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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

Proton Pump Inhibitor Preventing Upper Gastrointestinal Injury In Patients On Dual Antiplatelet Therapy After CABG

Phase 4
Active, not recruiting
Conditions
Anti-Platelet Therapy
Coronary Artery Bypass
Gastrointestinal Ulcer (Peptic) or Erosion
Interventions
First Posted Date
2019-04-09
Last Posted Date
2023-08-18
Lead Sponsor
Ruijin Hospital
Target Recruit Count
232
Registration Number
NCT03908593
Locations
🇨🇳

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

Esomeprazole or Pantoprazole in Renal Transplantation

Not Applicable
Completed
Conditions
Kidney Transplant; Complications
Interventions
First Posted Date
2019-01-23
Last Posted Date
2019-01-24
Lead Sponsor
Future University in Egypt
Target Recruit Count
47
Registration Number
NCT03812419

PPI and Microbiome in Healthy Volunteers and Functional Dyspepsia

Phase 4
Completed
Conditions
Dysbiosis
Interventions
Other: PPI withdrawal
First Posted Date
2018-06-04
Last Posted Date
2020-09-28
Lead Sponsor
Universitaire Ziekenhuizen KU Leuven
Target Recruit Count
79
Registration Number
NCT03545243
Locations
🇧🇪

UZ Leuven, Leuven, Belgium

Re-EValuating the Inhibition of Stress Erosions (REVISE) Trial

Phase 3
Completed
Conditions
Gastrointestinal Hemorrhage (Clinically Important, Upper)
Interventions
Drug: Placebo (0.9% saline)
First Posted Date
2017-12-15
Last Posted Date
2024-04-17
Lead Sponsor
McMaster University
Target Recruit Count
4800
Registration Number
NCT03374800
Locations
🇨🇦

Hamilton Health Science Center - General Hospital, Hamilton, Ontario, Canada

🇦🇺

Royal Melbourne Hospital, Melbourne, Victoria, Australia

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Sociedade Hospitalar Angelina Caron, Campina Grande Do Sul, Brazil

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Phase 1
Withdrawn
Conditions
Invasive Aspergillosis
Interventions
First Posted Date
2017-03-29
Last Posted Date
2017-11-01
Lead Sponsor
F2G Biotech GmbH
Registration Number
NCT03095547

Proton Pump Inhibitor Prevent Dual Antiplatelet Agents Induced Gastrointestinal Ulcer After Coronary Artery Bypass Graft

Phase 4
Withdrawn
Conditions
Ulcer of the Gastrointestinal Tract
Proton Pump Inhibitor
Gastric Ulcer Induced by Antiplatelet Agent
Interventions
First Posted Date
2017-01-31
Last Posted Date
2019-04-09
Lead Sponsor
Ruijin Hospital
Registration Number
NCT03038009
Locations
🇨🇳

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

To Investigate PK and PD of CJ-12420, Clarithromycin, Amoxicillin After Multiple Dose Administration

Phase 1
Completed
Conditions
Drug Interaction
Pharmacokinetic
Pharmacodynamic
Interventions
First Posted Date
2017-01-06
Last Posted Date
2017-05-12
Lead Sponsor
HK inno.N Corporation
Target Recruit Count
60
Registration Number
NCT03011996
Locations
🇰🇷

Inje University Busan Baik Hospital, Busan, Korea, Republic of

Dextromethorphan Use in Multimodal Analgesia Regimens for Total Knee Arthroplasty

First Posted Date
2016-12-09
Last Posted Date
2019-05-14
Lead Sponsor
University of Southern California
Target Recruit Count
23
Registration Number
NCT02987920

Pediatric Intensive Care Ulcer Prophylaxis Pilot Trial

Phase 3
Completed
Conditions
Gastrointestinal Hemorrhage
Interventions
Drug: Placebo (for pantoprazole)
First Posted Date
2016-10-11
Last Posted Date
2020-09-02
Lead Sponsor
McMaster University
Target Recruit Count
116
Registration Number
NCT02929563
Locations
🇨🇦

IWK Health Centre, Halifax, Nova Scotia, Canada

🇨🇦

McMaster Children's Hospital, Hamilton, Ontario, Canada

🇨🇦

Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada

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A Study To Assess The Efficacy And Safety Of Bismuth Tripotassium Dicitrate (De-Nol) In Combination With Pantoprazole And Pantoprazole Monotherapy In Treatment Of Subjects With Nonsteroidal Anti-Inflammatory Drugs (NSAID)-Induced Gastropathy

Phase 4
Terminated
Conditions
NSAID-induced Gastropathy
Interventions
Drug: bismuth tripotassium dicitrate
First Posted Date
2016-06-02
Last Posted Date
2017-09-21
Lead Sponsor
Astellas Pharma Europe B.V.
Target Recruit Count
9
Registration Number
NCT02788123
Locations
🇷🇺

Site RU70008, Saint-Petersburg, Russian Federation

🇷🇺

Site RU70012, Saint-Petersburg, Russian Federation

🇷🇺

Site RU70013, Volgograd, Russian Federation

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