{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT05564390","title":"MYELOMATCH: A Screening Study to Assign People With Myeloid Cancer to a Treatment Study or Standard of Care Treatment Within myeloMATCH (MyeloMATCH Screening Trial)","sponsor":"National Cancer Institute (NCI)","phases":["PHASE2"],"status":"RECRUITING","indication":{"slug":"aml","name":"Acute myeloid leukemia"},"disease":"acute myeloid leukemia"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of TOP2A, CDA has somatic-mutation evidence in acute myeloid leukemia","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: TOP2A in acute myeloid leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000131747/MONDO_0018874","date":"2026-11-11T22:51:13.126Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for TOP2A, CDA in acute myeloid leukemia","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: TOP2A in acute myeloid leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000131747/MONDO_0018874","date":"2026-11-11T22:51:13.126Z"},"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":"yes","detail":"Haematologic","rule":"From the indication, or the registry conditions when no indication matches","source":{"label":"ClinicalTrials.gov NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"},"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":"Azacitidine, Cytarabine, Daunorubicin, Fludarabine: standard agents, not counted in these flags."},{"label":"TOP2A (via Daunorubicin Hydrochloride)","text":"Evidence types in acute myeloid leukemia: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: TOP2A in acute myeloid leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000131747/MONDO_0018874","date":"2026-11-11T22:51:13.126Z"}},{"label":"CDA (via Decitabine and Cedazuridine)","text":"Evidence types in acute myeloid leukemia: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: CDA in acute myeloid leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000158825/MONDO_0018874","date":"2026-11-11T22:51:13.126Z"}}],"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":"no","detail":"Single group","rule":"Registry allocation field","source":{"label":"ClinicalTrials.gov NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"no","detail":"2000 planned; each patient moves a rate by 100 ÷ 2000 = 0.1 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"no","detail":"Timing of treatment Substudy or Tier Advancement Pathway (TAP) assignment","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"},"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 expected 2029-05-15; not yet due","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"},"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":"728 terminated, withdrawn or suspended trials of drugs against TOP2A; 3 of the 200 most recent give no reason. Reasons are quoted as the registry gives them on the target page.","source":{"label":"TOP2A: what already stopped","url":"/target/ENSG00000131747#stopped","date":"2026-11-11T22:51:13.174Z"}}],"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":"360 sites in 3 countries; 347 in the United States (96%)","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390?tab=locations","date":"2026-11-11T22:51:13.126Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"yes","detail":"EMEA-001858-PIP02-16-M04 (daunorubicin;cytarabine, Treatment of acute myeloid leukaemia): PM: decision on the application for modification of an agreed PIP, 25 Oct 2024","rule":"An EMA PIP decision (agreement, modification or waiver) lists the drug as its active substance, exact name","source":{"label":"EMA EMEA-001858-PIP02-16-M04","url":"https://www.ema.europa.eu/en/medicines/human/paediatric-investigation-plans/emea-001858-pip02-16-m04","date":"2026-11-11T09:12:26Z"},"context":[]},{"id":"eu_orphan","label":"EU orphan designation","value":"yes","detail":"EU/3/24/2945 positive 25 Jul 2024: Treatment of primary large B-cell lymphoma of immune-privileged sites; EU/3/11/942 positive 11 Jan 2012: Treatment of acute myeloid leukaemia; EU/3/00/011 expired 30 Dec 2000: Conditioning treatment prior to haematopoietic-progenitor-cell transplantation; EU/3/08/585 positive 3 Dec 2008: Treatment of acute myeloid leukaemia","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":"Vyxeos liposomal (previously Vyxeos): authorised since 23 Aug 2018, orphan medicine; Busulfan Fresenius Kabi: authorised since 22 Sept 2014; Busilvex: withdrawn since 9 Jul 2003","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":"Busulfan [Busulfex], 13 Jan 2003: For use in combination with cyclophosphamide as a conditioning regimen prior to allogeneic hematopoietic progenitor cell transplantation for chronic myelogenous leukemia; Daunorubicin Hydrochloride, 19 Dec 1979: In combination with other approved anticancer drugs, for remission induction in acute lymphocytic leukemia of children and adults","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":"2026-11-11T22:51:13.203Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"1104 interventional studies of Busulfan, Daunorubicin Hydrochloride, Decitabine and Cedazuridine, Emavusertib include patients under 18; 217 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=%22Busulfan%22+OR+%22Daunorubicin+Hydrochloride%22+OR+%22Decitabine+and+Cedazuridine%22+OR+%22Emavusertib%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-11T22:51:13.212Z"},"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 NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"}},{"label":"principal investigator","text":"Jerald P Radich, SWOG Cancer Research Network","source":{"label":"Person page","url":"/person/Jerald%20P%20Radich?ind=aml","date":"2026-11-11T22:51:13.126Z"}}],"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 NCT05564390","url":"https://clinicaltrials.gov/study/NCT05564390","date":"2026-11-11T22:51:13.126Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-11T22:51:13.126Z"},{"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":"2026-11-11T22:51:13.115Z"}