Clinical Trials Sponsored by Medipost America Inc.

Total 1226 results

Sumitomo Pharma America, Inc.

Completed

First-in-human Study of Oral TP-0184 in Patients With Advanced Solid Tumors

Advanced Solid Tumors

United States
Sumitomo Pharma America, Inc.

Completed

A Study of BBI608 in Adult Patients With Advanced Malignancies

Cancer, Advanced Malignancies

Canada, United States
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.

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
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
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

3

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