{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT07619898","title":"PHOENIX-ECP- Extracorporeal Photopheresis for Immune-related Colitis and/or Hepatitis in Advanced Melanoma With Inadequate Response to Steroid Exposure","sponsor":"Therakos LLC","phases":["PHASE2"],"status":"NOT_YET_RECRUITING","indication":null,"disease":"colitis"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of ITGA4, ITGB7, TNF, IMPDH1, IMPDH2 has somatic-mutation evidence in colitis","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: ITGA4 in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000115232/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for ITGA4, ITGB7, TNF, IMPDH1, IMPDH2 in colitis","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: ITGA4 in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000115232/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"},"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 NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"},"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":"ITGA4 (via Vedolizumab)","text":"Evidence types in colitis: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: ITGA4 in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000115232/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"}},{"label":"ITGB7 (via Vedolizumab)","text":"Evidence types in colitis: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: ITGB7 in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000139626/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"}},{"label":"TNF (via Infliximab)","text":"Evidence types in colitis: literature, clinical; literature listed separately from human genetics. Datasources: europepmc, clinical_precedence.","source":{"label":"Open Targets: TNF in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000232810/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"}},{"label":"IMPDH1 (via Mycophenolate Mofetil)","text":"Open Targets has no association between IMPDH1 and colitis.","source":{"label":"Open Targets: IMPDH1 in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000106348/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"}},{"label":"IMPDH2 (via Mycophenolate Mofetil)","text":"Evidence types in colitis: literature; literature listed separately from human genetics. Datasources: europepmc.","source":{"label":"Open Targets: IMPDH2 in colitis","url":"https://platform.opentargets.org/evidence/ENSG00000178035/MONDO_0005292","date":"2026-11-12T04:40:51.143Z"}}],"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 NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"no","detail":"112 planned; each patient moves a rate by 100 ÷ 112 = 0.9 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"no","detail":"Proportion of Participants Who are in Steroid-free response at Week 12 for the Randomized Immune-related Adverse Even…","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"},"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 2028-12; not yet due","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"},"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":"46 terminated, withdrawn or suspended trials of drugs against ITGA4; 6 give no reason. Reasons are quoted as the registry gives them on the target page.","source":{"label":"ITGA4: what already stopped","url":"/target/ENSG00000115232#stopped","date":"2026-11-12T04:40:51.179Z"}}],"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":"not published","detail":"The record lists no sites.","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898?tab=locations","date":"2026-11-12T04:40:51.143Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"yes","detail":"EMEA-000645-PIP01-09-M09 (vedolizumab, Treatment of Crohn's disease;Treatment of ulcerative colitis): PM: decision on the application for modification of an agreed PIP, 18 Jul 2024; EMEA-000645-PIP04-20-M02 (vedolizumab, Treatment of pouchitis): PM: decision on the application for modification of an agreed PIP, 7 Sept 2023; EMEA-000645-PIP03-18 (vedolizumab, Prevention of acute graft-versus-host disease): P: decision agreeing on a investigation plan, with or without partial waiver(s) and or deferral(s), 14 Aug 2019; EMEA-000549-PIP01-09-M01 (infliximab, Ankylosing spondylitis;Juvenile idiopathic arthritis;Psoriatic arthritis;Rheumatoid arthritis;Treatment of Crohn's disease;Treatment of psoriasis;Treatment of ulcerative colitis): PM: decision on the application for modification of an agreed PIP, 5 Nov 2010; compliance positive 16 Sept 2011","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/3/26/3236 positive 20 May 2026: Treatment of Kawasaki disease; EU/3/06/374 positive 22 May 2006: Treatment of graft-versus-host disease","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":"Entyvio: authorised since 22 May 2014; Remicade: authorised since 13 Aug 1999; Inflectra: withdrawn since 10 Sept 2013; CellCept: authorised since 14 Feb 1996; +8 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":"no","detail":"FDA's table lists no pediatric approval of methoxsalen, Vedolizumab, Infliximab, Mycophenolate Mofetil","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":"2026-11-12T04:40:51.186Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"487 interventional studies of methoxsalen, Vedolizumab, Infliximab, Mycophenolate Mofetil include patients under 18; 96 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=%22methoxsalen%22+OR+%22Vedolizumab%22+OR+%22Infliximab%22+OR+%22Mycophenolate+Mofetil%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-12T04:40:51.191Z"},"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":"Therakos LLC (industry)","source":{"label":"ClinicalTrials.gov NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"}},{"label":"study director","text":"Isabelle T Seemann, Ph.D, Therakos LLC","source":{"label":"Person page","url":"/person/Isabelle%20T%20Seemann%2C%20Ph.D","date":"2026-11-12T04:40:51.143Z"}}],"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 NCT07619898","url":"https://clinicaltrials.gov/study/NCT07619898","date":"2026-11-12T04:40:51.143Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-12T04:40:51.143Z"},{"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":"2026-11-12T04:40:51.138Z"}