Relaxin

drug
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Also known as Pig relaxinPorcine relaxinRelaxin (swine)Relaxin porcineRelaxin sus scrofa

Summary

Relaxin (CHEMBL2107882) is a phase-3 clinical-stage unknown targeting RXFP1, RXFP2, and RXFP3; indicated across 3 conditions including systemic sclerosis and congestive heart failure.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Targets: 3 (RXFP1, RXFP2, RXFP3)
  • Indications: 3 conditions
  • Clinical trials: 9

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2107882
NameRelaxin
TypeUnknown
Max phase3

Also known as: Pig relaxin, Porcine relaxin, Relaxin, Relaxin (swine), Relaxin porcine, Relaxin sus scrofa, RELAXIN

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
RXFP1RXFP1Full agonist10.370%Q9HBX9
RXFP2RXFP2Full agonist9.130%Q8WXD0
RXFP3RXFP3Full agonist100%Q9NSD7

Bioactivity

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

Target pathways

Aggregated over 3 target gene(s): RXFP1, RXFP2, RXFP3.

Top Reactome pathways

9 total, by targets touching each:

PathwayTargetsGenes
Relaxin receptors3RXFP1, RXFP2, RXFP3
Signal Transduction2RXFP1, RXFP2
Signaling by GPCR2RXFP1, RXFP2
Class A/1 (Rhodopsin-like receptors)2RXFP1, RXFP2
Peptide ligand-binding receptors2RXFP1, RXFP2
GPCR downstream signalling2RXFP1, RXFP2
G alpha (s) signalling events2RXFP1, RXFP2
GPCR ligand binding2RXFP1, RXFP2
G alpha (i) signalling events1RXFP3

Dominant GO biological processes

GO termTargets
signal transduction3
G protein-coupled receptor signaling pathway3
adenylate cyclase-activating G protein-coupled receptor signaling pathway2
hormone-mediated signaling pathway2
parturition1
extracellular matrix organization1
myofibroblast differentiation1
lung connective tissue development1
nipple morphogenesis1
adenylate cyclase-modulating G protein-coupled receptor signaling pathway1
oocyte maturation1
adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway1
negative regulation of cell population proliferation1
male gonad development1
negative regulation of apoptotic process1

Indications & clinical

Indications

3 indications (0 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
systemic sclerosis3MONDO:0005100EFO:0000717
congestive heart failure2MONDO:0005009EFO:0000373
preeclampsia1MONDO:0005081EFO:0000668

Clinical trials

Total trials: 9.

Phase distribution

PhaseTrials
PHASE23
Not specified3
PHASE2/PHASE31
PHASE31
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00520806PHASE2/PHASE3COMPLETEDEfficacy and Safety of Relaxin for the Treatment of Acute Heart Failure
NCT00704665PHASE3COMPLETEDRecombinant Human Relaxin in the Treatment of Diffuse Scleroderma
NCT07359872PHASE1/PHASE2NOT_YET_RECRUITINGRelaxin Therapy for Atrial Fibrillation
NCT00004380PHASE2COMPLETEDPhase II Study of Recombinant Relaxin for Progressive Systemic Sclerosis
NCT00259116PHASE2COMPLETEDA Pilot Study of Recombinant Human Relaxin (rhRlx) in Compensated Congestive Heart Failure
NCT03449251PHASE2UNKNOWNA Series of Pilot Studies to Evaluate the haemoDynamic and mEtabolic Effects oF apelIn aNd rElaxin
NCT06687486Not specifiedACTIVE_NOT_RECRUITINGEffect of Autogenic Relaxation Therapy on Caregivers on Perceived Stress Quality of Life and Caregiver Burden
NCT06933602Not specifiedACTIVE_NOT_RECRUITINGProgressive Relaxation for COPD: Effects on Insomnia and Satisfaction
NCT06808165Not specifiedCOMPLETEDRelaxin and Placental Volume in Placenta Accreta Spectrum

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

11 molecules share ≥1 primary target. Top 11 by shared-target count:

MoleculeSourceStatusShared targets
CLADRIBINEChEMBLPhase 4 (approved)RXFP1
EPINEPHRINE BITARTRATEChEMBLPhase 4 (approved)RXFP1
FAMCICLOVIRChEMBLPhase 4 (approved)RXFP1
ISOETHARINEChEMBLPhase 4 (approved)RXFP1
ISOPROTERENOLChEMBLPhase 4 (approved)RXFP1
METHYSERGIDEChEMBLPhase 4 (approved)RXFP1
PENTOXIFYLLINEChEMBLPhase 4 (approved)RXFP1
SUPROFENChEMBLPhase 4 (approved)RXFP1
COLFORSINChEMBLPhase 2RXFP1
FLUBENDAZOLEChEMBLPhase 2RXFP1
LOMIFYLLINEChEMBLPhase 2RXFP1