Search clinical trials for: Cefpodoxime proxetil

Total 40 results

Entasis Therapeutics

Completed

A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics (PK, the Measure of How the Human Body Processes a Substance) of ETX0282 When Administered Orally to Healthy Participants

Healthy Volunteers

Australia
St. Jude Children's Research Hospital
National Institutes of Health (NIH)

Completed

Prevention of Diarrhea in Patients Taking IV Irinotecan for Relapsed or Difficult to Treat Pediatric Solid Tumors

Diarrhea | Neoplasm

United States
St. Jude Children's Research Hospital
AstraZeneca; National Institutes of Health (NIH)

Completed

Study of ZD1839 Combined With Irinotecan and Vincristine in Pediatric Patients With Refractory Solid Tumors

Solid Tumors

United States
University of Washington

Completed

Cefpodoxime vs Ciprofloxacin for Acute Cystitis

Urinary Tract Infection

United States
Helsinki University Central Hospital

Completed

Nut Allergy Study: Double-blind Challenge and Oral Desensitization

Nut Allergy

Finland
Washington University School of Medicine

Completed

Healthy Patients & Effect of Antibiotics

Anti-bacterial Agents | Microbiota

United States
ProJenX
Worldwide Clinical Trials

Recruiting

A Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Doses of Prosetin in Healthy Volunteers (PRO-101)

Amyotrophic Lateral Sclerosis

United States
AstraZeneca

Completed

Study to Compare PT007 to Placebo MDI and Open-Label Proventil® HFA in Adult and Adolescent Subjects With Asthma

Asthma

United States
University of Michigan Rogel Cancer Center
Millennium Pharmaceuticals, Inc.

Completed

Study of Irinotecan and Bortezomib in Children With Recurrent/Refractory Neuroblastoma

Neuroblastoma

United States
Amphastar Pharmaceuticals, Inc.

Completed

Evaluation of Pharmacokinetics and Safety of A006 in Healthy Volunteers (A006-D)

Asthma

United States
Amphastar Pharmaceuticals, Inc.

Terminated

Controlled, 12-Week Study of Albuterol HFA Versus the Active Control, Proventil(R)-HFA in Asthmatic Patients

Asthma

United States
Amphastar Pharmaceuticals, Inc.

Completed

Albuterol DPI (A006) Clinical Study-B3:Efficacy, Dose-ranging and Safety Evaluation (A006-B3)

Asthma

United States
Nemours Children's Clinic

Completed

Dose-response of Albuterol in Asthmatics

Asthma

United States
Medical University of Vienna

Completed

Micronutrient Supplementation in PCO-syndrome

Polycystic Ovary Syndrome | Infertility, Female | Micronutrient Deficiency

Austria
University of Southern Denmark

Unknown

Paroxetines Effect on Tramadols Metabolism and Pharmakodynamics: a Dose Response Study

Depression | Pain
Lipomedix Pharmaceuticals Inc.

Terminated

Assessment of Safety and Therapeutic Efficacy of Promitil in Combination With Folfox in Patients With GI Malignancies

Cancer | Gastro-Intestinal Intraepithelial Neoplasia

Israel
Lipomedix Pharmaceuticals Inc.

Completed

Intravenously Administered Pegylated Liposomal Mitomycin-C Lipid-based Prodrug (PROMITIL) in Cancer Patients With Solid Tumors.

Cancer | Solid Tumor | Metastatic Colorectal Cancer (mCRC)

Israel
Lumbini Medical College

Completed

Efficacy and Cost Analysis of Steroids in Treatment of Otitis Media With Effusion

Otitis Media With Effusion

Nepal
Lipomedix Pharmaceuticals Inc.

Completed

Intravenously Administered Liposomal PROMITIL in Combination With External Beam Radiotherapy in Cancer Patients

Cancer | Solid Tumor | Metastatic Disease

Israel
University of Florida

Recruiting

Lung Disease and Its Affect on the Work of White Blood Cells in the Lungs

Alpha-1 Antitrypsin Deficiency | Cystic Fibrosis (CF) | AATD | AAT Deficiency

United States
Vanderbilt University Medical Center
National Heart, Lung, and Blood Institute (NHLBI)

Completed

Optimal Albuterol Regimens for Acute Asthma Exacerbations: DBRCT Pilot Study (OARS)

Acute Asthma
Amphastar Pharmaceuticals, Inc.

Completed

Escalating and Cumulative-Dose Study of Pharmacokinetics (PK), Pharmacodynamics (PD) and Safety of A006

Asthma | Chronic Obstructive Pulmonary Disease (COPD) | Bronchospasm

United States
AstraZeneca

Completed

Assessment of the Safety, Efficacy, PK, and Extrapulmonary Pharmacodynamics (PD) of Albuterol Sulfate Pressurized Inhalation Suspension (Hereafter Referred to as AS MDI) Compared to Proventil as an Active Control in Subjects With Asthma

Asthma

United States
University Medical Center of Southern Nevada

Completed

The Various Effects of Gaseous Albuterol on Serum Lactate

Asthma

United States
Children's Hospital Medical Center, Cincinnati

Completed

A Pilot Study of the Addition of Bevacizumab to VOIT Regimen for Relapsed/Refractory Pediatric Solid Tumors (VITAC)

Solid Tumor

United States
Amphastar Pharmaceuticals, Inc.

Completed

Dose-Ranging Study of A006 DPI, in Adult Asthma Patients

Asthma | Bronchospasm

United States
Seton Healthcare Family

Terminated

Comparison of Nebulizers in ED in Pediatric Asthma Patients

Asthma

United States
Oregon Health and Science University

Completed

Preterm Infant Inhaled Albuterol Dosing

Bronchopulmonary Dysplasia | Very Low Birth Weight

United States
Mayo Clinic
National Heart, Lung, and Blood Institute (NHLBI)

Completed

Inhaled Beta-adrenergic Agonists to Treat Pulmonary Vascular Disease in Heart Failure With Preserved EF (BEAT HFpEF): A Randomized Controlled Trial (BEAT HFpEF)

Congestive Heart Failure | Left-Sided Heart Failure | Heart Failure, Left-Sided

United States
Amphastar Pharmaceuticals, Inc.

Terminated

4-Week Study of Efficacy, Safety and PK of Albuterol-HFA Versus Proventil-HFA in Pediatric Asthma

Asthma

United States
Organon and Co
Integrated Therapeutics Group

Completed

Nasonex Compared With Placebo in Participants With Seasonal Allergic Rhinitis (SAR) and Concomitant Asthma (P03280)

Asthma | Rhinitis, Allergic, Seasonal
Teva Branded Pharmaceutical Products R&D, Inc.

Completed

Albuterol HFA MDI in Pediatric Participants With Asthma

Asthma

United States
University of Illinois at Chicago
Agency for Healthcare Research and Quality (AHRQ)

Completed

Reducing Diagnostic Error to Improve Patient Safety in COPD and Asthma (REDEFINE Study) (REDEFINE)

COPD Asthma

United States
NYU Langone Health

Completed

The Effects Of Bronchodilator Therapy On Respiratory And Autonomic Function In Patients With Familial Dysautonomia

Familial Dysautonomia

United States
West Virginia University

Enrolling by invitation

Comparing Oral Versus Parenteral Antimicrobial Therapy (COPAT)

Skin and Soft Tissue Infection | Gastrointestinal Infection | Pulmonary Infection | Bone and Joint Infection | Endovascular Infection | Genitourinary Infection

United States
Northwell Health
AstraZeneca; Jacobi Medical Center; Nassau University Medical Center

Completed

Study of Budesonide as an Addition to Standard Therapy in Adult Asthmatics in the Emergency Room.

Asthma

United States
Merck Sharp & Dohme LLC

Completed

Efficacy and Safety Study of RAGWITEK™ (MK-3641) in Children With Ragweed-Induced Rhinoconjunctivitis With or Without Asthma (MK-3641-008)

Rhinitis, Allergic, Seasonal
ALK-Abelló A/S

Completed

Efficacy and Safety of Grass Sublingual Tablet in Children and Adolescents (P05239 AM3)(COMPLETED)

Allergy | Rhinitis | Conjunctivitis | Rhinoconjunctivitis
ALK-Abelló A/S

Completed

Efficacy and Safety of Grass Sublingual Tablet in Adults (P05238 AM3)(COMPLETED)

Allergy | Rhinitis | Conjunctivitis | Rhinoconjunctivitis
Julio Ramirez
University of Louisville

Terminated

Patients Response to Early Switch To Oral:Osteomyelitis Study (PRESTO:Osteo)

Osteomyelitis

United States

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