Menotropins
Menopur (menotropins) is a protein pharmaceutical. Menotropins was first approved as Pergonal on 1975-08-22.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
Menopur (discontinued: Humegon, Pergonal, Repronex)
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Menotropins
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Menopur | menotropins | Ferring Pharmaceuticals Inc. | N-21663 RX | 2004-10-29 | 1 products |
Show 3 discontinued
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
menopur | Biologic Licensing Application | 2021-01-15 |
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
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ATC Codes
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HCPCS
Code | Description |
---|---|
S0122 | Injection, menotropins, 75 iu |
Clinical
Clinical Trials
2 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Osteoporosis | D010024 | EFO_0003882 | M81.0 | — | — | 1 | — | — | 1 |
Postmenopausal osteoporosis | D015663 | EFO_0003854 | — | 1 | 1 | — | — | 1 |
Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | MENOTROPINS |
INN | — |
Description | Menotropin (also called human menopausal gonadotropin or hMG) is a hormonally active medication for the treatment of fertility disturbances. Frequently the plural is used as the medication is a mixture of gonadotropins. Menotropins are extracted from the urine of postmenopausal women.
|
Classification | Protein |
Drug class | atropine derivatives |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | 61489-71-2 |
RxCUI | — |
ChEMBL ID | CHEMBL2108427 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB00032 |
UNII ID | — |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
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Trends
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Safety
Black-box Warning
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Adverse Events
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1 adverse events reported
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