Drug
Fedratinib clinical trials
Also written SAR302503, Inrebic and TG101348.
- studies test it
- 24
- open now
- 1
- in phase 3
- 3
- first study started
- 2008
Keep track of what changes. Save the fedratinib studies recruiting or about to start, and get an email each week — studies that open, close, add sites or post results.
Watch these studiesHow studies write it
Studies that test it under each name
Brand
Development codes
Studies by the year they started
24 studies that test it; most in 2012 (5)
| Year | Studies |
|---|---|
| 2008 | 2 |
| 2011 | 3 |
| 2012 | 5 |
| 2013 | 1 |
| 2019 | 5 |
| 2020 | 2 |
| 2021 | 3 |
| 2022 | 3 |
By phase
A phase 1/2 study counts in both.
- Phase 1
- 15
- Phase 2
- 9
- Phase 3
- 3
What it is tested for
Each study’s main condition, where its own words name it.
Who runs them
Industry 20 · Other 4
Bristol-Myers Squibb (13) · Celgene (6) · H. Lee Moffitt Cancer Center and Research Institute (2) · TargeGen (1) · University of Washington (1) · Joseph Jurcic (1)
Often tested with
Tested in the same studies.
Ruxolitinib (2) · Metoprolol (1) · Midazolam (1) · Fluconazole (1) · Digoxin (1) · Rosuvastatin (1) · Metformin (1) · Decitabine (1)
Studies
Open first, then newest update. How each study uses fedratinib is read from its arms, and is right about nine times in ten.
Testing it · 24
- Decitabine With Ruxolitinib, Fedratinib or Pacritinib for the Treatment of Accelerated/Blast Phase Myeloproliferative NeoplasmsRecruitingPhase 2University of WashingtonNCT04282187Written as Fedratinib
- A Long-Term Study of the Effects of Orally Administered SAR302503 in Patients With MyelofibrosisCompletedPhase 1/2Bristol-Myers SquibbNCT00724334Written as SAR302503 (TG101348)
- Phase III Study of SAR302503 in Intermediate-2 and High Risk Patients With MyelofibrosisTerminatedPhase 3Bristol-Myers SquibbNCT01437787Written as SAR302503
- Phase II, Open Label, Single Arm Study of SAR302503 In Myelofibrosis Patients Previously Treated With RuxolitinibTerminatedPhase 2Bristol-Myers SquibbNCT01523171Written as SAR302503
- Fedratinib in Myelodysplastic /Myeloproliferative Neoplasms (MDS/MPNs) and Chronic Neutrophilic Leukemia (CNL)CompletedPhase 2H. Lee Moffitt Cancer Center and Research InstituteNCT05177211Written as Fedratinib Pill
- A Study to Assess the Safety and Tolerability of BMS-986158 Alone and in Combination With Either Ruxolitinib or Fedratinib in Participants With Blood Cancer (Myelofibrosis)Active, not recruitingPhase 1/2Bristol-Myers SquibbNCT04817007Written as Fedratinib
- Maintenance Fedratinib to Prevent Post-Transplant Relapse in Myeloproliferative NeoplasmsTerminatedPhase 1H. Lee Moffitt Cancer Center and Research InstituteNCT05127174Written as Fedratinib Pill
- A Study of Fedratinib in Japanese Subjects With DIPSS (Dynamic International Prognostic Scoring System)- Intermediate or High-risk Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (Post-PV MF), or Post-essential Thrombocythemia Myelofibrosis (Post-ET MF)Active, not recruitingPhase 1/2Bristol-Myers SquibbNCT04446650Written as Fedratinib
- An Efficacy and Safety Study of Fedratinib Compared to Best Available Therapy in Subjects With DIPSS-intermediate or High-risk Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, or Post-essential Thrombocythemia Myelofibrosis and Previously Treated With RuxolitinibCompletedPhase 3CelgeneNCT03952039Written as FEDRATINIB
- Open Label Pharmacokinetic Study of SAR302503 in Subjects With Hepatic ImpairmentCompletedPhase 1Bristol-Myers SquibbNCT01762462Written as SAR302503
- Phase 2 Study in Japanese Patients With Intermediate-2 or High Risk Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, Post-Essential Thrombocythemia Myelofibrosis With SplenomegalyCompletedPhase 2Bristol-Myers SquibbNCT01692366Written as SAR302503
- Drug Interaction Study of SAR302503 in Patients With Solid TumorCompletedPhase 1Bristol-Myers SquibbNCT01585623Written as SAR302503
- Open Label Pharmacokinetic Study of SAR302503 in Subjects With Renal ImpairmentCompletedPhase 1Bristol-Myers SquibbNCT01763190Written as SAR302503
- Phase 2 Study of SAR302503 in Patients With MyelofibrosisCompletedPhase 2Bristol-Myers SquibbNCT01420770Written as SAR302503
- Effect of SAR302503 on ECG Activity in Patients With Solid TumorsCompletedPhase 1Bristol-Myers SquibbNCT01836705Written as SAR302503 (TG101348)
- Study With SAR302503 in Patients With Polycythemia Vera or Essential ThrombocythemiaCompletedPhase 2Bristol-Myers SquibbNCT01420783Written as SAR302503
- A Trial of Fedratinib in Subjects With DIPSS, Intermediate or High-Risk Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis and Previously Treated With RuxolitinibTerminatedPhase 3CelgeneNCT03755518Written as FEDRATINIB
- Combination of Fedratinib and Decitabine for Myeloproliferative Neoplasms (MPN)- Accelerated Phase (AP)/Blast Phase (BP)TerminatedPhase 1Joseph JurcicNCT05524857Written as Fedratinib Oral Capsule 300 mg
- A Pharmacokinetics and Tolerability Study of Fedratinib in Subjects With Moderate and Severe Hepatic ImpairmentCompletedPhase 1CelgeneNCT03983161Written as Fedratinib
- A Study to Evaluate the Bioavailability of Fedratinib When Administered in Different Ways to Healthy Adult ParticipantsCompletedPhase 1Bristol-Myers SquibbNCT05051553Written as Fedratinib
See all 24 studies that test fedratinib →
Given in every arm · 3 — fedratinib is usual care beside what is tested
- Revumenib in Patients With MyelofibrosisNot yet recruitingPhase 1/2John MascarenhasNCT07734077Written as FEDRATINIB
- Fedratinib in Combination With NivolumabCompletedPhase 2Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus NordwestNCT05393674Written as Fedratinib Oral Capsule [Inrebic]
- A Study of Fedratinib With IDH Inhibition in Advanced-Phase, IDH-Mutated Ph-Negative Myeloproliferative NeoplasmsWithdrawnPhase 1University of ChicagoNCT04955938Written as Fedratinib
Codes
What other systems call fedratinib · ClinicalTrials.gg INT005259
- MeSH (NLM) C528327fedratinibConfirmed ClinicalTrials.gov, NLM
- UNII (FDA) 6L1XP550I6FEDRATINIBConfirmed FDA, NLM, Wikidata
- RxNorm 2197490One source FDA
- Wikidata Q7670147fedratinibConfirmed FDA, NLM, Wikidata
- NCI Thesaurus C88293FedratinibOne source FDA
- DrugBank DB12500One source Wikidata
| System | Code | Name there | Checked by |
|---|---|---|---|
| MeSH (NLM) | C528327 | fedratinib | Confirmed ClinicalTrials.gov, NLM |
| UNII (FDA) | 6L1XP550I6 | FEDRATINIB | Confirmed FDA, NLM, Wikidata |
| RxNorm | 2197490 | — | One source FDA |
| Wikidata | Q7670147 | fedratinib | Confirmed FDA, NLM, Wikidata |
| NCI Thesaurus | C88293 | Fedratinib | One source FDA |
| DrugBank | DB12500 | — | One source Wikidata |
Also registered as fedratinib hydrochloride (UNII UH9J2HBQWJ · RxNorm 2197594).
“Confirmed” means two independent publishers link the code to this drug; “one source”, one does and its name agrees.