Acute respiratory distress syndrome
diseaseOn this page
Also known as acute lung injuryALIARDSincreased-permeability pulmonary edemaincreased-permeability pulmonary oedemanon-cardiogenic pulmonary edemanon-cardiogenic pulmonary oedemashock lungStiff lung
Summary
Acute respiratory distress syndrome (MONDO:0006502) is a disease with 5 cohort genes (8 GWAS associations across 6 studies) and 1,068 clinical trials. Top therapeutic interventions include cisatracurium, nitric oxide, and dexmedetomidine.
At a glance
- Cohort genes: 5
- GWAS associations: 8
- Clinical trials: 1,068
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | acute respiratory distress syndrome |
| Mondo ID | MONDO:0006502 |
| EFO | EFO:1000637 |
| ICD-10-CM | J80 |
| ICD-11 | 1189702844 |
| NCIT | C3353 |
| UMLS | C2887484 |
| MedGen | 1812214 |
| MedDRA | 10001052 |
| Is cancer (heuristic) | no |
Also known as: acute lung injury · acute respiratory distress syndrome · ALI · ARDS · increased-permeability pulmonary edema · increased-permeability pulmonary oedema · non-cardiogenic pulmonary edema · non-cardiogenic pulmonary oedema · shock lung · Stiff lung
Data availability: 8 GWAS associations (6 studies).
Disease family
An umbrella term covering 2 Mondo subtypes.
Classification path: disease › human disease › acute disease › acute respiratory failure › acute respiratory distress syndrome
Related subtypes (2): neonatal respiratory failure, pulmonary edema
Subtypes (2): adult acute respiratory distress syndrome, pediatric acute respiratory distress syndrome
Genetics & variants
GWAS landscape
8 GWAS associations across 6 studies. Top hits map to 6 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs11195238 | 4e-08 | SMC3 - Y_RNA | C | 1.67 |
| rs9508032 | 5e-08 | FLT1 | C | 1.64 |
| rs7967111 | 7e-08 | BORCS5 | G | 1.35 |
| rs619652 | 2e-07 | CHRM3 | G | 1.86 |
| rs116066418 | 2e-07 | ANKRD31 - HMGCR | A | 2.09 |
| rs59685452 | 3e-06 | OSTCP1, OSTCP1 | C | 1.84 |
| rs11111647 | 3e-06 | LINC02401 | A | 1.32 |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST012418 | Du M | 2021 | 1,250 | 1,583 | Integrative omics provide biological and clinical insights into acute respiratory distress syndrome. |
| GCST90473721 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 408 | 458,032 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90700332 | Guillen-Guio B | 2025 | 395 | 1,150 | Genome-wide association study of susceptibility to acute respiratory distress syndrome. |
| GCST010680 | Guillen-Guio B | 2020 | 274 | 0 | Sepsis-associated acute respiratory distress syndrome in individuals of European ancestry: a genome-wide association study. |
| GCST005805 | Bime C | 2018 | 232 | 0 | Genome Wide Association Study in African Americans with Acute Respiratory Distress Syndrome Identifies the Selectin P Ligand Gene as a Risk Factor. |
| GCST90093314 | Xu JY | 2021 | 70 | 0 | Nucleotide polymorphism in ARDS outcome: a whole exome sequencing association study. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 0 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 7 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 7 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 0 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| intron_variant | 5 |
| intergenic_variant | 2 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs11195238 | 10 | 110629099 | C>A,T | 0.13 | intergenic_variant | SMC3 - Y_RNA | 4e-08 | Tier 4: intronic/intergenic |
| rs9508032 | 13 | 28421803 | C>T | 0.25 | intron_variant | FLT1 | 5e-08 | Tier 4: intronic/intergenic |
| rs7967111 | 12 | 12449019 | G>A,C | 0.444 | intron_variant | BORCS5 | 7e-08 | Tier 4: intronic/intergenic |
| rs619652 | 1 | 239828684 | G>A,C,T | 0.402 | intron_variant | CHRM3 | 2e-07 | Tier 4: intronic/intergenic |
| rs116066418 | 5 | 75293073 | T>A | 0.05 | intergenic_variant | ANKRD31 - HMGCR | 2e-07 | Tier 4: intronic/intergenic |
| rs59685452 | 6 | 158856014 | G>C,T | 0.05 | intron_variant | OSTCP1, OSTCP1 | 3e-06 | Tier 4: intronic/intergenic |
| rs11111647 | 12 | 103551446 | G>A | 0.05 | intron_variant | LINC02401 | 3e-06 | Tier 4: intronic/intergenic |
Genes & proteins
Mendelian disease overlap and somatic drivers
GenCC: 0 · Orphanet: 4 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| CHRM3 | Orphanet:2970 | Prune belly syndrome |
| SMC3 | Orphanet:199 | Cornelia de Lange syndrome |
| RBM20 | Orphanet:154 | Familial isolated dilated cardiomyopathy |
| FLT1 | Orphanet:275555 | Preeclampsia |
Cohort genes → proteins
5 cohort genes, 5 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| gwas_only | 5 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| BORCS5 | HGNC:17950 | ENSG00000165714 | Q969J3 | BLOC-1-related complex subunit 5 | gwas |
| CHRM3 | HGNC:1952 | ENSG00000133019 | P20309 | Muscarinic acetylcholine receptor M3 | gwas |
| SMC3 | HGNC:2468 | ENSG00000108055 | Q9UQE7 | Structural maintenance of chromosomes protein 3 | gwas |
| RBM20 | HGNC:27424 | ENSG00000203867 | Q5T481 | RNA-binding protein 20 | gwas |
| FLT1 | HGNC:3763 | ENSG00000102755 | P17948 | Vascular endothelial growth factor receptor 1 | gwas |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| BORCS5 | BLOC-1-related complex subunit 5 | As part of the BORC complex may play a role in lysosomes movement and localization at the cell periphery. |
| CHRM3 | Muscarinic acetylcholine receptor M3 | The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. |
| SMC3 | Structural maintenance of chromosomes protein 3 | Central component of cohesin, a complex required for chromosome cohesion during the cell cycle. |
| RBM20 | RNA-binding protein 20 | RNA-binding protein that acts as a regulator of mRNA splicing of a subset of genes encoding key structural proteins involved in cardiac development, such as TTN (Titin), CACNA1C, CAMK2D or PDLIM5/ENH. |
| FLT1 | Vascular endothelial growth factor receptor 1 | Tyrosine-protein kinase that acts as a cell-surface receptor for VEGFA, VEGFB and PGF, and plays an essential role in the development of embryonic vasculature, the regulation of angiogenesis, cell survival, cell migration, macrophage funct… |
Protein-family classification
Druggable: 2 · Difficult: 1 · Unknown: 2 · Druggable fraction: 0.4
Family distribution
Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Kinase | 1 | 5.5× | 0.384 |
| GPCR | 1 | 4.8× | 0.384 |
| Transcription factor | 1 | 1.6× | 0.634 |
| Other/Unknown | 2 | 0.7× | 0.877 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| BORCS5 | Other/Unknown | no | TBORCS5 | |
| CHRM3 | GPCR | yes | GPCR_Rhodpsn, Musac_Ach_rcpt, Musac_Ach_M3_rcpt | |
| SMC3 | Other/Unknown | no | RecF/RecN/SMC_N, SMC_hinge, SMC | |
| RBM20 | Transcription factor | no | RRM_dom, Matrin/U1-C_Znf_C2H2, Matrin/U1-like-C_Znf_C2H2 | |
| FLT1 | Kinase | yes | 2.7.10.1 | Prot_kinase_dom, Ser-Thr/Tyr_kinase_cat_dom, Tyr_kinase_rcpt_3_CS |
Expression context
Cohort genes with no expression data: 0.
4 cohort genes are a single-cell marker in ≥1 SCXA experiment.
Breadth distribution (Bgee present_calls)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 5 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| endothelial cell | 2 |
| prefrontal cortex | 1 |
| primordial germ cell in gonad | 1 |
| sural nerve | 1 |
| Brodmann (1909) area 23 | 1 |
| middle temporal gyrus | 1 |
| oocyte | 1 |
| tendon of biceps brachii | 1 |
| ventricular zone | 1 |
| cardiac muscle of right atrium | 1 |
| left ventricle myocardium | 1 |
| myocardium | 1 |
| pericardium | 1 |
| placenta | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| BORCS5 | 139 | ubiquitous | yes | sural nerve, primordial germ cell in gonad, prefrontal cortex |
| CHRM3 | 222 | broad | marker | endothelial cell, Brodmann (1909) area 23, middle temporal gyrus |
| SMC3 | 276 | ubiquitous | marker | tendon of biceps brachii, ventricular zone, oocyte |
| RBM20 | 191 | broad | marker | left ventricle myocardium, cardiac muscle of right atrium, myocardium |
| FLT1 | 277 | broad | marker | pericardium, placenta, endothelial cell |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| SMC3 | 5,056 |
| RBM20 | 1,225 |
| CHRM3 | 1,178 |
| BORCS5 | 588 |
| FLT1 | 261 |
Structural data
PDB: 3 · AlphaFold-only: 2 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| SMC3 | Q9UQE7 | 12 |
| FLT1 | P17948 | 12 |
| CHRM3 | P20309 | 5 |
AlphaFold-only cohort genes (top 30 by pLDDT)
| Symbol | UniProt | pLDDT |
|---|---|---|
| BORCS5 | Q969J3 | 80.54 |
| RBM20 | Q5T481 | 48.52 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 37. Enrichment computed across 5 evidence-associated genes (3 with Reactome annotation).
Pathways by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 3 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| Neuropilin interactions with VEGF and VEGFR | 1 | 951.7× | 0.015 | FLT1 |
| Muscarinic acetylcholine receptors | 1 | 761.3× | 0.015 | CHRM3 |
| Mitotic Telophase/Cytokinesis | 1 | 475.8× | 0.015 | SMC3 |
| VEGF binds to VEGFR leading to receptor dimerization | 1 | 423.0× | 0.015 | FLT1 |
| Cohesin Loading onto Chromatin | 1 | 380.7× | 0.015 | SMC3 |
| Acetylcholine regulates insulin secretion | 1 | 380.7× | 0.015 | CHRM3 |
| Establishment of Sister Chromatid Cohesion | 1 | 346.1× | 0.015 | SMC3 |
| Amine ligand-binding receptors | 1 | 115.3× | 0.040 | CHRM3 |
| Meiosis | 1 | 95.2× | 0.043 | SMC3 |
| Regulation of insulin secretion | 1 | 73.2× | 0.045 | CHRM3 |
| Reproduction | 1 | 63.4× | 0.045 | SMC3 |
| S Phase | 1 | 60.4× | 0.045 | SMC3 |
| SUMO E3 ligases SUMOylate target proteins | 1 | 59.5× | 0.045 | SMC3 |
| Integration of energy metabolism | 1 | 58.6× | 0.045 | CHRM3 |
| SUMOylation | 1 | 54.4× | 0.045 | SMC3 |
| SUMOylation of DNA damage response and repair proteins | 1 | 48.8× | 0.046 | SMC3 |
| Meiotic synapsis | 1 | 47.0× | 0.046 | SMC3 |
| ESR-mediated signaling | 1 | 42.8× | 0.048 | SMC3 |
| Signaling by Nuclear Receptors | 1 | 34.0× | 0.052 | SMC3 |
| Mitotic Metaphase and Anaphase | 1 | 32.3× | 0.052 | SMC3 |
| Mitotic Anaphase | 1 | 32.3× | 0.052 | SMC3 |
| Signal Transduction | 2 | 6.8× | 0.052 | CHRM3, SMC3 |
| Resolution of Sister Chromatid Cohesion | 1 | 28.8× | 0.055 | SMC3 |
| Estrogen-dependent gene expression | 1 | 25.2× | 0.059 | SMC3 |
| Class A/1 (Rhodopsin-like receptors) | 1 | 24.7× | 0.059 | CHRM3 |
| Mitotic Prometaphase | 1 | 23.1× | 0.061 | SMC3 |
| M Phase | 1 | 22.0× | 0.061 | SMC3 |
| GPCR ligand binding | 1 | 21.4× | 0.061 | CHRM3 |
| Separation of Sister Chromatids | 1 | 20.2× | 0.062 | SMC3 |
| G alpha (q) signalling events | 1 | 19.1× | 0.063 | CHRM3 |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 5 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| vascular endothelial growth factor receptor-1 signaling pathway | 1 | 3370.4× | 0.012 | FLT1 |
| positive regulation of anterograde synaptic vesicle transport | 1 | 1685.2× | 0.012 | BORCS5 |
| establishment of meiotic sister chromatid cohesion | 1 | 842.6× | 0.012 | SMC3 |
| heart formation | 1 | 674.1× | 0.012 | RBM20 |
| spliceosome-depend formation of circular RNA | 1 | 674.1× | 0.012 | RBM20 |
| negative regulation of vascular endothelial cell proliferation | 1 | 674.1× | 0.012 | FLT1 |
| establishment of mitotic sister chromatid cohesion | 1 | 481.5× | 0.012 | SMC3 |
| hyaloid vascular plexus regression | 1 | 481.5× | 0.012 | FLT1 |
| adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway | 1 | 421.3× | 0.012 | CHRM3 |
| phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway | 1 | 421.3× | 0.012 | CHRM3 |
| saliva secretion | 1 | 421.3× | 0.012 | CHRM3 |
| regulation of lysosome size | 1 | 374.5× | 0.012 | BORCS5 |
| ligand-gated ion channel signaling pathway | 1 | 374.5× | 0.012 | CHRM3 |
| embryonic morphogenesis | 1 | 306.4× | 0.013 | FLT1 |
| regulation of endosome size | 1 | 306.4× | 0.013 | BORCS5 |
| regulation of smooth muscle contraction | 1 | 240.7× | 0.014 | CHRM3 |
| organelle transport along microtubule | 1 | 240.7× | 0.014 | BORCS5 |
| mitotic sister chromatid cohesion | 1 | 224.7× | 0.014 | SMC3 |
| G protein-coupled acetylcholine receptor signaling pathway | 1 | 210.7× | 0.014 | CHRM3 |
| positive regulation of RNA splicing | 1 | 210.7× | 0.014 | RBM20 |
| nervous system development | 2 | 18.4× | 0.014 | BORCS5, CHRM3 |
| positive regulation of smooth muscle contraction | 1 | 187.2× | 0.014 | CHRM3 |
| regulation of mRNA splicing, via spliceosome | 1 | 177.4× | 0.014 | RBM20 |
| smooth muscle contraction | 1 | 160.5× | 0.014 | CHRM3 |
| blood vessel morphogenesis | 1 | 160.5× | 0.014 | FLT1 |
| sister chromatid cohesion | 1 | 153.2× | 0.014 | SMC3 |
| negative regulation of mRNA splicing, via spliceosome | 1 | 153.2× | 0.014 | RBM20 |
| positive regulation of MAP kinase activity | 1 | 129.6× | 0.016 | FLT1 |
| acetylcholine receptor signaling pathway | 1 | 124.8× | 0.017 | CHRM3 |
| monocyte chemotaxis | 1 | 116.2× | 0.017 | FLT1 |
Therapeutics
Drugs indicated for this disease
2 approved, 18 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Beractant | Approved (phase 4) |
| Poractant Alfa | Approved (phase 4) |
| Alteplase | Phase 3 (in late-stage trials) |
| Betamethasone | Phase 3 (in late-stage trials) |
| Dexamethasone | Phase 3 (in late-stage trials) |
| Dornase Alfa | Phase 3 (in late-stage trials) |
| Esmolol | Phase 3 (in late-stage trials) |
| Fospropofol | Phase 3 (in late-stage trials) |
| Hydroxychloroquine | Phase 3 (in late-stage trials) |
| Ibuprofen | Phase 3 (in late-stage trials) |
| Methylprednisolone | Phase 3 (in late-stage trials) |
| Metoprolol | Phase 3 (in late-stage trials) |
| Nitric Oxide | Phase 3 (in late-stage trials) |
| Oxygen | Phase 3 (in late-stage trials) |
| Pirfenidone | Phase 3 (in late-stage trials) |
| Propofol | Phase 3 (in late-stage trials) |
| Protirelin | Phase 3 (in late-stage trials) |
| Ravulizumab | Phase 3 (in late-stage trials) |
| Remestemcel-L | Phase 3 (in late-stage trials) |
| Sevoflurane | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Adenosine, Anakinra, Aspirin, Aviptadil, Budesonide, Carbon Monoxide, Formoterol, Ginger, Isoflurane, Ketamine, Lactose, Anhydrous, Losartan, Lucinactant, Naltrexone, Remdesivir, Sodium Chloride, Soybean Oil, Tocilizumab, Ulinastatin.
Drug target analysis
Approved (phase 4): 2 · Phase ≥3: 2 · Phased (≥1): 3 · Undrugged: 2
Druggability breadth: 3 of 5 evidence-associated genes (60%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Genes with an approved drug
The molecule shown is one approved compound that hits the gene — not necessarily a drug of choice or one indicated for this disease.
| Symbol | Example approved molecule |
|---|---|
| CHRM3 | CARBACHOL |
| FLT1 | PONATINIB |
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| CHRM3 | 207 | 4 |
| FLT1 | 77 | 4 |
| SMC3 | 1 | 2 |
| BORCS5 | 0 | 0 |
| RBM20 | 0 | 0 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| CARBACHOL | 4 | CHRM3 |
| BETHANECHOL | 4 | CHRM3 |
| CLOZAPINE | 4 | CHRM3 |
| ATROPINE | 4 | CHRM3 |
| HALOPERIDOL | 4 | CHRM3 |
| OLANZAPINE | 4 | CHRM3 |
| QUETIAPINE | 4 | CHRM3 |
| RISPERIDONE | 4 | CHRM3 |
| CARBAMOYLCHOLINE | 4 | CHRM3 |
| PIRENZEPINE | 4 | CHRM3 |
| BEPRIDIL | 4 | CHRM3 |
| CANDESARTAN CILEXETIL | 4 | CHRM3 |
| CLOTRIMAZOLE | 4 | CHRM3 |
| PROPIVERINE | 4 | CHRM3 |
| VALPROIC ACID | 4 | CHRM3 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | 4 | CHRM3 |
| IMIPRAMINE | 4 | CHRM3 |
| BIPERIDEN | 4 | CHRM3 |
| AMOXAPINE | 4 | CHRM3 |
| IDARUBICIN | 4 | CHRM3 |
| DICYCLOMINE | 4 | CHRM3 |
| DESLORATADINE | 4 | CHRM3 |
| CHLOROPROCAINE | 4 | CHRM3 |
| ACETYLCHOLINE CHLORIDE | 4 | CHRM3 |
| ANISOTROPINE | 4 | CHRM3 |
| PALONOSETRON | 4 | CHRM3 |
| ACLIDINIUM | 4 | CHRM3 |
| CYCLACILLIN | 4 | CHRM3 |
| DIMENHYDRINATE | 4 | CHRM3 |
| TIOCONAZOLE | 4 | CHRM3 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 1.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| CHRM3 | 1,026 | Binding:764, Functional:244, ADMET:17, Unclassified:1 |
| FLT1 | 896 | Binding:852, Functional:38, ADMET:6 |
| SMC3 | 7 | Binding:7 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| FLT1 | 2.7.10.1 | receptor protein-tyrosine kinase |
Cohort genes with high screening signal
≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.
| Symbol | ChEMBL assays |
|---|---|
| CHRM3 | 1,026 |
| FLT1 | 896 |
Pharmacogenomics
Cohort genes with a PharmGKB record: 5; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Chemical tractability of cohort targets
30 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| CARBACHOL | 4 | CHRM3 |
| BETHANECHOL | 4 | CHRM3 |
| CLOZAPINE | 4 | CHRM3 |
| ATROPINE | 4 | CHRM3 |
| HALOPERIDOL | 4 | CHRM3 |
| OLANZAPINE | 4 | CHRM3 |
| QUETIAPINE | 4 | CHRM3 |
| RISPERIDONE | 4 | CHRM3 |
| CARBAMOYLCHOLINE | 4 | CHRM3 |
| PIRENZEPINE | 4 | CHRM3 |
| BEPRIDIL | 4 | CHRM3 |
| CANDESARTAN CILEXETIL | 4 | CHRM3 |
| CLOTRIMAZOLE | 4 | CHRM3 |
| PROPIVERINE | 4 | CHRM3 |
| VALPROIC ACID | 4 | CHRM3 |
| TRIHEXYPHENIDYL HYDROCHLORIDE | 4 | CHRM3 |
| IMIPRAMINE | 4 | CHRM3 |
| BIPERIDEN | 4 | CHRM3 |
| AMOXAPINE | 4 | CHRM3 |
| IDARUBICIN | 4 | CHRM3 |
| DICYCLOMINE | 4 | CHRM3 |
| DESLORATADINE | 4 | CHRM3 |
| CHLOROPROCAINE | 4 | CHRM3 |
| ACETYLCHOLINE CHLORIDE | 4 | CHRM3 |
| ANISOTROPINE | 4 | CHRM3 |
| PALONOSETRON | 4 | CHRM3 |
| ACLIDINIUM | 4 | CHRM3 |
| CYCLACILLIN | 4 | CHRM3 |
| DIMENHYDRINATE | 4 | CHRM3 |
| TIOCONAZOLE | 4 | CHRM3 |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 2 | CHRM3, FLT1 |
| B | Phased (≥1) drug, not yet approved | 1 | SMC3 |
| C | Druggable family + PDB, no drug | 0 | |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 2 | BORCS5, RBM20 |
Undrugged target profiles
2 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
| Symbol | ChEMBL assays | Drugged partners (top 3) |
|---|---|---|
| BORCS5 | 0 | — |
| RBM20 | 0 | — |
Clinical trials & evidence
Clinical trials
Clinical trials: 1,068.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 775 |
| PHASE2 | 101 |
| PHASE3 | 63 |
| PHASE1/PHASE2 | 42 |
| PHASE1 | 38 |
| PHASE4 | 25 |
| PHASE2/PHASE3 | 16 |
| EARLY_PHASE1 | 8 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06037330 | PHASE4 | RECRUITING | Nalbuphine in ARDS Patients After Surgery |
| NCT06934811 | PHASE4 | NOT_YET_RECRUITING | Ciprofol’s Impact on Oxygenator Function in Extracorporeal Membrane Oxygenation (ECMO) Patients |
| NCT07499154 | PHASE4 | NOT_YET_RECRUITING | Perioperative Lidocaine for Lung Protection in Infants Undergoing Cardiac Surgery |
| NCT00219375 | PHASE4 | COMPLETED | Study of Sivelestat Sodium Hydrate in Acute Lung Injury (ALI) Associated With Systemic Inflammatory Response Syndrome (SIRS) in Japan |
| NCT00299650 | PHASE4 | COMPLETED | Systematic Early Use of Neuromuscular Blocking Agents in ARDS Patients |
| NCT00773058 | PHASE4 | UNKNOWN | Effect of Treatment With Stress-Doses Glucocorticoid in Patients With Acute Respiratory Distress Syndrome (ARDS) |
| NCT01050699 | PHASE4 | COMPLETED | Sleep Intervention During Acute Lung Injury |
| NCT01573715 | PHASE4 | UNKNOWN | Effects of Neuromuscular Blocking Agents (NMBA) on the Alteration of Transpulmonary Pressures at the Early Phase of Acute Respiratory Distress Syndrome (ARDS) |
| NCT01600651 | PHASE4 | COMPLETED | Diffuse Acute Respiratory Distress Syndrome (ARDS), Recruitment Maneuver, and sRAGE (DAMAGE Study) |
| NCT01731795 | PHASE4 | COMPLETED | Efficacy Study of Dexamethasone to Treat the Acute Respiratory Distress Syndrome |
| NCT01763853 | PHASE4 | UNKNOWN | Impact of Fluid Resuscitation Therapy on Pulmonary Edema as Measured by Alveolar Fluid Clearance in Patients With Acute Respiratory Distress Syndrome (ARDS) |
| NCT01825304 | PHASE4 | UNKNOWN | The Study of Using Esophageal Pressure to Guide the PEEP Setting in Abdominal Hypertension Patients Who Undergoing Mechanical Ventilation |
| NCT02166853 | PHASE4 | COMPLETED | Effects of SEvoflurane on Gas Exchange and Inflammation in Patients With ARDS (SEGA Study) |
| NCT02902055 | PHASE4 | TERMINATED | Paediatric Ards Neuromuscular Blockade Study |
| NCT04014218 | PHASE4 | UNKNOWN | Effect of Inhalation Sedation Compared With Propofol on the Sepsis-related Acute Respiratory Distress Syndrome Course |
| NCT04133740 | PHASE4 | UNKNOWN | Oxygenation Targets in Cardiac Surgery Patients - a Before-and-after Study |
| NCT04335786 | PHASE4 | TERMINATED | Valsartan for Prevention of Acute Respiratory Distress Syndrome in Hospitalized Patients With SARS-COV-2 (COVID-19) Infection Disease |
| NCT04359862 | PHASE4 | TERMINATED | Sedation With Sevoflurane Versus Propofol in Patients With Acute Respiratory Distress Syndrome Caused by COVID19 Infection |
| NCT04397510 | PHASE4 | TERMINATED | Nebulized Heparin for the Treatment of COVID-19 Induced Lung Injury |
| NCT04663555 | PHASE4 | COMPLETED | Effect of Two Different Doses of Dexamethasone in Patients With ARDS and COVID-19 |
| NCT04909697 | PHASE4 | COMPLETED | Treatment of ARDS With Sivelestat Sodium |
| NCT05153525 | PHASE4 | UNKNOWN | Continuous Infusion Versus Intermittent Boluses of Cisatracurium in the Early Management of Pediatric ARDS |
| NCT05364385 | PHASE4 | UNKNOWN | Intra-tracheal Instillation of Budesonide to Prevent Chronic Lung Disease |
| NCT05514483 | PHASE4 | UNKNOWN | 5-HT3 Receptor Antagonist and Respiratory Drive in Patients With ARDS |
| NCT05658692 | PHASE4 | UNKNOWN | Platform Adaptive Embedded Trial for Acute Respiratory Distress Syndrome |
| NCT05075161 | PHASE3 | RECRUITING | Pirfenidone to Prevent Fibrosis in Ards. |
| NCT05354141 | PHASE3 | RECRUITING | Extracellular Vesicle Treatment for Acute Respiratory Distress Syndrome (ARDS) (EXTINGUISH ARDS) |
| NCT05497401 | PHASE3 | NOT_YET_RECRUITING | A Controlled Study to Evaluate the Efficacy of Allogeneic MesenCure for the Treatment of Patients With ARDS |
| NCT05847517 | PHASE3 | RECRUITING | Metoprolol in Acute Respiratory Distress Syndrome (MAIDEN) |
| NCT05849779 | PHASE3 | RECRUITING | Inhaled Sevoflurane for ARDS Prevention |
| NCT06013319 | PHASE3 | RECRUITING | Effect of Esmolol on Oxygenation Index in Patients With Acute Respiratory Distress Syndrome |
| NCT06066502 | PHASE3 | RECRUITING | Precision Ventilation vs Standard Care for Acute Respiratory Distress Syndrome |
| NCT06496997 | PHASE2/PHASE3 | RECRUITING | A Comparative Study of Glucocorticoids Efficacy in Acute Respiratory Distress Syndrome |
| NCT06526533 | PHASE3 | RECRUITING | RECOMMEND Platform Trial |
| NCT06640777 | PHASE3 | NOT_YET_RECRUITING | Efficacy and Safety of LEAF-4L6715 for Acute Respiratory Distress Syndrome |
| NCT06814340 | PHASE3 | RECRUITING | Continuous Positive Airway Pressure on Venovenous extracorporeaL Membrane Oxygenation for Acute respIratory Distress syndrOme |
| NCT07208591 | PHASE3 | RECRUITING | To Evaluate The Safety and Efficacy of STSA-1002 Injection in Patients With Acute Respiratory Distress Syndrome |
| NCT07317050 | PHASE3 | NOT_YET_RECRUITING | Clinical Trial With Aprotinin in the Acute Respiratory Distress Syndrome Treatment |
| NCT07342205 | PHASE2/PHASE3 | RECRUITING | A Study on the Treatment of Patients With Acute Lung Injury Caused by Sepsis Through Microbiota Transplantation |
| NCT07479043 | PHASE3 | NOT_YET_RECRUITING | To Evaluate the Safety and Potential Therapeutic Activity of JadiCell™, an Investigational Umbilical Cord-Derived Mesenchymal Stem Cell Therapy, in Patients Diagnosed With Acute Respiratory Distress Syndrome (ARDS). |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CISATRACURIUM | 4 | 9 |
| NITRIC OXIDE | 4 | 5 |
| DEXMEDETOMIDINE | 4 | 3 |
| HYDROCORTISONE | 4 | 3 |
| MEROPENEM | 4 | 3 |
| ONDANSETRON | 4 | 3 |
| HYDROXYCHLOROQUINE | 4 | 2 |
| ILOPROST | 4 | 2 |
| METOPROLOL | 4 | 2 |
| MIDAZOLAM | 4 | 2 |
| PIRFENIDONE | 4 | 2 |
| TENECTEPLASE | 4 | 2 |
| ALMITRINE | 4 | 1 |
| ANGIOTENSIN II | 4 | 1 |
| APROTININ | 4 | 1 |
| ARGATROBAN | 4 | 1 |
| ASCORBIC ACID | 4 | 1 |
| AXATILIMAB | 4 | 1 |
| BETAMETHASONE | 4 | 1 |
| BREXANOLONE | 4 | 1 |
| CALFACTANT | 4 | 1 |
| DAPSONE | 4 | 1 |
| DEXAMETHASONE | 4 | 1 |
| DOBUTAMINE | 4 | 1 |
| ECULIZUMAB | 4 | 1 |
| ESMOLOL | 4 | 1 |
| FENTANYL | 4 | 1 |
| FLUDROCORTISONE ACETATE | 4 | 1 |
| FOSTAMATINIB | 4 | 1 |
| FOSTAMATINIB DISODIUM | 4 | 1 |
Related Atlas pages
- Cohort genes: BORCS5, CHRM3, SMC3, RBM20, FLT1
- Drugs: Cisatracurium, Nitric Oxide, Dexmedetomidine, Hydrocortisone, Meropenem, Ondansetron, Hydroxychloroquine, Iloprost, Metoprolol, Midazolam, Pirfenidone, Tenecteplase, Almitrine, Angiotensin Ii, Aprotinin, Argatroban, Ascorbic Acid, Axatilimab, Betamethasone, Brexanolone, Calfactant, Dapsone, Dexamethasone, Dobutamine, Eculizumab, Esmolol, Fentanyl, Fludrocortisone Acetate, Fostamatinib