Target landscape
Open Targets · retrieved 2026-09-12 · weekly12 genes recurrently implicated in bladder cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 12 recurrently implicated genes, 8 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Bladder cancer does have labelled therapy — 11 drugs, listed in the next section.
Two different questions
The table below asks what can be aimed at 12 recurrently implicated genes. That is narrower than what is approved for the disease, and narrower again than what bladder cancer is actually treated with, which includes agents approved under broader indications. All three are on this page and they are kept apart deliberately.
| Gene | Drugs | Approval, and whether it reached this disease | Open Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it works | Cell therapy here |
|---|---|---|---|---|
| FGFR3 | 23 | 9 approvedE-7090, Erdafitinib, Futibatinib, Infigratinib, Masitinib, Nintedanib, Nintedanib Esylate, Pazopanib, PemigatinibApproved in bladder cancer: Erdafitinib.11 active of 35 bladder cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| ERBB2 across cancers → | 45 | 17 approvedAfatinib, Afatinib Dimaleate, Dacomitinib, Lapatinib, Lapatinib Ditosylate, Margetuximab, Masoprocol, Neratinib, Pertuzumab, Trastuzumab, Trastuzumab Deruxtecan, Trastuzumab Duocarmazine, Trastuzumab Emtansine, Tucatinib, Vandetanib, Zanidatamab, ZenocutuzumabApproved in non-small cell lung carcinoma, breast cancer, breast neoplasm and 10 other indications. No bladder cancer indication appears on these drugs’ labels.37 active of 84 bladder cancer trials | antibody, other clinical modality, protein degrader, small molecule | 1 active of 1 trial |
| NECTIN4 | 1 | 1 approvedEnfortumab VedotinApproved in bladder cancer: Enfortumab Vedotin.38 active of 45 bladder cancer trials | antibody, other clinical modality | 1 active of 1 trial |
| TACSTD2 across cancers → | 2 | 2 approvedDatopotamab Deruxtecan, Sacituzumab GovitecanApproved in breast cancer, breast neoplasm, non-small cell lung carcinoma and 2 other indications. No bladder cancer indication appears on these drugs’ labels.16 active of 20 bladder cancer trials | antibody, other clinical modality, protein degrader | — |
| CD274 across cancers → | 13 | 5 approvedAtezolizumab, Avelumab, Cosibelimab, Durvalumab, SugemalimabApproved in bladder cancer: Atezolizumab, Avelumab, Durvalumab.61 active of 138 bladder cancer trials | antibody, other clinical modality, protein degrader, small molecule | 0 active of 1 trial |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran2 trials, none active | other clinical modality, protein degrader, small molecule | — |
| RB1 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| KDM6A | 0 | No drug— | protein degrader, small molecule | — |
| ARID1A across cancers → | 0 | No drug— | protein degrader | — |
| PIK3CA across cancers → | 31 | 3 approvedAlpelisib, Copanlisib, InavolisibApproved in breast cancer, breast neoplasm, breast carcinoma and 3 other indications. No bladder cancer indication appears on these drugs’ labels.3 active of 5 bladder cancer trials | antibody, protein degrader, small molecule | — |
| TERT across cancers → | 1 | 1 approvedImetelstatApproved in anemia, myelodysplastic syndrome. No bladder cancer indication appears on these drugs’ labels.No bladder cancer trial of any of these drugs | antibody, other clinical modality, protein degrader, small molecule | — |
| STAG2 | 0 | No drug— | protein degrader | — |
Dataset evidence counts studies in the 457-study ranked set whose title or abstract names the gene; the bar is scaled to FGFR3. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-12. Clinical stage is the highest reached for any indication — see the per-drug indications noted in each row. Target-prioritisation reference only; not clinical or prescribing guidance.
What is actually approved here
openFDA drug labels · weekly11 drugs carry an FDA label naming bladder cancer: Atezolizumab, Avelumab, Durvalumab, Enfortumab Vedotin, Erdafitinib, Hexaminolevulinate, Mitomycin, Nadofaragene Firadenovec-Vncg, Nivolumab, Nogapendekin Alfa Inbakicept-Pmln, Pembrolizumab. Separately, 33 of the drugs returned for the genes in the table above are approved only for other diseases and reach bladder cancer through trials, not through their labels.
Every label that names bladder cancer
| Drug | Role | What the label says |
|---|---|---|
| AtezolizumabTECENTRIQ, Tecentriq Hybreza | Labelled here | Muscle Invasive Bladder Cancer (MIBC) as adjuvant treatment of adult patients with MIBC after cystectomy who have circulating tumor DNA molecular residual disease (ctDNA MRD) as determined by an FDA-authorized test. |
| AvelumabBAVENCIO | Labelled here | ( 1.1 , 14.1 ) Urothelial Carcinoma (UC) Maintenance treatment of patients with locally advanced or metastatic UC that has not progressed with first-line platinum-containing chemotherapy. |
| DurvalumabIMFINZI | Labelled here | Bladder Cancer • IMFINZI in combination with Bacillus Calmette-Guérin (BCG) is indicated for the treatment of adult patients with BCG-naive, high-risk non-muscle-invasive bladder cancer (NMIBC). • IMFINZI in combination with gemcitabine and cisplatin as neoadjuvant treatment, followed by single agent IMFINZI as adjuvant treatment following radical cystectomy, is indicated for the treatment of a... |
| Enfortumab VedotinPADCEV EJFV | Labelled here | ( 1 ) • in combination with pembrolizumab or pembrolizumab and berahyaluronidase alfa-pmph, for the treatment of adult patients with locally advanced or metastatic urothelial cancer (la/mUC). |
| ErdafitinibBALVERSA | Labelled here | BALVERSA is a kinase inhibitor indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (mUC) with susceptible FGFR3 genetic alterations whose disease has progressed on or after at least one line of prior systemic therapy. |
| HexaminolevulinateCysview | Labelled here | CYSVIEW is indicated for the cystoscopic detection of carcinoma of the bladder, including carcinoma in situ (CIS), in adult patients: With suspected or known lesion(s) based on a prior cystoscopy Undergoing surveillance cystoscopy for bladder cancer Limitations of Use CYSVIEW is not a replacement for random bladder biopsies or other procedures used in the detection of bladder cancer [see Warnin... |
| MitomycinJELMYTO, ZUSDURI | Labelled here | JELMYTO is an alkylating drug indicated for the treatment of adult patients with low-grade Upper Tract Urothelial Cancer (LG-UTUC). |
| Nadofaragene Firadenovec-VncgADSTILADRIN | Labelled here | ADSTILADRIN ® is indicated for the treatment of adult patients with high-risk Bacillus Calmette-Guérin (BCG)-unresponsive non-Muscle Invasive Bladder Cancer (NMIBC) with carcinoma in situ (CIS) with or without papillary tumors. |
| NivolumabOPDIVO, OPDIVO QVANTIG | Labelled here | Urothelial Carcinoma (UC) • adjuvant treatment of adult patients with UC who are at high risk of recurrence after undergoing radical resection of UC. |
| Nogapendekin Alfa Inbakicept-PmlnANKTIVA | Labelled here | ANKTIVA in combination with Bacillus Calmette-Guérin (BCG) is indicated for the treatment of adult patients with BCG-unresponsive nonmuscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) with or without papillary tumors. |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Urothelial Cancer in combination with enfortumab vedotin-ejfv, for the treatment of adult patients with locally advanced or metastatic urothelial cancer. |
| CisplatinCISPLATIN, CISplatin, Cisplatin | Backbone | Advanced bladder cancer |
| Gemcitabine IntravesicalINLEXZO | Backbone | INLEXZO is indicated for the treatment of adult patients with Bacillus Calmette-Guérin (BCG)-unresponsive, non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS), with or without papillary tumors. |
5 labels match indications_and_usage:"bladder cancer" OR indications_and_usage:"urothelial carcinoma" OR indications_and_usage:"urothelial cancer"; they collapse to 13 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-12. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Cell therapy against PD-1
ClinicalTrials.gov · retrieved 2026-09-12 · weeklyPD-1 is the busiest cell-therapy antigen in bladder cancer: 5 registered trials, 1 still active, 2 withdrawn before enrolling anyone. It has no gene entry of its own and is reached through PDCD1: a form or product of that gene.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT07410676 | 1/2 | Recruiting | EBNK-001 Allogeneic NK Cells With Low-Dose IL-15 ± Pembrolizumab in Advanced Solid Tumors | 2026-02-18 |
| NCT02863913 | 1 | Withdrawn | PD-1 Knockout Engineered T Cells for Muscle-invasive Bladder Cancer | 2019-03-06 |
| NCT03935347 | 2 | Withdrawn | Adoptive Cell Therapy With (LN-145) in Combination With Pembrolizumab in Treating Patients With Unresectable or Metastatic Transitional Cell Cancer Who Have Failed Cisplatin-Based Chemotherapy | 2020-01-02 |
| NCT03785925 | 2 | Completed | A Single-Arm Study of Bempegaldesleukin (NKTR-214) Plus Nivolumab in Cisplatin Ineligible Patients Who Have Locally Advanced or Metastatic Urothelial Cancer | 2023-03-28 |
| NCT04209114 | 3 | Completed | A Study of Nivolumab Plus Bempegaldesleukin (Bempeg/NKTR-214) vs Nivolumab Alone vs Standard of Care in Participants With Bladder Cancer That May Have Invaded The Muscle Wall of the Bladder and Who Cannot Get Cisplatin, A Type of Medicine Given To Treat Bladder Cancer | 2024-06-27 |
5 of 5 shown, most recently active first. Other antigens searched: Nectin-4 (1), PD-L1 (1), HER2 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-12. Trials are matched on the antigen named in the title or intervention, so a trial stating only a product code is missed.
Research momentum
PubMed MeSH · monthlyEvery term below is a share of the bladder cancer literature, not a count, because the field itself grew: 2015–2018 (n=6,000) against 2021–2025 (n=6,000). A topic whose papers doubled while the field doubled has not risen.
These are sample shares. The two windows hold 6,673 and 11,315 papers; MeSH terms were read from an evenly spaced sample of 6,000 and 6,000 of them, taken across the whole window rather than from its most recent papers. Percentages carry sampling error of roughly a percentage point and small differences between two terms are not meaningful.
Rising, with a real baseline
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Immunoconjugates | 0.12% | 0.97% | 8.28× | 58 papers |
| Single-Cell Analysis | 0.08% | 0.63% | 7.59× | 38 papers |
| Tumor Microenvironment | 1.0% | 6.8% | 6.8× | 408 papers |
| Nephroureterectomy | 0.1% | 0.62% | 6.16× | 37 papers |
| Pyrazoles | 0.08% | 0.5% | 5.99× | 30 papers |
| Platinum | 0.17% | 0.97% | 5.8× | 58 papers |
| Molecular Docking Simulation | 0.08% | 0.47% | 5.59× | 28 papers |
| Muscles | 0.83% | 4.42% | 5.3× | 265 papers |
| Microbiota | 0.1% | 0.47% | 4.66× | 28 papers |
| Killer Cells, Natural | 0.08% | 0.37% | 4.4× | 22 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Disease-Free Survival | 6.58% | 0.85% | 0.13× | 51 papers |
| Tumor Cells, Cultured | 1.82% | 0.32% | 0.17× | 19 papers |
| Time Factors | 4.67% | 0.9% | 0.19× | 54 papers |
| RNA, Small Interfering | 1.73% | 0.33% | 0.19× | 20 papers |
| Dose-Response Relationship, Drug | 1.2% | 0.23% | 0.19× | 14 papers |
| Neoplasm Grading | 5.82% | 1.18% | 0.2× | 71 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Carcinoma, Transitional Cell | 18.98% | 24.58% | 1.29× | 1475 papers |
| Cystectomy | 22.67% | 20.37% | 0.9× | 1222 papers |
| Prognosis | 15.33% | 15.25% | 0.99× | 915 papers |
| Neoplasm Invasiveness | 16.4% | 14.35% | 0.88× | 861 papers |
| Urinary Bladder | 9.92% | 14.07% | 1.42× | 844 papers |
| Biomarkers, Tumor | 14.38% | 12.23% | 0.85× | 734 papers |
| Treatment Outcome | 14.92% | 9.92% | 0.66× | 595 papers |
| Neoplasm Recurrence, Local | 11.98% | 9.48% | 0.79× | 569 papers |
| Gene Expression Regulation, Neoplastic | 11.32% | 8.92% | 0.79× | 535 papers |
| Cell Proliferation | 9.65% | 7.6% | 0.79× | 456 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.0% |
| Randomized Controlled Trial | 2.1% | 1.6% |
| Review | 12.7% | 8.9% |
| Meta-Analysis | 2.7% | 2.0% |
| Case Reports | 0.0% | 1.2% |
Query: Urinary Bladder Neoplasms[MeSH Major Topic] NOT ("Kidney Pelvis"[MeSH] OR "Ureteral Neoplasms"[MeSH] OR "Cystitis"[MeSH] OR "Urinary Bladder, Overactive"[MeSH]). Terms need at least 12 papers in the recent window and, in the rising table, at least 5 in the earlier one — a term going from 1 paper to 12 is a large fold change and no evidence of anything. Ubiquitous descriptors (Humans, Animals, age bands) and the disease’s own term are dropped. Windows are read whole where they fit and sampled where they do not; the totals and the sample sizes are both in the JSON beside this page. Source: PubMed MeSH, retrieved 2026-09-12.
Disease burden
What the public sources count, and how closely each category matches this disease. The same figures for every disease on the site are on one table.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 84,530 cases/year | direct | 2026 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| Deaths each year | 17,870 deaths/year | direct | 2026 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| Incidence rate | 17.9 cases per 100,000 people per year | direct | 2019-2023 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| Death rate | 4.1 deaths per 100,000 people per year | direct | 2020-2024 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| People living with it | 763,031 people living with the disease | direct | 2023 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| Median age at diagnosis | 73.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| median age at death | 79 years | direct | 2020-2024 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
| Five-year relative survival | 79.1% | direct | 2016-2022 SEER Cancer Stat Facts, Bladder Cancer, retrieved 2026-09-12 |
Years of life lost
1.1 years per case, 95,401 a year, from survival and age at diagnosis rather than from a death count. derived proxy What this costs to fund is in Funding.
3 assumptions behind this estimate
- Five-year relative survival stands in for cure; a death after five years is not counted.
- The median age at diagnosis stands in for the whole age distribution.
- Life expectancy at birth (78.4 years) is the reference, rather than remaining expectancy at the age of death from a life table.
- Each assumption moves the result by more than the difference between the two diseases currently on this site, so this figure separates a disease from one ten times its size, not from a close neighbour.
Funding
NIH RePORTER · quarterlyNIH obligations naming bladder cancer, after removing the 3,246 records across all years that matched the search but are about something else. That filter is not cosmetic: without it this section reports another field’s funding as this disease’s.
NIH obligations by fiscal year
| Year | Obligations | Awards | Distinct projects | Dropped as off-topic |
|---|---|---|---|---|
| FY2013 | $21.6M | 59 | 50 | 224 |
| FY2014 | $28.2M | 77 | 65 | 235 |
| FY2015 | $32.3M | 67 | 57 | 229 |
| FY2016 | $30.5M | 69 | 59 | 230 |
| FY2017 | $29.0M | 67 | 60 | 220 |
| FY2018 | $38.0M | 90 | 69 | 311 |
| FY2019 | $35.8M | 84 | 68 | 262 |
| FY2020 | $42.9M | 90 | 73 | 275 |
| FY2021 | $49.4M | 114 | 88 | 265 |
| FY2022 | $57.4M | 114 | 93 | 266 |
| FY2023 | $60.3M | 119 | 106 | 265 |
| FY2024 | $58.1M | 121 | 103 | 249 |
| FY2025 | $63.6M | 108 | 93 | 215 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Division Of Cancer Epidemiology And Genetics | $6.9M | 0 |
| Cedars-Sinai Medical Center | $5.7M | 10 |
| University Of Tx Md Anderson Can Ctr | $4.5M | 6 |
| Roswell Park Cancer Institute Corp | $3.7M | 3 |
| Division Of Basic Sciences - Nci | $3.5M | 4 |
| Methodist Hospital Research Institute | $3.2M | 5 |
| Sloan-Kettering Inst Can Research | $3.1M | 5 |
| Northwestern University | $3.0M | 0 |
| Vanderbilt University | $3.0M | 0 |
| Dana-Farber Cancer Inst | $2.3M | 4 |
Text search bladder cancer over project title, terms and abstract, per fiscal year. Awards are individual funding actions; distinct projects collapse them by core project number, so a multi-year grant counts once. The most recent year may be incomplete. Source: NIH RePORTER, retrieved 2026-09-12.
What that buys
Against 95,401 years of life lost a year, FY2025 obligations are $667 per life-year — $752 per case. The estimate and its assumptions are in Disease burden.
Who funds it, FY2025
The total says how much. These say who from, through what kind of award, and to whom — which a dollar figure cannot.
NIH institutes
Projects by administering institute. The rows above are the top 4 and account for 108 of 108.
Award mechanisms
R01 is an investigator-initiated grant; ZIA is NIH intramural, meaning the work happens inside NIH rather than being funded outside it. The rows above are the top 15 and account for 104 of 108.
Where it lands
Share of $63.6M in FY2025. The top three hold 27%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly772 human GEO series match bladder cancer. Keyword relevance cannot tell a 972-sample patient cohort from a six-well cell-line experiment, so this ranking scores four things GEO does not expose: how often the accession is named in full-text papers, field-normalised citation impact, clinical annotation, and cohort type.
Composition of the 457-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE32894 | A Molecular Taxonomy of Urothelial Carcinoma2012 · array | 308 | 419 | 18.9 | APT 0.95stagemolecularERBB2FGFR3HER2755 cites |
| GSE13507 | Predective Value of Prognosis-Related Gene Expression Study in Primary Bladder Cancer2010 · array | 256 | 951 | 7.4 | patient cohortAPT 0.95survival336 cites |
| GSE176307 | Fibroblast Growth Factor Receptor 3 Alterations and Response to Immune Checkpoint Inhibition in Metastatic Urothelial Cancer: A Real World Experience2021 · sequencing | 90 | 165 | 6.4 | patient cohortAPT 0.95survivalmolecularFGFR3149 cites |
| GSE145281 | High gene expression of IL8 in peripheral blood mononuclear cells from bladder cancer patients is associated with nonresponders to atezolizumab2020 · sequencing | 18 | 78 | 13.2 | patient cohortAPT 0.95survivalmolecularATEZOLIZUMABPD-L1364 cites |
| GSE19915 | Subtype classification, grading, and outcome prediction of urothelial carcinomas by combined mRNA profiling and aCGH2010 · array | 285 | 53 | 5.4 | APT 0.95survivalstagemolecularFGFR3PIK3CATP53242 cites |
| GSE31684 | Combination of a novel gene expression signature with a clinical nomogram improves the prediction of survival in high-risk bladder cancer2012 · array | 93 | 394 | 4.6 | APT 0.75survivalstage186 cites |
| GSE113486 | Circulating miRNA panels for specific and early detection in bladder cancer2018 · array | 972 | 78 | 8.7 | patient cohortAPT 0.95195 cites |
| GSE3167 | Classification of carcinoma in situ lesions in human bladder cancer2005 · array | 60 | 161 | 7.3 | patient cohortAPT 0.75stage385 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE222315 | Gene expression profile at single cell level of bladder cancer and normal adjacent tissues2024 · single-cell | 13 | 52 | 17.1 | APT 0.75142 cites |
| GSE279390 | Basal/squamous and mixed subtype bladder cancers present poor outcomes after neoadjuvant chemotherapy in the VESPER trial2024 · sequencing | 540 | 2 | 7.0 | patient cohortAPT 0.95survival26 cites |
| GSE216037 | TP53-related signature for predicting prognosis and tumor microenvironment characteristics in bladder cancer: a multi-omics study 1 microenvironment characteristic2022 · single-cell | 52 | 7 | 1.1 | patient cohortAPT 0.25survivalstagemolecularTP5317 cites |
| GSE244266 | Association of Molecular Subtypes with Pathologic Response, PFS and OS in a Phase II Study of Coexpression Extrapolation (COXEN) with Neoadjuvant Chemotherapy (NAC) for Localized, Muscle-Invasive Bladder Cancer (SWOG S1314; NCT02177695)2023 · array | 189 | 2 | 6.9 | patient cohortAPT 0.95survival27 cites |
| GSE267718 | Single cell RNA sequencing (scRNAseq) of urine-derived cells, peripheral blood mononuclear (PBMC), and tumor cells from bladder cancer patients.2024 · single-cell | 33 | 18 | 2.4 | patient cohortAPT 0.524 cites |
| GSE318164 | Molecular Heterogeneity and Immune Infiltration Drive Clinical Outcomes in Upper Tract Urothelial Carcinoma2026 · sequencing | 113 | 0 | 5.1 | patient cohortAPT 0.75survivalmolecularFGFR317 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-12. SubSeries are collapsed to one row per study by linked PMID. Of 772 series retrieved, 6 were dropped by the profile’s exclusion rules and 200 named the disease only in passing. The ranked set is a relevance-ranked sample, not a census, so the composition figures describe the sample only.
Where the gaps are
Derived from the sections above · recomputed on every refreshEach card below is a disagreement between two of the tables on this page — a drug that exists but was never tried here, a target that looks tested and was not, a gene with no drug whose product has a busy clinical programme. They are computed from the same facts as the tables, so they cannot contradict them.
RB1
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
KDM6A
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
ARID1A
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
TERT
1 approved drug (Imetelstat) and no registered trial in bladder cancer. The molecules exist; nobody has tested them here.
STAG2
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
How a machine reads this page
StaticThis page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite.
Fully server-rendered
Every figure is in the HTML at first byte. No JavaScript runs, no figure is fetched after load, and nothing on this page requires a renderer to see.
Every number carries a source
Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-12), ClinicalTrials.gov (2026-09-12), openFDA (2026-09-12), NCBI GEO (2026-09-12), PubMed (2026-09-12), NIH RePORTER (2026-09-12).
Negatives stated explicitly
Where nothing exists for bladder cancer — no drug, no trial, no approval — the page says so in those words rather than omitting the row. An absent row is unquotable; a stated negative is the finding.
Denominators, not just percentages
Every share is printed with the count and the total it came from, so a figure can be checked rather than taken.
The filters are published
2 exclusion patterns are applied to free text before anything is ranked, because T24 is used as a model system in generic invasion and drug-cytotoxicity work. What was removed and why is stated in each section rather than silently applied.
{
"disease": "Bladder cancer",
"mesh": "Urinary Bladder Neoplasms",
"facts": "https://usebiotransfer.org/disease/bladder-cancer.json",
"methods": "https://usebiotransfer.org/methods/",
"note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}