Target landscape
Open Targets · retrieved 2026-09-12 · weekly12 genes recurrently implicated in ovarian cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 12 recurrently implicated genes, 6 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Ovarian cancer does have labelled therapy — 9 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 ovarian 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 |
|---|---|---|---|---|
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran6 trials, none active | other clinical modality, protein degrader, small molecule | — |
| BRCA1 across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| BRCA2 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| CCNE1 | 0 | No drug— | protein degrader, small molecule | — |
| FOLR1 | 4 | 2 approvedMirvetuximab Soravtansine, VintafolideApproved in ovarian cancer: Mirvetuximab Soravtansine.28 active of 60 ovarian cancer trials | antibody, other clinical modality, protein degrader, small molecule | 2 active of 3 trials |
| MUC16 | 4 | 1 approvedIgovomabApproved in radiologic finding, ovarian neoplasm. No ovarian cancer indication appears on these drugs’ labels.4 active of 19 ovarian cancer trials | antibody, other clinical modality, protein degrader | 3 active of 3 trials |
| MSLN across cancers → | 5 | Phase 2Amatuximab, Anetumab Ravtansine, Lmb-100, Rg-7600, Ss1(Dsfv)-Pe381 active of 8 ovarian cancer trials | antibody, other clinical modality, protein degrader | 8 active of 15 trials |
| KRAS across cancers → | 3 | 2 approvedAdagrasib, SotorasibApproved in non-small cell lung carcinoma. No ovarian cancer indication appears on these drugs’ labels.1 active of 1 ovarian cancer trial | antibody, 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 ovarian cancer indication appears on these drugs’ labels.9 active of 25 ovarian cancer trials | antibody, protein degrader, small molecule | — |
| PTEN across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| NF1 across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
Dataset evidence counts studies in the 1053-study ranked set whose title or abstract names the gene; the bar is scaled to BRCA1. 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 · weekly9 drugs carry an FDA label naming ovarian cancer: Air Polymer-Type A Intrauterine Foam, Avutometinib Potassium And Defactinib, Bevacizumab, Mirvetuximab Soravtansine, Niraparib, Olaparib, Pembrolizumab, Relacorilant, Rucaparib. Separately, 7 of the drugs returned for the genes in the table above are approved only for other diseases and reach ovarian cancer through trials, not through their labels.
Every label that names ovarian cancer
| Drug | Role | What the label says |
|---|---|---|
| Air Polymer-Type A Intrauterine FoamExEm Foam | Labelled here | ExEm ® Foam is indicated for sonohysterosalpingography to assess fallopian tube patency in women with known or suspected infertility. |
| Avutometinib Potassium And DefactinibAVMAPKI FAKZYNJA CO-PACK | Labelled here | AVMAPKI FAKZYNJA CO-PACK is indicated for the treatment of adult patients with KRAS -mutated recurrent low-grade serous ovarian cancer (LGSOC) who have received prior systemic therapy. |
| BevacizumabALYMSYS, Avastin, JOBEVNE | Labelled here | Epithelial ovarian, fallopian tube, or primary peritoneal cancer: in combination with carboplatin and paclitaxel, followed by MVASI as a single agent, for stage III or IV disease following initial surgical resection |
| Mirvetuximab SoravtansineELAHERE | Labelled here | ELAHERE ® is indicated for the treatment of adult patients with folate receptor-alpha (FRα) positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received one to three prior systemic treatment regimens. |
| NiraparibZEJULA | Labelled here | Maintenance Treatment of Recurrent Germline BRCA -Mutated Ovarian Cancer ZEJULA is indicated for the maintenance treatment of adult patients with deleterious or suspected deleterious germline BRCA -mutated (g BRCA mut) recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in a complete or partial response to platinum-based chemotherapy. |
| OlaparibLynparza | Labelled here | Maintenance Treatment of BRCA-mutated Recurrent Ovarian Cancer Lynparza is indicated for the maintenance treatment of adult patients with deleterious or suspected deleterious germline or somatic BRCA-mutated recurrent epithelial ovarian, fallopian tube or primary peritoneal cancer, who are in complete or partial response to platinum-based chemotherapy. |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Ovarian Cancer KEYTRUDA, in combination with paclitaxel, with or without bevacizumab, is indicated for the treatment of adult patients with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal carcinoma whose tumors express PD-L1 (CPS ≥1) as determined by an FDA-authorized test [see Dosage and Administration |
| RelacorilantLifyorli | Labelled here | LIFYORLI is indicated in combination with nab-paclitaxel for the treatment of adults with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens, at least one of which included bevacizumab . |
| RucaparibRubraca | Labelled here | Maintenance Treatment of BRCA -mutated Recurrent Ovarian Cancer RUBRACA is indicated for the maintenance treatment of adult patients with a deleterious BRCA mutation (germline and/or somatic)-associated recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in a complete or partial response to platinum-based chemotherapy. |
| AmifostineEthyol | Backbone | ETHYOL is a cytoprotective agent indicated for: – reduction of cumulative renal toxicity associated with repeated administration of cisplatin in patients with advanced ovarian cancer. |
| CisplatinCisplatin | Backbone | Advanced ovarian cancer |
| DoxorubicinDOXIL, DOXORUBICIN HYDROCHLORIDE, Doxorubicin Hydrochloride | Backbone | Ovarian Cancer DOXIL liposomal infusion is indicated for the treatment of patients with ovarian cancer whose disease has progressed or recurred after platinum-based chemotherapy. |
| GemcitabineAVGEMSI, GEMCITABINE, Gemcitabine | Backbone | Ovarian Cancer AVGEMSI in combination with carboplatin is indicated for the treatment of patients with advanced ovarian cancer that has relapsed at least 6 months after completion of platinum-based therapy. |
| TopotecanHYCAMTIN, Topotecan Hydrochloride, Topotecan hydrochloride | Backbone | Ovarian Cancer HYCAMTIN ® for injection, as a single agent, is indicated for the treatment of patients with metastatic ovarian cancer after disease progression on or after initial or subsequent chemotherapy. |
| PafolacianineCytalux | Not a therapy | CYTALUX is indicated as an adjunct for intraoperative identification of: Malignant lesions in adult patients with ovarian cancer. |
19 labels match indications_and_usage:"ovarian cancer" OR indications_and_usage:"epithelial ovarian" OR indications_and_usage:"fallopian tube"; they collapse to 15 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Diagnostic and contrast agents (Pafolacianine) are listed but are not treatments. 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 mesothelin
ClinicalTrials.gov · retrieved 2026-09-12 · weeklymesothelin is the busiest cell-therapy antigen in ovarian cancer: 15 registered trials, 8 still active. It has no gene entry of its own and is reached through MSLN: a form or product of that gene.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT05410717 | 1 | Recruiting | CLDN6/GPC3/Mesothelin/AXL-CAR-NK Cell Therapy for Advanced Solid Tumors | 2024-06-25 |
| NCT07480954 | 1/2 | Recruiting | Dual-Targeting CAR-NK Cells for Recurrent Ovarian Cancer (MSLN, FRα, MUC16) | 2026-03-18 |
| NCT07523529 | 1/2 | Recruiting | Biomarker-Guided Dual-Target CAR-T Cells for Advanced Solid Tumors | 2026-04-13 |
| NCT07589543 | 1/2 | Recruiting | Dual-Target CAR-NK Cells in Recurrent or Refractory Epithelial Ovarian Cancer | 2026-05-15 |
| NCT07617753 | 1/2 | Recruiting | Dual-Targeting CAR-NK Cells for Recurrent Ovarian Cancer (MSLN, FRα, MUC16) pt2 | 2026-06-01 |
| NCT06051695 | 1/2 | Recruiting | A Study to Evaluate the Safety and Efficacy of Mesothelin-Targeting Logic-gated CAR T, in Participants With Solid Tumors That Express MSLN and Have Lost HLA-A*02 Expression | 2026-06-12 |
| NCT06885697 | 1 | Recruiting | Anti-Mesothelin TNaive/SCM hYP218 (TNhYP218) CAR T Cells in Participants With Mesothelin-Expressing Solid Tumors Including Mesothelioma | 2026-08-26 |
| NCT05963100 | 1/2 | Active | Clinical Study of TCR-like CAR-T Cell Targeted MSLN in the Treatment of Ovarian Cancer | 2025-04-02 |
| NCT02580747 | 1 | Unknown | Treatment of Relapsed and/or Chemotherapy Refractory Advanced Malignancies by CART-meso | 2015-10-20 |
| NCT03692637 | EARLY/1 | Unknown | Study of Anti-Mesothelin Car NK Cells in Epithelial Ovarian Cancer | 2019-01-31 |
10 of 15 shown, most recently active first. Other antigens searched: HER2 (6), MUC1 (4), FRalpha (3), CA-125 (3), CLDN6 (2), PD-L1 (2), TROP2 (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 ovarian 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 10,510 and 14,666 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 |
|---|---|---|---|---|
| Machine Learning | 0.13% | 1.2% | 8.99× | 72 papers |
| Nomograms | 0.15% | 1.27% | 8.44× | 76 papers |
| Molecular Docking Simulation | 0.13% | 0.98% | 7.37× | 59 papers |
| Extracellular Vesicles | 0.13% | 0.88% | 6.62× | 53 papers |
| Exome Sequencing | 0.08% | 0.52% | 6.19× | 31 papers |
| RNA, Circular | 0.13% | 0.75% | 5.62× | 45 papers |
| Coordination Complexes | 0.08% | 0.4% | 4.8× | 24 papers |
| Genital Neoplasms, Female | 0.27% | 1.27% | 4.75× | 76 papers |
| Ubiquitination | 0.13% | 0.62% | 4.62× | 37 papers |
| Ligands | 0.12% | 0.53% | 4.57× | 32 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Neoplasms, Glandular and Epithelial | 16.48% | 1.02% | 0.06× | 61 papers |
| Time Factors | 2.5% | 0.23% | 0.09× | 14 papers |
| Neoplasms, Cystic, Mucinous, and Serous | 2.15% | 0.2% | 0.09× | 12 papers |
| Survival Analysis | 3.67% | 0.37% | 0.1× | 22 papers |
| Disease-Free Survival | 7.08% | 0.78% | 0.11× | 47 papers |
| Gene Expression | 1.68% | 0.25% | 0.15× | 15 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Carcinoma, Ovarian Epithelial | 19.73% | 21.82% | 1.11× | 1309 papers |
| Prognosis | 16.35% | 12.82% | 0.78× | 769 papers |
| Biomarkers, Tumor | 14.58% | 11.03% | 0.76× | 662 papers |
| Gene Expression Regulation, Neoplastic | 14.08% | 10.45% | 0.74× | 627 papers |
| Cell Proliferation | 12.18% | 10.17% | 0.83× | 610 papers |
| Antineoplastic Agents | 12.25% | 9.1% | 0.74× | 546 papers |
| Tumor Microenvironment | 1.8% | 8.18% | 4.55× | 491 papers |
| Drug Resistance, Neoplasm | 9.07% | 7.63% | 0.84× | 458 papers |
| Neoplasm Recurrence, Local | 7.2% | 7.3% | 1.01× | 438 papers |
| Cystadenocarcinoma, Serous | 7.13% | 6.83% | 0.96× | 410 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 1.8% | 1.3% |
| Review | 10.2% | 9.9% |
| Meta-Analysis | 2.5% | 1.5% |
| Case Reports | 0.0% | 2.1% |
Query: Ovarian Neoplasms[MeSH Major Topic] NOT ("Neoplasms, Germ Cell and Embryonal"[MeSH] OR "Sex Cord-Gonadal Stromal Tumors"[MeSH] OR "Granulosa Cell Tumor"[MeSH] OR "Polycystic Ovary Syndrome"[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 | 21,010 cases/year | direct | 2026 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| Deaths each year | 12,450 deaths/year | direct | 2026 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| Incidence rate | 10.4 cases per 100,000 women per year | direct | 2019-2023 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| Death rate | 5.7 deaths per 100,000 women per year | direct | 2020-2024 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| People living with it | 254,621 women living with the disease | direct | 2023 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| Median age at diagnosis | 63.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| median age at death | 71 years | direct | 2020-2024 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
| Five-year relative survival | 52.0% | direct | 2016-2022 SEER Cancer Stat Facts, Ovarian Cancer, retrieved 2026-09-12 |
Years of life lost
7.4 years per case, 155,306 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 ovarian cancer, after removing the 9,128 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 | $79.2M | 197 | 145 | 642 |
| FY2014 | $68.8M | 170 | 146 | 629 |
| FY2015 | $65.2M | 169 | 146 | 627 |
| FY2016 | $75.1M | 188 | 158 | 653 |
| FY2017 | $87.7M | 207 | 173 | 666 |
| FY2018 | $97.7M | 233 | 181 | 883 |
| FY2019 | $91.1M | 241 | 196 | 707 |
| FY2020 | $92.9M | 223 | 190 | 682 |
| FY2021 | $101.8M | 260 | 206 | 727 |
| FY2022 | $108.0M | 263 | 210 | 722 |
| FY2023 | $107.1M | 260 | 214 | 689 |
| FY2024 | $106.5M | 261 | 202 | 790 |
| FY2025 | $111.6M | 229 | 185 | 711 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| University Of Tx Md Anderson Can Ctr | $12.0M | 22 |
| University Of Pennsylvania | $7.4M | 10 |
| Mayo Clinic Rochester | $6.5M | 18 |
| Johns Hopkins University | $5.3M | 10 |
| University Of Pittsburgh At Pittsburgh | $4.8M | 8 |
| Roswell Park Cancer Institute Corp | $3.9M | 8 |
| Massachusetts General Hospital | $3.7M | 5 |
| Division Of Basic Sciences - Nci | $3.3M | 0 |
| Sloan-Kettering Inst Can Research | $3.1M | 0 |
| Division Of Cancer Epidemiology And Genetics | $2.5M | 0 |
Text search ovarian 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 155,306 years of life lost a year, FY2025 obligations are $718 per life-year — $5,310 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 10 and account for 228 of 229.
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 206 of 229.
Where it lands
Share of $111.6M in FY2025. The top three hold 23%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly2,065 human GEO series match ovarian cancer. Keyword relevance cannot tell a 4,046-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 1053-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE26712 | A Gene Signature Predicting for Survival in Suboptimally Debulked Patients with Ovarian Cancer2011 · array | 195 | 500 | 6.7 | patient cohortAPT 0.75survivalstage340 cites |
| GSE65821 | Whole genome characterisation of chemoresistant ovarian cancer2015 · methylation | 356 | 16 | 37.6 | patient cohortAPT 0.95survivalstagemolecularBRCA1BRCA2CCNE11,276 cites |
| GSE106817 | Integrated extracellular microRNA profiling for ovarian cancer screening2018 · array | 4,046 | 99 | 10.4 | patient cohortAPT 0.95253 cites |
| GSE32062 | Immune-activation as a therapeutic direction for patients with high-risk ovarian cancer based on gene expression signature (1)2012 · array | 270 | 187 | 3.7 | patient cohortAPT 0.95survivalstage163 cites |
| GSE26193 | Control of oxidative stress by miRNA and impact on ovarian tumorigenesis2011 · array | 107 | 286 | 10.2 | patient cohortAPT 0.75stage407 cites |
| GSE3149 | Ovarian Cancer Dataset2005 · array | 153 | 100 | 29.9 | mixedAPT 0.95survival1,565 cites |
| GSE40595 | A cancer associated fibroblasts (CAFs) specific gene signature in high grade serous ovarian cancer2014 · array | 77 | 160 | 9.6 | patient cohortAPT 0.75survivalstage344 cites |
| GSE9899 | Expression profile of ovarian tumour samples2008 · array | 295 | 483 | 24.4 | patient cohortAPT 0.951,171 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE180661 | Ovarian cancer mutational processes drive site-specific immune evasion2022 · single-cell | 283 | 20 | 15.8 | patient cohortAPT 0.75stagemolecularBRCA1BRCA2272 cites |
| GSE184880 | Single-cell RNA sequencing reveals tissue architecture during human high-grade serous ovarian cancer progression2022 · single-cell | 12 | 128 | 15.7 | patient cohortAPT 0.75stage236 cites |
| GSE211956 | Spatial transcriptomics reveals ovarian cancer subclones with different microenvironments2022 · single-cell | 13 | 34 | 14.6 | APT 0.75stage130 cites |
| GSE266577 | Chemotherapy induces myeloid-driven spatial T-cell exhaustion in ovarian cancer2024 · single-cell | 48 | 8 | 6.9 | patient cohortAPT 0.75stage71 cites |
| GSE276935 | The activity of tertiary lymphoid structures in high grade serous ovarian cancer is governed by site, stroma, and cellular interactions2024 · spatial | 417 | 1 | 7.2 | patient cohortAPT 0.75survivalstage71 cites |
| GSE211687 | The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer2022 · methylation | 262 | 8 | 6.2 | APT 0.95stage105 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-12. SubSeries are collapsed to one row per study by linked PMID. Of 2,065 series retrieved, 86 were dropped by the profile’s exclusion rules and 653 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.
BRCA1
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
BRCA2
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
CCNE1
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
MSLN
15 cell-therapy trials against mesothelin, 8 active, and no approved product. The clinical activity is real and none of it has reached a label.
ARID1A
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
PTEN
No drug, no trial, no clinical programme of any kind. Whatever the biology says, nothing has been built.
NF1
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 ovarian 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
3 exclusion patterns are applied to free text before anything is ranked, because SKOV3 and A2780 is used as a model system in generic cisplatin-sensitivity and drug-resistance work. What was removed and why is stated in each section rather than silently applied.
{
"disease": "Ovarian cancer",
"mesh": "Ovarian Neoplasms",
"facts": "https://usebiotransfer.org/disease/ovarian-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."
}