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AboutPricing
Drug ReportsZalcitabine
Zalcitabine
Hivid (zalcitabine) is a small molecule pharmaceutical. Zalcitabine was first approved as Hivid on 1992-06-19. It is used to treat acquired immunodeficiency syndrome in the USA.
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Financial
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Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
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Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
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Primary completion date
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Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
urogenital diseasesD000091642
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)
Zalcitabine
Tradename
Company
Number
Date
Products
HIVIDRocheN-020199 DISCN1992-06-19
2 products
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FDA
EMA
No data
Indications
FDA
EMA
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
J: Antiinfectives for systemic use
— J05: Antivirals for systemic use
— J05A: Direct acting antivirals
— J05AF: Nucleoside and nucleotide reverse transcriptase inhibitors
— J05AF03: Zalcitabine
HCPCS
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Clinical
Clinical Trials
75 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hiv infectionsD015658EFO_0000764B20618103945
Parkinson diseaseD010300EFO_0002508G205642218
Acquired immunodeficiency syndromeD000163EFO_0000765B201831417
LipodystrophyD008060HP_0009125E88.1———2—2
Hemophilia aD006467EFO_0007267D66———1—1
AcidosisD000138EFO_1000014E87.2———1—1
Lactic acidosisD000140HP_0003128E87.20———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfectionsD007239EFO_0000544—163—212
Communicable diseasesD003141——152—19
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Central nervous system diseasesD002493HP_0002011G96.912———3
Brain diseasesD001927HP_0001298G93.4012———3
Nervous system diseasesD009422—G00-G9912———3
Movement disordersD009069HP_0100022—12———3
Neurodegenerative diseasesD019636EFO_0005772G31.912———3
Disease progressionD018450———2———2
DyskinesiasD020820HP_0002310G24—1———1
LeukoencephalopathiesD056784HP_0002352——1———1
Progressive multifocal leukoencephalopathyD007968EFO_0007455A81.2—1———1
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Aids-related complexD000386EFO_0007137B201———12
Inborn errors amino acid metabolismD000592—E72.91———12
Hepatitis cD006526—B19.21————1
HepatitisD006505HP_0012115K75.91————1
Hepatitis aD006506EFO_0007305B151————1
Parkinsonian disordersD020734HP_0001300G20.C1————1
Basal ganglia diseasesD001480HP_0002134—1————1
SarcomaD012509——1————1
Kaposi sarcomaD012514—C461————1
Argininosuccinic aciduriaD056807——1————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple myelomaD009101—C90.0————11
Plasma cell neoplasmsD054219——————11
HypoxiaD000860HP_0012418R09.02————11
Virus diseasesD014777—B34————11
Immunologic deficiency syndromesD007153HP_0002721D84.9————11
KeratitisD007634HP_0000491H16————11
Autoimmune hepatitisD019693——————11
SyndromeD013577——————11
Autoimmune polyendocrinopathiesD016884—E31.0————11
PancreatitisD010195HP_0001733K85————11
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameZalcitabine
INNzalcitabine
Description
Zalcitabine is a pyrimidine 2',3'-dideoxyribonucleoside compound having cytosine as the nucleobase. It has a role as an antiviral drug, an antimetabolite and a HIV-1 reverse transcriptase inhibitor.
Classification
Small molecule
Drug classnucleoside antiviral or antineoplastic agents, cytarabine or azarabine derivatives
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Nc1ccn([C@H]2CC[C@@H](CO)O2)c(=O)n1
Identifiers
PDB—
CAS-ID7481-89-2
RxCUI—
ChEMBL IDCHEMBL853
ChEBI ID10101
PubChem CID24066
DrugBankDB00943
UNII ID6L3XT8CB3I (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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243 adverse events reported
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