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Clinical Trials About "Reckitt Benckiser" RSS

13:24 EDT 20th September 2018 | BioPortfolio

We list hundreds of Clinical Trials about "Reckitt Benckiser" on BioPortfolio. We draw our references from global clinical trials data listed on ClinicalTrials.gov and refresh our database daily.

More Information about "Reckitt Benckiser" on BioPortfolio

We have published hundreds of Reckitt Benckiser news stories on BioPortfolio along with dozens of Reckitt Benckiser Clinical Trials and PubMed Articles about Reckitt Benckiser for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of Reckitt Benckiser Companies in our database. You can also find out about relevant Reckitt Benckiser Drugs and Medications on this site too.

Showing "Reckitt Benckiser" Clinical Trials, all 3

Extremely Relevant

Efficacy of Gaviscon-Advance® in Suppressing Post-supper Acid-pocket and Night-time Acid-reflux in Obese Participants

A randomized, open-label study with antacid-control will be performed over 48 hours period by continuous pH impedance and bravo capsule monitoring. Asymptomatic obese patients will be separated into either groups according to alginate antacid group [Gaviscon Advance (GA)®, Reckitt Benckiser, UK] and non antacid alginate group [simple antacid]. Both groups will be studied for 48 hours using the ambulatory wireless capsule and pH impedance. Participants according to their group ...


Buprenorphine 8 mg Sublingual Tablets Under Fasting Conditions

The object of this study is to compare the rate and extent of absorption of an investigational formulation of buprenorphine 8 mg sublingual tablets manufactured by Barr Laboratories, Inc. to an equivalent oral dose of the commercially available reference product, Subutex® manufactured by Reckitt Benckiser, following and overnight fast of at least 10 hours.

Relevant

Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg/5ml and Nurofen®, Oral Suspension 100 mg/5 ml in Healthy Volunteers Under Fasting Conditions

To demonstrate bioequivalence of single dose test formulation of Ibuprofen,oral suspension 200 mg/5 ml (containing ibuprofen 200 mg) of Pharmtechnology LLC, Republic of Belarus with reference Nurofen® for Children, oral suspension 100 mg / 5 ml (containing ibuprofen 100 mg) of "Reckitt Benckiser Healthcare International Ltd, .", UK in normal, healthy, adult, human subjects under fasting conditions.To monitor adverse events and ensure the safety



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