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Generated: December 10, 2018

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CLINICAL TRIALS PROFILE FOR PROTONIX

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Clinical Trials for Protonix

Trial ID Title Status Sponsor Phase Summary
NCT00133770 Intravenous (IV) Pantoprazole in Erosive Esophagitis Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 4 The aim of this study is to examine whether pantoprazole (Protonix) given through continuous intravenous infusion for 72 hours is superior to Protonix given through once a day IV injection in the treatment of erosive esophagitis.
NCT00133770 Intravenous (IV) Pantoprazole in Erosive Esophagitis Completed Emory University Phase 4 The aim of this study is to examine whether pantoprazole (Protonix) given through continuous intravenous infusion for 72 hours is superior to Protonix given through once a day IV injection in the treatment of erosive esophagitis.
NCT00206050 Study of Intragastric pH Profile After 5 Days Pantoprazole 40 mg iv Followed by Oral Esomeprazole 40 mg po or Oral Pantoprazole 40 mg po Completed AstraZeneca Phase 4 This Phase IV study is intended to compare intragastric acid suppression of oral esomeprazole (NEXIUM ® Delayed-Release Capsules) with that of oral pantoprazole (PROTONIX ® Delayed Release Tablets ), in subjects who continue to require acid-suppressive therapy following a course of intravenous (iv) pantoprazole (PROTONIX ® I.V. for Injection).
NCT00625274 A Randomized, Open-Label, Comparative 3-Way Treatment Crossover Study of 24-Hour Intragastric pH Profile of Once Daily Oral Administration of Esomeprazole 40mg, Lansoprazole 30mg, and Pantoprazole 40mg at Steady State in NSAID-Using Patients Completed AstraZeneca Phase 4 This study looks at controlling intragastric pH following administration of esomeprazole 40 mg, lansoprazole 30 mg and pantoprazole 40 mg taken orally, once daily in patients taking either non-selective or cyclooxygenase-2 (COX-2) selective nonsteroidal anti-inflammatory drugs (NSAIDs).
NCT00674245 Effect of Pantoprazole 40mg Daily vs Placebo on Power Spectral Analysis of the Sleep EEG of Patients With GERD. Completed Southern Arizona VA Health Care System Phase 2/Phase 3 The purpose of this research study is to determine if treatment with pantoprazole 40 mg daily versus a placebo improves sleep quality in patients with gastroesophageal reflux disease (GERD). Another purpose is to determine if treatment with pantoprazole 40 mg once daily versus a placebo improves sleep outcomes in patients with gastroesophageal reflux disease using spectral analysis of sleep electroencephalogram (EEG).
NCT00699361 Influence of Pantoprazole on Human Myocardial Contractility at Patients With Congestive Heart Failure Withdrawn Johann Wolfgang Goethe University Hospital Phase 3 Recently literature revealed facts, that show H+/K+ ATPase expression is not limited tot he stomach. H+/K+ ATPase was also found in smooth muscle cells and in other tissues (McCabe, R.D. et al., Am J Physiol. 1992). For myocard a localisation is only proven for rats yet (Beisvag, V. et al., Acta Physiol Scand. 2003). Moreover biochemical hints lead us to a highly probability of a myocardial H+/K+ ATPase (Nagashima, R. et al., Jpn Heart J. 1999).
NCT00744419 Intravenous (IV) Pantoprazole for Gastroesophageal Reflux Disease (GERD) in Neonates and Infants Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 1 The purpose of this study is to determine how the body uses and eliminates pantoprazole, a drug used to treat GERD. This is a pharmacokinetic (PK) study. PK is a measure of how much drug is in the blood and how long it takes to leave the body. It is hypothesized that younger infants will need a lower dose than older children to achieve the same PK measurement. The results of this study will be used to determine the best dose of the drug to use in each age group. Pantoprazole is a drug used to decrease acid production. The use of pantoprazole has not been approved for use in children. Pantoprazole is approved for use of acid-related and stomach disorders in adults.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Protonix

Condition Name

Condition Name for Protonix
Intervention Trials
Healthy 10
Gastroesophageal Reflux 2
Pain, Postoperative 1
Esophagitis 1
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Condition MeSH

Condition MeSH for Protonix
Intervention Trials
Gastroesophageal Reflux 5
Psychotic Disorders 2
Mental Disorders 2
Fractures, Bone 1
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Clinical Trial Locations for Protonix

Trials by Country

Trials by Country for Protonix
Location Trials
United States 16
India 6
Canada 2
Netherlands 1
Serbia 1
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Trials by US State

Trials by US State for Protonix
Location Trials
Missouri 4
Texas 2
New Jersey 1
Pennsylvania 1
Kentucky 1
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Clinical Trial Progress for Protonix

Clinical Trial Phase

Clinical Trial Phase for Protonix
Clinical Trial Phase Trials
Phase 4 7
Phase 3 2
Phase 2/Phase 3 2
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Clinical Trial Status

Clinical Trial Status for Protonix
Clinical Trial Phase Trials
Completed 17
Unknown status 2
Not yet recruiting 2
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Clinical Trial Sponsors for Protonix

Sponsor Name

Sponsor Name for Protonix
Sponsor Trials
Dr. Reddy's Laboratories Limited 2
Kremers Urban Development Company 2
Wyeth is now a wholly owned subsidiary of Pfizer 2
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Sponsor Type

Sponsor Type for Protonix
Sponsor Trials
Industry 19
Other 13
U.S. Fed 1
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Serving hundreds of leading biopharmaceutical companies globally:

AstraZeneca
McKesson
Harvard Business School
Express Scripts
Cantor Fitzgerald
Cipla
Boehringer Ingelheim
Queensland Health
Colorcon

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