^
2years
A Safety and Preliminary Efficacy Study of SBT6290 Alone and in Combination With PD-(L)1 Inhibitors in Select Advanced Solid Tumors (clinicaltrials.gov)
P1/2, N=0, Withdrawn, Silverback Therapeutics | N=225 --> 0 | Trial completion date: May 2025 --> Mar 2022 | Recruiting --> Withdrawn | Trial primary completion date: Jan 2025 --> Mar 2022
Enrollment change • Trial completion date • Trial withdrawal • Trial primary completion date • Combination therapy
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HER-2 (Human epidermal growth factor receptor 2) • NECTIN4 (Nectin Cell Adhesion Molecule 4)
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HER-2 negative • NECTIN4 expression
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Keytruda (pembrolizumab) • SBT6290
2years
Enrollment open • Combination therapy
|
HER-2 (Human epidermal growth factor receptor 2) • NECTIN4 (Nectin Cell Adhesion Molecule 4)
|
HER-2 negative • NECTIN4 expression
|
Keytruda (pembrolizumab) • SBT6290
over2years
New P1/2 trial • Combination therapy
|
HER-2 (Human epidermal growth factor receptor 2) • NECTIN4 (Nectin Cell Adhesion Molecule 4)
|
HER-2 negative • NECTIN4 expression
|
Keytruda (pembrolizumab) • SBT6290
3years
[VIRTUAL] SBT6290, a systemically administered Nectin4-directed TLR8 ImmunoTAC™ product candidate, is designed for tumor-localized activation of myeloid cells (AACR 2021)
Systemic administration of a SBT6290 surrogate in mice bearing Nectin4-expressing tumors results in intra-tumoral myeloid and T cell activation and increased overall survival. The preclinical data described here demonstrate the potential for SBT6290 to drive anti-tumor responses and support continued preclinical development of SBT6290 for Nectin4-expressing tumors.
IO biomarker
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TIGIT (T Cell Immunoreceptor With Ig And ITIM Domains 2) • NECTIN4 (Nectin Cell Adhesion Molecule 4) • TLR8 (Toll Like Receptor 8)
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NECTIN4 expression
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SBT6290