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vistusertib
- Development stage
- Phase 2
- Lead developer
- AstraZeneca
- Modality
- Small Molecules
- Administration
- Oral
01
Overview
Vistusertib is an orally bioavailable small molecule inhibitor of the mammalian target of rapamycin (mTOR), specifically acting as a dual inhibitor of both mTORC1 and mTORC2 complexes. By inhibiting mTOR, a serine/threonine kinase involved in the PI3K/Akt/mTOR signaling pathway, vistusertib can induce tumor cell apoptosis and decrease tumor cell proliferation. It was developed for potential antineoplastic activity across various cancers, including advanced gastric adenocarcinoma, breast cancer, ovarian cancer, lung cancer, renal carcinoma, diffuse large B-cell lymphoma, meningioma, and others. Vistusertib has demonstrated blood-brain barrier penetration and has been evaluated in combination with other therapies such as paclitaxel or aromatase inhibitors[1][2][3][4][6][7].
- Brand names
- vistusertib
- Other names
- vistusertib [INN]
02
Targets
mTOR (Mammalian target of rapamycin kinase)
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