Clinical Trials Sponsored by Link America, Inc.

Total 1225 results

American Regent, Inc.

Completed

Safety and Tolerability of a Single Dose of FCM vs. Standard of Care in Treating Iron Deficiency Anemia

Anemia

United States
American Regent, Inc.

Completed

Safety and Tolerability of Ferric Carboxymaltose (FCM) Versus Standard of Care in Treating Iron Deficiency Anemia

Anemia

United States
American Regent, Inc.

Completed

Hypophosphatemia With Ferric Carboxymaltose Vs. Iron Dextran in Iron Deficiency Secondary to Heavy Uterine Bleeding

Iron Deficiency Anemia
American Regent, Inc.

Completed

Taxoprexin Plus Carboplatin Treatment for Advanced Lung Cancer

Non-Small Cell Lung Cancer

United States
American Regent, Inc.

Completed

Comparison of Oral Iron With IV Iron in Patients With Anemia of Chronic Renal Failure Not on Dialysis

Anemia
American Regent, Inc.

Completed

Pharmacokinetic Study of Intravenous Iron Sucrose in Adolescents on Hemodialysis or Peritoneal Dialysis Receiving Epoetin

Anemia
American Regent, Inc.

Completed

Taxoprexin Treatment for Advanced Skin Melanoma

Metastatic Melanoma
American Regent, Inc.

Unknown

Trial to Evaluate the Utility of Serum Hepcidin Levels to Predict Response to Oral or IV Iron and to Compare Safety, Effect on Quality of Life, and Resource Utilization of Injectafer vs Intravenous Standard of Care for the Treatment of IDA in an Infusion Center Setting

Iron Deficiency Anemia (IDA)
American Regent, Inc.

Terminated

Randomized Double Blind Placebo Controlled Trial of Sodium Thiosulfate for the Treatment of Pain Associated With Calcific Uremic Arteriolopath

Calciphylaxis | Calcific Uremic Arteriolopathy

United States
American Regent, Inc.

Completed

Study of the Safety, Tolerability and Analgesic Efficacy of Multiple Doses of Ketorolac Tromethamine (IN) for Postoperative Pain

Postoperative Pain

New Zealand
Main Line Health
Ananda Hemp, Inc.

Active, not recruiting

Effect of Hemp-CBD on Patients With CIPN (Coala-T-CBD)

Breast Cancer | Pancreatic Cancer | Ovarian Cancer | Colorectal Cancer Stage II | Colorectal Cancer Stage III | Chemotherapy-induced Peripheral Neuropathy | Uterine Cancer

United States
Ulthera, Inc

Completed

Evaluation of the Ulthera System for Treating Axillary Hyperhidrosis (ULT-218)

Axillary Hyperhidrosis

Germany
Ulthera, Inc

Completed

Ultherapy® for Treating the Face and Neck Using Standard Versus Simulines Transducers

Skin Laxity

United States
Ulthera, Inc

Completed

Clinical Study on the Application of a Non-Invasive Micro-Focused Ultrasound With Visualization System for Skin Laxity (ULT-215) (ULT-215)

Facial Skin Laxity
Ulthera, Inc

Completed

Ultherapy® for the Treatment of Erythematotelangiectatic Rosacea

Rosacea | Erythematotelangiectatic Rosacea

United States, Canada
Ulthera, Inc

Completed

Ultherapy for Buttock Lift

Buttock Ptosis

United States
Ulthera, Inc

Completed

Feasibility Study: Evaluation of the Treatment of Striae Using Ultherapy® in Combination With Laser Treatment

Scars | Striae

United States
Ulthera, Inc

Completed

Histological Analysis Following Ulthera System Treatment for Hyperhidrosis

Hyperhidrosis

United States
Ulthera, Inc

Completed

Lifting and Tightening of the Face and Neck Utilizing the Ulthera® System

Facial and Neck Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Heavy Water Tissue Labeling Protocol

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Compare the Effectiveness Between Two Pain Medications When Used Prior to Ultherapy™ Treatments

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Higher Density Ulthera® System Treatment With Vectoring for Treatment of the Face and Neck

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Lifting and Tightening of the Elbows

Skin Laxity

United States
Ulthera, Inc

Completed

Retrospective Evaluation of Combination Treatment With the Ulthera System

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera Treatment of the Buttocks and Thighs

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Safety and Efficacy of the Ulthera® System for Treatment of Axillary Hyperhidrosis

Hyperhidrosis

United States
Ulthera, Inc

Completed

Evaluation of the Effectiveness and Safety of the Ulthera™ System for the Treatment of Wrinkles Around the Eyes

Periorbital Wrinkles

United States
American Regent, Inc.

Not yet recruiting

Tralement Versus a Fixed-dose Trace Element Combination Product of Zinc, Copper, and Selenious Acid to Evaluate Product Safety in Adult Patients Requiring Long-term Parenteral Nutrition

Manganese Safety in Adults
American Regent, Inc.

Withdrawn

Safety, Tolerability, PK and PD of Intravenous Ferric Carboxymaltose in Infants With Iron Deficiency Anemia

Iron Deficiency, Anaemia

United States
American Regent, Inc.

Terminated

Randomized, Placebo-controlled Trial of Ferric Carboxymaltose in RLS Patients With Iron-deficiency Anemia

Restless Legs Syndrome (RLS)

United States
American Regent, Inc.

Completed

A Study to Characterize the PK and PD Profile of IV FCM in Pediatric Subjects 1-17 Years Old With IDA

Iron Deficiency Anemia (IDA)

Poland, Russian Federation
American Regent, Inc.

Completed

Multicenter Randomized Active-controlled Study to Investigate Efficacy & Safety of IV FCM in Pediatric Patients With IDA

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Efficacy and Safety of Venofer (Iron Sucrose Injection USP) in Patients Receiving Peritoneal Dialysis

Anemia
American Regent, Inc.

Completed

Can Iron Lessen Anemia Due to Cancer and Chemotherapy: A Study to Investigate the Efficacy and Safety of Injectafer® (IRON CLAD)

Cancer and Chemotherapy Related Anemia

United States
American Regent, Inc.

Completed

Treatment Response of Injectafer vs Oral Iron to Baseline Hepcidin Levels in Patients With Iron Deficiency Anemia (IDA) Secondary to Inflammatory Bowel Disease (IBD) or Gastric Bypass

Iron Deficiency Anemia Secondary to IBD or Gastric Bypass
American Regent, Inc.

Completed

Registry to Evaluate Maintenance Treatment With Venofer in Pediatric Patients With Chronic Kidney Disease

Chronic Kidney Disease

United States
American Regent, Inc.

Completed

Safety and Tolerability of FCM vs Standard of Care in Treating Iron Deficiency Anemia in Chronic Kidney Disease Patients

Anemia

United States
American Regent, Inc.

Completed

Long Term Safety Study of (VIT45) Extension Study: Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease

Anemia

United States
American Regent, Inc.

Completed

Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in the Treatment of Anemia Secondary to Heavy Uterine Bleeding

Anemia

United States
American Regent, Inc.

Completed

Blinded Randomized Placebo-Controlled Study Efficacy and Safety of Injectafer in ID Patients With Fibromyalgia

Fibromyalgia | Iron Deficiency

United States
American Regent, Inc.

Completed

Evaluation of Efficacy and Safety of Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia and Impaired Renal Function (REPAIR-IDA)

Iron Deficiency Anemia | Impaired Renal Function

United States
American Regent, Inc.

Completed

Safety and Tolerability of Ferric Carboxymaltose (FCM) Versus Iron Dextran in Treating Iron Deficiency Anemia

Anemia

United States
American Regent, Inc.

Completed

Iron Sucrose in Non-Dialysis Dependent (NDD-CKD) Pediatric Patients

Anemia

United States
American Regent, Inc.

Completed

Intravenous Ferric Carboxymaltose vs IV Iron Sucrose or IV Iron Dextran in Treating Iron Deficiency Anemia in Women

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Safety, Tolerability, and Pharmacokinetic Study of Methylene Blue Following a 1 mg/kg Intravenous Dose in Healthy Adults

Methemoglobinemia | Congenital Methemoglobinemia
American Regent, Inc.

Completed

Study of Taxoprexin Injection vs. Dacarbazine in Patients With Metastatic Malignant Melanoma

Malignant Melanoma

United States
American Regent, Inc.

Completed

Bioequivalence Trial of Luitpold Azacitidine Versus Vidaza® in Patients With Myelodysplastic Syndrome, Myelofibrosis, Chronic Myeloid Leukemia or Chronic Lymphocytic Leukemia

Myelofibrosis | Chronic Lymphocytic Leukemia | Chronic Myeloid Leukemia | Myelodysplastic Syndrome

United States
American Regent, Inc.

Completed

Observational Study on the Use of IV (Intravenous) Iron Therapy Among Subjects With Iron Deficiency Anemia

Iron Deficiency Anemia (IDA)

United States
American Regent, Inc.

Terminated

Taxoprexin® Treatment for Advanced Primary Cancers of the Liver

Cancer of the Liver

United States

3

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