Disease Briefing

Bladder cancer: research and therapeutic landscape

A live synthesis of what is being targeted, what is being trialled, which datasets exist, and where the actionable gaps sit — assembled from public APIs, with every figure traceable to its source.

Generated 2026-09-12Sources Open Targets · ClinicalTrials.gov · openFDA · GEO · PubMed · Europe PMC · iCite · RePORTERRanked 457 studies · 20,005 GEO samples
Reading as
Reorders emphasis only — nothing is hidden or loaded on demand.

Answer block

12 genes recurrently implicated in bladder cancer — FGFR3, ERBB2, NECTIN4, TACSTD2, CD274, TP53, RB1, KDM6A, ARID1A, PIK3CA, TERT, STAG2 — triaged for what can actually be aimed at them, alongside the trials, public datasets, literature and funding around the disease. Every figure below carries its source and retrieval date in the section it comes from.

11
drugs carry an FDA label naming bladder cancer: Atezolizumab, Avelumab, Durvalumab, Enfortumab Vedotin, Erdafitinib, Hexaminolevulinate and 5 more. This counts labels, not treatment — the disease is also treated with agents approved under broader indications
3
of the 12 genes above carry a drug that is approved in bladder cancer itself — CD274, FGFR3, NECTIN4. Across all of them 132 drug entries reach these genes, 124 distinct once salt forms are merged
5
registered PD-1 cell-therapy trials in bladder cancer, 1 active and 2 withdrawn. Counted from ClinicalTrials.gov across 3 synonyms, deduplicated by NCT id, interventional studies only — the query is published in the JSON beside this page so the number can be re-derived
5
targets carry an Open Targets tractability signal and have no clinical programme of any kind: RB1, KDM6A, ARID1A, TERT, STAG2. ERBB2, NECTIN4, CD274 all have cell-therapy trials, so they are undrugged rather than untouched
772
human GEO series match the disease; 457 survive on-topic filtering, and only 26 are patient cohorts of 100+ samples
951
Europe PMC full-text papers name GSE13507 — the highest accession-mention count in the set. A mention is not proof of reanalysis, so read it as reach rather than reuse
$63.6M
NIH obligations in FY2025, up 195% since 2013 — while distinct core projects went 50 to 93. Both more projects (+86%) and larger awards, the latter carrying more of the growth; core projects are not the same unit as laboratories

Target landscape

Open Targets · retrieved 2026-09-12 · weekly

12 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.

GeneDrugsApproval, and whether it reached this diseaseOpen Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it worksCell 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 · weekly

11 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.

11Labelled for bladder cancerFDA INDICATIONS AND USAGE names the disease
33Approved, but for another diseasereturned for the genes in the table above
2Backbone agents listing itbroad cytotoxics whose labels name many tumours
1Active PD-1 cell-therapy trialsof 5 registered

Every label that names bladder cancer

DrugRoleWhat the label says
AtezolizumabTECENTRIQ, Tecentriq HybrezaLabelled hereMuscle 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.
AvelumabBAVENCIOLabelled 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.
DurvalumabIMFINZILabelled hereBladder 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 EJFVLabelled 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).
ErdafitinibBALVERSALabelled hereBALVERSA 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.
HexaminolevulinateCysviewLabelled hereCYSVIEW 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, ZUSDURILabelled hereJELMYTO is an alkylating drug indicated for the treatment of adult patients with low-grade Upper Tract Urothelial Cancer (LG-UTUC).
Nadofaragene Firadenovec-VncgADSTILADRINLabelled hereADSTILADRIN ® 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 QVANTIGLabelled hereUrothelial 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-PmlnANKTIVALabelled hereANKTIVA 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 QLEXLabelled hereUrothelial Cancer in combination with enfortumab vedotin-ejfv, for the treatment of adult patients with locally advanced or metastatic urothelial cancer.
CisplatinCISPLATIN, CISplatin, CisplatinBackboneAdvanced bladder cancer
Gemcitabine IntravesicalINLEXZOBackboneINLEXZO 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 · weekly

PD-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.

TrialPhaseStatusTitleLast update
NCT074106761/2RecruitingEBNK-001 Allogeneic NK Cells With Low-Dose IL-15 ± Pembrolizumab in Advanced Solid Tumors2026-02-18
NCT028639131WithdrawnPD-1 Knockout Engineered T Cells for Muscle-invasive Bladder Cancer2019-03-06
NCT039353472WithdrawnAdoptive Cell Therapy With (LN-145) in Combination With Pembrolizumab in Treating Patients With Unresectable or Metastatic Transitional Cell Cancer Who Have Failed Cisplatin-Based Chemotherapy2020-01-02
NCT037859252CompletedA Single-Arm Study of Bempegaldesleukin (NKTR-214) Plus Nivolumab in Cisplatin Ineligible Patients Who Have Locally Advanced or Metastatic Urothelial Cancer2023-03-28
NCT042091143CompletedA 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 Cancer2024-06-27

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 · monthly

Every 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 term2015–182021–25ChangeShare now
Immunoconjugates0.12%0.97%8.28×58 papers
Single-Cell Analysis0.08%0.63%7.59×38 papers
Tumor Microenvironment1.0%6.8%6.8×408 papers
Nephroureterectomy0.1%0.62%6.16×37 papers
Pyrazoles0.08%0.5%5.99×30 papers
Platinum0.17%0.97%5.8×58 papers
Molecular Docking Simulation0.08%0.47%5.59×28 papers
Muscles0.83%4.42%5.3×265 papers
Microbiota0.1%0.47%4.66×28 papers
Killer Cells, Natural0.08%0.37%4.4×22 papers

Cooling

MeSH term2015–182021–25ChangeShare now
Disease-Free Survival6.58%0.85%0.13×51 papers
Tumor Cells, Cultured1.82%0.32%0.17×19 papers
Time Factors4.67%0.9%0.19×54 papers
RNA, Small Interfering1.73%0.33%0.19×20 papers
Dose-Response Relationship, Drug1.2%0.23%0.19×14 papers
Neoplasm Grading5.82%1.18%0.2×71 papers

Biggest topics now

MeSH term2015–182021–25ChangeShare now
Carcinoma, Transitional Cell18.98%24.58%1.29×1475 papers
Cystectomy22.67%20.37%0.9×1222 papers
Prognosis15.33%15.25%0.99×915 papers
Neoplasm Invasiveness16.4%14.35%0.88×861 papers
Urinary Bladder9.92%14.07%1.42×844 papers
Biomarkers, Tumor14.38%12.23%0.85×734 papers
Treatment Outcome14.92%9.92%0.66×595 papers
Neoplasm Recurrence, Local11.98%9.48%0.79×569 papers
Gene Expression Regulation, Neoplastic11.32%8.92%0.79×535 papers
Cell Proliferation9.65%7.6%0.79×456 papers

Publication mix

Type2015–182021–25
Clinical Trial0.0%0.0%
Randomized Controlled Trial2.1%1.6%
Review12.7%8.9%
Meta-Analysis2.7%2.0%
Case Reports0.0%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.

MeasureValueMatchWhat it counts
New cases each year84,530 cases/yeardirect2026
Deaths each year17,870 deaths/yeardirect2026
Incidence rate17.9 cases per 100,000 people per yeardirect2019-2023
Death rate4.1 deaths per 100,000 people per yeardirect2020-2024
People living with it763,031 people living with the diseasedirect2023
Median age at diagnosis73.0 yearsdirect2019-2023
median age at death79 yearsdirect2020-2024
Five-year relative survival79.1%direct2016-2022

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 · quarterly

NIH 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.

$63.6MNIH obligations, FY2025from $21.6M in FY2013 · +195%
93distinct projects funded50 in FY2013
$63.6Mpeak year was FY2025obligations, all institutes
91%of FY2025 awards from NCI98 of 108

NIH obligations by fiscal year

$16M$32M$48M$64M13151719212325
YearObligationsAwardsDistinct projectsDropped as off-topic
FY2013$21.6M5950224
FY2014$28.2M7765235
FY2015$32.3M6757229
FY2016$30.5M6959230
FY2017$29.0M6760220
FY2018$38.0M9069311
FY2019$35.8M8468262
FY2020$42.9M9073275
FY2021$49.4M11488265
FY2022$57.4M11493266
FY2023$60.3M119106265
FY2024$58.1M121103249
FY2025$63.6M10893215

Where FY2025 money went

InstitutionObligationsAwards
Division Of Cancer Epidemiology And Genetics$6.9M0
Cedars-Sinai Medical Center$5.7M10
University Of Tx Md Anderson Can Ctr$4.5M6
Roswell Park Cancer Institute Corp$3.7M3
Division Of Basic Sciences - Nci$3.5M4
Methodist Hospital Research Institute$3.2M5
Sloan-Kettering Inst Can Research$3.1M5
Northwestern University$3.0M0
Vanderbilt University$3.0M0
Dana-Farber Cancer Inst$2.3M4

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

NCI98 · 91%
VA8 · 7%
NCATS1 · 1%
NIBIB1 · 1%

Projects by administering institute. The rows above are the top 4 and account for 108 of 108.

Award mechanisms

R0140 · 37%
P0110 · 9%
ZIA8 · 7%
U017 · 6%
K087 · 6%
R216 · 6%

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

Division Of Cancer Epidemiology And Gene$6.9M · 10.9%
Cedars-Sinai Medical Center$5.7M · 9.0%
University Of Tx Md Anderson Can Ctr$4.5M · 7.1%
Roswell Park Cancer Institute Corp$3.7M · 5.8%
Division Of Basic Sciences - Nci$3.5M · 5.5%
Methodist Hospital Research Institute$3.2M · 5.0%

Share of $63.6M in FY2025. The top three hold 27%.

Public datasets, ranked

NCBI GEO + Europe PMC + iCite · weekly

772 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

patient 144unspecified 136cell line 127mixed 49xenograft 1
144 patient136 unspecified127 cell line49 mixed1 xenograft218 carry clinical annotation158 carry survival26 patient cohorts ≥100 GEO samples20,005 GEO samples totalin 25 single-cell series a GEO sample is one cell, not one patient

Established

high reuse, older
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE32894A Molecular Taxonomy of Urothelial Carcinoma2012 · array30841918.9
APT 0.95stagemolecularERBB2FGFR3HER2755 cites
GSE13507Predective Value of Prognosis-Related Gene Expression Study in Primary Bladder Cancer2010 · array2569517.4
patient cohortAPT 0.95survival336 cites
GSE176307Fibroblast Growth Factor Receptor 3 Alterations and Response to Immune Checkpoint Inhibition in Metastatic Urothelial Cancer: A Real World Experience2021 · sequencing901656.4
patient cohortAPT 0.95survivalmolecularFGFR3149 cites
GSE145281High gene expression of IL8 in peripheral blood mononuclear cells from bladder cancer patients is associated with nonresponders to atezolizumab2020 · sequencing187813.2
patient cohortAPT 0.95survivalmolecularATEZOLIZUMABPD-L1364 cites
GSE19915Subtype classification, grading, and outcome prediction of urothelial carcinomas by combined mRNA profiling and aCGH2010 · array285535.4
APT 0.95survivalstagemolecularFGFR3PIK3CATP53242 cites
GSE31684Combination of a novel gene expression signature with a clinical nomogram improves the prediction of survival in high-risk bladder cancer2012 · array933944.6
APT 0.75survivalstage186 cites
GSE113486Circulating miRNA panels for specific and early detection in bladder cancer2018 · array972788.7
patient cohortAPT 0.95195 cites
GSE3167Classification of carcinoma in situ lesions in human bladder cancer2005 · array601617.3
patient cohortAPT 0.75stage385 cites

Recent

2022 onward, by score
AccessionStudySamplesMentionsEurope PMCRCREvidence
GSE222315Gene expression profile at single cell level of bladder cancer and normal adjacent tissues2024 · single-cell135217.1
APT 0.75142 cites
GSE279390Basal/squamous and mixed subtype bladder cancers present poor outcomes after neoadjuvant chemotherapy in the VESPER trial2024 · sequencing54027.0
patient cohortAPT 0.95survival26 cites
GSE216037TP53-related signature for predicting prognosis and tumor microenvironment characteristics in bladder cancer: a multi-omics study 1 microenvironment characteristic2022 · single-cell5271.1
patient cohortAPT 0.25survivalstagemolecularTP5317 cites
GSE244266Association 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 · array18926.9
patient cohortAPT 0.95survival27 cites
GSE267718Single cell RNA sequencing (scRNAseq) of urine-derived cells, peripheral blood mononuclear (PBMC), and tumor cells from bladder cancer patients.2024 · single-cell33182.4
patient cohortAPT 0.524 cites
GSE318164Molecular Heterogeneity and Immune Infiltration Drive Clinical Outcomes in Upper Tract Urothelial Carcinoma2026 · sequencing11305.1
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 refresh

Each 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

Static

This 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."
}