{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT03779854","title":"Naive T Cell Depletion for Preventing Chronic Graft-versus-Host Disease in Children and Young Adults With Blood Cancers Undergoing Donor Stem Cell Transplant","sponsor":"Fred Hutchinson Cancer Center","phases":["PHASE2"],"status":"ACTIVE_NOT_RECRUITING","indication":{"slug":"pediatric-all","name":"Childhood acute lymphoblastic leukemia"},"disease":"childhood acute lymphoblastic leukemia"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of FKBP1A has somatic-mutation evidence in childhood acute lymphoblastic leukemia","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: FKBP1A in childhood acute lymphoblastic leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000088832/MONDO_0000870","date":"2026-11-11T21:25:45.931Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for FKBP1A in childhood acute lymphoblastic 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: FKBP1A in childhood acute lymphoblastic leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000088832/MONDO_0000870","date":"2026-11-11T21:25:45.931Z"},"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 NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"},"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":"Fludarabine, Cyclophosphamide, Methotrexate: standard agents, not counted in these flags."},{"label":"FKBP1A (via Tacrolimus)","text":"Open Targets has no association between FKBP1A and childhood acute lymphoblastic leukemia.","source":{"label":"Open Targets: FKBP1A in childhood acute lymphoblastic leukemia","url":"https://platform.opentargets.org/evidence/ENSG00000088832/MONDO_0000870","date":"2026-11-11T21:25:45.931Z"}}],"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 NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"no","detail":"45 enrolled; each patient moves a rate by 100 ÷ 45 = 2.2 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"no","detail":"Feasibility achievement; Engraftment of neutrophils by day 28 (Feasibility); Current-graft versus host disease (GVHD)-free, relapse-free survival (Randomized Controlled Trial [RCT])","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"},"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 2027-08-31; not yet due","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"},"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":"578 terminated, withdrawn or suspended trials of drugs against FKBP1A; 8 of the 200 most recent give no reason. Reasons are quoted as the registry gives them on the target page.","source":{"label":"FKBP1A: what already stopped","url":"/target/ENSG00000088832#stopped","date":"2026-11-11T21:25:45.945Z"}}],"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":"yes","detail":"All 9 sites in United States","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854?tab=locations","date":"2026-11-11T21:25:45.931Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"yes","detail":"EMA/PE/0000232771 (tacrolimus, Treatment of vernal keratoconjunctivitis): P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s), 21 Mar 2025; EMEA-001642-PIP02-20 (tacrolimus, Prevention of solid organ transplant rejection;Treatment of solid organ transplant rejection): P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s), 17 Mar 2021","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/3/06/424 withdrawn 29 Jan 2007: Conditioning treatment prior to haematopoietic-progenitor-cell transplantation; EU/3/17/1912 positive 23 Aug 2017: Treatment of pulmonary arterial hypertension; EU/3/00/011 expired 30 Dec 2000: Conditioning treatment prior to haematopoietic-progenitor-cell transplantation","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":"Advagraf: authorised since 23 Apr 2007; Thiotepa Riemser: authorised since 26 Mar 2021; Tepadina: authorised since 15 Mar 2010; Protopic: authorised since 27 Feb 2002; +6 more","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","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":"2026-11-11T21:25:45.963Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"924 interventional studies of Thiotepa, Busulfan, Tacrolimus include patients under 18; 176 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=%22Thiotepa%22+OR+%22Busulfan%22+OR+%22Tacrolimus%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-11T21:25:45.971Z"},"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":"Fred Hutchinson Cancer Center (academic or other)","source":{"label":"ClinicalTrials.gov NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"}},{"label":"principal investigator","text":"Marie Bleakley, Fred Hutch/University of Washington Cancer Consortium","source":{"label":"Person page","url":"/person/Marie%20Bleakley?ind=pediatric-all","date":"2026-11-11T21:25:45.931Z"}}],"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 NCT03779854","url":"https://clinicaltrials.gov/study/NCT03779854","date":"2026-11-11T21:25:45.931Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-11T21:25:45.931Z"},{"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":"2026-11-11T21:25:45.896Z"}