completed

Evaluation of Use of Brain Activity Monitoring Dynamics in ADHD

ADHD

Israel
ProCore Ltd.

Completed

A Phase I, Prospective, Randomized, Open-label, Active-Controlled Clinical Trial for Safety Evaluation of Intra-articular Injection of RegenoGel-SP for the Treatment of Moderate to Severe Osteoarthritis

Osteoarthritis

Israel
Alcobra Ltd.

Completed

A 6 Week Study of MG01CI 1400 mg Compared With Placebo in Adults With ADHD ( Attention Deficit/Hyperactivity )

ADHD | Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

United States, Israel
Egalet Ltd

Completed

The Pharmacokinetics of Ketorolac Tromethamine Administered Intranasally (IN) for Postoperative Pain in Children Aged 12 Through 17 Years

Postoperative Pain

United States
Egalet Ltd

Completed

Study to Determine the Tolerability, Safety and Pharmacokinetics of Ketorolac Tromethamine by Intranasal Administration in Healthy Volunteers

Healthy Volunteers

United Kingdom
Alcobra Ltd.

Completed

Efficacy Study of Metadoxine SR Formulation in Attention Deficit Hyperactivity Disorder (ADHD) Subjects

Attention Deficit Hyperactivity Disorder

Israel
Kerecis Ltd.

Completed

Use of Fish Skin Extracellular Matrix (ECM) to Facilitate Chronic Wound Healing

Pressure Ulcers | Venous Ulcers | Trauma-related Wound | Diabetic Ulcers | Chronic Ulcer of Foot

Iceland
Egalet Ltd

Completed

Assessment of Nasal Deposition and Clearance of Ketorolac Solution Administered Using the Valois Nasal Spray Device

Healthy Subjects

United Kingdom
Egalet Ltd

Completed

Safety and Efficacy of Multiple Doses of Intranasal Ketorolac in Postoperative Pain Following Major Abdominal Surgery

Postoperative Pain

United States, New Zealand
Egalet Ltd

Completed

Safety and Efficacy of Multiple Doses of Ketorolac Tromethamine Administered Intranasally for Postoperative Pain

Postoperative Pain

New Zealand
Polyphor Ltd.

Terminated

Safety, Efficacy and PK/PD of POL7080 in Patients With Exacerbation of Non-cystic Fibrosis Bronchiectasis.

Bronchiectasis | Lower Respiratory Infection

Spain, United Kingdom
Vibrant Ltd.

Withdrawn

Ease of Use, Tolerability, Efficacy and Safety of the Vibrant Capsule Administered in the Home Environment

Constipation

United States
EarlySense Ltd.

Completed

Monitoring Changes in Blood Pressure

Blood Pressure

Israel
PeerMedical Ltd.

Completed

Polyp Detection With The Peerscope System™

Colon Cancer | Colon Polyps and Adenomas

Israel, United States, Netherlands
BioMAS Ltd

Unknown

Safety and Efficacy Double Blind Vehicle Controlled Study of 15% AS101 Gel to Treat External Genital Warts

External Genital Warts

Israel
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

3

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