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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
Associated Therapies
-

Symptomatic Relief of Acute Dyspeptic Pain in Emergency Department With Pantoprazole

Phase 4
Completed
Conditions
Dyspepsia
Emergency
Pain
Interventions
Drug: Normal saline
Drug: Pantoprazole
Drug: Oral antacid
Drug: Hyoscine butylbromide
First Posted Date
2011-01-24
Last Posted Date
2013-09-18
Lead Sponsor
Chulalongkorn University
Target Recruit Count
87
Registration Number
NCT01281501
Locations
🇹🇭

Emergency Medicine Unit, King Chulalongkorn Memorial Hospital, Patumwan, Bangkok, Thailand

Is Rebamipide Effective on the Healing of Iatrogenic Gastric Ulcer After Endoscopic Mucosal Resection?

Not Applicable
Completed
Conditions
Stomach Ulcer
Interventions
First Posted Date
2010-07-22
Last Posted Date
2015-09-04
Lead Sponsor
Kangdong Sacred Heart Hospital
Target Recruit Count
290
Registration Number
NCT01167101
Locations
🇰🇷

Kangdong Sacred Heart Hospital, Seoul, Korea, Republic of

Pantoprazole With Doxorubicin for Advanced Cancer Patients With Extension Cohort of Patients With Solid Tumours

Phase 1
Completed
Conditions
Advanced Solid Tumours
Interventions
First Posted Date
2010-07-16
Last Posted Date
2015-07-15
Lead Sponsor
University Health Network, Toronto
Target Recruit Count
24
Registration Number
NCT01163903
Locations
🇨🇦

Princess Margaret Hospital, Toronto, Ontario, Canada

Interaction Study of Clopidogrel 300/75 mg Given Alone or Concomitantly With Pantoprazole 80 mg in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2010-05-24
Last Posted Date
2011-12-15
Lead Sponsor
Sanofi
Target Recruit Count
66
Registration Number
NCT01129427
Locations
🇺🇸

Sanofi-Aventis Administrative Office, Bridgewater, New Jersey, United States

Clopidogrel Proton-Pump Inhibitors Study

Phase 4
Withdrawn
Conditions
Coronary Artery Disease
Interventions
First Posted Date
2009-11-19
Last Posted Date
2016-10-21
Lead Sponsor
Sheba Medical Center
Registration Number
NCT01016717
Locations
🇮🇱

Leviev Heart Center, Sheba Medical Center, Tel Hashomer, Israel

Drug-Drug Interaction of Cladribine and Pantoprazole in Multiple Sclerosis Subjects

Phase 1
Completed
Conditions
Multiple Sclerosis
Interventions
First Posted Date
2009-07-13
Last Posted Date
2016-04-14
Lead Sponsor
Merck KGaA, Darmstadt, Germany
Target Recruit Count
18
Registration Number
NCT00938366

Symptom Evaluation After Cessation of a Proton Pump Inhibitor in Healthy Volunteers

Not Applicable
Completed
Conditions
Healthy
Interventions
Drug: Pantoprazole
Drug: Placebo
First Posted Date
2009-06-05
Last Posted Date
2009-06-05
Lead Sponsor
Sahlgrenska University Hospital, Sweden
Target Recruit Count
50
Registration Number
NCT00915239
Locations
🇸🇪

Sahlgrenska Univeristy Hospital, Gothenburg, Sweden

Esomeprazole Versus Pantoprazole to Prevent Peptic Ulcer Rebleeding

Phase 4
Withdrawn
Conditions
Peptic Ulcer
Interventions
First Posted Date
2009-04-15
Last Posted Date
2015-04-08
Lead Sponsor
Lotung Poh-Ai Hospital
Registration Number
NCT00881413

Open Label Safety Study of Enteric-Coated Spheroid Suspension in Infants Aged Less Than 12 Months With Presumed Gastroesophageal Reflux Disease (GERD)

Phase 3
Completed
Conditions
Gastroesophageal Reflux
Interventions
First Posted Date
2009-03-24
Last Posted Date
2010-05-04
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
58
Registration Number
NCT00868296

Comparison of 7-day and 14-day Bismuth Based Quadruple Therapy for Secondary Helicobacter Pylori Eradication

Phase 4
Completed
Conditions
Helicobacter Infection
Interventions
First Posted Date
2009-02-11
Last Posted Date
2016-12-06
Lead Sponsor
Asan Medical Center
Target Recruit Count
199
Registration Number
NCT00841854
Locations
🇰🇷

Asan Medical Center, Seoul, Korea, Republic of

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