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Drug ReportsPanobinostat
Panobinostat
Farydak (panobinostat) is a small molecule pharmaceutical. Panobinostat was first approved as Farydak on 2015-02-23. It is used to treat multiple myeloma in the USA. It has been approved in Europe to treat multiple myeloma. It is known to target histone deacetylase 7, histone deacetylase 6, histone deacetylase 9, histone deacetylase 4, histone deacetylase 3, histone deacetylase 8, histone deacetylase 1, and histone deacetylase 2.
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Novartis Pharmaceuticals
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
cardiovascular diseasesD002318
hemic and lymphatic diseasesD006425
immune system diseasesD007154
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Panobinostat lactate
Tradename
Company
Number
Date
Products
FARYDAKSecura BioN-205353 DISCN2015-02-23
3 products, RLD
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Labels
FDA
EMA
Brand Name
Status
Last Update
farydakNew Drug Application2021-07-27
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
multiple myeloma—D009101C90.0
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
Flag
FDA Information
Panobinostat Lactate, Farydak, Secura
88838422028-06-13U-1669
79894942028-01-17DS, DP
ATC Codes
L: Antineoplastic and immunomodulating agents
— L01: Antineoplastic agents
— L01X: Other antineoplastic agents in atc
— L01XH: Histone deacetylase (hdac) inhibitors
— L01XH03: Panobinostat
HCPCS
No data
Clinical
Clinical Trials
152 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Myeloid leukemiaD007951—C92117—1—15
Myeloid leukemia acuteD015470—C92.011511—14
Primary myelofibrosisD055728—D47.443—1—6
Graft vs host diseaseD006086—D89.8113—1—4
Polycythemia veraD011087—D4522—1—4
PolycythemiaD011086EFO_0005804D75.122—1—4
ThalassemiaD013789EFO_1001996D56———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple myelomaD009101—C90.017181—332
Plasma cell neoplasmsD054219——16161—330
LymphomaD008223—C85.913191——29
Myelodysplastic syndromesD009190—D46761——11
PreleukemiaD011289——761——11
Hodgkin diseaseD006689—C81641——9
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
LeukemiaD007938—C951413———21
NeoplasmsD009369—C80151———16
Breast neoplasmsD001943EFO_0003869C5085———10
SyndromeD013577——76———10
Non-hodgkin lymphomaD008228—C85.954———8
GliomaD005910EFO_0000520—64———8
Lung neoplasmsD008175HP_0100526C34.9071———8
Prostatic neoplasmsD011471—C6162———7
RecurrenceD012008——53———7
T-cell lymphomaD016399——26———7
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-small-cell lung carcinomaD002289——6————6
Liver neoplasmsD008113EFO_1001513C22.02————2
Head and neck neoplasmsD006258——2————2
Triple negative breast neoplasmsD064726——2————2
Castration-resistant prostatic neoplasmsD064129——1————1
Myeloproliferative disordersD009196—D47.11————1
AnemiaD000740HP_0001903D64.91————1
Leukemia myeloid chronic atypical bcr-abl negativeD054438—C92.21————1
Myelodysplastic-myeloproliferative diseasesD054437——1————1
AdenocarcinomaD000230——1————1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePanobinostat
INNpanobinostat
Description
Panobinostat is a hydroxamic acid obtained by formal condensation of the carboxy group of (2E)-3-[4-({[2-(2-methylindol-3-yl)ethyl]amino}methyl)phenyl]prop-2-enoic acid with the amino group of hydroxylamine. A histone deacetylase inhibitor used (as its lactate salt) in combination with bortezomib and dexamethasone for the treatment of multiple myeloma. It has a role as an EC 3.5.1.98 (histone deacetylase) inhibitor, an antineoplastic agent and an angiogenesis modulating agent. It is a hydroxamic acid, a member of cinnamamides, a secondary amino compound and a methylindole. It is a conjugate base of a panobinostat(1+).
Classification
Small molecule
Drug classenzyme inhibitors: histone deacetylase inhibitors
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Cc1[nH]c2ccccc2c1CCNCc1ccc(/C=C/C(=O)NO)cc1
Identifiers
PDB—
CAS-ID404950-80-7
RxCUI—
ChEMBL IDCHEMBL483254
ChEBI ID85990
PubChem CID6918837
DrugBankDB06603
UNII ID9647FM7Y3Z (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
HDAC9
HDAC9
HDAC6
HDAC6
HDAC7
HDAC7
Organism
Homo sapiens
Gene name
HDAC9
Gene synonyms
HDAC7, HDAC7B, HDRP, KIAA0744, MITR
NCBI Gene ID
Protein name
histone deacetylase 9
Protein synonyms
HD7, HD7b, histone deacetylase 4/5-related protein, Histone deacetylase 7B, Histone deacetylase-related protein, MEF-2 interacting transcription repressor (MITR) protein, MEF2-interacting transcription repressor MITR
Uniprot ID
Mouse ortholog
Hdac9 (79221)
histone deacetylase 9 (Q99N13)
Variants
No data
Financial
No data
Trends
PubMed Central
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Safety
Black-box Warning
Black-box warning for: Farydak
Adverse Events
Top Adverse Reactions
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1,993 adverse events reported
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