Search clinical trials for: Phenylephrine HCl (Sinus Comfort, BAY112476)

Total 47 results

Bayer

Completed

Study to Find Out Whether Participants With a History of Stuffy Nose Due to Allergic Reactions in the Nose Would Intend to Buy Drug Phenylephrine Hydrochloride Extended Release Tablets After Receiving it Once in This Study

Nasal Congestion Due to Allergic Rhinitis

United States
Bayer

Completed

Bioequivalence of Single Dose Phenylephrine Extended Release Tablets and Phenylephrine HCl Immediate Release Tablets Dosed Every Four Hours (P08340)(COMPLETED)

Nasal Congestion
University of Minnesota

Completed

ValGanciclovir Versus ValAcyclovir for Viral Prophylaxis in Kidney Transplantation

Epstein-Barr Virus Infections | Cytomegalovirus Infections | Transplantation Infection

United States
Johnson & Johnson Consumer Inc. (J&JCI)

Terminated

Randomized, Double-blind, Placebo-Controlled, Efficacy Study of a New Formulation of Phenylephrine HCL in the Common Cold (PIER)

Common Cold

Canada
Bayer

Completed

Consumer Preference Study of Two Formulations of Phenylephrine Hydrochloride (Study CL2008-15)(P07530)(COMPLETED)

Seasonal Allergic Rhinitis | Vasomotor Rhinitis
Novartis

Withdrawn

Safety of Phenylephrine Hydrochloride, Acetaminophen, Dimethindene Maleate Compared to Phenylephrine Hydrochloride Alone in Healthy Volunteers

Blood Pressure | Arrhythmias | Heart Rate

Brazil
Bayer

Completed

Continuous Dosing of BAY73-4506 in Patients With Advanced Malignancies

Neoplasm

United States
Omeros Corporation

Completed

A Randomized Study in Children Ages Birth Through Three Years Undergoing Unilateral Cataract Extraction With or Without Lens Replacement (ILR7)

Congenital Cataract | Unilateral Cataract Extraction

United States
Bayer

Completed

Safety Study Comparing Phenylephrine HCL Extended Release Tablets 30 mg and Placebo (Study CL2007-07)(P07529)(COMPLETED)

Blood Pressure | Human Experimentation
McNeil AB

Completed

To Test Bioequivalence Between Two Formulations of Paracetamol/Phenylephrine

Respiratory Tract Infections

Ireland
Allergan

Completed

Safety and Efficacy of Oxymetazoline HCl Cream 1.0% in Patients With Persistent Erythema Associated With Rosacea

Erythema | Rosacea

United States
Johnson & Johnson Consumer and Personal Products...

Completed

Phenylephrine Pediatric Pharmacokinetic Study

Rhinitis

United States
St. Renatus, LLC
Rho, Inc.; Triligent International

Terminated

Comparison of Intranasal Kovacaine Mist, Tetracaine Alone, and Placebo for Anesthetizing Maxillary Teeth

Anesthesia

United States
Boehringer Ingelheim

Completed

Single Dose of BI 1744 CL in Patients With Mild and Moderate Hepatic Impairment Compared to Subjects With Normal Hepatic Function

Liver Diseases | Healthy
St. Renatus, LLC
Rho, Inc.; Triligent International

Completed

Comparison of Intranasal Kovacaine Mist, Tetracaine Alone, and Placebo for Anesthetizing Maxillary Teeth in Adults

Anesthesia

United States
Boehringer Ingelheim

Completed

A Study to Assess Safety, Tolerability and Pharmacokinetics of Single Rising Inhaled Doses of BI 1744 CL in Healthy Male and Female Volunteers

Healthy
Boehringer Ingelheim

Terminated

Safety, Tolerability and Pharmacokinetics Study of BI 1744 CL in Healthy Male Subjects

Healthy
Bayer

Completed

Effects of Phenylephrine on Nasal Congestion in Participants With Seasonal Allergic Rhinitis (P08156 AM2)(Completed)

Rhinitis | Seasonal Rhinitis
University of North Carolina, Chapel Hill

Withdrawn

Efficacy of Tetracaine/Oxymetazoline Nasal Spray for Endodontic Treatment

Local Anesthesia | Endodontic Disease | Endodontic Inflammation | Dental Anesthesia
St. Renatus, LLC
Rho, Inc.; Triligent International; Analytical Bio-Chemistry Laboratories, Inc.

Completed

Safety and Pharmacokinetics of Kovacaine Nasal Spray (24 Hour Blood Collection)

Anesthesia

United States
GlaxoSmithKline

Withdrawn

An Efficacy and Safety Study of Theraflu Day Powder as Oral Solution for Cold and Flu

Infections, Respiratory Tract
St. Renatus, LLC
Rho, Inc.; Ground Zero Pharmaceuticals

Completed

Dose-Escalation Safety and Pharmacokinetic Study of K305

Anesthesia

United States
St. Renatus, LLC
Rho, Inc.; Triligent International; Analytical Bio-Chemistry Laboratories, Inc.

Completed

Safety and Pharmacokinetics of Kovacaine Nasal Spray in Pediatric Subjects

Anesthesia

United States
St. Renatus, LLC
Rho, Inc.; Triligent International

Completed

Comparison of Intranasal Kovacaine Mist, and Placebo for Anesthetizing Maxillary Teeth in Pediatric Patients

Anesthesia

United States
St. Renatus, LLC
Rho, Inc.; Triligent International

Completed

Comparison of Intranasal Kovacaine Mist, and Placebo for Anesthetizing Maxillary Teeth in Adults

Anesthesia

United States
St. Renatus, LLC

Completed

Comparison of Anesthetic Efficacy of Bilateral and Unillateral Application of Kovacaine Mist in Healthy Volunteers

Anesthesia

United States
St. Renatus, LLC
Rho, Inc.; Triligent International

Completed

Dose-Ranging Study of Intranasal Kovacaine Mist in Pediatric Subjects

Anesthesia

United States
Emalex Biosciences Inc.
Syneos Health; Nuventra

Terminated

Drug-Drug Interaction Study to Evaluate the Effects of Ecopipam on the Pharmacokinetics of Multiple Substrates

Drug-Interactions

United States
Cancer Insight, LLC
Bristol-Myers Squibb; Cancer Research Institute, New York City; Akamis Bio

Active, not recruiting

Exploratory Platform Trial to Evaluate Immunotherapy Combinations With Chemotherapy for the Treatment of Patients With Previously Untreated Metastatic Pancreatic Adenocarcinoma (REVOLUTION)

Metastatic Pancreatic Adenocarcinoma

United States
Aclaris Therapeutics, Inc.

Completed

Safety and Tolerability of Oxymetazoline and Energy-Based Therapy in Participants With Rosacea

Rosacea

United States
GlaxoSmithKline

Withdrawn

An Efficacy and Safety Study of Theraflu Night Powder as Oral Solution for Cold and Flu

Infections, Respiratory Tract
Allergan

Completed

A Long-Term Safety and Efficacy Study AGN-19920 in Patients With Persistent Erythema Associated With Rosacea

Erythema | Rosacea

United States
Hepa C

Completed

Effectiveness, Safety and Clinical Outcomes of Elbasvir/Grazoprevir: Results From a Spanish Real World Cohort

Hepatitis C

Spain
Eisai Inc.

Completed

A Dose-ranging Study to Evaluate the Safety and Efficacy of LUSEDRA (Fospropofol Disodium) as an Intravenous Sedative for Diagnostic or Therapeutic Colonoscopy in Adult Special Populations

Sedation

United States
St. Renatus, LLC
Rho, Inc.; Ground Zero Pharmaceuticals

Completed

Safety and Effectiveness of Kovacaine Nasal Spray for Dental Anesthesia

Dental Anesthesia Efficacy

United States
Johnson & Johnson Consumer and Personal Products...

Completed

A Bioequivalence Study Between Two Brands of Medications to Treat Cough & Cold Symptoms

Healthy Volunteers | Bioequivalence

Russian Federation
Eye Therapies, LLC
ORA, Inc.

Completed

A Single-Center, Randomized, Double-Masked, Placebo and Active Controlled, Dose-Ranging Evaluation of the Duration of Action of Brimonidine Tartrate Ophthalmic Solution in the Control of Ocular Redness Induced by Conjunctival Allergen Challenge (CAC)

Allergic Conjunctivitis

United States
Candela Corporation

Completed

Pulsed Dye Laser Treatment and Oxymetazoline Hydrochloride (HCL) 1% Cream for Erythematotelangiectatic Rosacea

Erythematotelangiectatic Rosacea

United States
Dr. Reddy's Laboratories Limited

Completed

Bioequivalence Study of Naproxen Sodium 220 mg & Pseudoephedrine HCl 120 mg ER Tablets of Dr. Reddy's Under Fed Conditions

Healthy

India
Dr. Reddy's Laboratories Limited

Completed

Bioequivalence Study of Naproxen Sodium 220 mg & Pseudoephedrine HCl 120 mg ER Tablets of Dr. Reddy's Under Fasting Conditions

Healthy

India
University of South Florida

Completed

Minocycline in the Treatment of Angelman Syndrome

Angelman Syndrome

United States
Louisiana State University Health Sciences Center...

Unknown

: Pulpal Blood Flow With the Use of Intra-nasal Anesthetic

Local Anesthetic Drug Adverse Reaction | Local Infiltration | Pulp Disease, Dental
HTL-Strefa S.A.

Completed

Capillary Blood Volume and Pain Perception Obtained in a Process of Puncturing With Different Safety Lancets

Healthy

Poland
ProgenaBiome
Topelia Therapeutics

Active, not recruiting

Trial of Combination Therapy to Treat COVID-19 Infection

Coronavirus Infection | Covid-19 | COVID | Corona Virus Infection | SARS-CoV Infection | SARS-CoV2 | Coronavirus-19

United States
M.D. Anderson Cancer Center
National Cancer Institute (NCI)

Active, not recruiting

Ixazomib, Gemcitabine, and Doxorubicin in Treating Patients With Locally Advanced or Metastatic Kidney Cancer

Metastatic Renal Cell Carcinoma | Stage III Renal Cell Cancer AJCC v8 | Stage IV Renal Cell Cancer AJCC v8 | Metastatic Kidney Medullary Carcinoma | SMARCB1 Negative

United States
Rutgers, The State University of New Jersey
National Cancer Institute (NCI); Rutgers Cancer Institute of New Jersey

Active, not recruiting

Pegylated Liposomal Doxorubicin Hydrochloride and Carboplatin Followed by Surgery and Paclitaxel in Treating Patients With Triple Negative Stage II-III Breast Cancer

Stage IIIA Breast Cancer | Stage IIIB Breast Cancer | Triple-negative Breast Cancer | Stage IIA Breast Cancer | Stage IIB Breast Cancer | Stage IIIC Breast Cancer | Estrogen Receptor-negative Breast Cancer | Progesterone Receptor-negative Breast Cancer | HER2-negative Breast Cancer

United States
Vanderbilt University

Completed

Treatment of Orthostatic Hypotension in Autonomic Failure

Orthostatic Hypotension | Autonomic Failure

United States

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