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DRUG:

abituzumab (EMD 525797)

i
Other names: EMD 525797, DI 17E6, DI17E6, EMD525797, DI-17E6, EMD-525797
Associations
Company:
EMD Serono, SFJ Pharma
Drug class:
Integrin α chain inhibitor
Related drugs:
Associations
10ms
Inside a Metastatic Fracture: Molecular Bases and New Potential Therapeutic Targets. (PubMed, Cancer Med)
This paper underscores the importance of advanced molecular biology and transcriptomics in identifying novel therapeutic targets. The integration of these biomarkers with clinical and radiological assessments using artificial intelligence tools could revolutionize the diagnostics and treatment strategies for patients with bone metastases.
Review • Journal
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ISLR (Immunoglobulin Superfamily Containing Leucine Rich Repeat) • TNFRSF11B (Tumor necrosis factor receptor superfamily member 11B)
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Cilcane (cilengitide) • abituzumab (EMD 525797) • andecaliximab (GS-5745) • volociximab (M200)
over4years
Combining bintrafusp alfa with abituzumab enhances suppression of the TGF-β signaling pathway (SITC 2021)
In vivo, the combination led to increased tumor growth inhibition of Detroit 562 xenograft tumors relative to either monotherapy, further supporting the potential of this combination. Conclusions Collectively, these preclinical findings support clinical development of bintrafusp alfa and abituzumab combination therapy to maximally suppress TGF-β signaling in the TME.
PD(L)-1 Biomarker • IO biomarker
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TGFB1 (Transforming Growth Factor Beta 1)
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bintrafusp alfa (M7824) • abituzumab (EMD 525797)