Search clinical trials for: Vildagliptin and Metformin Hydrochloride 50/1000 mg FCT

Total 474563 results

Inmunotek S.L.

Completed

Dose Finding for the Treatment of Rhinitis/Rhinoconjunctivitis Against Grass Pollen Allergy (MG56)

Rhinitis | Rhinoconjunctivitis

Spain
Pfizer's Upjohn has merged with Mylan to form Viatris...

Completed

A Study to Assess if Epanutin Infatabs 50 mg From Germany Are Similar to Dilantin Infatabs 50 mg From Australia

Healthy

Singapore
Woolsthorpe Technologies, LLC

Completed

Cardiac Output Pulmonary Arterial Catheter Compared to FloWave™ 1000

Aortic Valve Disease | Mitral Regurgitation | Mitral Valve Prolapse | Congestive Heart Failure | Ischemic Cardiomyopathy | Tricuspid Regurgitation

United States
ApoPharma

Completed

Safety and Acceptability of Deferiprone Delayed Release Tablets in Patients With Systemic Iron Overload (TWICE)

Iron Overload Due to Repeated Red Blood Cell Transfusions

United States, Canada, Greece, Italy
Muğla Sıtkı Koçman University

Completed

The Effect of Kinesio Taping Tension on the Pain Threshold and Tolerance

PRESSURE PAIN THRESHOLD | PAIN TOLERANCE | KINESIOTAPING

Turkey
Chong Kun Dang Pharmaceutical

Completed

A Clinical Study to Compare the Pharmacokinetic Characteristics of CKD-395 0.5/1000 mg in Healthy Male Volunteers

Diabetes Mellitus, Type II

Korea, Republic of
Pamukkale University

Unknown

Comparison of Dexketoprofen, Paracetamol and Ibuprofen in the Treatment of Primary Dysmenorrhea

Dysmenorrhea

Turkey
Global Alliance for TB Drug Development

Completed

Food Effect Study on the Bioavailability and PK of PA-824 Tablets in Healthy Adult Subjects (CL-009) (CL-009)

Tuberculosis

United States
German University in Cairo

Recruiting

Drug Repurposing Using Metformin for Improving the Therapeutic Outcome in Multiple Sclerosis Patients

Multiple Sclerosis

Egypt
National Natural Science Foundation of China

Active, not recruiting

A Study on Relationship Between Resected Normal Liver Parenchymal Volume（RNLV）and Post-Hepatectomy Liver Failure (PHLF) (RNLV)

Liver Failure

China
Air Liquide Santé International

Completed

Use of 50% Nitrous Oxide / 50% Oxygen Premix During Liver Biopsy of Focal Lesion

Liver Biopsy

France
GlaxoSmithKline

Completed

Safety, Tolerability and Pharmacokinetics of Single and Repeat Doses of GSK2292767 in Healthy Participants Who Smoke Cigarettes

Asthma

United Kingdom
Sandoz

Completed

Relative Bioavailability Study of Bicalutamide 50 mg Tablet and Casodex Following a 50 mg Dose in Healthy Subjects Under Fed Conditions

Prostate Cancer | Hirsutism
Nutricia Research

Completed

Glucose Response to a Formula for Patients at Risk of Hypoglycaemia (EFFECT)

Postprandial Hypoglycemia

Netherlands
Centre hospitalier de l'Université de Montréal...

Completed

Impact of MELD Score for 1000 Consecutive Liver Transplantations

End Stage Liver Disease

Canada
Yonsei University

Completed

Dose-ranging Study of Ramosetron for the Prevention of Nausea and Vomiting After Gynecologic Laparoscopic Surgery

Postoperative Nausea and Vomiting

Korea, Republic of
Egalet Ltd

Completed

A Efficacy and Safety Trial of Controlled Release (CR) Morphine in Cancer Patients

Pain | Cancer

Lithuania, Poland
Janssen Research & Development, LLC

Completed

A Study to Evaluate the Effects of JNJ-54861911 on Amyloid Beta Processing in Cerebrospinal Fluid and Plasma in Patients With Prodromal Alzheimer's Disease

Alzheimer Disease

Spain, Netherlands, Belgium, Sweden
Johnson & Johnson Pharmaceutical Research & Development...

Completed

A Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-40411813 in Male and Female Elderly Patients

Healthy

Belgium
Armed Forces Institute of Urology, Rawalpindi

Completed

Comparison of Post-Operative Analgesia After Percutaneous Nephrolithotomy.

Pain | Postoperative Pain

Pakistan
S1 Biopharma, Inc.

Completed

Phase 1b/2a Unblinded Study of Responses in Premenopausal Women With HSDD to Lorexys Evaluating Efficacy and Safety (PURPLE)

Hypoactive Sexual Desire Disorder (DSM-IV-TR Defined) | Sexual Interest/Arousal Disorder (DSM-5 Defined)

United States
Poznan University of Life Sciences

Unknown

Polyunsaturated Fatty Acids Supplementation and Blood Metabolome

Healthy

Poland
Italfarmaco

Completed

ITF2984 Repeated Doses Study in Healthy Volunteers (MAD)

Healthy Male Volunteers

Italy, United Kingdom
Dong-A ST Co., Ltd.

Completed

A Study to Investigate the Bioequivalence Test of DA-1229_01(A) at Fed State

Type2 Diabetes

Korea, Republic of
Hoffmann-La Roche

Completed

Tocilizumab Real-Life Human Factors (RLHFs) Validation Study

Rheumatoid Arthritis

United States
Astellas Pharma Europe Ltd.

Completed

A Study to Determine Pharmacokinetics of Children Receiving Modigraf (Tacrolimus Granules) Following Solid Organ Transplantation (OPTION)

Liver Transplantation | Kidney Transplantation | Heart Transplantation

Belgium, France, Germany, Poland, Spain, United Kingdom
Novartis Vaccines

Completed

Safety and Immunogenicity of A/H1N1-SOIV (Swine Flu) Vaccine With and Without Adjuvant in Children, Adolescents and Adults (3 to 64 Years)

Novel 2009 Influenza H1N1

Costa Rica
Takeda

Terminated

Fasiglifam 25 mg BID vs 50 mg QD

Type 2 Diabetes Mellitus

United States, Poland, Ukraine, Taiwan, Bulgaria, Romania, Slovakia
Dr. Falk Pharma GmbH

Completed

TID 1000 mg Mesalazine Versus TID 2x500 mg Mesalazine in Active Ulcerative Colitis (UC)

Active Ulcerative Colitis

Germany
Dr. Reddy's Laboratories Limited

Completed

Bioavailability Study of Ciprofloxacin 1000 mg ER Tablets of Dr. Reddy's Under Fasting Conditions

Fasting

United States
Geisinger Clinic

Recruiting

Virtual Reality vs Nitrous Oxide in Pediatric Dentistry

Pediatric Dentistry

United States
Genetesis Inc.

Recruiting

A Registry of Cardiac PET and CardioFlux Magnetocardiography in Patients With Suspected Coronary Ischemia. (Magneto-PET)

Coronary; Ischemic

United States
Second Affiliated Hospital, School of Medicine,...
Changxing People's Hospital

Recruiting

Serplulimab Combined With FOLFIRI and Bevacizumab in the Treatment of Colon Cancer Peritoneal Metastases

Unresectable Colon Cancer Peritoneal Metastases | PMMR/Ras/BRAF Wild-type

China
Ophthotech Corporation

Completed

A Phase 1, Safety, Tolerability and Pharmacokinetic Profile of Intravitreous Injections of E10030 (Anti-PDGF Pegylated Aptamer) in Subjects With Neovascular Age-Related Macular Degeneration

Age-related Macular Degeneration

United States
Dr.Gerhard Kaufmann

Completed

Short-term Results After Minimally Invasive Chevron Osteotomy for Hallux Valgus Correction

Hallux Valgus | Minimally Invasive Surgical Procedures

Austria
Bristol-Myers Squibb

Completed

A Study to Assess the Effect of BMS-986419 on the Single Dose Drug Levels of Probe Substrates in Healthy Participants

Healthy Volunteers

United States
Genetesis Inc.

Completed

Acute Coronary Syndrome CardioFlux TM Study (ACCMED) (MAGNETO)

Acute Myocardial Injuries

United States
Genetesis Inc.

Suspended

Mason Heart Study With MCG (MHS-MCG)

Acute Myocardial Injuries

United States
Invitae Corporation

Completed

PROCLAIM: Germline Genetic Testing for Prostate Cancer Patients

Prostate Cancer

United States
FRESCA Medical

Completed

Non-Inferiority Study of the FRESCA Mask Versus Existing CPAP Mask for Treatment of Obstructive Sleep Apnea

Obstructive Sleep Apnea | Sleep Apnea | OSA

United States
Aesculap AG

Completed

Treatment of Coronary Artery Disease (CAD) With Bare Metal Stent (BMS) Followed by Paclitaxel-Coated Balloon Catheter Versus Paclitaxel-Eluting Stent

Coronary Artery Disease

Poland
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Evaluating Single Ascending Doses Of ILS-920

Acute Ischemic Stroke
Wyeth is now a wholly owned subsidiary of Pfizer

Terminated

Study Evaluating HTC-867 in Healthy Young and Elderly Subjects

Healthy Subjects

United States
Wyeth is now a wholly owned subsidiary of Pfizer
Solvay Pharmaceuticals

Terminated

Study Evaluating the Safety and Tolerability of Single Ascending Dose (SAD) SLV-351 in Healthy Subjects

Healthy
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Evaluating the Safety, Tolerability, and Pharmacokinetics (PK) of HKI-357 Administered Orally to Healthy Subjects

Healthy
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Single Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously

Arrhythmia

United States
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study of the Safety, Tolerability, and PK of PRA-027 Administered to Women of Nonchildbearing Potential

Fibroid

United States
GlaxoSmithKline

Completed

Evaluation of Single Doses of GSK962040 in Critically Ill Patients With Enteral Feed Intolerance

Gastroparesis

Australia
Repros Therapeutics Inc.

Terminated

Evaluate PK and Safety of Proellex® in Females With Various Stages of Impaired Renal Function and Healthy Females

Renal Impairment

United States
Sandoz

Completed

Relative Bioavailability Study of Bicalutamide 50 mg Tablet and Casodex Following a 50 mg Dose in Healthy Subjects Under Fasting Conditions

Prostate Cancer | Hirsutism

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