Lutropin Alfa

drug
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Also known as ATC G03 GA GONADOTROPINSLuteinising hormoneLuteinising hormone (human)Lutropin alfa component of pergoverisLutropina alfaLutropine alfaLuveris

Summary

Lutropin Alfa (CHEMBL1201419) is an approved protein (ATC G03GA07) targeting LHCGR; indicated across 4 conditions including female infertility and infertility disorder.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Protein
  • ATC class: G03GA07
  • Targets: 1 (LHCGR)
  • Indications: 4 conditions
  • Clinical trials: 11

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201419
NameLutropin Alfa
TypeProtein
Max phase4
ATCG03GA07

Also known as: ATC G03 GA GONADOTROPINS, Luteinising hormone, Luteinising hormone (human), Lutropin alfa, Lutropin alfa component of pergoveris, Lutropina alfa, Lutropine alfa, Luveris, LUTROPIN ALFA

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
LHCGRLH receptorFull agonist10.90%P22888

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): LHCGR.

Top Reactome pathways

7 total, by targets touching each:

PathwayTargetsGenes
Signal Transduction1LHCGR
Signaling by GPCR1LHCGR
Class A/1 (Rhodopsin-like receptors)1LHCGR
Hormone ligand-binding receptors1LHCGR
GPCR downstream signalling1LHCGR
G alpha (s) signalling events1LHCGR
GPCR ligand binding1LHCGR

Dominant GO biological processes

GO termTargets
ovarian follicle development1
G protein-coupled receptor signaling pathway1
G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger1
adenylate cyclase-activating G protein-coupled receptor signaling pathway1
phospholipase C-activating G protein-coupled receptor signaling pathway1
spermatogenesis1
male gonad development1
hormone-mediated signaling pathway1
ovulation cycle process1
male genitalia development1
positive regulation of inositol trisphosphate biosynthetic process1
luteinizing hormone signaling pathway1
development of animal secondary male sexual characteristics1
cognition1
uterus development1

Indications & clinical

Indications

4 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
female infertility4MONDO:0021124EFO:0008560
infertility disorder3MONDO:0005047EFO:0000545
hypogonadism2MONDO:0002146MONDO:0002146

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE45
PHASE32
PHASE22
PHASE12

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00439829PHASE4COMPLETEDSynchronization of Follicle Wave Emergence and Ovarian Stimulation
NCT01504139PHASE4COMPLETEDThe Luteal Phase After GnRHa Trigger - a Proof of Concept Study
NCT02140515PHASE4UNKNOWNComparison of Assisted Reproductive Technology (ART) Outcomes Between Two Protocols of Induction of Ovulation in Patients With Hypogonadotropic Hypogonadism
NCT03177538PHASE4COMPLETEDCorifollitropin Alfa Combined With Menotropin Versus Follitropin and Lutropin Alfa in Expected Suboptimal Responders
NCT05405686PHASE4WITHDRAWNEffect of LH Supplementation on the Endometrial Gene Expression Profile in Poor Ovarian Responders
NCT06227949PHASE3NOT_YET_RECRUITINGFSH and LH Versus FSH Alone for Ovarian Stimulation in Non-hormone Sensitive Onco-fertility Patients
NCT07340827PHASE3RECRUITINGA Study to Compare the Efficacy and Safety of Follitropin Alfa/Lutropin Alfa Versus hMG in Japanese Participants With LH and FSH Deficiency Undergoing ART (HINATA)
NCT01029470PHASE2UNKNOWNTo Describe the Effect of rhLH Supplementation in Women With Hyporesponse to rhFSH After Pituitary Downregulation
NCT04189133PHASE2UNKNOWNRec-LH PD and Safety Profile in Hypogonadotropic Hypogonadism Men
NCT04899193PHASE1COMPLETEDPergoveris FD and Liquid China BE Study
NCT07269327PHASE1COMPLETEDAn Ethno-bridging Study of Pergoveris in Healthy Premenopausal Participants of Japanese or Caucasian Origin

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).