{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT02152982","title":"Temozolomide With or Without Veliparib in Treating Patients With Newly Diagnosed Glioblastoma Multiforme","sponsor":"National Cancer Institute (NCI)","phases":["PHASE2","PHASE3"],"status":"ACTIVE_NOT_RECRUITING","indication":{"slug":"gbm","name":"Glioblastoma"},"disease":"glioblastoma"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of PARP1, PARP3, PARP2 has somatic-mutation evidence in glioblastoma","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: PARP1 in glioblastoma","url":"https://platform.opentargets.org/evidence/ENSG00000143799/MONDO_0018177","date":"2026-11-11T19:27:15.274Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for PARP1, PARP3, PARP2 in glioblastoma","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: PARP1 in glioblastoma","url":"https://platform.opentargets.org/evidence/ENSG00000143799/MONDO_0018177","date":"2026-11-11T19:27:15.274Z"},"context":[]},{"id":"pediatric_target","label":"Pediatric target","value":"no","detail":"Not 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 NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982","date":"2026-11-11T19:27:15.274Z"},"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":"Background therapy","text":"Temozolomide: standard agents, not counted in these flags."},{"label":"PARP1 (via Veliparib)","text":"Evidence types in glioblastoma: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: PARP1 in glioblastoma","url":"https://platform.opentargets.org/evidence/ENSG00000143799/MONDO_0018177","date":"2026-11-11T19:27:15.274Z"}},{"label":"PARP3 (via Veliparib)","text":"Evidence types in glioblastoma: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: PARP3 in glioblastoma","url":"https://platform.opentargets.org/evidence/ENSG00000041880/MONDO_0018177","date":"2026-11-11T19:27:15.274Z"}},{"label":"PARP2 (via Veliparib)","text":"Evidence types in glioblastoma: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: PARP2 in glioblastoma","url":"https://platform.opentargets.org/evidence/ENSG00000129484/MONDO_0018177","date":"2026-11-11T19:27:15.274Z"}}],"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 NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982","date":"2026-11-11T19:27:15.274Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"no","detail":"447 enrolled; each patient moves a rate by 100 ÷ 447 = 0.2 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982","date":"2026-11-11T19:27:15.274Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"yes","detail":"Overall Survival (OS)","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982","date":"2026-11-11T19:27:15.274Z"},"context":[]},{"id":"results_overdue","label":"Results overdue","value":"no","detail":"Results posted 2023-04-04","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982?tab=results","date":"2026-11-11T19:27:15.274Z"},"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":"164 terminated, withdrawn or suspended trials of drugs against PARP1; 9 give no reason. Reasons are quoted as the registry gives them on the target page.","source":{"label":"PARP1: what already stopped","url":"/target/ENSG00000143799#stopped","date":"2026-11-11T19:27:15.292Z"}}],"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":"391 sites in 2 countries; 390 in the United States (100%)","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982?tab=locations","date":"2026-11-11T19:27:15.274Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"yes","detail":"EMEA-000499-PIP02-10-M01 (veliparib, Treatment of high-grade glioma): PM: decision on the application for modification of an agreed PIP, 4 Dec 2020; EMEA-000499-PIP05-18 (veliparib, Treatment of fallopian tube cancer;Treatment of ovarian cancer;Treatment of peritoneal carcinoma): W: decision granting a waiver in all age groups for all conditions or indications, 14 Aug 2018; EMEA-000499-PIP04-17 (veliparib, Treatment of lung carcinoma (small cell and non-small cell carcinoma)): W: decision granting a waiver in all age groups for all conditions or indications, 16 Mar 2018; EMEA-000499-PIP03-17 (veliparib, Treatment of breast cancer): W: decision granting a waiver in all age groups for all conditions or indications, 31 Oct 2017","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":"yes","detail":"EU/3/10/830 withdrawn 17 Dec 2010: Treatment of ovarian cancer","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 EU/3/10/830","url":"https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu-3-10-830","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"eu_authorised","label":"Authorised in the EU","value":"no","detail":"EMA lists no centrally authorised medicine of Veliparib","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":"no","detail":"FDA's table lists no pediatric approval of Veliparib","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":"2026-11-11T19:27:15.314Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"4 interventional studies of Veliparib include patients under 18; 1 is 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=%22Veliparib%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-11T19:27:15.325Z"},"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":"National Cancer Institute (NCI) (academic or other)","source":{"label":"ClinicalTrials.gov NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982","date":"2026-11-11T19:27:15.274Z"}},{"label":"principal investigator","text":"Jann N Sarkaria, Alliance for Clinical Trials in Oncology","source":{"label":"Person page","url":"/person/Jann%20N%20Sarkaria?ind=gbm","date":"2026-11-11T19:27:15.274Z"}}],"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 NCT02152982","url":"https://clinicaltrials.gov/study/NCT02152982","date":"2026-11-11T19:27:15.274Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-11T19:27:15.274Z"},{"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":"2026-11-11T19:27:15.268Z"}