Giardiasis
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Sign up freeTop drugs studied for this disease
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CLINICAL_TRIALS research · 2026-03-16Clinical Trial Update: Evaluation, Treatment and Monitoring of Patients With a Known or Suspected Parasitic Infection
A National Institute of Allergy and Infectious Diseases sponsored clinical trial evaluating how to evaluate, treat, and monitor patients wit…
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FDA approval · 2026-02-13FDA Approved: METRONIDAZOLE — Original Application (Viona Pharmaceuticals Inc)
FDA approved the original ANDA for metronidazole from Viona Pharmaceuticals Inc, enabling a generic version of the antibiotic to be marketed…
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CLINICAL_TRIALS research · 2025-04-04Clinical Trial Update: Anti-protozoal Effect of Steroid Hormone 20-hydroxyecdysone [Phase 2, Phase 3]
A Phase 2/3 trial evaluating the anti-protozoal effects of the steroid hormone 20-hydroxyecdysone for Giardia lamblia infection. The study i…
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FDA approval · 2025-02-14FDA Approved: METRONIDAZOLE — Supplemental Application (Alembic Pharmaceuticals Limited)
FDA approved a supplemental application for metronidazole from Alembic Pharmaceuticals Limited.
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FDA approval · 2025-02-03FDA Approved: NITAZOXANIDE — Original Application (ANI Pharmaceuticals, Inc.)
FDA approved ANI Pharmaceuticals' original application for nitazoxanide, a generic treatment for infections caused by Giardia lamblia and Cr…
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FDA approval · 2024-12-17FDA Approved: METRONIDAZOLE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for Metronidazole from Sun Pharmaceutical Industries, Inc., resulting in continued approval of this …
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FDA approval · 2024-10-25FDA Approved: METRONIDAZOLE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved a supplemental application for metronidazole from Heritage Pharmaceuticals d/b/a Avet Pharmaceuticals Inc. under an ANDA.
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FDA approval · 2024-10-25FDA Approved: METRONIDAZOLE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Metronidazole filed by Aurobindo Pharma Limited, authorizing the generic product under the suppl…
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FDA approval · 2024-10-25FDA Approved: METRONIDAZOLE — Supplemental Application (Alembic Pharmaceuticals Limited)
FDA approves a supplemental application for Metronidazole from Alembic Pharmaceuticals Limited, confirming continued approval of the generic…
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FDA approval · 2024-09-04FDA Approved: ALBENDAZOLE — Original Application (Alembic Pharmaceuticals Inc.)
FDA approves Alembic Pharmaceuticals' original application for albendazole, adding a generic version to the market.
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CLINICAL_TRIALS research · 2024-08-01Clinical Trial Update: A Comparison of Microscopy and Enzyme Linked Immunosorbent Assay for Diagnosis of Giardia Lamblia in Children, Sohag
A clinical trial by Sohag University compares microscopy and enzyme-linked immunosorbent assay for diagnosing Giardia lamblia infection in c…
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FDA approval · 2024-06-18FDA Approved: METRONIDAZOLE — Supplemental Application (Alembic Pharmaceuticals Limited)
FDA approved a supplemental application for Metronidazole from Alembic Pharmaceuticals Limited, granting approval for a generic version of t…
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FDA approval · 2024-06-18FDA Approved: METRONIDAZOLE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
The FDA approved a supplemental application for metronidazole from Heritage Pharmaceuticals Inc. (d/b/a Avet Pharmaceuticals Inc.) to modify…
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FDA approval · 2024-01-09FDA Approved: METRONIDAZOLE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Metronidazole from Aurobindo Pharma Limited.
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FDA label_change · 2023-11-22FDA Approved: METRONIDAZOLE — Supplemental Application (Prasco Laboratories)
FDA approved a supplemental application for metronidazole from Prasco Laboratories, indicating an updated labeling/approval for an additiona…
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FDA approval · 2023-10-17FDA Approved: METRONIDAZOLE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for Metronidazole filed by Sun Pharmaceutical Industries, Inc., updating the drug’s labeling as …
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FDA approval · 2023-09-12FDA Approved: TINDAZOLE — Supplemental Application (Rising Pharma Holdings, Inc.)
FDA approved a supplemental application for TINDAZOLE (tinidazole) from Rising Pharma Holdings, Inc., granting additional regulatory authori…
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FDA approval · 2023-07-12FDA Approved: METRONIDAZOLE — Original Application (Cosette Pharmaceuticals, Inc.)
FDA approved Cosette Pharmaceuticals, Inc.'s original application for a generic metronidazole.
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FDA approval · 2023-04-21FDA Approved: METRONIDAZOLE — Original Application (Viona Pharmaceuticals Inc)
The FDA approved Viona Pharmaceuticals' original application for metronidazole, granting a generic version of the antibiotic/antiprotozoal.
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CLINICAL_TRIALS trial_result · 2023-01-26Clinical Trial Update: Auranofin for Giardia Protozoa [Phase 2]
A Phase 2 clinical trial evaluating auranofin for Giardia and amoebic dysentery has completed with posted results.
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FDA approval · 2022-08-11FDA Approved: NITAZOXANIDE — Supplemental Application (Rising Pharma Holdings, Inc.)
FDA approved a supplemental application for nitazoxanide submitted by Rising Pharma Holdings, Inc. (Nitazoxanide).
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FDA label_change · 2022-07-25FDA Approved: TINIDAZOLE — Supplemental Application (Lupin Pharmaceuticals,Inc.)
The FDA approved a supplemental application for tinidazole from Lupin Pharmaceuticals, Inc., indicating changes to the product's labeling.
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FDA approval · 2022-07-25FDA Approved: TINIDAZOLE — Supplemental Application (Edenbridge Pharmaceuticals LLC.)
FDA approved a supplemental application for Tinidazole from Edenbridge Pharmaceuticals LLC., confirming regulatory approval of a generic Tin…
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FDA approval · 2022-03-31FDA Approved: METRONIDAZOLE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for metronidazole from Aurobindo Pharma Limited, indicating a supplemental approval for this generic…
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FDA approval · 2022-03-16FDA Approved: METRONIDAZOLE — Supplemental Application (Prasco Laboratories)
FDA approved a supplemental application for METRONIDAZOLE submitted by Prasco Laboratories.