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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

Bioavailability of BIBR 963 ZW After 50 mg of BIBR 1048 MS With and Without of Pantoprazole in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BIBR 1048 MS Capsule D
Drug: BIBR 1048 MS tartaric acid solution
Drug: BIBR 1048 MS Capsule C
Drug: BIBR 1048 MS Capsule A
Drug: BIBR 1048 MS Capsule B
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
16
Registration Number
NCT02170896

Bioavailability of BIBR 953 ZW in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BIBR 1048 low1
Drug: BIBR 1048 low2
Drug: BIBR 1048 medium
Drug: BIBR 1048 high
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
48
Registration Number
NCT02170766

Assessment of Safety, Pharmacokinetics and the Effect of BIBR 1048 MS on Coagulation Parameters in Healthy Volunteer Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BIBR 1048 MS - low dose
Drug: BIBR 1048 MS - high dose
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
26
Registration Number
NCT02170740

Bioavailability of BIBR 1048 MS With and Without Pantoprazole Under Influence of Food in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
18
Registration Number
NCT02170610

Bioavailability of BIBR 953 ZW After Oral Administration of BIBR 1048 MS in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BIBR 1048 MS Capsule E
Drug: BIBR 1048 MS Capsule F
Drug: BIBR 1048 MS Capsule G
Drug: BIBR 1048 MS Tablet H
Drug: BIBR 1048 MS Drinking solution
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
15
Registration Number
NCT02170636

Bioavailability of BIBR 953 ZW After Administration of BIBR 1048 MS in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BIBR 1048 MS Capsule I
Drug: BIBR 1048 MS Capsule K
Drug: BIBR 1048 MS drinking solution
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
12
Registration Number
NCT02170623

Bioavailability of BIBR 1048 MS Single Doses With or Without Pantoprazole in Healthy Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BIBR 1048 MS capsule formulation A
Drug: BIBR 1048 MS capsule formulation B
Drug: BIBR 1048 MS powder plus solution
First Posted Date
2014-06-23
Last Posted Date
2014-06-23
Lead Sponsor
Boehringer Ingelheim
Target Recruit Count
24
Registration Number
NCT02170805

Stereotactic Radiosurgery in Metastatic Spinal Cord Compression

Not Applicable
Terminated
Conditions
Spinal Cord Compression
Neoplasm Metastasis
Interventions
Procedure: Decompression surgery
Radiation: Radiosurgery
Radiation: Fractionated Radiotherapy
Drug: Glucocorticoids
First Posted Date
2014-06-19
Last Posted Date
2021-03-11
Lead Sponsor
Rigshospitalet, Denmark
Target Recruit Count
10
Registration Number
NCT02167633
Locations
🇩🇰

Rigshospitalet, Copenhagen, Denmark

Compare Sequential and Quadruple Therapy for the Eradication of Helicobacter Pylori in Korea

Not Applicable
Completed
Conditions
Helicobacter Pylori Infection
Interventions
First Posted Date
2014-06-10
Last Posted Date
2019-05-13
Lead Sponsor
Seoul National University Bundang Hospital
Target Recruit Count
390
Registration Number
NCT02159976
Locations
🇰🇷

Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, Korea, Republic of

Histamine Glutamate Antagonism in Stroke

Phase 2
Completed
Conditions
Acute Cerebrovascular Accident
Cerebral Edema
Interventions
First Posted Date
2014-05-20
Last Posted Date
2015-12-15
Lead Sponsor
University of Florida
Target Recruit Count
3
Registration Number
NCT02142712
Locations
🇺🇸

Shands Hospital at University of Florida, Gainesville, Florida, United States

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