{"ok":true,"data":{"subject":{"kind":"trial","nctId":"NCT05590377","title":"A Study of Modakafusp Alfa Together With Daratumumab Adults With Relapsed or Refractory Multiple Myeloma","sponsor":"Teva Branded Pharmaceutical Products R&D LLC","phases":["PHASE1","PHASE2"],"status":"TERMINATED","indication":{"slug":"myeloma","name":"Multiple myeloma"},"disease":"plasma cell myeloma"},"rows":[{"n":1,"question":"Is the biology right?","flags":[{"id":"somatic_driver","label":"Somatic driver evidence","value":"no","detail":"None of CD38 has somatic-mutation evidence in plasma cell myeloma","rule":"Open Targets has somatic-mutation evidence for the target in this cancer","source":{"label":"Open Targets: CD38 in plasma cell myeloma","url":"https://platform.opentargets.org/evidence/ENSG00000004468/MONDO_0009693","date":"2026-11-11T22:29:17.933Z"},"context":[]},{"id":"human_genetic","label":"Human genetic evidence","value":"no","detail":"No germline or somatic evidence for CD38 in plasma cell myeloma","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: CD38 in plasma cell myeloma","url":"https://platform.opentargets.org/evidence/ENSG00000004468/MONDO_0009693","date":"2026-11-11T22:29:17.933Z"},"context":[]},{"id":"pediatric_target","label":"Pediatric target","value":"yes","detail":"CD38 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 NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377","date":"2026-11-11T22:29:17.933Z"},"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":"CD38 (via Daratumumab)","text":"Evidence types in plasma cell myeloma: literature, clinical; literature listed separately from human genetics. Datasources: clinical_precedence, europepmc.","source":{"label":"Open Targets: CD38 in plasma cell myeloma","url":"https://platform.opentargets.org/evidence/ENSG00000004468/MONDO_0009693","date":"2026-11-11T22:29:17.933Z"}}],"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 NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377","date":"2026-11-11T22:29:17.933Z"},"context":[]},{"id":"small_denominator","label":"Small denominator","value":"yes","detail":"15 enrolled; each patient moves a rate by 100 ÷ 15 = 6.7 points","rule":"Enrolment under 30; the arithmetic is shown, not a benchmark","source":{"label":"ClinicalTrials.gov NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377","date":"2026-11-11T22:29:17.933Z"},"context":[]},{"id":"primary_os","label":"Primary endpoint is overall survival","value":"no","detail":"Phase 1: Number of Participants With Dose Limiting Toxicities (DLT); Phase 1: Number of Participants Reporting One or More TEAEs and Per Severity; Phase 2a: Overall Response Rate (ORR)","rule":"A registered primary outcome measure names overall survival","source":{"label":"ClinicalTrials.gov NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377","date":"2026-11-11T22:29:17.933Z"},"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":"Results posted 2025-08-06","rule":"Primary completion (actual) more than 12 months ago and no results posted to the registry","source":{"label":"ClinicalTrials.gov NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377?tab=results","date":"2026-11-11T22:29:17.933Z"},"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":"75 terminated, withdrawn or suspended trials of drugs against CD38. Reasons are quoted as the registry gives them on the target page.","source":{"label":"CD38: what already stopped","url":"/target/ENSG00000004468#stopped","date":"2026-11-11T22:29:17.948Z"}}],"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":"27 sites in 7 countries; 13 in the United States (48%)","rule":"All listed sites are in one country; the share of US sites is shown","source":{"label":"ClinicalTrials.gov NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377?tab=locations","date":"2026-11-11T22:29:17.933Z"},"context":[]},{"id":"eu_pip","label":"EU paediatric investigation plan","value":"yes","detail":"EMEA-002152-PIP01-17-M04 (daratumumab, Treatment of lymphoid malignancies (except mature B-cell neoplasms)): PM: decision on the application for modification of an agreed PIP, 13 Sept 2024; compliance positive 13 Dec 2024; EMEA-003217-PIP01-22 (modakafusp alfa, Treatment of Multiple Myeloma): W: decision granting a waiver in all age groups for all conditions or indications, 11 Aug 2022; EMEA-002152-PIP03-19 (daratumumab, Treatment of systemic light chain amyloidosis): W: decision granting a waiver in all age groups for all conditions or indications, 18 Mar 2020; EMEA-002152-PIP02-17-M01 (daratumumab, Treatment of lymphoid malignancies (except mature B-cell neoplasms)): PM: decision on the application for modification of an agreed PIP, 12 Jun 2019","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/3/18/2020 withdrawn 25 May 2018: Treatment of AL amyloidosis; EU/3/13/1153 expired 17 Jul 2013: Treatment of plasma-cell myeloma","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":"Darzalex: authorised since 20 May 2016","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 EPAR Darzalex","url":"https://www.ema.europa.eu/en/medicines/human/EPAR/darzalex","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 Modakafusp Alfa, Daratumumab","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":"2026-11-11T22:29:17.964Z"},"context":[]},{"id":"studies_under_18","label":"Registered studies open to children","value":"yes","detail":"23 interventional studies of Modakafusp Alfa, Daratumumab include patients under 18; 15 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=%22Modakafusp+Alfa%22+OR+%22Daratumumab%22&aggFilters=ages%3Achild%2CstudyType%3Aint","date":"2026-11-11T22:29:17.977Z"},"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":"Teva Branded Pharmaceutical Products R&D LLC (industry)","source":{"label":"ClinicalTrials.gov NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377","date":"2026-11-11T22:29:17.933Z"}}],"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 NCT05590377","url":"https://clinicaltrials.gov/study/NCT05590377","date":"2026-11-11T22:29:17.933Z"},{"label":"Open Targets Platform","url":"https://platform.opentargets.org","date":"2026-11-11T22:29:17.933Z"},{"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":"2026-11-11T22:29:17.927Z"}