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1000 Titel
  • Comprehensive biomarker and modeling approach to support dose finding for BI 836880, a VEGF/Ang-2 inhibitor
1000 Autor/in
  1. Keller, Sascha |
  2. Kunz, Ulrich |
  3. Schmid, Ulrike |
  4. Beusmans, Jack |
  5. Büchert, Martin |
  6. He, Min |
  7. Jayadeva, Girish |
  8. Le Tourneau, Christophe |
  9. Luedtke, Doreen |
  10. Niessen, Heiko G. |
  11. Oum’hamed, Zohra |
  12. Pleiner, Sina |
  13. Wang, Xiaoning |
  14. Graeser, Ralph |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-10-14
1000 Erschienen in
1000 Quellenangabe
  • 22(1):934
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12967-024-05612-x |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11476076/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!BI 836880 is a humanized bispecific nanobody® that binds to and blocks vascular endothelial growth factor (VEGF) and angiopoietin-2 (Ang-2). A comprehensive biomarker and modeling approach is presented here that supported dose finding for BI 836880.!##!Methods!#!Two Phase I dose-escalation studies (1336.1 [NCT02674152], 1336.6 [NCT02689505]) assessed BI 836880 in adults with confirmed locally advanced or metastatic solid tumors, refractory to standard therapy or for which standard therapy was not reliably effective. Two dosing schedules were investigated, 3 weeks (q3w) or once weekly (qw), starting at a dose of 40 mg. In a comprehensive biomarker approach, soluble pharmacodynamic markers (free and total plasma VEGF-A and Ang-2), as well as circulating angiogenic factors (soluble VEGF3, soluble Tie2 and placenta growth factor, amongst others) were analyzed to assess target engagement in peripheral blood for q3w doses. A Population based pharmacokinetics/pharmacodynamics (PopPK/PD) model was built using the limited Phase I dataset to support dose finding by simulations. In order to demonstrate drug activity in the tumor, dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) was applied.!##!Results!#!DCE-MRI scans supported target engagement in the tumor. Free VEGF-A was depleted at all doses, whereas free Ang-2 decreased dose-dependently, reaching depletion in most patients from 360 mg q3w onwards. While total VEGF-A levels increased in a dose-dependent manner, reaching saturation at 360 mg q3w, total Ang-2 levels increased, but did not plateau. Angiogenic biomarkers showed changes from doses ≥ 360 mg q3w. PopPK/PD modeling showed that doses ≥ 360 mg q3w led to > 90% inhibition of free Ang-2 at steady-state in most patients. By increasing the dose to ≥ 500 mg q3w, > 90% of patients are expected to achieve this level.!##!Conclusions!#!The comprehensive analyses of multiple target engagement markers support BI 836880 720 mg q3w as a biologically relevant monotherapy dose schedule.!##!Trial registration!#!NCT02674152 and NCT02689505.
1000 Sacherschließung
lokal Angiogenesis Inhibitors/pharmacology [MeSH]
lokal Vascular Endothelial Growth Factor A/blood [MeSH]
lokal Biomarkers
lokal Aged [MeSH]
lokal Models, Biological [MeSH]
lokal Male [MeSH]
lokal VEGF
lokal Ang-2
lokal Dose-Response Relationship, Drug [MeSH]
lokal Female [MeSH]
lokal Angiopoietin-2/blood [MeSH]
lokal Adult [MeSH]
lokal Angiogenesis Inhibitors/administration
lokal Biomarkers/blood [MeSH]
lokal Humans [MeSH]
lokal BI 836880
lokal Middle Aged [MeSH]
lokal Pharmacodynamics
lokal Angiopoietin-2/antagonists
lokal Disease Biomarkers
lokal Biomarkers, Tumor/blood [MeSH]
lokal Neoplasms/drug therapy [MeSH]
lokal Pharmacokinetics
lokal Research
lokal Angiogenesis Inhibitors/therapeutic use [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/S2VsbGVyLCBTYXNjaGE=|https://frl.publisso.de/adhoc/uri/S3VueiwgVWxyaWNo|https://frl.publisso.de/adhoc/uri/U2NobWlkLCBVbHJpa2U=|https://frl.publisso.de/adhoc/uri/QmV1c21hbnMsIEphY2s=|https://frl.publisso.de/adhoc/uri/QsO8Y2hlcnQsIE1hcnRpbg==|https://frl.publisso.de/adhoc/uri/SGUsIE1pbg==|https://frl.publisso.de/adhoc/uri/SmF5YWRldmEsIEdpcmlzaA==|https://frl.publisso.de/adhoc/uri/TGUgVG91cm5lYXUsIENocmlzdG9waGU=|https://frl.publisso.de/adhoc/uri/THVlZHRrZSwgRG9yZWVu|https://frl.publisso.de/adhoc/uri/Tmllc3NlbiwgSGVpa28gRy4=|https://frl.publisso.de/adhoc/uri/T3Vt4oCZaGFtZWQsIFpvaHJh|https://frl.publisso.de/adhoc/uri/UGxlaW5lciwgU2luYQ==|https://frl.publisso.de/adhoc/uri/V2FuZywgWGlhb25pbmc=|https://orcid.org/0000-0002-3600-2484
1000 Hinweis
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1000 Label
1000 Förderer
  1. Boehringer Ingelheim |
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1000 Dateien
1000 Förderung
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    1000 Förderer Boehringer Ingelheim |
    1000 Förderprogramm -
    1000 Fördernummer -
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1000 Erstellt am 2025-07-05T12:30:20.765+0200
1000 Erstellt von 322
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1000 Zuletzt bearbeitet 2025-08-15T20:39:00.006+0200
1000 Objekt bearb. Fri Aug 15 20:39:00 CEST 2025
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