Drug Type Small molecule drug |
Synonyms |
Target |
Mechanism FLT3 inhibitors(Tyrosine-protein kinase receptor FLT3 inhibitors), MEK1 inhibitors(Dual specificity mitogen-activated protein kinase kinase 1 inhibitors) |
Therapeutic Areas |
Active Indication |
Inactive Indication |
Originator Organization |
Active Organization |
Inactive Organization |
Drug Highest PhasePhase 2 |
First Approval Date- |
Regulation- |
Molecular FormulaC21H27NO6 |
InChIKeyMWUFVYLAWAXDHQ-HMNLTAHHSA-N |
CAS Registry603987-35-5 |
KEGG | Wiki | ATC | Drug Bank |
---|---|---|---|
- | - | - |
Indication | Highest Phase | Country/Location | Organization | Date |
---|---|---|---|---|
Acute Lymphoblastic Leukemia | Phase 2 | - | - | |
Acute Lymphoblastic Leukemia | Phase 2 | - | - | |
Chronic Myelomonocytic Leukemia | Phase 2 | - | - | |
Chronic Myelomonocytic Leukemia | Phase 2 | - | - | |
Myelodysplastic Syndromes | Phase 2 | - | - | |
Myelodysplastic Syndromes | Phase 2 | - | - | |
Acute Myeloid Leukemia | Discovery | US | 10 Apr 2015 | |
Myeloproliferative Disorders | Discovery | US | 10 Apr 2015 |
Phase 1 | 4 | (Monotherapy Safety Run-in: E6201) | (xquoadwsak) = lsretsmrzk iqvjzeicfu (ljtoniptyo, fqvjhxkjxb - qhoduyzvvs) View more | - | 20 May 2022 | ||
E6201 plus dabrafenib (Combination Safety Run-in: E6201 Plus Dabrafenib) | jmswuyquso(tzatonddbv) = ksebnmcdka funnpsrhoz (sodqwmxodz, zuolqkpnfp - wipaduqevw) View more | ||||||
Phase 1/2 | 27 | zjcptjblpg(fswhmlyugh) = fymwbigyoi ntfgseglrs (zzdgshdsmu, qgvetorzaw - hqjnzcuwzv) | - | 05 Mar 2019 | |||
NCT00794781 (Pubmed) Manual | Phase 1 | 55 | (Part A) | (tmjxxtbizb) = Adverse events included QT prolongation (n = 4) and eye disorders (n = 3). kaobnsqtvc (npssnhbwgv ) View more | Positive | 01 Jun 2018 | |
(Part B) | |||||||
Phase 1 | 25 | (yxbuxyslsg) = tkrrcwdpqc qhyrmnxqvz (zohvcnpbtf ) | - | 20 May 2010 |