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DRUG:

ST316

i
Other names: ST316
Company:
Sapience Therap
Drug class:
β-catenin antagonist
over1year
A Phase 1-2 of ST316 With Selected Advanced Unresectable and Metastatic Solid Tumors (clinicaltrials.gov)
P1, N=156, Recruiting, Sapience Therapeutics | Not yet recruiting --> Recruiting
Enrollment open • Metastases
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PD-L1 (Programmed death ligand 1) • MSI (Microsatellite instability) • BRCA (Breast cancer early onset)
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PD-L1 expression • MSI-H/dMMR • BRCA mutation
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ST316
over1year
New P1 trial
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PD-L1 (Programmed death ligand 1) • MSI (Microsatellite instability) • BRCA (Breast cancer early onset)
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PD-L1 expression • MSI-H/dMMR • BRCA mutation
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ST316
over1year
Immunotherapeutic potential of ST316, a peptide antagonist of β-catenin (AACR 2023)
Anti-tumor activity was accompanied by an increase the M1/M2 ratio. Overall, these results support the immuno-therapeutic potential of ST316 and extend the application range of ST316 to include Wnt-driven cancers with poor clinical response to immune checkpoint blockade and other immunotherapeutic agents.
Late-breaking abstract • PD(L)-1 Biomarker • IO biomarker
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IFNG (Interferon, gamma) • CTNNB1 (Catenin (cadherin-associated protein), beta 1) • CD163 (CD163 Molecule) • BCL9 (BCL9 Transcription Coactivator) • CD80 (CD80 Molecule) • CD86 (CD86 Molecule)
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ST316
over2years
β-catenin antagonist peptide, ST316, attenuates Wnt-dependent oncogenic activity (AACR 2022)
ST316 (5 mg/kg) administered three times weekly by subcutaneous injection resulted in 99.6% tumor growth inhibition vs. vehicle controls (p<0.05), while a negative control peptide had no significant impact on tumor growth. These data demonstrate the potential of ST316 as a potent therapeutic candidate for Wnt/β-catenin-dependent cancers.
Late-breaking abstract
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CDK4 (Cyclin-dependent kinase 4) • CTNNB1 (Catenin (cadherin-associated protein), beta 1) • APC (APC Regulator Of WNT Signaling Pathway) • BCL9 (BCL9 Transcription Coactivator)
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APC mutation
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ST316