{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT03288545","title":"A Study of Enfortumab Vedotin Alone or With Other Therapies for Treatment of Urothelial Cancer","sponsor":"Astellas Pharma Global Development, Inc.","phases":["PHASE1","PHASE2"],"status":"TERMINATED","indication":null,"disease":"cervical squamous cell carcinoma"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of NECTIN4, TUBB4B, TUBB1, PDCD1 has somatic-mutation evidence in cervical squamous cell carcinoma","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: NECTIN4 in cervical squamous cell carcinoma","url":"https://platform.opentargets.org/evidence/ENSG00000143217/MONDO_0006143","date":"2026-11-11T15:32:30.709Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for NECTIN4, TUBB4B, TUBB1, PDCD1 in cervical squamous cell carcinoma","rule":"Any germline or somatic human genetic evidence for the target in this cancer, counted apart from animal-model and literature evidence","source":{"label":"Open Targets: NECTIN4 in cervical squamous cell carcinoma","url":"https://platform.opentargets.org/evidence/ENSG00000143217/MONDO_0006143","date":"2026-11-11T15:32:30.709Z"},"context":[]},{"id":"pediatric_target","label":"Pediatric target","value":"yes","detail":"PDCD1 on the FDA list","rule":"Target is on FDA's Pediatric Molecular Target List (relevant targets); membership alone neither requires nor waives a study","source":{"label":"FDA Pediatric Molecular Target List (Listed as February 2026 on the FDA Pediatric Oncology page; the file served is 9.7.22_the_relevant_molecular_target_list.xlsx, whose Summary of Changes sheet is headed 'SEPTEMBER 2022 UPDATE' (footnote date 2022-09-01))","url":"https://www.fda.gov/media/191157/download?attachment","date":"2026-11-11T07:05:03Z"},"context":[]},{"id":"haematologic","label":"Haematologic cancer","value":"no","detail":"Solid tumour","rule":"From the indication, or the registry conditions when no indication matches","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"},"context":[{"figure":"Likelihood of approval from phase 1: 7.5% haematologic vs 4.6% solid","dataset":"BIO / Informa / QLS 2021","years":"2011–2020","caveat":"Population-level, not a prediction."}]}],"facts":[{"label":"NECTIN4 (via enfortumab vedotin)","text":"Open Targets has no association between NECTIN4 and cervical squamous cell carcinoma.","source":{"label":"Open Targets: NECTIN4 in cervical squamous cell carcinoma","url":"https://platform.opentargets.org/evidence/ENSG00000143217/MONDO_0006143","date":"2026-11-11T15:32:30.709Z"}},{"label":"TUBB4B (via enfortumab vedotin)","text":"Evidence types in cervical squamous cell carcinoma: clinical. Datasources: clinical_precedence.","source":{"label":"Open Targets: TUBB4B in cervical squamous cell carcinoma","url":"https://platform.opentargets.org/evidence/ENSG00000188229/MONDO_0006143","date":"2026-11-11T15:32:30.709Z"}},{"label":"TUBB1 (via enfortumab vedotin)","text":"Evidence types in cervical squamous cell carcinoma: clinical. Datasources: clinical_precedence.","source":{"label":"Open Targets: TUBB1 in cervical squamous cell carcinoma","url":"https://platform.opentargets.org/evidence/ENSG00000101162/MONDO_0006143","date":"2026-11-11T15:32:30.709Z"}},{"label":"PDCD1 (via pembrolizumab)","text":"Evidence types in cervical squamous cell carcinoma: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: PDCD1 in cervical squamous cell carcinoma","url":"https://platform.opentargets.org/evidence/ENSG00000188389/MONDO_0006143","date":"2026-11-11T15:32:30.709Z"}}],"pending":[{"what":"Normal-tissue expression in vital organs","source":"Human Protein Atlas (ticket 36)"},{"what":"Pan-essential in cell lines","source":"DepMap (ticket 36)"},{"what":"Approved drug on this target","source":"Drugs@FDA (ticket 30)"}]},{"n":2,"question":"Can the result be trusted?","flags":[{"id":"randomised","label":"Randomised","value":"yes","detail":"Randomised allocation","rule":"Registry allocation field","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"no","detail":"348 enrolled; each patient moves a rate by 100 ÷ 348 = 0.3 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"no","detail":"Type, incidence, severity, seriousness, and relatedness of adverse events (Dose escalation and Expansion Parts 1 to 3…; Type, incidence, and severity of laboratory abnormalities (Dose escalation and Expansion Parts 1 to 3 cohorts only); Confirmed objective response rate (ORR) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) by … (and 1 more)","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"},"context":[{"figure":"Non-OS primary endpoint: odds ratio 2.79 for a positive phase 3","dataset":"Otsuka 2021, 400 phase 3 oncology trials","years":"to 2020","caveat":"Shown with the next figure: a surrogate is easier to hit, and often a weak guide to survival."},{"figure":"52% of surrogate-to-OS correlations are low","dataset":"Prasad 2015","years":"published to 2014","caveat":"Shown with the figure above."}]},{"id":"results_overdue","label":"Results overdue","value":"no","detail":"Primary completion 2026-02-20, 8 months ago; within 12 months","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"},"context":[]}],"facts":[],"pending":[{"what":"Treated and evaluable counts, assessor, confirmed response, follow-up and data cutoff","source":"Readout extraction (ticket 32)"},{"what":"Primary endpoint changed between registry versions","source":"Registry versions in the store (ticket 32)"}]},{"n":3,"question":"What must it beat?","flags":[],"facts":[],"pending":[{"what":"Control-arm result and approved therapies for the same segment, with label links","source":"Drugs@FDA, FDA labels and readouts (tickets 30, 32)"}]},{"n":4,"question":"Too crowded, or too late?","flags":[],"facts":[{"label":"Stopped on this target","text":"5 terminated, withdrawn or suspended trials of drugs against NECTIN4. Reasons are quoted as the registry gives them on the target page.","source":{"label":"NECTIN4: what already stopped","url":"/target/ENSG00000143217#stopped","date":"2026-11-11T15:32:30.713Z"}}],"pending":[{"what":"Programs on the target by phase and months behind the leader","source":"Programs and Drugs@FDA (ticket 33)"}]},{"n":5,"question":"Can it be approved, and stay approved?","flags":[{"id":"single_country","label":"Single-country","value":"no","detail":"106 sites in 6 countries; 83 in the United States (78%)","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545?tab=locations","date":"2026-11-11T15:32:30.709Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"yes","detail":"EMEA-002299-PIP01-17 (Enfortumab vedotin, Treatment of urothelial carcinoma): W: decision granting a waiver in all age groups for all conditions or indications, 11 Apr 2018; EMEA-003104-PIP02-22 (Favezelimab;pembrolizumab, Treatment of Hodgkin lymphoma): P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s), date not given; EMEA-003063-PIP03-22 (vibostolimab;pembrolizumab, Treatment of melanoma): P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s), 27 Oct 2023; EMEA-003063-PIP02-22 (vibostolimab;pembrolizumab, Treatment of Hodgkin lymphoma): P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s), date not given; +7 more","rule":"An EMA PIP decision (agreement, modification or waiver) lists the drug as its active substance, exact name","source":{"label":"EMA data download (dated snapshot)","url":"https://www.ema.europa.eu/en/documents/report/medicines-output-paediatric_investigation_plans-output-json-report_en.json","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"eu_orphan","label":"EU orphan designation","value":"no","detail":"No EU orphan designation names enfortumab vedotin, pembrolizumab","rule":"An EU orphan designation lists the drug as its active substance (exact name) or belongs to a medicine that does; withdrawn and expired designations are listed with their status","source":{"label":"EMA data download (dated snapshot)","url":"https://www.ema.europa.eu/en/documents/report/medicines-output-orphan_designations-json-report_en.json","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"eu_authorised","label":"Authorised in the EU","value":"yes","detail":"Keytruda: authorised since 17 Jul 2015; Padcev: authorised since 13 Apr 2022","rule":"An EMA medicine record lists the drug as its active substance or INN, exact name; national-only authorisations are not in this file","source":{"label":"EMA data download (dated snapshot)","url":"https://www.ema.europa.eu/en/documents/report/medicines-output-medicines_json-report_en.json","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"fda_orphan","label":"FDA orphan designation","value":"not published","detail":"FDA's orphan designation database turns away automated requests, so this app does not read it; search it by hand at the link","rule":"Would be: an FDA orphan designation names the drug","source":{"label":"FDA orphan designations search","url":"https://www.accessdata.fda.gov/scripts/opdlisting/oopd/","date":""},"context":[]},{"id":"fda_ped_approval","label":"FDA pediatric oncology approval","value":"yes","detail":"Pembrolizumab and berahyaluronidase alfa-pmph [Keytruda Qlex], 19 Sept 2025: Treatment of adult and pediatric patients 12 years and older with unresectable or metastatic tumor mutational burden high (TMB-H) [≥10 mutations/megabase (mut/Mb)] solid tumors, as determined by an FDA-approved test, that have progressed following prior treatment and who have no satisfactory alternative treatment options; Pembrolizumab and berahyaluronidase alfa-pmph [Keytruda Qlex], 19 Sept 2025: Adjuvant treatment of adult and pediatric patients 12 years and older with Stage IIB, IIC, or III melanoma following complete resection; Pembrolizumab and berahyaluronidase alfa-pmph [Keytruda Qlex], 19 Sept 2025: Treatment of adult and pediatric patients 12 years and older with unresectable or metastatic microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) solid tumors, as determined by an FDA-approved test, that have progressed following prior treatment and who have no satisfactory alternative treatment options; +7 more","rule":"FDA's Pediatric Oncology Drug Approvals table names the drug","source":{"label":"FDA Pediatric Oncology Drug Approvals (content current as of 2026-03-03)","url":"https://www.fda.gov/about-fda/oncology-center-excellence/pediatric-oncology-drug-approvals","date":"2026-11-11T15:32:30.715Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"75 interventional studies of enfortumab vedotin, pembrolizumab include patients under 18; 44 are recruiting, not yet recruiting or active","rule":"The registry's age group includes Child (birth to 17 years), which also counts studies that set no minimum age","source":{"label":"ClinicalTrials.gov search","url":"https://clinicaltrials.gov/search?intr=%22enfortumab+vedotin%22+OR+%22pembrolizumab%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-11T15:32:30.719Z"},"context":[]}],"facts":[{"label":"Caveat","text":"Site counts are not patients per country, and trials registered only outside ClinicalTrials.gov are not covered. Where the sites are is a fact about the record, not a judgement of its quality."},{"label":"Rare pediatric disease voucher","text":"FDA, content current as of 29 Apr 2026: “As of February 3, 2026, enactment of the Consolidated Appropriations Act, 2026, the rare pediatric disease PRV program will sunset after September 30, 2029. FDA may not award any PRVs under this program after September 30, 2029.” Voucher sale prices are not shown here; they appear only as company-reported news.","source":{"label":"FDA: Rare Pediatric Disease Designation and Priority Review Voucher Programs","url":"https://www.fda.gov/industry/medical-products-rare-diseases-and-conditions/rare-pediatric-disease-designation-and-priority-review-voucher-programs","date":"2026-11-11"}}],"pending":[{"what":"Precedent approvals for target, modality and endpoint; accelerated-approval status","source":"Drugs@FDA and FDA accelerated-approval tables (ticket 30)"}]},{"n":6,"question":"Can the sponsor finish?","flags":[],"facts":[{"label":"Sponsor","text":"Astellas Pharma Global Development, Inc. (industry)","source":{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"}},{"label":"study director","text":"Changting Meng, MD, Seagen Inc.","source":{"label":"Person page","url":"/person/Changting%20Meng%2C%20MD","date":"2026-11-11T15:32:30.709Z"}},{"label":"study director","text":"Jason Lukas, MD, PhD, Seagen Inc.","source":{"label":"Person page","url":"/person/Jason%20Lukas%2C%20MD%2C%20PhD","date":"2026-11-11T15:32:30.709Z"}}],"pending":[{"what":"Filed cash, quarterly spend and the runway arithmetic","source":"SEC XBRL company facts (ticket 37)"},{"what":"Sponsor's completed vs stopped oncology trials and results-reporting record","source":"Registry, by company (ticket 37)"}]}],"limits":"Public records cannot show: sales forecasts; a probability of success for this asset; full deal terms and net prices; FDA designations and action dates before approval (shown only as company-reported); clinical holds unless the company disclosed them; manufacturing; patents on unapproved drugs; whether preclinical findings have been replicated.","sources":[{"label":"ClinicalTrials.gov NCT03288545","url":"https://clinicaltrials.gov/study/NCT03288545","date":"2026-11-11T15:32:30.709Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-11T15:32:30.709Z"},{"label":"FDA Pediatric Molecular Target List (Listed as February 2026 on the FDA Pediatric Oncology page; the file served is 9.7.22_the_relevant_molecular_target_list.xlsx, whose Summary of Changes sheet is headed 'SEPTEMBER 2022 UPDATE' (footnote date 2022-09-01))","url":"https://www.fda.gov/media/191157/download?attachment","date":"2026-11-11T07:05:03Z"}]},"source":"ClinicalTrials.gov + Open Targets","fetchedAt":"2026-11-11T15:32:30.708Z"}