Panobinostat
Phase 1Completed 0 views this week 0 watching💤 Quiet
Interest: 29/100
29
Development Stage
✓
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Myelodysplastic Syndromes (MDS)
Conditions
Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML), Acute Myeloid Leukemia (AML)
Trial Timeline
Aug 1, 2012 → May 1, 2014
NCT ID
NCT01613976About Panobinostat
Panobinostat is a phase 1 stage product being developed by Novartis for Myelodysplastic Syndromes (MDS). The current trial status is completed. This product is registered under clinical trial identifier NCT01613976. Target conditions include Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML), Acute Myeloid Leukemia (AML).
What happened to similar drugs?
7 of 19 similar drugs in Myelodysplastic Syndromes (MDS) were approved
Approved (7) Terminated (7) Active (7)
Hype Score Breakdown
Clinical
6
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (16)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02568943 | Pre-clinical | Completed |
| NCT02204553 | Pre-clinical | Completed |
| NCT02722941 | Phase 2 | Completed |
| NCT01802879 | Phase 2 | Completed |
| NCT01680094 | Phase 1/2 | Completed |
| NCT01613976 | Phase 1 | Completed |
| NCT01324635 | Phase 1 | Terminated |
| NCT01242774 | Phase 1 | Completed |
| NCT01115036 | Phase 2 | Withdrawn |
| NCT00931762 | Phase 2 | Terminated |
| NCT00742027 | Phase 2 | Completed |
| NCT00670553 | Phase 1 | Completed |
| NCT00667862 | Phase 2 | Completed |
| NCT00594230 | Phase 2 | Terminated |
| NCT00490776 | Phase 2 | Terminated |
| NCT00425555 | Phase 2 | Completed |
Competing Products
20 competing products in Myelodysplastic Syndromes (MDS)
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| NEX-18a injection + Azacitidine Injection | Nanexa AB | Phase 1 | 23 |
| JSP191 | Jasper Therapeutics | Phase 1 | 11 |
| Humanized anti-CD117 Monoclonal Antibody (JSP191) | Jasper Therapeutics | Phase 1 | 15 |
| GTB-3550 TriKE® Phase I + GTB-3550 TriKE® Phase II | GT Biopharma | Phase 1/2 | 14 |
| Erlotinib Hydrochloride | Astellas Pharma | Phase 2 | 35 |
| Decitabine + Decitabine + Decitabine | Eisai | Phase 2 | 35 |
| Decitabine + Valproic Acid | Eisai | Phase 2 | 35 |
| decitabine + decitabine | Eisai | Phase 2 | 35 |
| decitabine + azacitidine | Eisai | Approved | 35 |
| Decitabine | Eisai | Phase 2 | 27 |
| decitabine + decitabine + decitabine + decitabine | Eisai | Phase 1 | 29 |
| Decitabine, Arsenic Trioxide and Ascorbic Acid | Eisai | Phase 2 | 35 |
| Subcutaneous Decitabine | Eisai | Phase 1 | 21 |
| Decitabine | Eisai | Phase 2 | 35 |
| Galunisertib + Placebo | Eli Lilly | Phase 2/3 | 38 |
| DSP-7888 | Sumitomo Pharma | Phase 1/2 | 32 |
| TP-0184 | Sumitomo Pharma | Phase 1/2 | 24 |
| Decitabine | Johnson & Johnson | Phase 2 | 35 |
| Epoetin alfa | Johnson & Johnson | Phase 2 | 27 |
| ZARNESTRA, tipifarnib, R115777 | Johnson & Johnson | Phase 2 | 35 |