Ondansetron
Other / unclassified targets HTR3A via inhibition
Regulatory milestones approvals, filings & regulatory actions · 9 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansions (8) | US (FDA) | ZOFRAN | — | 1993-02-02 – 2005-03-25 | fda.gov ↗ |
| Approved | US (FDA) | ZOFRAN | — | 1991-01-04 | fda.gov ↗ |
Trials 190 · started per year
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 04 trials | ||||||
| Phase 0 | NCT05819619 | Jul 2023 → Apr 2024 | — | Hackensack Meridian Health | Terminated | No outcome recorded Stop: Enrollment |
| Phase 0 | NCT04891484 | Apr 2021 → Apr 2022 | nephrolithiasis | Mansoura University | Completed | No outcome recorded |
| Phase 0 | NCT03125811 | Jul 2017 → Mar 2023 | — | Texas Tech University Health Sciences Center, El Paso | Completed | No outcome recorded |
| Phase 0 | NCT01851993 | Jun 2013 → Sep 2014 | — | McGill University | Completed | No outcome recorded |
| Phase 128 trials · 2 met primary | ||||||
| Phase 1 | NCT07310563 | Dec 2024 → May 2025 | obesity disorder | Amgen | Completed | No outcome recorded |
| Phase 1 | NCT06297499 | Aug 2024 → Aug 2025 overdue | — | Wayne State University | Recruiting | No outcome recorded |
| Phase 1 | NCT05124067 | Oct 2021 → Jan 2022 | delirium | Tanta University | Completed | No outcome recorded |
| Phase 1 | NCT03809234 | May 2019 → Nov 2020 | neuropathy, painful | Washington University School of Medicine | Terminated | No outcome recorded |
| Phase 1 | NCT03583489 | Jul → Aug 2018 | — | Acacia Pharma Ltd | Completed | No outcome recorded |
| Phase 1 | NCT02614586 | Dec 2015 → Apr 2016 | schizophrenia | Takeda | Terminated | No outcome recorded |
| Phase 1 | NCT02460341 | Aug 2015 → Feb 2017 | — | Icahn School of Medicine at Mount Sinai | Completed | No outcome recorded |
| Phase 1 | NCT02473887 | Sep 2014 → Jan 2015 | gastroenteritis | Hamad Medical Corporation | Completed | No outcome recorded |
| Phase 1 | NCT01815125 | Mar 2013 → Feb 2014 | traumatic brain injury | St. Justine's Hospital | Completed | No outcome recorded |
| Phase 1 | NCT01572012 | Feb 2012 → Nov 2013 | — | Halozyme Therapeutics | Completed | No outcome recorded |
| Phase 1 | NCT01290276 | Dec 2010 → Aug 2012 | — | Tong Lee | Completed | No outcome recorded |
| Phase 1 | NCT00981487 | Feb → Mar 2009 | — | Forest Laboratories | Completed | No outcome recorded |
| Phase 1 | NCT01036854 | Feb → Apr 2009 | — | Forest Laboratories | Completed | No outcome recorded |
| Phase 1 | NCT00905190 | Feb → Mar 2009 | — | Forest Laboratories | Completed | No outcome recorded |
| Phase 1 | NCT01113164 | Sep 2008 → Feb 2012 | alcohol dependence | Brown University | Completed | Mixed |
| Phase 1 | NCT01220167 | Aug 2008 | — | Aquestive Therapeutics | Completed | No outcome recorded |
| Phase 1 | NCT00437229 | Feb → May 2007 | chemotherapy-induced toxicity | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT00649363 | Jul 2005 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00947128 | Sep → Oct 2004 | — | Sandoz | Completed | No outcome recorded |
| Phase 1 | NCT00946387 | Sep 2004 | — | Sandoz | Completed | No outcome recorded |
| Phase 1 | NCT00659685 | Nov 2003 → ? | — | Par Pharmaceutical, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT00659074 | Oct 2003 → Jan 2004 | — | Par Pharmaceutical, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT00649532 | Jul 2003 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00648583 | Jul 2003 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00934921 | Feb 2003 | — | Teva Pharmaceuticals USA | Completed | Met primary |
| Phase 1 | NCT00934180 | Dec 2002 | — | Teva Pharmaceuticals USA | Completed | Met primary |
| Phase 1 | NCT00654277 | Aug → Sep 2002 | — | Par Pharmaceutical, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT00653458 | Aug → Sep 2002 | — | Par Pharmaceutical, Inc. | Completed | No outcome recorded |
| Phase 1/22 trials · 1 missed | ||||||
| Phase 1/2 | NCT04603066 | Jan 2021 → Oct 2023 | neuropathy, painful | Washington University School of Medicine | Completed | Missed primary |
| Phase 1/2 | NCT01217190 | Sep 2008 | chemotherapy-induced toxicity | MonoSol Rx | Completed | No outcome recorded |
| Phase 234 trials · 1 met primary · 3 missed | ||||||
| Phase 2 | NCT07795060 | Mar → Dec 2027 expected | cholera | Public Interest Science Center | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT07381634 | Mar → Dec 2026 expected | hepatocellular carcinoma | First Affiliated Hospital of Wenzhou Medical University | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT04226170 | Nov 2023 → Apr 2025 | AChR+ myasthenia gravis | DAS-MG, Inc | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2 | NCT05378113 | May → Aug 2023 | — | Emory University | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2 | NCT05342818 | Apr → Jul 2022 | gastroparesis | Tanta University | Completed | No outcome recorded |
| Phase 2 | NCT05202574 | Sep 2021 → Feb 2022 | intracranial hypotension | Minia University | Unknown | No outcome recorded |
| Phase 2 | NCT04557189 | Oct 2020 → Mar 2022 | — | Takeda | Completed | Met primary |
| Phase 2 | NCT06289335 | Aug 2020 → Sep 2021 | — | Hospital Central "Dr. Ignacio Morones Prieto" | Completed | No outcome recorded |
| Phase 2 | NCT04468685 | Jul → Dec 2020 | cholecystitis | National Hepatology & Tropical Medicine Research Institute | Completed | No outcome recorded |
| Phase 2 | NCT03865290 | Apr 2019 → Mar 2028 expected | diabetes mellitus, dyspepsia | Mayo Clinic | Recruiting | No outcome recorded |
| Phase 2 | NCT03785691 | Mar 2019 → Jul 2022 | hyperemesis gravidarum | Nordsjaellands Hospital | Terminated | Mixed Stop: Enrollment |
| Phase 2 | NCT04362449 | Jan 2019 → Feb 2023 | gallbladder cancer | Imperial College Healthcare NHS Trust | Unknown | No outcome recorded |
| Phase 2 | NCT03572829 | Mar 2018 → Jan 2020 | chemotherapy-induced toxicity, head and neck squamous cell carcinoma | Chinese Academy of Medical Sciences | Completed | No outcome recorded |
| Phase 2 | NCT02757105 | May 2016 → Jun 2017 | irritable bowel syndrome | RedHill Biopharma Limited | Completed | No outcome recorded |
| Phase 2 | NCT00890149 | Sep 2015 → Sep 2016 | alcohol abuse, alcohol dependence | University of Maryland, Baltimore | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2 | NCT02354703 | Aug 2015 → Mar 2020 | alcohol-related disorders | University of Maryland, Baltimore | Completed | Missed primary |
| Phase 2 | NCT01965704 | Sep 2014 → Sep 2020 | drug dependence, neonatal abstinence syndrome | Stanford University | Completed | Missed primary |
| Phase 2 | NCT02006056 | Nov 2013 → Jun 2014 | — | Sunnybrook Health Sciences Centre | Completed | No outcome recorded |
| Phase 2 | NCT01841606 | Mar → Dec 2013 | — | University of British Columbia | Completed | No outcome recorded |
| Phase 2 | NCT01370408 | Feb 2012 → Mar 2016 | chemotherapy-induced toxicity | Northside Hospital, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01275248 | Jan 2011 → Sep 2015 | obsessive-compulsive disorder | Transcept Pharmaceuticals | Terminated | No outcome recorded |
| Phase 2 | NCT01254877 | Dec 2010 → Jan 2017 | alcohol abuse, alcohol dependence | Johns Hopkins University | Completed | No outcome recorded |
| Phase 2 | NCT00795769 | Aug 2008 → Jun 2009 | Burkitt lymphoma, Hodgkins lymphoma, MALT lymphoma, acute myeloid leukemia with 11q23 abnormalities +29 | Fred Hutchinson Cancer Center | Completed | No outcome recorded |
| Phase 2 | NCT00689572 | Jul 2008 → Dec 2013 | cocaine dependence | University of Virginia | Completed | Missed primary |
| Phase 2 | NCT01543945 | Mar 2008 → Dec 2011 | — | Prince of Songkla University | Completed | No outcome recorded |
| Phase 2 | NCT00678457 | Jan 2007 → May 2008 | alcohol dependence | University of Virginia | Completed | No outcome recorded |
| Phase 2 | NCT00285051 | Nov 2005 → Feb 2009 | cancer | Rafa Laboratories | Terminated | No outcome recorded |
| Phase 2 | NCT00183222 | May → Dec 2005 | alcohol dependence | Medical University of South Carolina | Completed | No outcome recorded |
| Phase 2 | NCT00006205 | Mar 2005 → Jun 2013 | alcohol dependence | Bankole Johnson | Unknown | No outcome recorded |
| Phase 2 | NCT00040053 | Jun 2002 → Feb 2004 | methamphetamine dependence | National Institute on Drug Abuse (NIDA) | Completed | No outcome recorded |
| Phase 2 | NCT00027079 | Sep 2001 → Aug 2004 | alcohol dependence | National Institute on Alcohol Abuse and Alcoholism (NIAAA) | Completed | No outcome recorded |
| Phase 2 | NCT00033085 | May 2001 → Dec 2002 | substance-related disorder | National Institute on Drug Abuse (NIDA) | Completed | No outcome recorded |
| Phase 2 | NCT00000289 | May 1998 → Dec 2001 | nicotine dependence | National Institute on Drug Abuse (NIDA) | Completed | No outcome recorded |
| Phase 2 | NCT00000443 | ? → Apr 2000 | alcohol dependence | National Institute on Alcohol Abuse and Alcoholism (NIAAA) | Completed | No outcome recorded |
| Phase 2/34 trials · 1 missed | ||||||
| Phase 2/3 | NCT07588217 | Oct 2026 → Oct 2028 expected | acute lung injury, acute respiratory distress syndrome | Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT03052361 | Jul 2017 → Sep 2020 | gastroenteritis | St. Justine's Hospital | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2/3 | NCT01591291 | Jun 2012 → Dec 2017 | alcohol dependence | University of Virginia | Withdrawn | No outcome recorded |
| Phase 2/3 | NCT01414777 | Nov 2009 → Jun 2011 | hypotensive disorder, pregnancy disorder | University of Virginia | Completed | Missed primary |
| Phase 327 trials · 2 met primary · 3 missed | ||||||
| Phase 3 | NCT05876585 | Jun 2025 overdue | gastroenteritis | Genuine Research Center, Egypt | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT06282211 | Feb → Mar 2024 | — | The First Affiliated Hospital of Xinxiang Medical College | Unknown | No outcome recorded |
| Phase 3 | NCT06208917 | Jul 2023 → Jul 2026 overdue | childhood neoplasm | Yizhuo Zhang | Recruiting | No outcome recorded |
| Phase 3 | NCT05872893 | Jun 2023 → Jan 2025 | childhood malignant neoplasm | Immune Oncology Research Institute | Completed | No outcome recorded |
| Phase 3 | NCT05620641 | Oct 2022 → Feb 2025 | morbid obesity | Tanta University | Completed | No outcome recorded |
| Phase 3 | NCT04703088 | Jun → Aug 2021 | hypotensive disorder | Laval University | Unknown | No outcome recorded |
| Phase 3 | NCT05087615 | Mar → Aug 2021 | — | Shahid Beheshti University of Medical Sciences | Completed | No outcome recorded |
| Phase 3 | NCT04101227 | Feb 2020 → Feb 2022 | alcohol-related disorders | Adial Pharmaceuticals | Completed | Missed primary |
| Phase 3 | NCT03817970 | Nov 2019 → Sep 2027 expected | cisplatin toxicity | University of Colorado, Denver | Active not recruiting | No outcome recorded |
| Phase 3 | NCT03851835 | Sep 2019 → Jun 2024 | diarrheal disease, gastroenteritis, viral infectious disease | University of Calgary | Completed | Met primary |
| Phase 3 | NCT03555188 | Mar 2018 → Aug 2020 | irritable bowel syndrome | University of Leeds | Completed | Missed primary |
| Phase 3 | NCT03330119 | Oct 2017 → Jun 2018 | pregnancy disorder, substance-related disorder | Brest, Norman A., M.D. | Terminated | No outcome recorded Stop: Business |
| Phase 3 | NCT02619201 | Nov 2015 → May 2016 | gastroenteritis | Hospital General Naval de Alta Especialidad - Escuela Medico Naval | Unknown | No outcome recorded |
| Phase 3 | NCT02246439 | Dec 2014 → Feb 2017 | gastritis, gastroenteritis | RedHill Biopharma Limited | Completed | Met primary |
| Phase 3 | NCT02028910 | Jan → Oct 2014 | gastroenteritis | Assistance Publique - Hôpitaux de Paris | Terminated | No outcome recorded |
| Phase 3 | NCT01536392 | Mar 2012 → Oct 2019 | cervical cancer | M.D. Anderson Cancer Center | Completed | No outcome recorded |
| Phase 3 | NCT01432977 | Sep 2011 → Jun 2012 | pain agnosia | University Hospital, Limoges | Completed | No outcome recorded |
| Phase 3 | NCT01257672 | Jul 2011 → Nov 2013 | gastroenteritis | IRCCS Burlo Garofolo | Completed | No outcome recorded |
| Phase 3 | NCT00768508 | Sep 2008 → Dec 2012 | alcohol dependence | Bankole Johnson | Completed | No outcome recorded |
| Phase 3 | NCT00382642 | Jun 2006 → Mar 2009 | alcohol dependence | Bankole Johnson | Completed | No outcome recorded |
| Phase 3 | NCT00147355 | Nov 2005 → Nov 2008 | HIV infectious disease | Kirby Institute | Terminated | No outcome recorded Stop: Enrollment |
| Phase 3 | NCT00149734 | Jan 2005 → May 2010 | schizophrenia | University of Colorado, Denver | Completed | No outcome recorded |
| Phase 3 | NCT00090246 | May 2004 → Apr 2005 | — | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT00090155 | Sep 2003 → Nov 2004 | — | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT00642512 | Jul 2003 → Jul 2004 | chemotherapy-induced toxicity | Solvay Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00020657 | Jul 2001 → Oct 2004 | cancer of unknown primary site | Gary Morrow | Completed | Missed primary |
| Phase 3 | NCT00006348 | Oct 2000 → Sep 2001 | childhood malignant neoplasm, leukemia, myelodysplastic syndrome, myeloproliferative neoplasm +3 | Alliance for Clinical Trials in Oncology | Completed | No outcome recorded |
| Phase 445 trials · 4 met primary · 6 missed | ||||||
| Phase 4 | NCT07858149 | Sep 2026 → Jan 2027 expected | — | Istanbul University | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT07681076 | Sep → Nov 2026 expected | — | Karuna Therapeutics, Inc. | Recruiting | No outcome recorded |
| Phase 4 | NCT07638527 | Sep 2026 → Mar 2027 expected | — | Faisalabad Medical University | Recruiting | No outcome recorded |
| Phase 4 | NCT07740577 | Jul 2026 → Jan 2027 expected | — | Sanliurfa Education and Research Hospital | Recruiting | No outcome recorded |
| Phase 4 | NCT07336680 | Feb → Jul 2026 | — | Peking Union Medical College Hospital | Completed | No outcome recorded |
| Phase 4 | NCT06632184 | Dec 2025 → Mar 2026 overdue | — | Mexican Social Security Institute | Active not recruiting | Met primary |
| Phase 4 | NCT07264738 | Jul → Sep 2025 overdue | — | Peking Union Medical College Hospital | Active not recruiting | No outcome recorded |
| Phase 4 | NCT05844501 | Apr 2025 → Dec 2027 expected | atrial fibrillation | Indiana University | Recruiting | No outcome recorded |
| Phase 4 | NCT07217600 | Mar 2025 → Mar 2026 overdue | childhood malignant neoplasm, radiation-induced disorder | Chongqing University Cancer Hospital | Recruiting | No outcome recorded |
| Phase 4 | NCT06747975 | Jan 2025 → Jan 2026 overdue | — | Assiut University | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT06729307 | Jan 2025 → Jan 2026 overdue | — | Peking Union Medical College Hospital | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT06704139 | Dec 2024 → Dec 2026 expected | — | Assiut University | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT06697782 | Jul → Dec 2024 | thyroid cancer | The First Affiliated Hospital of Zhengzhou University | Completed | No outcome recorded |
| Phase 4 | NCT05583214 | Oct → Dec 2022 | — | Muhammad Mubariz | Unknown | No outcome recorded |
| Phase 4 | NCT05127876 | Jan → Mar 2022 | — | Ain Shams University | Completed | No outcome recorded |
| Phase 4 | NCT04318847 | Oct 2021 → Apr 2023 | — | Lizar Aguirre Pascasio | Unknown | No outcome recorded |
| Phase 4 | NCT05439772 | Jan 2021 → Jul 2023 | diarrheal disease, eosinophilic gastroenteritis, inflammatory bowel disease | State University of New York - Downstate Medical Center | Completed | Missed primary |
| Phase 4 | NCT06927817 | Nov 2020 → Nov 2021 | cholecystitis | University of Health Sciences | Completed | No outcome recorded |
| Phase 4 | NCT03833999 | Oct 2018 → Jun 2019 | intestinal motility disease | University of Nottingham | Completed | No outcome recorded |
| Phase 4 | NCT07068230 | Oct 2018 → Sep 2019 | headache disorder | Minia University | Completed | No outcome recorded |
| Phase 4 | NCT03503292 | May 2018 → Dec 2019 | — | Mayo Clinic | Completed | No outcome recorded |
| Phase 4 | NCT03262038 | Dec 2017 → Aug 2019 | — | University of Michigan | Terminated | Missed primary |
| Phase 4 | NCT03297021 | Oct 2017 → Apr 2019 | — | Icahn School of Medicine at Mount Sinai | Completed | No outcome recorded |
| Phase 4 | NCT03035942 | Jan 2017 → Oct 2018 | disease of bone structure, poisoning | Pontifical Catholic University of São Paulo | Completed | No outcome recorded |
| Phase 4 | NCT02928601 | Nov 2016 → Aug 2017 | — | Cukurova University | Completed | No outcome recorded |
| Phase 4 | NCT02468323 | Oct 2015 → Feb 2017 | — | Hospital de Base | Completed | No outcome recorded |
| Phase 4 | NCT02541019 | Oct 2015 → Jan 2017 | — | Bonsucesso Federal Hospital | Completed | No outcome recorded |
| Phase 4 | NCT02803788 | Jul 2015 → Jul 2016 | — | Government Medical College, Haldwani | Unknown | No outcome recorded |
| Phase 4 | NCT01870635 | May 2014 → Jan 2017 | diarrheal disease, gastroenteritis | Dr. Stephen Freedman | Completed | Missed primary |
| Phase 4 | NCT01870648 | May 2014 → Dec 2017 | diarrheal disease, gastroenteritis | Dr. Stephen Freedman | Completed | Missed primary |
| Phase 4 | NCT02985840 | Jan 2014 → Nov 2016 | — | OhioHealth | Terminated | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT01876290 | May 2013 → Jan 2014 | — | Hopital Foch | Completed | Missed primary |
| Phase 4 | NCT02382146 | Apr 2012 → Dec 2014 | — | Yeditepe University Hospital | Completed | No outcome recorded |
| Phase 4 | NCT01913990 | Sep 2011 → Aug 2017 | — | Ottawa Hospital Research Institute | Unknown | Met primary |
| Phase 4 | NCT01050270 | Sep 2010 → Dec 2012 | poisoning | University of Edinburgh | Completed | Met primary |
| Phase 4 | NCT01303536 | Dec 2009 → Mar 2010 | obsessive-compulsive disorder | Institute of Neuroscience, Florence, Italy | Completed | No outcome recorded |
| Phase 4 | NCT00878228 | Apr 2009 → Jan 2010 | — | Hospital for Special Surgery, New York | Completed | No outcome recorded |
| Phase 4 | NCT00745004 | Jan 2009 → Jul 2011 | irritable bowel syndrome | University of Nottingham | Completed | No outcome recorded |
| Phase 4 | NCT00793663 | Nov 2008 → Apr 2011 | — | RWTH Aachen University | Completed | No outcome recorded |
| Phase 4 | NCT01165866 | Jun → Dec 2008 | gastroenteritis | Hamad Medical Corporation | Completed | Missed primary |
| Phase 4 | NCT00796497 | Mar → Nov 2008 | obsessive-compulsive disorder | Institute of Neuroscience, Florence, Italy | Completed | No outcome recorded |
| Phase 4 | NCT00674713 | Jan 2006 → Sep 2007 | cholelithiasis | Catholic University of the Sacred Heart | Completed | No outcome recorded |
| Phase 4 | NCT00090207 | Jan → Sep 2004 | — | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 4 | NCT00429832 | Oct 2003 → Nov 2005 | — | University of New Mexico | Completed | Met primary |
| Phase 4 | NCT00092183 | Oct 2002 → Dec 2003 | breast cancer | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase not applicable46 trials · 4 met primary · 1 missed | ||||||
| — | NCT07632144 | Jun → Jul 2026 overdue | — | Mongi Slim Hospital | Not yet recruiting | No outcome recorded |
| — | NCT07511491 | Apr → Aug 2026 overdue | — | Tanta University | Recruiting | No outcome recorded |
| — | NCT07489742 | Mar → Sep 2026 overdue | — | Tanta University | Recruiting | No outcome recorded |
| — | NCT07377903 | Feb → Jul 2026 overdue | — | Sohag University | Not yet recruiting | No outcome recorded |
| — | NCT06898268 | Jul → Dec 2024 | gastroesophageal reflux disease | Muhammad Aamir Latif | Completed | No outcome recorded |
| — | NCT06423820 | May 2024 → Jan 2025 | strabismus | Tanta University | Completed | No outcome recorded |
| — | NCT06423807 | May → Sep 2024 | benign shuddering attacks | Tanta University | Completed | No outcome recorded |
| — | NCT06371014 | May → Dec 2024 | — | Shanghai Children's Medical Center | Unknown | No outcome recorded |
| — | NCT06300346 | Mar → Aug 2024 | — | Sohag University | Unknown | No outcome recorded |
| — | NCT06254131 | Feb → Oct 2024 | — | Tanta University | Completed | No outcome recorded |
| — | NCT06080880 | Dec 2023 → Nov 2025 overdue | chemotherapy-induced toxicity | Hubei Cancer Hospital | Recruiting | No outcome recorded |
| — | NCT06444737 | Nov 2023 → Jun 2024 | intracranial hypotension | Mongi Slim Hospital | Unknown | No outcome recorded |
| — | NCT06175806 | Sep → Nov 2023 | — | Ain Shams University | Completed | No outcome recorded |
| — | NCT05475873 | Jun → Oct 2023 | — | General Hospital of Ningxia Medical University | Completed | Met primary |
| — | NCT04499274 | Sep 2020 → Nov 2023 | blood coagulation disease | Seoul National University Bundang Hospital | Unknown | No outcome recorded |
| — | NCT07334223 | Jul 2020 → Jan 2021 | benign shuddering attacks | Mayo Hospital Lahore | Completed | No outcome recorded |
| — | NCT05076461 | Jul 2020 → Jun 2021 | gastroenteritis | Tehsil Headquarter Hospital | Completed | No outcome recorded |
| — | NCT04294992 | Apr → Sep 2020 | — | Kasr El Aini Hospital | Unknown | No outcome recorded |
| — | NCT04169828 | Aug 2019 → Jan 2025 | juvenile idiopathic arthritis | University of British Columbia | Completed | No outcome recorded |
| — | NCT03859102 | Dec 2018 → Oct 2019 | aneurysm or dilatation of ascending aorta, aortic valve disorder, cardiac valvular defect, coronary artery disorder +2 | James Cook University Hospital | Unknown | No outcome recorded |
| — | NCT02966041 | Mar → Jul 2018 | — | University of British Columbia | Completed | Met primary |
| — | NCT05590936 | Jan 2018 → Dec 2022 | — | University of Thessaly | Completed | No outcome recorded |
| — | NCT03182179 | Nov 2016 → Nov 2021 | rectal cancer | Ente Ospedaliero Cantonale, Bellinzona | Completed | No outcome recorded |
| — | NCT02901054 | Aug → Nov 2016 | — | Washington University School of Medicine | Completed | No outcome recorded |
| — | NCT02793843 | Jun 2016 → Jun 2017 | — | Makassed General Hospital | Completed | No outcome recorded |
| — | NCT02883192 | Feb → Oct 2016 | — | Bnai Zion Medical Center | Unknown | No outcome recorded |
| — | NCT02862873 | Mar → May 2015 | hypotensive disorder | Centre Hospitalier Universitaire Dijon | Terminated | No outcome recorded |
| — | NCT03685032 | Aug 2014 → Feb 2016 | — | Khon Kaen University | Completed | No outcome recorded |
| — | NCT02026778 | Dec 2013 → Nov 2014 | — | Yonsei University | Completed | No outcome recorded |
| — | NCT01668069 | Oct 2012 | hyperemesis gravidarum | United States Naval Medical Center, San Diego | Completed | Met primary |
| — | NCT01843868 | Jan 2012 → Jun 2015 | non-Hodgkin lymphoma | Australasian Leukaemia and Lymphoma Group | Withdrawn | No outcome recorded Stop: Enrollment |
| — | NCT01477242 | Nov 2011 → May 2012 | — | Seoul National University Hospital | Unknown | No outcome recorded |
| — | NCT01549652 | Apr 2011 → Apr 2015 | drug dependence, substance withdrawal syndrome | Stanford University | Completed | Missed primary |
| — | NCT01640340 | Jan → Aug 2011 | cancer | Ohio State University Comprehensive Cancer Center | Completed | No outcome recorded |
| — | NCT01006707 | Nov 2010 → Jul 2013 | substance-related disorder | Stanford University | Completed | No outcome recorded |
| — | NCT01759706 | Oct 2010 → Dec 2012 | pancreatic neoplasm | Vita-Salute San Raffaele University | Completed | No outcome recorded |
| — | NCT01169805 | Aug 2010 → Jun 2011 | non-congenital cyst of kidney | Yonsei University | Completed | No outcome recorded |
| — | NCT01067677 | Feb 2010 → Feb 2012 | — | Franklyn Cladis | Withdrawn | No outcome recorded Stop: Business |
| — | NCT01216410 | Dec 2008 → Apr 2011 | — | Duke University | Completed | Met primary |
| — | NCT00695864 | May 2008 → Jul 2009 | substance withdrawal syndrome | Stanford University | Completed | No outcome recorded |
| — | NCT00599573 | Oct 2007 → Jul 2010 | HIV infectious disease, cocaine dependence | University of Virginia | Unknown | No outcome recorded |
| — | NCT00499668 | Aug 2007 → Jan 2008 | leukemia, lymphoproliferative syndrome, myelodysplastic syndrome, myeloproliferative neoplasm +1 | Vanderbilt-Ingram Cancer Center | Withdrawn | No outcome recorded Stop: Enrollment |
| — | NCT00199329 | Jan 2005 → ? | — | Khon Kaen University | Completed | No outcome recorded |
| — | NCT00120744 | Jan 2004 → Apr 2005 | diarrheal disease, gastroenteritis | The Hospital for Sick Children | Completed | No outcome recorded |
| — | NCT00387556 | Dec 2002 → Dec 2006 | — | University of Colorado, Denver | Completed | No outcome recorded |
| — | NCT00018850 | Jun 1998 → Jun 2003 | schizophrenia | US Department of Veterans Affairs | Completed | No outcome recorded |
| Comparator or background therapy271 trials | ||||||
| Phase 0 | NCT07662200 Comparator | Aug 2026 → Aug 2027 expected | malignant germ cell tumor | Ottawa Hospital Research Institute | Not yet recruiting | No outcome recorded |
| Phase 0 | NCT04682743 Comparator | Jan 2021 → Jan 2022 | — | Cairo University | Completed | No outcome recorded |
| Phase 0 | NCT03593811 Comparator | Aug 2018 → Apr 2021 | — | Vanderbilt University Medical Center | Completed | No outcome recorded |
| Phase 0 | NCT03475693 Background | Sep 2017 → Nov 2019 | traumatic encephalopathy | Corewell Health South | Completed | No outcome recorded |
| Phase 0 | NCT00314743 Background | Oct 2005 → Dec 2008 | — | Washington University School of Medicine | Completed | No outcome recorded |
| Show all 271 trials opens the full record — a long page | ||||||
News releases announcing trial results or a regulatory action · 35
| Date | Issuer | Release |
|---|---|---|
| 2026-06-09 | Nasus Pharma | Results Nasus Pharma Announces Positive Results from Preclinical Pharmacokinetic and Safety Study of Intranasal Ondansetron (NS003) nasuspharma.com ↗
Data showed that NS003 had a PK profile comparable to IV, with similar time to maximum concentration (Tmax) and area under the curve (AUC) results. |
| 2026-04-27 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Submits Application to FDA Commissioner's National Priority Voucher (CNPV) Pilot Program for AD04 Clinical Development Program adial.com ↗ |
| 2025-05-08 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Granted End of Phase 2 Meeting from the U.S. Food and Drug Administration adial.com ↗
Adial Pharmaceuticals, Inc. ( NASDAQ: ADIL ) (“Adial” or the “Company”), a clinical-stage biopharmaceutical company focused on developing therapies for the treatment and prevention of addiction and related disorders, today announced that the FDA has granted Adial’s request for an End of Phase 2 meeting to discuss Adial’s proposed clinical development plan and seek FDA guidance on the Phase 3 adaptive with enrichment design of the upcoming clinical trial for AD04. |
| 2025-02-25 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Receives Positive Response from FDA Meeting Regarding Proposed In Vitro Bridging Strategy for AD04 adial.com ↗
Adial Pharmaceuticals, Inc. (NASDAQ: ADIL) (“Adial” or the “Company”), a clinical-stage biopharmaceutical company focused on developing therapies for the treatment and prevention of addiction and related disorders, today announced a positive response from the U.S. Food and Drug Administration (FDA) regarding its proposed in vitro bridging strategy for AD04. |
| 2025-01-29 | Adial Pharmaceuticals | Results Adial Pharmaceuticals Announces Positive Clinical Study Results from the AD04-103 Pharmacokinetics Study of AD04 for the Treatment of Alcohol Use Disorder adial.com ↗
These study results support the near micro-dosing regimen planned for use in the upcoming registration trials for AD04 and conform with the FDA’s bridging requirements for a 505(b)(2) registration pathway. |
| 2024-11-14 | Adial Pharmaceuticals | Results Adial Pharmaceuticals Announces Positive Topline Results from the AD04-103 Pharmacokinetics Study of AD04 for the Treatment of Alcohol Use Disorder adial.com ↗
Completion of this study also satisfied an FDA requirement for the upcoming Phase 3 clinical trials of AD04. |
| 2024-06-20 | Adial Pharmaceuticals | Results Adial Pharmaceuticals Announces Publication in Leading Peer-Reviewed Journal Supporting the Potential Efficacy of AD04 as a Precision Medicine for the Treatment of Alcohol Use Disorder adial.com ↗
The publication findings showed a significant difference in the monthly percentage of heavy drinking days between the Company’s lead asset, AD04 (low-dose ondansetron), and the placebo group among heavy drinking patients with Alcohol Use Disorder (AUD) and specific genotypic variants. |
| 2024-04-10 | Adial Pharmaceuticals | Results Adial Pharmaceuticals Announces Peer-Reviewed Publication Highlighting Promising Safety Data and High Patient Compliance in a Clinical Trial of AD04 as a Potential Treatment for Alcohol Use Disorder adial.com ↗
According to the publication, low-dose AD04 did not significantly change biochemical markers of liver injury, such as ALT, AST, and Serum Bilirubin. |
| 2022-07-20 | Adial Pharmaceuticals | Results Adial Pharmaceuticals Announces Topline Results For Onward™ Phase 3 Trial for AD04 in Patients with Alcohol Use Disorder adial.com ↗
AD04 achieved statistically significant mean reduction in heavy drinking days among the pre-specified group of “heavy drinkers” (defined below). |
| 2021-06-24 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Provides Regulatory and Development Update adial.com ↗
The Company is reporting that on June 23, 2021, it received notice from the FDA that its request for Fast Track Designation has been denied at this time. |
| 2020-10-21 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Announces FDA Reactivation of its Investigational New Drug Application for AD04 in Alcohol Use Disorder adial.com ↗
today announced that the U.S. Food and Drug Administration (FDA) has reactivated Adial’s U.S. Investigational New Drug (IND) application and lifted the clinical hold from AD04, a genetically-targeted therapeutic agent for the treatment of Alcohol Use Disorder (AUD). |
| 2020-07-28 | RedHill Biopharma Limited | Results RedHill Biopharma Publishes Positive IBS-D Phase 2 Study Data in The American Journal of Gastroenterology redhillbio.com ↗
The newly published positive data in patients who received RHB-102 for IBS-D, are a demonstration of RedHill’s ongoing ability to successfully execute its R&D programs to meet specified endpoints. |
| 2020-07-22 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Receives European Medicines Agency (EMA) Agreement on the Pediatric Investigation Plan (PIP) for AD04 in Alcohol Use Disorder adial.com ↗ |
| 2020-06-11 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Announces Approval to Commence Landmark ONWARD(TM) Pivotal Phase 3 Trial in Poland adial.com ↗ |
| 2020-01-09 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Receives Approval to Commence Phase 3 Trial in Finland adial.com ↗
today announced that it has received favorable opinions from the Finnish Medicines Agency (FIMEA) and National Committee on Medical Research Ethics (TUKIJA) to commence its Phase 3 study |
| 2019-12-19 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Submits Clinical Trial Applications in Six Additional European Countries adial.com ↗
today announced that it has submitted Clinical Trial Applications (CTAs) to commence its first Phase 3 trial in Finland, Estonia, Latvia, Poland, Bulgaria, and Croatia. |
| 2019-11-12 | RedHill Biopharma Limited | Results RedHill Biopharma Announces Publication of RHB-102 Gastroenteritis Phase 3 Study Results in JAMA redhillbio.com ↗
The GUARD study met its primary endpoint, prevention of further vomiting for at least 24 hours among adolescents and adults with gastroenteritis-related emesis without the usage of intravenous hydration or rescue medication. |
| 2019-10-01 | Adial Pharmaceuticals | Regulatory Adial Files Clinical Trial Application to Commence Phase 3 Trial adial.com ↗
today announced that it has submitted its Clinical Trial Application (CTA) to commence the Phase 3 clinical trial |
| 2019-09-05 | Adial Pharmaceuticals | Regulatory Adial Pharmaceuticals Completes Key Regulatory Milestone Prior to Commencing European Phase 3 Clinical Trial of AD04 for the Treatment of Alcohol Use Disorder adial.com ↗
today announced that the European Medicines Agency (EMA) has validated the Pediatric Investigation Plan (PIP) waiver application for AD04, the Company’s lead investigational new drug product for the treatment of Alcohol Use Disorder (AUD). |
| 2018-05-30 | RedHill Biopharma Limited | Results RedHill Biopharma to Present Positive Phase II Results of BEKINDA® for IBS-D at Digestive Disease Week 2018 redhillbio.com ↗
The Phase II study with BEKINDA® 12 mg successfully met its primary endpoint, improving the primary efficacy outcome of stool consistency (per FDA guidance definition) by an absolute difference of 20.7% vs. placebo (p-value=0.036). |
| 2018-03-26 | RedHill Biopharma Limited | Results RedHill Biopharma Announces DDW 2018 Poster of Distinction on Positive Phase II Results with BEKINDA® for IBS-D redhillbio.com ↗
The Phase II study with BEKINDA® 12 mg successfully met its primary endpoint, improving the primary efficacy outcome of stool consistency (per FDA guidance definition) by an absolute difference of 20.7% vs. placebo (p-value=0.036). |
| 2018-01-16 | RedHill Biopharma Limited | Results RedHill Biopharma Announces Final Results from Phase II Study with BEKINDA® for IBS-D redhillbio.com ↗
RedHill Biopharma Ltd. (NASDAQ:RDHL) (Tel-Aviv Stock Exchange:RDHL) ("RedHill" or the "Company"), a specialty biopharmaceutical company primarily focused on late clinical-stage development and commercialization of proprietary drugs for gastrointestinal diseases and cancer, today announced top-line final results1 from the Phase II clinical study with BEKINDA® 12 mg (RHB-102)2 for the treatment of diarrhea-predominant irritable bowel syndrome (IBS-D). |
| 2017-10-03 | RedHill Biopharma Limited | Results RedHill Biopharma Announces Positive Top-Line Results from Phase II Study of BEKINDA in Patients with IBS-D redhillbio.com ↗
BEKINDA®i 12 mg Phase II study successfully met its primary endpoint, improving primary efficacy outcome of stool consistency by an absolute difference of 19.4% vs. placebo |
| 2017-10-03 | RedHill Biopharma Limited | Results RedHill Biopharma Announces Positive Top-Line Results from Phase II Study of BEKINDA® in Patients with Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D) redhillbio.com ↗
BEKINDA®i 12 mg Phase II study successfully met its primary endpoint, improving primary efficacy outcome of stool consistency by an absolute difference of 19.4% vs. placebo and comparing favorably with previously reported outcomes from studies of Xifaxan® (rifaximin) and Viberzi® (eluxadoline)ii |
| 2017-06-14 | RedHill Biopharma Limited | Results RedHill Biopharma Announces Successful Phase III Top-Line Results with BEKINDA® for Acute Gastroenteritis redhillbio.com ↗
RedHill Biopharma Ltd. (NASDAQ:RDHL) (Tel-Aviv Stock Exchange:RDHL) ("RedHill" or the "Company"), a specialty biopharmaceutical company primarily focused on late clinical-stage development and commercialization of proprietary, orally-administered, small molecule drugs for gastrointestinal and inflammatory diseases and cancer, today announced positive top-line results from the Phase III GUARD study with BEKINDA® (RHB-102)1 24 mg for acute gastroenteritis and gastritis. |
| 2016-02-11 | RedHill Biopharma Limited | Results RedHill Biopharma Announces Successful PK Study With BEKINDA™ 12 mg and Submission to FDA of IBS-D Phase II Study Protocol redhillbio.com ↗ |
| 2015-09-28 | Heron Therapeutics | Results Heron Therapeutics Announces Oral Presentation of Data from Completed Phase 3 MAGIC Study for SUSTOL® at the ASCO Breast Cancer Symposium herontx.com ↗
These data were presented in an oral presentation and poster titled “Phase III Study of APF530 versus Ondansetron with a Neurokinin 1 Antagonist + Corticosteroid in Preventing Highly Emetogenic Chemotherapy-Induced Nausea and Vomiting: MAGIC Trial.” |
| 2014-12-31 | RedHill Biopharma Limited | Regulatory RedHill Biopharma Announces Acceptance for Review of BEKINDA(TM) European Marketing Application for Oncology Support redhillbio.com ↗
The UK MHRA has validated the European marketing application for the indications of chemotherapy and radiotherapy-induced nausea and vomiting; MHRA's feedback is expected during H2/2015 |
| 2014-12-09 | RedHill Biopharma Limited | Regulatory RedHill Biopharma Submits BEKINDA™ (RHB-102) European Marketing Authorization Application for Oncology Support redhillbio.com ↗
The European marketing authorization application (MAA) seeks approval of BEKINDA™ for cancer patients suffering from chemotherapy and radiotherapy-induced nausea and vomiting |
| 2014-05-22 | RedHill Biopharma Limited | Regulatory RedHill Biopharma Announces FDA Clearance for Phase III Study with RHB-102 Planned to Commence in Q3 2014 redhillbio.com ↗
FDA’s clearance of RedHill’s Investigational New Drug (“IND”) amendment allows the initiation of a Phase III clinical study for a new undisclosed indication with RHB-102[1], a proprietary, once-daily, extended release oral pill formulation of the antiemetic drug ondansetron |
| 2014-04-30 | RedHill Biopharma Limited | Results RedHill Biopharma Reports Successful RHB-102 Bioavailability Clinical Trial and Planned Submission of European Marketing Application in Q3/2014 redhillbio.com ↗
RedHill received positive results from a comparative bioavailability clinical trial which included 20 healthy volunteers |
| 2013-10-08 | RedHill Biopharma Limited | Results RedHill Biopharma Reports Positive PK Clinical Studies Towards Planned NDA with RHB-102 (Anti-Emetic) redhillbio.com ↗
today reported positive results from two supplementary pharmacokinetic (PK) studies with RHB-102, an anti-emetic oncology-support drug. |
| 2010-08-06 | Lannett Company, Inc. | Regulatory LANNETT RECEIVES FDA APPROVAL FOR ONDANSETRON INJECTION, USP 2 MG/ML SINGLE-DOSE VIALS PDF Version investorroom.com ↗
Philadelphia, PA – August 6, 2010 – Lannett Company, Inc. (AMEX: LCI), a manufacturer of generic pharmaceuticals, announced today that it has received approval from the U.S. Food and Drug Administration (FDA) of its Abbreviated New Drug Application (ANDA) for Ondansetron Injection USP, 2 mg/mL, Single-Dose Vials. |
| 2007-06-26 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Announces Approval Of Ondansetron Hcl Tablets And Ondansetron Orally Disintegrating Tablets USP tevapharm.com ↗
Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) announced today that the U.S. Food and Drug Administration has granted approval for the Company's Abbreviated New Drug Applications (ANDA) to market Ondansetron Hydrochloride Tablets, 4 mg, 8 mg and 24 mg and Ondansetron Orally Disintegrating Tablets USP, 4 mg and 8 mg. |
| 2006-02-26 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Announces Tentative Approval of Ondansetron Injection USP tevapharm.com ↗
Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) announced today that the U.S. Food and Drug Administration has granted tentative approval for the Company's ANDAs for Ondansetron Injection USP |
All press releases naming this drug 118 releases
| Date | Issuer | Release |
|---|---|---|
| Show all 118 releases opens the full record — a long page | ||
Evidence & citations 44 cited values
Every value below carries the sentence it was read from. 463 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Ondansetron | “METHODS: Women scheduled for elective cesarean delivery were randomized to one of three groups: placebo (placebo plus placebo); metoclopramide (metoclopramide 10 mg plus...” PMID 23635626 ↗ Mar 2013444“5HT3 (5-Hydroxytryptamine 3) antagonists (ondansetron, granisetron or tropisetron) used as the local institutional standard of care will be permitted, although the preferential...” NCT01843868 ↗ “Comparing the Effects of Ondansetron Versus Dexamethasone on the Incidence of Post-dural Puncture Headache (PDPH) , Nausea and Vomiting After Spinal Anaesthesia of Parturients...” NCT05202574 ↗ “30 minutes prior to emergence 0.2 μg/kg total body weight Sufentanil IV and 1 gram of paracetamol IV (if 6hrs since preoperative medicine) and 4 mg ondansetron IV (PONV...” NCT04248179 ↗ “Placebo, given orally Ranitide 50 mg, IV, before chemotherapy (D1) Ondansetron 8 mg, IV, before chemotherapy (D1) Dexamethasone 10 mg, IV, before chemotherapy (D1)...” NCT01052844 ↗ “Anesthesia will be maintained with Sevoflurane, Magnesium, Lidocaine, Ketamine, Decadron, Ondansetron, and Ketorolac at a concentration range/dose(s) based on the clinical need...” NCT03367988 ↗ “Day 1: Aprepitant 125mg QD (once daily); Ondansetron 8mg BD (twice daily); Dexamethasone 12mg QD (Aprepitant, Ondansetron and Dexamethasone to be take 60 minutes before...” NCT07455955 ↗ “Granisetron Transdermal Delivery System (GTDS) efficacy compared with the ondansetron efficacy with regard to Complete Response (CR) of Chemotherapy Induced Nausea and Vomiting (CINV).” NCT01659775 ↗ “Pramipexole group: Consenting individuals meeting accession criteria will start pramipexole 2.0mg daily dose (1.0mg twice a day) with ondansetron 16mg daily dose (8mg twice a day).” NCT03642964 ↗ “Patients will receive ondansetron (0.1 mg / kg dose of 4mg cap) associated with dexamethasone (0.15 mg / kg dose of 5mg ceiling) or dexamethasone (0.15 mg / kg) or placebo” NCT01297010 ↗ “Comparison Between Propofol, Ondansetron and Pregabalin for Control of Emetic Attacks During Caesarean Delivery With Spinal Anesthesia: Randomized Clinical Trial” NCT06300346 ↗ |
| Known as | A04AA01 | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | AD04 | “AD04 (ondansetron)” NCT04101227 ↗ |
| Known as | BEKINDA | “Randomized, Placebo-Controlled, Phase 3 Trial of RHB-102 (BEKINDA) (Ondansetron 24 mg Bimodal Release Tablets) for Acute Gastroenteritis.” NCT02246439 ↗1“BEKINDA (Ondansetron 12 mg Bimodal Release Tablets)” NCT02757105 ↗ |
| Known as | Demorem | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Desmethylondansetron | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | EUR-1025 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01036854 ↗ |
| Known as | GR 38032F | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | GR-38032 | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | GR-C507/75 | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | NS003 | “NS003 Ondansetron HCl microspheres powder for nasal application” NCT07868861 ↗ |
| Known as | NSC-665799 | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | NSC-757870 | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Odansetron hydrochloride | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | OND | “The combination of dexamethasone (DEX), ondansetron (OND) and droperidol (DRO) is efficacious in preventing postoperative nausea and vomiting in adults, but has not been well...” PMID 28505233 ↗ Jun 2017 |
| Known as | Ond-PR1 | “Single oral dose of 8 mg of ondansetron pulsatile-release formulation 1 (Ond-PR1)” NCT01290276 ↗ |
| Known as | Ond-PR2 | “Single oral dose of 8 mg ondansetron pulsatile-release formulation 2 (Ond-PR2)” NCT01290276 ↗ |
| Known as | Ondalenz | “oral ondansetron in the form of an oral soluble film 4 mg strip (Ondalenz, 4 mg orodispersible films of Nerhadou International Co.)” NCT07088601 ↗5“Pediatric patients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery as a study group.” NCT06423820 ↗ “Patients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery.” NCT06254131 ↗ “Patients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery.” NCT07511491 ↗ “Patients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery.” NCT06423807 ↗ “Patients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery.” NCT07489742 ↗ |
| Known as | Ondansetron (as hydrochloride) | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Ondansetron (Zofran) | “Ondansetron (Zofran)” NCT00781768 ↗1“ondansetron (Zofran)” NCT02724033 ↗ |
| Known as | Ondansetron Accord | “Ondansetron (Ondansetron Accord 2mg/ml, 2 ml solution, Accord Healthcare Limited, Great Britain) in a dose of 4 mg will be administered intravenously” NCT06609993 ↗ |
| Known as | Ondansetron HCl | “Ondansetron HCl 8 mg OD Tablet (test) dosed in first period followed by Zofran® 8 mg ODT (reference) dosed in second period” NCT00934180 ↗3“NS003 Ondansetron HCl microspheres powder for nasal application” NCT07868861 ↗ “Ondansetron HCl 24 mg Tablets (Sandoz, Inc.)” NCT00946387 ↗ “Ondansetron HCl 24 mg Tablets (Sandoz, Inc.)” NCT00947128 ↗ |
| Known as | Ondansetron Hydrochloride | “ondansetron hydrochloride(8mg, i.v. day 1-day 3)” NCT04536558 ↗ |
| Known as | Ondansetron hydrochloride dihydrate | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Ondansetron hydrochloride hydrate | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Ondansetron hydrochloride preservative free | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Ondansetron monohydrochloride | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Ondasetron | “Drug: Ondasetron 4mg” NCT07084753 ↗ |
| Known as | Ondemet | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | RHB-102 | “Randomized, Placebo-Controlled, Phase 3 Trial of RHB-102 (BEKINDA) (Ondansetron 24 mg Bimodal Release Tablets) for Acute Gastroenteritis.” NCT02246439 ↗ |
| Known as | Setofilm | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | SN 307 | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | ZOFATRONE | “Patients will receive 8 mg of ondansetron (ZOFATRONE®, 8 mg/4 mL, EVA Pharma, Egypt)” NCT06850740 ↗ |
| Known as | Zofran | “Treatment B: single dose of Zofran ODT (containing ondansetron 8 mg) was orally administered, allowed to dissolve, swallowed with saliva, followed with 240 mL room temperature...” NCT01217190 ↗30“Ondansetron HCl 8 mg OD Tablet (test) dosed in first period followed by Zofran® 8 mg ODT (reference) dosed in second period” NCT00934180 ↗ “Eligible patients were randomized to Sancuso patch or Zofran groups and received the assigned treatment for 5days.” NCT01659775 ↗ “ondansetron (Zofran) tablets combined with a medicine called dexamethasone given IV” NCT00781768 ↗ “To compare the single-dose bioavailability of Ondansetron ODT 8 mg and Zofran 8 mg” NCT00653458 ↗ “D1 Zofran 8mg pre-Cyclophosphamide 300mg/mg2 po and D3 Ipilimumab 10mg/kg iv” NCT01740401 ↗ “The usual treatment for nausea/vomiting is a drug called Zofran” NCT03125811 ↗ “ondansetron 4mg (Zofran; GlaxoSmithKline, Alexandria, USA” NCT06017167 ↗ “Zofran (Ondansetron HCl) 24 mg Tablets (GlaxoSmithKline)” NCT00947128 ↗ “Zofran (Ondansetron HCl) 24 mg Tablets (GlaxoSmithKline)” NCT00946387 ↗ “ondansetron (Zofran)” NCT00027079 ↗ |
| Known as | zofran - ondansetron | “zofran - ondansetron” NCT01536691 ↗ |
| Known as | Zofran ODT | “Ondansetron HCl with the already marketed reference formulation Zofran ODT under fasting conditions” NCT00934180 ↗1“Single dose of Zofran ODT (containing ondansetron 8 mg) administered without water” NCT01220167 ↗ |
| Known as | Zofran preservative free | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Zofran, Ondansetron hydrochloride | “Zofran (ondansetron hydrochloride)” NCT01290276 ↗1“Zofran, Ondansetron hydrochloride” NCT05378113 ↗ |
| Known as | Zophren | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Known as | Zuplenz | ChEMBL registry synonym — accepted as the source's own label CHEMBL46 ↗ |
| Action | Inhibit | “Serotonin 3a (5-HT3a) receptor antagonist” CHEMBL46 ↗1“a 5HT3 antagonist” NCT00000289 ↗ |
| Modality | Other / unclassified | “Ondansetron is a selective 5-HT3 receptor antagonist.” NCT00967499 ↗ |
| Route | Oral | “ondansetron orally” NCT00005994 ↗ |
| Target | HTR3A | “Serotonin 3a (5-HT3a) receptor antagonist” CHEMBL46 ↗ |