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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

Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients.

Not Applicable
Completed
Conditions
Clostridium Difficile Colitis
Gastrointestinal Hemorrhage
Interventions
First Posted Date
2011-11-22
Last Posted Date
2018-01-16
Lead Sponsor
Mohamed Saad
Target Recruit Count
124
Registration Number
NCT01477320
Locations
🇺🇸

University of Louisville hospital, Louisville, Kentucky, United States

Structured Treatment of Osteoarthritis of the Knee With or Without Total Knee Replacement

Not Applicable
Completed
Conditions
Osteoarthritis of the Knee
Interventions
Other: Neuromuscular training (NEMEX-TJR)
Drug: Burana
Behavioral: Dietary counseling
Behavioral: Patient education
Procedure: TKR
Other: Insoles
First Posted Date
2011-08-05
Last Posted Date
2017-10-16
Lead Sponsor
Northern Orthopaedic Division, Denmark
Target Recruit Count
100
Registration Number
NCT01410409
Locations
🇩🇰

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

🇩🇰

Vendsyssel Hospital, Frederikshavn, Frederikshavn, Denmark

🇩🇰

Farsoe Hospital, Farsø, Denmark

The Clinical Significance of Acid Rebound in Functional Dyspepsia

Phase 4
Terminated
Conditions
Functional Dyspepsia
Interventions
First Posted Date
2011-06-15
Last Posted Date
2013-12-06
Lead Sponsor
Zealand University Hospital
Target Recruit Count
184
Registration Number
NCT01373970
Locations
🇩🇰

Koege Hospital, Koege, Denmark

A Bioequivalence Study of SCH 530348 2.5 mg Tablets (P06558)

Phase 1
Completed
Conditions
Acute Coronary Syndrome
Interventions
Drug: SCH 530348 (standard percentage)
Drug: SCH 530348 (high percentage)
First Posted Date
2011-05-23
Last Posted Date
2015-09-29
Lead Sponsor
Merck Sharp & Dohme LLC
Target Recruit Count
173
Registration Number
NCT01358344

Bioequivalence Study of Pantoprazole Sodium DR Tablets 40 mg of Dr. Reddy's Laboratories Limited Under Fasting Condition

Phase 1
Completed
Conditions
Fasting
Interventions
First Posted Date
2011-01-26
Last Posted Date
2011-01-26
Lead Sponsor
Dr. Reddy's Laboratories Limited
Target Recruit Count
42
Registration Number
NCT01283919
Locations
🇮🇳

VimtaLabsLtd., Hyderabad, Andhrapradesh, India

Bioequivalence Study of Pantoprazole Sodium DR Tablets 40 mg of Dr. Reddy's Laboratories Limited Under Fed Condition

Phase 1
Completed
Conditions
FED
Interventions
First Posted Date
2011-01-26
Last Posted Date
2011-01-26
Lead Sponsor
Dr. Reddy's Laboratories Limited
Target Recruit Count
52
Registration Number
NCT01283932
Locations
🇮🇳

VimtaLabsLtd., Hyderabad, Andhrapradesh, India

Symptomatic Relief of Acute Dyspeptic Pain in Emergency Department With Pantoprazole

Phase 4
Completed
Conditions
Dyspepsia
Emergency
Pain
Interventions
Drug: Normal saline
Drug: Oral antacid
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

Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hydrogen (pH) in Patients From Acid Peptic Disorder After Single and Repeated Dosing.

Phase 4
Completed
Conditions
Acid Peptic Disorder
Interventions
First Posted Date
2010-10-05
Last Posted Date
2012-12-28
Lead Sponsor
Abbott
Target Recruit Count
47
Registration Number
NCT01214408
Locations
🇮🇳

Site Reference ID/Investigator# 42043, Chennai, India

Oral Versus IV Proton Pump Inhibitor in High-risk Bleeding Peptic Ulcers After Endoscopic Hemostasis

Phase 3
Conditions
Peptic Ulcers
Interventions
First Posted Date
2010-08-17
Last Posted Date
2012-06-21
Lead Sponsor
National Taiwan University Hospital
Target Recruit Count
190
Registration Number
NCT01182597
Locations
🇨🇳

National Taiwan Univeristy Hospital, Taipei, Taiwan

🇨🇳

National Taiwan Univeristy Hospital Yunlin Branch, Dou-liou, Taiwan

Bioequivalence Study of Pantoprazole 40 mg DR Tablets and Protonix 40 mg Tablets

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2010-08-11
Last Posted Date
2010-08-11
Lead Sponsor
Kremers Urban Development Company
Target Recruit Count
48
Registration Number
NCT01179646
Locations
🇺🇸

MDS Pharma Services, Lincoln, Nebraska, United States

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