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Pantoprazole

Generic Name
Pantoprazole
Brand Names
Protonix, Somac Control, Tecta, Pantozol Control, Controloc Control
Drug Type
Small Molecule
Chemical Formula
C16H15F2N3O4S
CAS Number
102625-70-7
Unique Ingredient Identifier
D8TST4O562
Background

Pantoprazole is a first-generation proton pump inhibitor (PPI) used for the management of gastroesophageal reflux disease (GERD), for gastric protection to prevent recurrence of stomach ulcers or gastric damage from chronic use of NSAIDs, and for the treatment of pathological hypersecretory conditions including Zollinger-Ellison (ZE) Syndrome. It can also be found in quadruple regimens for the treatment of H. pylori infections along with other antibiotics including amoxicillin, clarithromycin, and metronidazole, for example. Its efficacy is considered similar to other medications within the PPI class including omeprazole, esomeprazole, lansoprazole, dexlansoprazole, and rabeprazole.

Pantoprazole exerts its stomach acid-suppressing effects by preventing the final step in gastric acid production by covalently binding to sulfhydryl groups of cysteines found on the (H+, K+)-ATPase enzyme at the secretory surface of gastric parietal cell. This effect leads to inhibition of both basal and stimulated gastric acid secretion, irrespective of the stimulus. As the binding of pantoprazole to the (H+, K+)-ATPase enzyme is irreversible and new enzyme needs to be expressed in order to resume acid secretion, pantoprazole's duration of antisecretory effect persists longer than 24 hours.

Due to their good safety profile and as several PPIs are available over the counter without a prescription, their current use in North America is widespread. Long term use of PPIs such as pantoprazole have been associated with possible adverse effects, however, including increased susceptibility to bacterial infections (including gastrointestinal C. difficile), reduced absorption of micronutrients including iron and B12, and an increased risk of developing hypomagnesemia and hypocalcemia which may contribute to osteoporosis and bone fractures later in life.

PPIs such as pantoprazole have also been shown to inhibit the activity of dimethylarginine dimethylaminohydrolase (DDAH), an enzyme necessary for cardiovascular health. DDAH inhibition causes a consequent accumulation of the nitric oxide synthase inhibitor asymmetric dimethylarginie (ADMA), which is thought to cause the association of PPIs with increased risk of cardiovascular events in patients with unstable coronary syndromes.

Pantoprazole doses should be slowly lowered, or tapered, before discontinuing as rapid discontinuation of PPIs such as pantoprazole may cause a rebound effect and a short term increase in hypersecretion.

Indication

Pantoprazole Injection:

Treatment of gastroesophageal reflux disease associated with a history of erosive esophagitis

Pantoprazole for injection is indicated for short-term treatment (7-10 days) of patients having gastroesophageal reflux disease (GERD) with a history of erosive esophagitis, as an alternative to oral medication in patients who are unable to continue taking pantoprazole delayed-release tablets. Safety and efficacy of pantoprazole injection as the initial treatment of patients having GERD with a history of erosive esophagitis have not been demonstrated at this time.

Pathological Hypersecretion Associated with Zollinger-Ellison Syndrome

Pantoprazole for injection is indicated for the treatment of pathological hypersecretory conditions associated with Zollinger-Ellison Syndrome or other neoplastic conditions.

Pantoprazole delayed-release oral suspension:

Short-Term Treatment of erosive esophagitis associated with gastroesophageal reflux disease (GERD)

Indicated in adults and pediatric patients five years of age and above for the short-term treatment (up to 8 weeks) in the healing and symptomatic relief of erosive esophagitis. For adult patients who have not healed after 8 weeks of treatment, an additional 8-week course of pantoprazole may be considered. Safety of treatment beyond 8 weeks in pediatric patients has not been determined.

Maintenance of healing of erosive esophagitis

Indicated for maintenance of healing of erosive esophagitis and reduction in relapse rates of daytime and nighttime heartburn symptoms in adult patients with GERD.

Pathological hypersecretory conditions including Zollinger-Ellison syndrome

Indicated for the long-term treatment of the above conditions.

Associated Conditions
Erosive Esophagitis, GERD With Erosive Esophagitis, Gastro-esophageal Reflux Disease (GERD), Healing, Heartburn, Helicobacter Pylori Infection, Stress Ulcers, Zollinger-Ellison Syndrome, Conditions where a reduction of gastric acid secretion is required, Pathological hypersecretory conditions

Omeprazole and Pantoprazole Antiplatelet Effect of Clopidogrel Clinical Trials(OPEN)

Phase 4
Conditions
Acute Coronary Syndromes
Interventions
First Posted Date
2012-11-28
Last Posted Date
2012-11-28
Lead Sponsor
Yaling Han
Target Recruit Count
620
Registration Number
NCT01735227
Locations
🇨🇳

OPEN trail, Shenyang, Liaoning, China

🇨🇳

ShenyangNH, Shenyang, Liaoning, China

Clinical Study, Multicenter, Randomized With 2 Arms of Pantoprazole + Domperidone and Pantoprazole Isolated at the Gastroesophageal Reflux Disease

Phase 3
Withdrawn
Conditions
Gastroesophageal Reflux Disease
Interventions
First Posted Date
2012-10-19
Last Posted Date
2015-07-24
Lead Sponsor
Eurofarma Laboratorios S.A.
Registration Number
NCT01710462
Locations
🇧🇷

Goiania, Goiania, Goias, Brazil

🇧🇷

Curitiba, Curitiba, Paraná, Brazil

🇧🇷

Campinas, Campinas, São Paulo, Brazil

and more 5 locations

Study to Investigate the Relative Bioavailability, Influence of Pantoprazole Coadministration and Food Effect of Different Oral Formulation of BI 113608

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2012-10-11
Last Posted Date
2017-01-20
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
15
Registration Number
NCT01703858
Locations
🇩🇪

1314.3.1 Boehringer Ingelheim Investigational Site, Ingelheim, Germany

Bioequivalence Study of Pantoprazole Sodium 40 mg Delayed Release Tablets Fasting Study

Not Applicable
Completed
Conditions
Healthy
Interventions
First Posted Date
2012-08-01
Last Posted Date
2012-08-01
Lead Sponsor
Ranbaxy Laboratories Limited
Target Recruit Count
80
Registration Number
NCT01654705
Locations
🇮🇳

Clinical Pharmacology Unit, Ranbaxy Laboratories Limited, Noida, Uttar Pradesh, India

Bioequivalence Study of Pantoprazole Sodium 40 mg Delayed Release Tablets Fed Study

Not Applicable
Completed
Conditions
Healthy
Interventions
First Posted Date
2012-08-01
Last Posted Date
2012-08-01
Lead Sponsor
Ranbaxy Laboratories Limited
Target Recruit Count
40
Registration Number
NCT01654718
Locations
🇮🇳

Clinical Pharmacology Unit, Ranbaxy Laboratories Limited, Noida, Uttar Pradesh, India

The Efficacy of Pantoprazole Treatment in Patients With Functional Dyspepsia

Phase 4
Conditions
Nonulcer Dyspepsia
Interventions
First Posted Date
2012-05-31
Last Posted Date
2012-05-31
Lead Sponsor
Bezmialem Vakif University
Target Recruit Count
200
Registration Number
NCT01608750
Locations
🇹🇷

Bezmialem medical faculty, Istanbul, Turkey

Pantoprazole on Insulin Secretion in Diabetes

Phase 2
Completed
Conditions
Type 2 Diabetes
Interventions
Drug: placebo
First Posted Date
2012-03-01
Last Posted Date
2014-02-21
Lead Sponsor
Coordinación de Investigación en Salud, Mexico
Target Recruit Count
14
Registration Number
NCT01541735
Locations
🇲🇽

Instituto Mexicano del Seguro Social. Hospital de Especialidades., Guadalajara, Jalisco, Mexico

Structured Non-operative Treatment of Knee Osteoarthritis

Not Applicable
Completed
Conditions
Osteoarthritis of the Knee
Interventions
Other: Neuromuscular training (NEMEX-TJR)
Behavioral: Information
Drug: Burana
Behavioral: Dietary counseling
Behavioral: Patient education
Other: Insoles
First Posted Date
2012-02-17
Last Posted Date
2017-10-16
Lead Sponsor
Northern Orthopaedic Division, Denmark
Target Recruit Count
100
Registration Number
NCT01535001
Locations
🇩🇰

Department of Occupational and Physiotherapy, Aalborg Hospital-Aarhus University Hospital, Aalborg, Denmark

🇩🇰

Vendsyssel Hospital, Frederikshavn, Frederikshavn, Denmark

🇩🇰

Farsoe Hospital, Farsø, Denmark

Proton Pump Inhibitors in the Prevention of Iron Reaccumulation in Patient With Hereditary Hemochromatosis

Not Applicable
Conditions
Hemochromatosis
Interventions
First Posted Date
2012-02-02
Last Posted Date
2012-02-02
Lead Sponsor
Maastricht University Medical Center
Target Recruit Count
48
Registration Number
NCT01524757
Locations
🇧🇪

University hospital Gasthuisberg, Leuven, Limburg, Belgium

🇳🇱

Atrium MC Parkstad, Heerlen, Limburg, Netherlands

🇳🇱

Maastricht university medical center, Maastricht, Limburg, Netherlands

A Prospective, Open Label Study Evaluating Two Management Strategies on Gastrointestinal Symptoms in Patients Newly on Treatment With Pradaxa for the Prevention of Stroke and Systemic Embolism With Non-valvular Atrial Fibrillation

Phase 4
Completed
Conditions
Atrial Fibrillation
Interventions
Drug: Pradaxa, within 30 minutes after a meal
First Posted Date
2011-12-16
Last Posted Date
2015-10-05
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
1067
Registration Number
NCT01493557
Locations
🇺🇸

1160.128.1011 Boehringer Ingelheim Investigational Site, Kalispell, Montana, United States

🇺🇸

1160.128.1041 Boehringer Ingelheim Investigational Site, Columbia, Maryland, United States

🇺🇸

1160.128.1068 Boehringer Ingelheim Investigational Site, Roswell, Georgia, United States

and more 100 locations
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