Zollinger-ellison Syndrome
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Sign up freeTop drugs studied for this disease
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FDA approval · 2018-06-07FDA Approved: OMEPRAZOLE — Supplemental Application (Golden State Medical Supply, Inc.)
The FDA approved a supplemental application for the generic omeprazole from Golden State Medical Supply, Inc., authorizing changes to the ap…
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FDA approval · 2018-06-07FDA Approved: OMEPRAZOLE — Supplemental Application (Lannett Company, Inc.)
The FDA approved a supplemental application for the generic Omeprazole from Lannett Company, Inc., granting continued approval for this prod…
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FDA approval · 2018-05-31FDA Approved: OMEPRAZOLE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for omeprazole from Aurobindo Pharma Limited, authorizing their generic omeprazole product.
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FDA approval · 2018-05-31FDA Approved: OMEPRAZOLE — Supplemental Application (Glenmark Pharmaceuticals Inc., USA)
The FDA approved Glenmark's supplemental application for omeprazole, granting approval for the generic proton pump inhibitor product. This a…
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FDA approval · 2017-12-20FDA Approved: PROTONIX I.V. — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
The FDA approved a supplemental application for PROTONIX I.V., approving its intravenous pantoprazole sodium formulation. This expands treat…
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FDA approval · 2017-10-30FDA Approved: GOOD NEIGHBOR PHARMACY OMEPRAZOLE — Supplemental Application (Amerisource Bergen)
The FDA approved a supplemental application for Good Neighbor Pharmacy Omeprazole (omeprazole), with AmerisourceBergen as the manufacturer, …
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FDA approval · 2017-08-30FDA Approved: LANSOPRAZOLE — Original Application (Lifestar Pharma LLC.)
FDA approves a generic lansoprazole under an Original Application (ANDA) for Lifestar Pharma LLC.
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FDA approval · 2017-08-18FDA Approved: KIRKLAND SIGNATURE ESOMEPRAZOLE MAGNESIUM — Original Application (Costco Wholesale Company)
The FDA approved the original generic application for Kirkland Signature Esomeprazole Magnesium, a generic version of esomeprazole magnesium…
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FDA approval · 2017-07-06FDA Approved: PROTONIX DELAYED-RELEASE — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
FDA approved a supplemental application for Protonix Delayed-Release (pantoprazole sodium) from Wyeth/Pfizer to update the drug's labeling.
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FDA approval · 2017-07-06FDA Approved: PROTONIX I.V. — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
The FDA approved a supplemental application to authorize the intravenous formulation of Protonix (pantoprazole sodium) for specified indicat…
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FDA approval · 2017-07-03FDA Approved: OMEPRAZOLE — Original Application (Golden State Medical Supply, Inc.)
FDA approves a generic omeprazole from Golden State Medical Supply, Inc. under an Original Application (ANDA 203481).
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CLINICAL_TRIALS trial_result · 2017-07-02Clinical Trial Update: The Use of Oral Omeprazole and Intravenous Pantoprazole in Patients With Hypersecretion of Gastric Acid [Phase 2]
Phase 2 trial evaluating oral omeprazole and IV pantoprazole for hypersecretion of gastric acid in patients with gastrinoma and Zollinger-El…
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CLINICAL_TRIALS trial_result · 2017-07-02Clinical Trial Update: Interferon and Octreotide to Treat Zollinger-Ellison Syndrome and Advanced Non-B Islet Cell Cancer [Phase 2]
A Phase 2 clinical trial evaluating the combination of interferon and octreotide for Zollinger-Ellison syndrome and advanced non-B islet cel…
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CLINICAL_TRIALS trial_result · 2017-07-02Clinical Trial Update: Treatment of Zollinger-Ellison Syndrome
A completed clinical trial update documenting the treatment of Zollinger-Ellison syndrome.
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FDA approval · 2017-06-30FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Civica, Inc.)
The FDA approved Civica, Inc.'s pantoprazole sodium original application (NDA 209463), a proton pump inhibitor for acid-related conditions a…
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FDA approval · 2017-02-17FDA Approved: RABEPRAZOLE SODIUM — Original Application (Aurobindo Pharma Limited)
FDA approved an original ANDA for a generic rabeprazole sodium product from Aurobindo Pharma Limited.
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CLINICAL_TRIALS trial_result · 2017-01-19Clinical Trial Update: A Phase I/III Study of D961H 10 mg and 20 mg in Japanese Paediatric Patients With Gastrointestinal Acid Related Diseases [Phase 3]
Phase III results for D961H at 10 mg and 20 mg in Japanese pediatric patients with gastrointestinal acid-related diseases have been complete…
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FDA approval · 2016-04-22FDA Approved: ESOMEPRAZOLE MAGNESIUM — Supplemental Application (NorthStar Rx LLC)
FDA approved a supplemental application for Esomeprazole Magnesium (generic esomeprazole magnesium) submitted by NorthStar Rx LLC.
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FDA approval · 2016-04-21FDA Approved: ESOMEPRAZOLE MAGNESIUM — Original Application (Aurobindo Pharma Limited)
FDA approved the original application for esomeprazole magnesium from Aurobindo Pharma Limited, making a generic version of this proton pump…
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FDA approval · 2016-03-30FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Eugia US LLC)
The FDA approved Pantoprazole sodium from Eugia US LLC under an original ANDA, making a generic pantoprazole product available. It is indica…
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FDA approval · 2016-03-18FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (XLCare Pharmaceuticals Inc.)
FDA approved a supplemental application for Pantoprazole Sodium from XLCare Pharmaceuticals Inc., approving a change to this generic product…
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FDA approval · 2016-02-25FDA Approved: OMEPRAZOLE — Supplemental Application (Lannett Company, Inc.)
FDA approved a supplemental application for omeprazole from Lannett Company, Inc., effectively updating the product labeling under the ANDA.
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FDA approval · 2016-01-26FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Amneal Pharmaceuticals LLC)
FDA approved Amneal Pharmaceuticals' original application for pantoprazole sodium, a generic pantoprazole product, expanding access to a pro…
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FDA approval · 2015-12-22FDA Approved: FAMOTIDINE — Original Application (Aurobindo Pharma Limited)
FDA approved the original application for famotidine from Aurobindo Pharma Limited, enabling a generic version of famotidine to be marketed.
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FDA approval · 2015-09-25FDA Approved: ESOMEPRAZOLE MAGNESIUM — Original Application (NorthStar Rx LLC)
FDA approved the original application for esomeprazole magnesium from NorthStar Rx LLC, a generic version of the proton pump inhibitor esome…