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Gonal-f(follitropin alfa)
Gonal-f, Gonal-f RFF, Pergoveris (follitropin alfa) is a protein pharmaceutical. Follitropin alfa was first approved as Gonal-f on 1995-10-20. It is used to treat infertility in the USA. It has been approved in Europe to treat anovulation, assisted reproductive techniques, female infertility, and hypogonadism.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
urogenital diseasesD000091642
endocrine system diseasesD004700
therapeuticsD013812
investigative techniquesD008919
reproductive and urinary physiological phenomenaD012101
Trade Name
FDA
EMA
Gonal-f, Gonal-f rff, Gonal-f rff rediject
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)
Follitropin alfa
Tradename
Proper name
Company
Number
Date
Products
Gonal-ffollitropin alfaEMD SeronoN-20378 RX2001-02-28
2 products
Gonal-f RFF RediJectfollitropin alfaEMD SeronoN-21684 RX2004-05-25
3 products
Gonal-f RFFfollitropin alfaEMD SeronoN-21765 RX2004-03-25
1 products
Show 2 discontinued
Labels
FDA
EMA
Brand Name
Status
Last Update
gonal-f rffBiologic Licensing Application2022-08-08
gonal-f rffBiologic Licensing Application2022-08-08
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
infertilityEFO_0000545D007246—
Agency Specific
FDA
EMA
Expiration
Code
follitropin alfa, Gonal-f, EMD Serono, Inc.
2107-05-24Orphan excl.
Patent Expiration
No data
ATC Codes
G: Genito urinary system and sex hormones
— G03: Sex hormones and modulators of the genital system
— G03G: Gonadotropins and other ovulation stimulants
— G03GA: Gonadotropins
— G03GA05: Follitropin alfa
HCPCS
Code
Description
S0126
Injection, follitropin alfa, 75 iu
Clinical
Clinical Trials
176 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfertilityD007246EFO_00005454826302187
Female infertilityD007247EFO_0008560N974—74116
Fertilization in vitroD005307—128314
Ovulation inductionD010062—452112
Polycystic ovary syndromeD011085EFO_0000660E28.21134211
AnovulationD000858——4116
HypogonadismD007006E23.0—11215
Healthy volunteers/patients—4——1—5
Intracytoplasmic sperm injectionsD020554———4—4
Assisted reproductive techniquesD027724——2114
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
PregnancyD011247EFO_0002950Z33.1——1—45
FertilityD005298——1—12
Embryo transferD004624——1——1
Male infertilityD007248EFO_0004248N46—11——1
Oocyte donationD018587——1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
FertilizationD005306—1———1
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Area under curveD0195401————1
PharmacokineticsD0105991————1
AbsorptionD0000421————1
Therapeutic equivalencyD0138101————1
Ovarian neoplasmsD010051EFO_0003893C561————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Primary ovarian insufficiencyD016649EFO_0004266E28.3————22
Pregnancy rateD018873————11
Prostatic neoplasmsD011471C61————11
ThalassemiaD013789EFO_1001996D56————11
Pregnancy outcomeD011256————11
EndometriosisD004715EFO_0001065N80————11
Female genital diseasesD005831EFO_0009549N85————11
Oxidative stressD018384EFO_1001905————11
In vitro oocyte maturation techniquesD059471————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameFOLLITROPIN ALFA
INNfollitropin alfa
Description
Follitropin beta chain precursor (Follicle-stimulating hormone beta subunit) (FSH-beta)
Classification
Protein
Drug classatropine derivatives
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
RxCUI—
ChEMBL IDCHEMBL1201692
ChEBI ID—
PubChem CID—
DrugBank—
UNII IDVV3HN9ZPB5 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
Mock data
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Additional graphs summarizing 573 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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33 adverse events reported
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