Clinical Trials Sponsored by Link America, Inc

Total 1226 results

Sumitomo Pharma America, Inc.

Completed

A Study of DSP-7888 Dosing Emulsion in Adult Patients With Advanced Malignancies

Melanoma | Sarcoma | Renal Cell Carcinoma | Acute Myeloid Leukemia | Myelodysplastic Syndromes | Pancreatic Cancer | Ovarian Cancer | Non-Small Cell Lung Cancer | Glioblastoma Multiforme

United States
Sumitomo Pharma America, Inc.

Completed

First-in-human Study of Oral TP-0903 (a Novel Inhibitor of AXL Kinase) in Patients With Advanced Solid Tumors

Advanced Solid Tumors | Recurrent Ovarian Carcinoma | Colorectal Carcinoma | EGFR Positive Non-small Cell Lung Cancer | BRAF-Mutated Melanoma

United States
Merz North America, Inc.

Completed

Evaluation of Effectiveness and Safety of Radiesse (+) to Improve the Contour of Jawline by Adding Volume to the Jawline

Improvement of Jawline Contour

United States
Sumitomo Pharma America, Inc.

Completed

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Drug Interaction Potential of Napabucasin in Healthy Volunteers

Drug-drug Interactions

United States
Sumitomo Pharma America, Inc.

Completed

A Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors

Cancer | Advanced Solid Tumors

United States
Sumitomo Pharma America, Inc.

Completed

A Study to Evaluate the Mass Balance of 14C-Napabucasin in Healthy Adult Male Subjects

Healthy | ADME

United States
Teijin America, Inc.
Parexel

Completed

A Study to Investigate Safety, Tolerability, and Pharmacokinetics of Oral Doses of TCK-276 in Patients With Rheumatoid Arthritis

Rheumatoid Arthritis

United States
Merz North America, Inc.

Completed

A Prospective, Multicenter, Randomized, Comparator-controlled, Evaluator-blinded Study to Evaluate the Safety and Effectiveness of VP1 Lido US for Volume Augmentation of the Cheek (BCheek)

Cheek Volume Augmentation

Germany
Merz North America, Inc.

Completed

Evaluation of the MJGS Following Radiesse (+) Injection Into the Jawline

Volume Loss of the Jawline
Merz North America, Inc.

Completed

Radiesse® Safety Study For the Treatment of Hands

Volume Loss in the Dorsum of the Hand

United States
Toray Industries (America), Inc.

Completed

Pilot Study Evaluating the Toray Satake Balloon Thermal Ablation System for Treatment of Paroxysmal Atrial Fibrillation

Paroxysmal Atrial Fibrillation

United States
Merz North America, Inc.

Withdrawn

Efficacy and Safety Study of MSRD-100 in Subjects With Atopic Dermatitis >=3 Months of Age and Older (MSRD-100)

Atopic Dermatitis
Maruho North America Inc.

Completed

Long Term Study to Evaluate Safety and Efficacy of M518101 in Subjects With Plaque Psoriasis

Psoriasis

United States
Maruho North America Inc.

Completed

Evaluate the Efficacy and Safety of M518101 in Subjects With Plaque Psoriasis

Psoriasis

United States
Merz North America, Inc.

Completed

Belotero Post Approval Study

Nasolabial Folds

United States
Merz North America, Inc.

Completed

Multicenter Study of the Safety and Efficacy of Dermal Filler, Belotero® Soft

Facial Wrinkles

United States
Merz North America, Inc.

Completed

Multicenter Study of the Safety and Efficacy of NAFT-500 in Tinea Pedis

Tinea Pedis | Athlete's Foot

United States
Merz North America, Inc.

Completed

Radiesse® Injectable Dermal Filler for the Treatment of Nasolabial Folds in Persons of Color

Nasolabial Folds

United States
Merz North America, Inc.

Completed

Multicenter Study of the Safety and Effectiveness of Dermal Filler, Belotero®.

Facial Wrinkles

United States
Massachusetts General Hospital
Takeda Pharmaceuticals North America, Inc.; American College of Gastroenterology

Recruiting

Identification/Characterization of Changes in Microscopic Colitis

Colitis, Microscopic

United States
American Regent, Inc.

Completed

Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients With Iron Deficiency Anemia and Unsatisfactory Response Oral Iron Under Study Protocol 1VIT17044

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Safety and Efficacy of Iron Sucrose in Children

Anemia | Chronic Kidney Disease

United States
American Regent, Inc.

Completed

Efficacy and Safety of Intravenous Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia (IDA)

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Intravenous (IV) Iron vs. No Iron as the Treatment of Anemia in Cancer Patients Undergoing Chemotherapy and Erythropoietin Therapy

Anemia
American Regent, Inc.

Completed

Intravenous (IV) Iron Preparation (VIT-45) in the Treatment of Restless Legs Syndrome (RLS)

Restless Legs Syndrome (RLS)
American Regent, Inc.

Completed

Safety of FCM vs. Standard of Care in Treating Iron Deficiency Anemia in Heavy Uterine Bleeding and Post Partum Patients

Anemia

United States
American Regent, Inc.

Completed

Iron Sucrose In The Treatment of Restless Legs Syndrome: Safety of Three Dose Regimens as Evaluated by Clinical Assessments

Restless Legs Syndrome
American Regent, Inc.

Completed

Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in Subjects Who Display Postpartum Anemia

Anemia

United States
American Regent, Inc.

Withdrawn

Safety Assessment of Iron Sucrose (Venofer) in Patients With Chronic Kidney Disease Who Cannot Tolerate Ferumoxytol (Feraheme) or Iron Dextran (INFed or Dexferrum) (ASSURED)

Iron Deficiency Anemia

United States
American Regent, Inc.

Completed

Taxoprexin® Treatment for Advanced Eye Melanoma

Metastatic Melanoma

United States
American Regent, Inc.

Completed

Pharmacokinetics, Safety, and Efficacy of SPRIX in 12 to 17 Year Old Patients vs. Adult Patients Undergoing Open Surgical Procedures

Pain

United States
American Regent, Inc.

Completed

Safety and Tolerability of Intravenous VIT-45 in Patients With Iron Deficiency Anemia

Anemia

United States
Merz North America, Inc.
Ulthera, Inc

Completed

A Study of Octave System for Improving Lines and Wrinkles of the Décolleté

Décolleté Wrinkles

United States
Ulthera, Inc

Terminated

Simulines Non-Inferiority Pivotal Study

Skin Laxity

United States
Merz North America, Inc.
Ulthera, Inc

Completed

Study of the Cabochon System for Improvement in the Appearance of Cellulite

Gynoid Lipodystrophy

United States
Ulthera, Inc

Completed

A Retrospective Study to Evaluate the Effectiveness of the Ulthera System

Wrinkles | Skin Laxity

United States
Ulthera, Inc

Completed

Ulthera® System for Treating Axillary Hyperhidrosis

Primary Axillary Hyperhidrosis

United States
Ulthera, Inc

Completed

Reducing Wrinkles Around the Eyes Using the Ulthera® System

Periorbital Wrinkles

United States
Ulthera, Inc

Completed

Treatment of the Face and Neck With Lower Ulthera System Energy Settings

Skin Laxity

United States
Ulthera, Inc

Completed

Evaluation of the Ulthera® System for Treatment of the Brachia

Brachial Ptosis

United States
Ulthera, Inc

Completed

Feasibility Study: Evaluate the Effectiveness of Using a Topical Anesthetic Prior to Ultherapy™ Treatment

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Lifting and Tightening Neck Skin in Patients

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera System for the Treatment of Rosacea

Erythematotelangiectatic Rosacea

Canada
Ulthera, Inc

Completed

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

Hyperhidrosis

United States
Ulthera, Inc

Terminated

Feasibility Study: Histological Characterization After Treatment With the Ulthera® System

Skin Laxity

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 Pediatric Patients >3 to 17 Years of Age Requiring Long-term Parenteral Nutrition

Manganese Safety in Pediatric Patients
American Regent, Inc.

Completed

Placebo-Controlled Study to Investigate the Efficacy & Safety of Injectafer in the Treatment of RLS

Restless Legs Syndrome (RLS)

United States
American Regent, Inc.

Completed

Comparison of Safety and Efficacy of Intravenous Iron Versus Oral Iron in Chronic Renal Failure Subjects With Anemia

Anemia

United States
American Regent, Inc.

Completed

Safety and Efficacy of a Hematinic Agent in the Treatment of Postpartum Patients

Postpartum Anemia

United States
American Regent, Inc.

Completed

VIT45 Versus Oral Iron in the Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease

Anemia

United States

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