Clinical Trials Sponsored by Reckitt Benckiser Inc.

Total 59 results

Reckitt Benckiser Inc.

Completed

Study to Evaluate the Pharmacokinetics of Mucinex 600 mg Extended-release Bi-layer Tablet in Healthy Volunteers

Healthy Subjects
Reckitt Benckiser Inc.

Completed

Mucinex® ER 600 mg Bi-layer Tablet Versus Guaifenesin Immediate Release (IR) 200 mg q4h

Healthy Subjects
Reckitt Benckiser Inc.

Completed

Mucinex Exploratory Cold Study

Common Cold

United States
Reckitt Benckiser Inc.

Completed

Safety and Efficacy Study of Guaifenesin and Pseudoephedrine for Symptomatic Therapy to Treat Acute RTI (Wait and See)

Acute Upper Respiratory Track Infection

United States
Reckitt Benckiser Inc.

Completed

Bioequivalence Study Comparing Mucinex Extended-release 600 mg Tablets to Immediate-release Guaifenesin 600 mg in Healthy Volunteers

Healthy Subjects
Reckitt Benckiser Inc.

Completed

Study to Characterize the Pharmacokinetics of 3 Marketed Products Containing 200 mg Guaifenesin in Healthy Volunteers.

Healthy Subjects
Reckitt Benckiser LLC

Completed

Study to Evaluate the Pharmacokinetics of Guaifenesin in Adults and Adolescents

Healthy Subjects
Reckitt Benckiser LLC

Completed

Safety & Performance Study of Verruca Treatment Device

Plantar Wart | Verruca

United Kingdom
Reckitt Benckiser LLC

Completed

Study to Evaluate Drug-drug Interactions of Guaifenesin and Hydrocodone Bitartrate

Healthy Subjects
Reckitt Benckiser LLC

Completed

Study to Evaluate the Safety and Tolerability of Mucinex™(Guaifenesin) 600 mg Extended-Release Bi-Layer Tablets in the Treatment of Otherwise Healthy Patients With Symptoms of Cough, Thickened Mucus and Chest Congestion

Healthy Subjects
Reckitt Benckiser LLC

Completed

Study to Evaluate the Pharmacokinetics of Mucinex® 1200 mg Extended-Release Tablet

Healthy Subjects
Reckitt Benckiser LLC

Completed

Evaluating the Effect of Mucinex 1200mg on Mucociliary and Cough Clearance During an Acute Respiratory Infection (MCC/CC)

Acute Respiratory Infection

United States
Reckitt Benckiser LLC

Completed

Evaluation of Tolerance and Acceptability of a Coated Condom

Tolerance and Acceptability of a New Condom Coating

United Kingdom
Indivior Inc.
Reckitt Benckiser LLC

Completed

Study of Two Formulations of Buprenorphine HCl in Opioid-dependent Subjects on Buprenorphine Maintenance Therapy (Study P04451) (COMPLETED)

Opioid Dependency
Reckitt Benckiser LLC

Completed

Mucinex® ER 600 mg Bi-Layer Tablet Fed and Fasted

Healthy Subjects
Reckitt Benckiser LLC

Completed

Placebo-Controlled Onset-of-Action Study of Flurbiprofen Utilizing the Double-Stopwatch Method

Sore Throat | Acute Pharyngitis

United States
Reckitt Benckiser LLC

Completed

A Study of Flurbiprofen 8.75 mg Lozenge in Patients With Pharyngitis

Pharyngitis

United States
Reckitt Benckiser LLC

Completed

A Study of Flurbiprofen 8.75 mg Lozenge in Patient With Pharyngitis

Pharyngitis

United States
Reckitt Benckiser LLC

Completed

Safety and Efficacy of Mucinex and IR Guaifenesin the Treatment of Symptoms of Acute Upper Respiratory Tract Infections

Acute Upper Respiratory Tract Infection

United States
Reckitt Benckiser Healthcare (UK) Limited

Recruiting

A Clinical Investigation to Assess the Effectiveness of Benzocaine in NRL Condoms in Healthy Adult Men Who Feel They Ejaculate Too Quickly During Vaginal Sex

Ejaculation Delayed

Germany
Reckitt Benckiser Healthcare (UK) Limited

Completed

A Clinical Investigation to Assess the Performance of Natural Rubber Latex Condoms in Couples

Control of Pregnancy | Prevention of Sexually Transmitted Infections

Thailand
Reckitt Benckiser Healthcare (UK) Limited

Completed

Ibuprofen Suspension Bioequivalence Study

Healthy Volunteer Study

United Kingdom
Reckitt Benckiser Healthcare (UK) Limited

Withdrawn

A Clinical Investigation to Assess the Effectiveness of Benzocaine Condoms in Healthy Adult Men

Ejaculation Delayed
Reckitt Benckiser Healthcare (UK) Limited

Unknown

An Internet Mediated Research Study to Assess the Quality of Life of Consumers With Self-reported Fungal Nail Infection (Onychomycosis) During Treatment With Scholl Fungal Nail.

Onychomycosis of Toenail

United Kingdom
Reckitt Benckiser Healthcare (UK) Limited

Terminated

Gamma Scintigraphy Study to Investigate Tablet Disintegration in Healthy Volunteers.

Healthy Subjects
Reckitt Benckiser Healthcare (UK) Limited

Completed

Compound Sodium Alginate Oral Suspension Sachet Symptomatic Relief Study

Gastro-esophageal Reflux Disease (GERD)

China
Reckitt Benckiser Healthcare (UK) Limited

Completed

Compound Sodium Alginate Double Action Chewable Tablet Symptomatic Relief Study

Dyspepsia | Gastroesophageal Reflux Disease

China
Reckitt Benckiser Healthcare (UK) Limited

Completed

Effectiveness and Safety of a Water-based and a Silicone-based Personal Lubricants With Sensory Action

Vaginal Dryness | Dyspareunia

Germany
Reckitt Benckiser Healthcare (UK) Limited

Completed

Clinical Investigation to Assess the Acid Neutralisation Activity of a Calcite Chewing Gum

Esophagitis | Gastro Oesophageal Reflux Disease

Ireland
Reckitt Benckiser Healthcare (UK) Limited

Completed

Ibuprofen 4% (w/v) Pivotal Bioequivalence Study

Bioequivalence of the Test Formulation
Reckitt Benckiser Healthcare (UK) Limited

Completed

Francis Biomechanics Study

Healthy Subject

Belgium
Reckitt Benckiser Healthcare (UK) Limited

Terminated

Compound Sodium Alginate Oral Suspension Sachet 4-hour Esophageal pH Study in GERD Patients

Gastro-esophageal Reflux Disease (GERD)

China
Reckitt Benckiser Healthcare (UK) Limited

Completed

A Clinical Investigation to Evaluate the Safety and Performance of a Treatment Kit for Ingrowing Toenail

Onychomycosis of Toenails

United Kingdom
Reckitt Benckiser Healthcare (UK) Limited

Completed

Compound Sodium Alginate Double Action Chewable Tablets 4-hour Esophageal pH Study in GERD Patients

Gastroesophageal Reflux Disease

China
Reckitt Benckiser LLC
Premier Research Group plc; Aptuit Inc.

Completed

Ibuprofen/Acetaminophen Versus Nurofen Plus® and Panadeine® Extra Dental Pain Study

Post-operative Pain

United States
Northumbria University
Reckitt Benckiser Group PLC

Recruiting

Evaluating the Effects of Prebiotics on Sleep, the Gut Microbiome, Cognition, Immune Function and Stress

Sleep

United Kingdom
Reckitt Benckiser Healthcare (UK) Limited
Intertek

Completed

To Evaluate the in Use Tolerance of E45 Eczema Repair Emollient in Babies and Children With (Very(Dry/Atopic Skin

Atopic Dermatitis / Eczema
Reckitt Benckiser Healthcare (UK) Limited
Simbec Research

Completed

Naproxen Sodium (2 x 220 mg) Fasted Comparative Bioavailability Study

Healthy
University of Melbourne
Reckitt Benckiser LLC

Recruiting

Effect of Over-the-counter NSAIDS on Cough Reflex Sensitivity in Patients With Upper Respiratory Tract Infections

Cough | Upper Respiratory Tract Infections

Australia
Reckitt Benckiser Healthcare (UK) Limited
Intertek

Completed

Evaluation of the Performance of a Fungal Nail Treatment on the Visual Signs of Onychomycosis

Onychomycosis of Toenails

United Kingdom
University of North Carolina, Chapel Hill
Reckitt Benckiser Inc.

Completed

Evaluating the Effect of Mucinex® 1200 mg on Mucociliary and Cough Clearance From the Human Lung

Mucociliary Clearance

United States
Reckitt Benckiser Healthcare (UK) Limited
proDERM GmbH

Completed

A Clinical Investigation Into the Effectiveness and Safety of Five Water Based Personal Lubricants.

Vaginal Dryness | Dyspareunia

Germany
Reckitt Benckiser Healthcare (UK) Limited
Simbec Research

Completed

Ibuprofen Bioavailability Study

Healthy

United Kingdom
Reckitt Benckiser Healthcare (UK) Limited
Simbec Research

Completed

Ibuprofen and Paracetamol Pharmacokinetic Study

Healthy Volunteer Study
Reckitt Benckiser Healthcare (UK) Limited
SynteractHCR Deutschland GmbH

Terminated

Effectiveness of Four Orthotic Insoles on Pain in the Lower Body Associated With Musculoskeletal Stress

Musculoskeletal Pain

United Kingdom
Washington University School of Medicine
Reckitt Benckiser LLC

Completed

Buprenorphine Used With Treatment Resistant Depression in Older Adults (IRLGreyB)

Depression | Major Depressive Disorder

United States
Reckitt Benckiser Healthcare (UK) Limited
Alba Science Ltd

Completed

A 24 Hour Occlusive Single Patch Test to Assess Acute Tolerance of Pre Lubricated Condom on a Panel of Healthy Adult Subjects

Healthy

United Kingdom
Reckitt Benckiser Healthcare (UK) Limited
Skin Investigation Technology

Completed

A 47 Hour Occlusive Cutaneous Skin Patch Test on Adult Subjects With Dry/Atopic Skin

Eczema

Germany
Reckitt Benckiser Healthcare (UK) Limited
O4 Research

Completed

A 3 Day In-use Assessment of the Scholl Corn Foam Cushions on Pain Levels Associated With Heloma Durum.

Heloma Durum

Ireland
Reckitt Benckiser Healthcare (UK) Limited
Simbec Research

Terminated

Nurofen Ibuprofen Orodispersible Tablet Disintegration Study

Healthy

United Kingdom

3

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