Clinical Trials Sponsored by GlycoMimetics Incorporated

Total 1171 results

Cook Group Incorporated

Completed

Zenith(R) Fenestrated Abdominal Aortic Aneurysm (AAA) Endovascular Graft Clinical Study

Abdominal Aortic Aneurysms | Aorto-iliac Aneurysms | Juxtarenal Aneurysms

United States
Cook Group Incorporated

Completed

Cook Micronized Small Intestinal Submucosa (SIS) for Critical Limb Ischemia

Ischemia | Peripheral Arterial Disease | Peripheral Vascular Diseases

Canada
Cook Group Incorporated

Completed

Evaluation of the Zilver® Vena™ Venous Stent (VIVO EU)

Iliofemoral Venous Outflow Obstruction

Switzerland, United Kingdom, Ireland, Germany, Spain
Vertex Pharmaceuticals Incorporated

Completed

A Study of Lumacaftor in Combination With Ivacaftor in Cystic Fibrosis Subjects Aged 12 Years and Older Who Are Homozygous for the F508del-CFTR Mutation (TRANSPORT)

Cystic Fibrosis, Homozygous for the F508del CFTR Mutation

United States, France, Spain, Belgium, Canada, Austria, Australia, Germany, United Kingdom, Denmark
Sound Pharmaceuticals, Incorporated

Completed

Study to Evaluate the Safety and Pharmacokinetics of SPI-1005

Cancer | Hearing Loss

United States
Cook Group Incorporated

Completed

Evaluation of the Cook Biodesign® Nipple Reconstruction Cylinder (NRC) (NRC)

Breast Cancer | Breast Reconstruction | Nipple Reconstruction

United States
Inflamax Research Incorporated

Completed

Irritation and Sensitization Potential of Repeat Applications of Rotigotine Patch

Bioequivalence - Irritation and Sensitization Potential of Transdermal Patch

United States, Canada
Cook Group Incorporated

Completed

Zilver PTX Drug-Eluting Peripheral Stent Study

Peripheral Arterial Disease

Germany, Switzerland
Cook Group Incorporated

Completed

Clinical Evaluation of the Surgisis Biodesign Vesico-Vaginal Fistula Plug (VVP)

Vesico-vaginal Fistula

Uganda
Cook Group Incorporated

Completed

Zilver® Flex™ Vascular Stent Study

Peripheral Arterial Disease (PAD)

Germany
Vertex Pharmaceuticals Incorporated

Completed

A Phase 2/3 Open-label Extension Study to Evaluate Long-Term Safety and Efficacy With VX-509 in Subjects With Rheumatoid Arthritis

Rheumatoid Arthritis

United States, Estonia, Lithuania, South Africa
Vertex Pharmaceuticals Incorporated

Completed

24-week Study With Open Label Extension of VX-509, an Oral JAK3 Inhibitor, in Subjects Taking Methotrexate

Rheumatoid Arthritis

United States, Argentina, Bulgaria, Czech Republic, Estonia, Germany, Hungary, Mexico, Poland, Romania, Russian Federation, Serbia, Slovakia, Ukraine
Vertex Pharmaceuticals Incorporated

Completed

Study of VX-809 Alone and in Combination With VX-770 in Cystic Fibrosis (CF) Patients Homozygous or Heterozygous for the F508del-CFTR Mutation

Cystic Fibrosis

United States, France, United Kingdom, Germany, Australia, New Zealand, Belgium
Vertex Pharmaceuticals Incorporated

Terminated

Telaprevir, Peg-IFN-alfa-2a, and RBV in Treatment-Experienced Black/African American and Non-Black/African American Subjects With Genotype 1 Chronic Hepatitis C

Hepatitis C

United States
Cook Group Incorporated

Terminated

Rubber Band Ligation and Mucosectomy for Gastroesophageal Reflux Disease (GERD) (GERD)

Dyspepsia | Gastroesophageal Reflux Disease | Heartburn | Regurgitation

United States
Vertex Pharmaceuticals Incorporated

Terminated

An Open Label Study of the Effect of Telaprevir in Combination With Ribavirin and Peginterferon on HCV Infection in Stable Liver Transplant Patients

Hepatitis C

Canada, United States
Vertex Pharmaceuticals Incorporated

Completed

Pilot Study Testing the Effect of Ivacaftor on Lung Function in Subjects With Cystic Fibrosis and Residual CFTR Function

Cystic Fibrosis

United States
Vertex Pharmaceuticals Incorporated

Completed

A Phase 2 Study to Evaluate the Safety and Efficacy of VX-135 With Ribavirin in Treatment-Naïve Subjects With Chronic Hepatitis C

Chronic Hepatitis C

United States
Bausch & Lomb Incorporated

Completed

Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery

Cataract

United States
Bausch & Lomb Incorporated

Completed

A Study to Determine if 0.6% ISV-403 is Safe and Effective in the Treatment of Bacterial Conjunctivitis.

Acute Bacterial Conjunctivitis
Bausch & Lomb Incorporated

Completed

Safety and Efficacy of a Bausch & Lomb Multipurpose Solution When Compared to Ciba Vision Aquify Multipurpose Solution

Contact Lens Solutions

United States
Cook Group Incorporated

Completed

Zenith® AAA Endovascular Graft Clinical Study

Abdominal Aortic Aneurysm
Bausch & Lomb Incorporated

Completed

One-Day Dispensing Clinical Evaluation of SofLens Daily Disposable Lenses Compared to a Marketed 1 Day Contact Lens

Myopia

United States
Cook Group Incorporated

Completed

Surgisis Anal Fistula Plug Study: An Experience in Saudi Arabia (SurgiSIS AFP)

Anal Fistula

Saudi Arabia
Cook Group Incorporated

Completed

Ligation of the Intersphincteric Fistula Tract (LIFT) + Biodesign for Anal Fistula (LIFT+Graft)

Anal Fistula

United States
Cook Group Incorporated

Completed

SX ELLA Esophageal Degradable BD Stent System (DESTINY)

Benign Esophageal Lesions

Belgium, Italy, Netherlands, Spain, United Kingdom
Cook Group Incorporated

Completed

Return of Continence Following Robot-Assisted Radical Prostatectomy With or Without a Urethrovesical Sling

Urinary Incontinence | Prostate Cancer

United States
Cook Group Incorporated

Terminated

Evaluation of the Goldstein SonoBiopsy™ Catheter for Diagnosing Endometrial Pathology

Uterine Neoplasms | Polycystic Ovary Syndrome | Endometrial Neoplasms | Menorrhagia

Panama
Bausch & Lomb Incorporated

Terminated

Accommodation Measurements After Bilateral Implantation of an Aspheric Accommodating Lens and Monofocal Aspheric Lenses

Cataract

United States
Bausch & Lomb Incorporated

Terminated

Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis

Bacterial Conjunctivitis

United States
Acetylon Pharmaceuticals Incorporated

Completed

Alternative 10 mg/mL Liquid Formulation of ACY 1215 (Ricolinostat) in Healthy Subjects

Healthy

United States
Bausch & Lomb Incorporated

Completed

Toric Intraocular Lens Following Cataract Surgery

Cataract | Astigmatism

United States
Bausch & Lomb Incorporated

Terminated

Besifloxacin Ophthalmic Suspension Verses Gatifloxacin Ophthalmic Solution in Neonates With Bacterial Conjunctivitis

Bacterial Conjunctivitis

United States
Vertex Pharmaceuticals Incorporated

Completed

Phase 1, QT/QTC Interval Study in Healthy Subjects

Cystic Fibrosis

Netherlands
Vertex Pharmaceuticals Incorporated

Completed

Phase 2 Study of VX-950, Pegasys® With and Without Copegus® in Hepatitis C

Chronic Hepatitis C

Austria, France, Germany, United Kingdom
Vertex Pharmaceuticals Incorporated

Completed

VX-222 + Telaprevir + Ribavirin for 12 or 16 Weeks in Treatment-Naive Subjects With Genotype 1a Hepatitis C

Chronic Hepatitis C Virus

United States
Bausch & Lomb Incorporated

Completed

A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens

Myopia

United States
Vertex Pharmaceuticals Incorporated

Completed

A Phase 1 Study to Investigate the Food Effect of Lumacaftor in Combination With Ivacaftor

Cystic Fibrosis

United States
Gen-Probe, Incorporated

Completed

Female Urine, Vaginal & Endocervical Swab & Cervical Specimen Collections for APTIMA Trichomonas Vaginalis Assay Testing

Trichomonas Vaginalis

United States
Bausch & Lomb Incorporated

Completed

Efficacy of Fluocinolone Acetonide Intravitreal Implant in Diabetic Macular Edema

Diabetic Macular Edema
Gen-Probe, Incorporated

Completed

Prospective Collection of Female and Male Specimens for PANTHER® System Testing

Gonorrhea | Chlamydia Infections

United States
Vertex Pharmaceuticals Incorporated

Terminated

VX-710, Doxorubicin, and Vincristine for the Treatment of Patients With Recurrent Small Cell Lung Cancer

Lung Cancer

United States
Vertex Pharmaceuticals Incorporated

Completed

Phase 1 PK Interaction Study Between VX-509 and Prednisone or Methylprednisolone in Healthy Male Subjects

Drug Interactions

United States
Bausch & Lomb Incorporated

Completed

Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs.

Myopia

Japan
Bausch & Lomb Incorporated

Completed

Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome

Dry Eye Syndromes

United States
Bausch & Lomb Incorporated

Completed

Hypersensitivity Reaction to Vitrase (Ovine Hyaluronidase)

Drug Hypersensitivity

United States
Bausch & Lomb Incorporated

Completed

Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome

Dry Eye Syndromes

United States
Cook Group Incorporated

Completed

Zenith Low Profile AAA Endovascular Graft (ZLP) Clinical Study (ZLP)

Abdominal Aortic Aneurysm | Iliac Aneurysm | Aorto-iliac Aneurysm

Japan
Bausch & Lomb Incorporated

Completed

Evaluation of the Onset and Duration of Action of Bepotastine Besilate Ophthalmic Solution in Acute Allergic Conjunctivitis

Conjunctivitis, Allergic

United States
Bausch & Lomb Incorporated

Completed

Safety/Efficacy of Bromfenac Ophthalmic Solution for Ocular Inflammation and Pain Associated With Cataract Surgery

Pain | Inflammation

United States

Clinical Trials Sponsored by GlycoMimetics Incorporated

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Madagascar

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations