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Drug ReportsTafluprost
Tafluprost
Tafluprost, Zioptan (tafluprost) is a small molecule pharmaceutical. Tafluprost was first approved as Zioptan on 2012-02-10. It is used to treat open-angle glaucoma in the USA. The pharmaceutical is active against prostaglandin F2-alpha receptor.
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Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
eye diseasesD005128
Trade Name
FDA
EMA
Tafluprost, Zioptan (discontinued: Tafluprost)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Tafluprost
Tradename
Company
Number
Date
Products
ZIOPTANThea PharmaN-202514 RX2012-02-10
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
tafluprostANDA2022-06-09
tafluprost ophthalmicNDA authorized generic2022-06-01
zioptanNew Drug Application2024-04-17
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
open-angle glaucomaEFO_0004190D005902H40.1
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
Flag
FDA Information
Tafluprost, Zioptan, Thea Pharma
99995932029-05-28DP
108641592029-05-28DPU-778
ATC Codes
S: Sensory organ drugs
— S01: Ophthalmologicals
— S01E: Antiglaucoma preparations and miotics
— S01EE: Prostaglandin analogues, antiglaucoma drugs and miotics
— S01EE05: Tafluprost
HCPCS
No data
Clinical
Clinical Trials
36 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
GlaucomaD005901EFO_0000516H40231114634
Ocular hypertensionD009798EFO_1001069H40.02199424
Open-angle glaucomaD005902EFO_0004190H40.1—199423
HypertensionD006973EFO_0000537I102185318
Graves ophthalmopathyD049970EFO_1001466————1—1
Eye diseasesD005128EFO_0003966H44———1—1
Thyroid diseasesD013959HP_0000820E00-E07———1—1
Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Macular edemaD008269———1———1
CataractD002386HP_0000518H26.9—1———1
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients———1————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Corneal diseasesD003316—H18.9————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameTafluprost
INNtafluprost
Description
Tafluprost (trade names Taflotan by Santen Pharmaceutical, Zioptan by Merck in the US and Saflutan by Mundipharma in Australia) is a prostaglandin analogue. It is used topically (as eye drops) to control the progression of open-angle glaucoma and in the management of ocular hypertension, alone or in combination with other medication. It reduces intraocular pressure by increasing the outflow of aqueous fluid from the eyes.
Classification
Small molecule
Drug classprostaglandins
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
CC(C)OC(=O)CCC/C=C\C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1/C=C/C(F)(F)COc1ccccc1
Identifiers
PDB—
CAS-ID209860-87-7
RxCUI—
ChEMBL IDCHEMBL1963683
ChEBI ID66899
PubChem CID6433101
DrugBankDB08819
UNII ID1O6WQ6T7G3 (ChemIDplus, GSRS)
Target
Agency Approved
PTGFR
PTGFR
Organism
Homo sapiens
Gene name
PTGFR
Gene synonyms
NCBI Gene ID
Protein name
prostaglandin F2-alpha receptor
Protein synonyms
FP prostanoid receptor, PGF receptor, PGF2 alpha receptor, prostaglandin receptor (2-alpha), Prostanoid FP receptor
Uniprot ID
Mouse ortholog
Ptgfr (19220)
prostaglandin F2-alpha receptor (P43117)
Alternate
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
Zioptan – Akorn
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Tabular view
Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 766 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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1,993 adverse events reported
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