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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

Study of Pantoprazole for Sleepiness Associated With Acid Reflux and Sleep Apnea

Phase 4
Completed
Conditions
Acid Reflux Disease
Obstructive Sleep Apnea
First Posted Date
2006-03-28
Last Posted Date
2007-12-12
Lead Sponsor
University of Cincinnati
Target Recruit Count
68
Registration Number
NCT00307944
Locations
🇺🇸

University Ear, Nose and Throat Specialists, Cincinnati, Ohio, United States

Comparison of the Nighttime Effects of Two Different Drugs on Subjects With GERD

Phase 4
Completed
Conditions
Gastroesophageal Reflux Disease
First Posted Date
2006-03-17
Last Posted Date
2007-09-17
Lead Sponsor
VA Greater Los Angeles Healthcare System
Target Recruit Count
23
Registration Number
NCT00304421
Locations
🇺🇸

VA Greater Los Angeles Healthcare System, Los Angeles, California, United States

Study Evaluating Pantoprazole in Children With Gastroesophageal Reflux Disease (GERD)

Phase 3
Completed
Conditions
Gastroesophageal Reflux
Interventions
First Posted Date
2006-03-09
Last Posted Date
2010-05-19
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
60
Registration Number
NCT00300755

Effects of 2 Different Doses of Pantoprazole on Gastric pH and Recurrent Bleeding in Patients Who Bled From Peptic Ulcers

Phase 4
Completed
Conditions
Peptic Ulcer Hemorrhage
First Posted Date
2006-01-19
Last Posted Date
2006-01-19
Lead Sponsor
Kwong Wah Hospital
Registration Number
NCT00279123
Locations
🇨🇳

Department of Surgery, Kwong Wah Hospital, Hong Kong, China

Determination of a Questionnaire After Treatment With Pantoprazole at Full Dose and Half Dose in Adult Patients With Symptoms of Acid Reflux (Gastroesophageal Reflux Disease) (BY1023/UK-506)

Phase 4
Completed
Conditions
Gastroesophageal Reflux
GERD
GORD
First Posted Date
2005-12-05
Last Posted Date
2012-05-07
Lead Sponsor
Takeda
Target Recruit Count
300
Registration Number
NCT00261339
Locations
🇬🇧

Altana Pharma/Nycomed, Watford, United Kingdom

Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints (BY1023/VMG-708)

Phase 3
Completed
Conditions
Gastroesophageal Reflux Disease (GERD)
Peptic Ulcers
Interventions
First Posted Date
2005-12-05
Last Posted Date
2012-05-07
Lead Sponsor
Takeda
Target Recruit Count
100
Registration Number
NCT00261300
Locations
🇩🇪

Altana Pharma/Nycomed, Hannover, Germany

Study Evaluating Pantoprazole Sodium Enteric-Coated Spheroid Suspension In Infants With Presumed GERD

Phase 3
Completed
Conditions
Gastroesophageal Reflux
Interventions
First Posted Date
2005-11-28
Last Posted Date
2010-05-07
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
67
Registration Number
NCT00259012

Comparison of a "Step-Up" Versus a "Step-Down" Treatment Strategy for Patients With New Onset Dyspepsia in General Practice (The DIAMOND-Study)

Not Applicable
Completed
Conditions
Dyspepsia
Gastrointestinal Diseases
Interventions
Drug: algeldrate/magnesium oxide
First Posted Date
2005-11-02
Last Posted Date
2007-08-29
Lead Sponsor
Radboud University Medical Center
Target Recruit Count
664
Registration Number
NCT00247715
Locations
🇳🇱

Maastricht University, Maastricht, Limburg, Netherlands

🇳🇱

Radboud University Nijmegen Medical Center, Nijmegen, Gelderland, Netherlands

🇳🇱

UMC Utrecht, Utrecht, Netherlands

Determination of the Minimal Clinically Important Difference After Treatment With Pantoprazole in Patients With Symptoms of Acid Reflux (Gastroesophageal Reflux Disease) (BY1023/M3-340)

Phase 4
Completed
Conditions
Gastroesophageal Reflux
First Posted Date
2005-11-01
Last Posted Date
2012-05-07
Lead Sponsor
Takeda
Target Recruit Count
600
Registration Number
NCT00246909
Locations
🇺🇸

Altana Pharma/Nycomed, Milwaukee, Wisconsin, United States

Study of Intragastric pH Profile After 5 Days Pantoprazole 40 mg iv Followed by Oral Esomeprazole 40 mg po or Oral Pantoprazole 40 mg po

Phase 4
Completed
Conditions
Healthy
First Posted Date
2005-09-21
Last Posted Date
2011-01-21
Lead Sponsor
AstraZeneca
Target Recruit Count
40
Registration Number
NCT00206050
Locations
🇺🇸

Research Site, Oklahoma City, Oklahoma, United States

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