Clinical Trials Sponsored by Kerecis Ltd.

Total 16910 results

Kerecis Ltd.

Completed

Healing of Punch Graft Wounds. Comparative Study Between MariGen and Oasis: a Non-inferiority Study

Punch Biopsy Wounds | Healing Times

Iceland
Kerecis Ltd.

Completed

Viruxal Oral and Nasal Spray for Treating the Symptoms of COVID-19 (KONS-COVID19)

COVID-19

Iceland
Kerecis Ltd.

Not yet recruiting

Kerecis Real World Registry

Surgical Wound | Diabetic Foot Ulcer | Venous Leg Ulcer | Pressure Ulcer | Wounds | Soft Tissue Reinforcement
Kerecis Ltd.

Recruiting

Kerecis Case Registry for SurgiBind : Soft Tissue Reinforcement

Surgery-Complications

United States
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
Kerecis Ltd.

Recruiting

Prospective Case Registry for Wounds

Wound Healing Delayed

United States
Kerecis Ltd.

Active, not recruiting

Omega3 Wound Fish Skin Graft in the Treatment of DFUs

Diabetic Foot Ulcer

United States
Kerecis Ltd.
MedStar Health

Completed

Fish Skin Compared to Cadaver Skin as Temporary Cover for Full Thickness Burns (Kereburn)

Burns

United States
Kerecis Ltd.
Tufts University School of Dental Medicine

Completed

A Clinical Trial to Evaluate Kerecis Oral™ Compared to Autogenous Free Gingival Graft (AFGG) Tissue to Augment Gingival Soft Tissue and Wound Healing

Mucogingival Deformity - Insufficient Keratinized Tissue
Kerecis Ltd.
Joseph M. Still Research Foundation, Inc.

Recruiting

AFS Compared to AHC in Treatment of Necrotizing Fasciitis NF (NF)

Necrotizing Fasciitis

United States
Cerecin

Completed

Study to Compare the Pharmacokinetics of Daily Administration of Tricaprilin on Ketone Body Production

Alzheimer Disease

United States
Cerecin

Completed

Taste-masking Study for Tricaprilin in Sensory Panelists (TMS)

Taste Profile Assessments

United States
Cerecin

Completed

Pharmacokinetics of Tricaprilin Including Food Effect on Ketone Body Production

Alzheimer Disease

Australia
Cerecin

Withdrawn

Medical Food Formulation Pharmacokinetic (PK) Study in Medium Chain Triglycerides

Alzheimer Disease
Cerecin

Withdrawn

AC-1204 Long-term Efficacy Response Trial (ALERT Protocol) (ALERT)

Alzheimer's Disease

United States
Cerecin

Completed

A Phase 1, Two-part, Randomized Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of a Liquid Formulation of Tricaprilin and Matching Placebo in Healthy Subjects

Alzheimer Disease

United States
Cerecin

Terminated

Tricaprilin Liquid Formulation PK Study

Alzheimer Disease

Australia
Cerecin

Withdrawn

A Phase III Multi Regional Clinical Trial (MRCT) of Tricaprilin in Mild to Moderately Severe Probable Alzheimer's Disease With Optional Open Label Extension

Alzheimer's Disease
Cerecin

Completed

Safety of Three Formulations of Ketasyn Administered for 14 Days in Healthy Elderly

Alzheimer's Disease

United States
Cerecin

Not yet recruiting

Tricaprilin Phase 3 AD Study

Alzheimer Disease
Cerecin

Completed

Tricaprilin Phase 2 Pilot Study in Migraine

Migraine

Australia
Cerecin

Completed

AC-OLE-01-VA Tolerability Study in Healthy Participants Under Different Dosing Conditions

Alzheimer Disease

Australia
Cerecin

Active, not recruiting

Tricaprilin Infantile Spasms Pilot Study

Infantile Spasm

Singapore, Australia
Cerecin

Completed

AC-1204 26-Week Long Term Efficacy Response Trial With Optional Open-label Ext (NOURISH-AD)

Alzheimer's Disease

United States
Cerecin

Completed

Tricaprilin in Mild to Moderate Alzheimer's Disease

Alzheimer's Disease

United States
Cerecin

Completed

Tricaprilin In Age-Associated Memory Impairment

Age-Associated Memory Impairment

United States
Cerecin

Completed

Study to Compare the Pharmacokinetics of Tricaprilin Formulations and a Placebo on Ketone Body Production

Alzheimer Disease

Australia
Cerecin

Completed

Retrospective Cohort Study Of The Efficacy Of Axona® (Medium Chain Triglycerides) In Patients With Alzheimer's Disease (ACT)

Alzheimer's Disease
Cerecin
Celerion

Completed

Evaluation of PK of AC-1204 Mixed in Water, AC-1202 Mixed in Water, and AC-1202 Mixed in Ensure® on Ketone Body Production

Healthy

United States
Cerecin
Celerion

Completed

Study to Compare the Pharmacokinetics of AC 1202 and Two Doses of AC-SD-01 on Ketone Body Production

Healthy

United States
Cerecin
Celerion

Completed

Evaluation of PK of Caprylic Triglyceride Oil, AC-1202, AC-1204, and Axona on Ketone Body Production

Healthy

United States
Cerecin
Celerion

Completed

Evaluation of PK of AC1204 v Caprylic Triglyceride Oil Incl Food Effect on Ketone Body Production

Healthy

United States
Cerenis Therapeutics, SA

Completed

Exploratory Study of Plaque Regression (EXPRESS)

Heterozygous Familial Hypercholesterolemia

Canada
Cerenis Therapeutics, SA

Terminated

CER-001 Therapy as a Novel Approach to Treat Genetic Orphan Diseases (TANGO)

Familial Hypoalphalipoproteinemia

France, United States, Belgium, Canada, Israel, Italy, Netherlands
Cerenis Therapeutics, SA

Completed

Effect of CER-001 on Plaque Volume in Homozygous Familial Hypercholesterolemia (HoFH) Subjects (MODE)

Homozygous Familial Hypercholesterolemia

United States, Canada, Italy, Netherlands, United Kingdom
Cerenis Therapeutics, SA

Completed

Effect of CER-001 on Atherosclerosis in Acute Coronary Syndrome (ACS) Patients - Efficacy and Safety: The CHI SQUARE Trial (CHI SQUARE)

Acute Coronary Syndrome

Canada, United States, France, Netherlands
Centre d'Etudes et de Recherche pour l'Intensification...
Kerecis Ltd.; RCTs; Clininfo S.A.

Completed

Interventional Clinical Trial Comparing Kerecis Omega3 Wound Versus SOC in Diabetic Foot Wounds (KereFish)

Diabetes | Diabetic Foot Ulcer

France
Kerecis Ltd.
Centre d'Etudes et de Recherche pour l'Intensification du Traitement du Diabète and other collaborators

Completed

Kerecis Omega3 Wound Plus SOC vs. SOC Alone in Treating Severe Diabetic Foot Ulcers and Forefoot Amputations (Odinn)

Amputation | Diabetic Foot Ulcer | Dehiscence of Amputation Stump

France
University of Miami
National Multiple Sclerosis Society; Cerecin

Completed

Caprylic Triglyceride for Treatment of Cognitive Impairments in Multiple Sclerosis

Relapsing Remitting MS | Secondary Progressive MS | Primary Progressive MS

United States
Cerenis Therapeutics, SA
South Australian Health and Medical Research Institute

Completed

CER-001 Atherosclerosis Regression ACS Trial (CARAT)

Acute Coronary Syndromes

United States, Australia, Netherlands, Hungary
Salus Ltd.
TheraVitae Ltd.

Completed

Autologous Angiogenic Cell Precursors (ACPs) for the Treatment of Peripheral Artery Disease

Critical Limb Ischemia

Hungary
Mirka Ltd
Clinius Ltd

Completed

A Pre-market Study to Evaluate the Performance and Safety of a Skin Preparation Device for Removal of Dry Crusty Skin

Keratosis, Actinic | Hyperkeratotic Callus | Actinic Lesion | Solar Keratosis/Sunburn | Hyperkeratosis | Hyperkeratotic; Lesion | Hyperkeratotic Actinic Keratosis

Finland
Janssen-Cilag Farmaceutica Ltda.
Janssen Korea, Ltd., Korea

No longer available

An Expanded Access Program for Decitabine in Patients With Myelodysplastic Syndrome (MDS)

Myelodysplastic Syndromes

Hong Kong, Brazil, Thailand
Paion UK Ltd.
Chiltern International Ltd.; HFL Ltd.

Completed

An Efficacy and Safety Study to Compare Morphine 6-glucuronide (M6G) and Morphine in Patients Suffering With Post-Operative Pain for at Least 24 Hours

Postoperative Pain

France, Germany, Netherlands, Poland, United Kingdom, Czechia
Calcivis Ltd
Medsource UK Ltd.

Completed

Caries Lesion Activity in Orthodontic Patients - Calcivis System

Dental Caries

United Kingdom
TyrNovo Ltd.

Active, not recruiting

A Study to Evaluate NT219 Alone and in Combination With ERBITUX® (Cetuximab) in Adults With Advanced Solid Tumors and Head and Neck Cancer

Head and Neck Cancer | Squamous Cell Carcinoma of Head and Neck | Metastatic Solid Tumor | Colorectal Adenocarcinoma | Solid Tumor, Adult | Recurrent Solid Tumor

United States, Israel
Xention Ltd
Ario Pharma Ltd

Completed

A Study to Assess the Efficacy of XEN-D0501 in Reducing the Cough Frequency in Patients With Chronic Idiopathic Cough

Chronic Idiopathic Cough

United Kingdom, Ireland
Cardiovalve Ltd.
Meditrial Europe Ltd.

Recruiting

Cardiovalve Transfemoral System - FIM Study

Mitral Regurgitation

Lithuania
Vensica Therapeutics Ltd.
Blueclinical, Ltd.

Completed

Clinical Trial for the Assessment of Safety, Usability and Efficacy of the Vixe Combination for OAB in Female Subjects (XAVIER)

Overactive Bladder

Portugal
Nanomedic Technologies Ltd.

Completed

Evaluation of the SpinCare™ System in the Treatment of Partial Thickness Burns (SPINCARE2)

Partial Thickness Burn

Israel

Clinical Trials Sponsored by Kerecis Ltd.

Sponsors and Collaborators

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CROs in Belarus

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