Drug intelligence / Profile preview

ipatasertib + atezolizumab + docetaxel

Development stage
Discontinued
Lead developer
Roche
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral (ipatasertib), Intravenous (atezolizumab), Intravenous (docetaxel)
01

Overview

This is a **combination regimen** comprising three active agents: - **Ipatasertib** is a potent and selective pan-AKT inhibitor (small molecule), targeting the AKT pathway involved in cell survival, proliferation, and therapy resistance in cancer[4][5]. - **Atezolizumab** is a monoclonal antibody immune checkpoint inhibitor targeting Programmed Death-Ligand 1 (PD-L1), intended to activate anti-tumor immune responses[5]. - **Docetaxel** is a taxane-class cytotoxic anti-neoplastic agent inhibiting microtubule depolymerization, resulting in cell cycle arrest and apoptosis[1]. This combination has been investigated in Phase 1 trials for **metastatic castration-resistant prostate cancer (mCRPC),** as well as advanced breast cancer (notably triple-negative breast cancer, TNBC), where it seeks to leverage synergy between targeted AKT inhibition, immune checkpoint blockade, and cytotoxic chemotherapy[1][5]. The development status for prostate cancer is terminated[1]; there is no evidence of ongoing late-phase trials for breast cancer specifically with docetaxel in combination with ipatasertib and atezolizumab, though related taxanes (paclitaxel, nab-paclitaxel) have been studied extensively[5].

Brand names
atezolizumab (Tecentriq)docetaxel (Taxotere)
Other names
ipatasertib + atezolizumab + docetaxel
02

Targets

RPS6KB1 (Ribosomal protein S6 kinase beta-1)PKG (cGMP-dependent protein kinase I alpha)AKT2 (Rac-beta serine/threonine-protein kinase)CD274 (Programmed cell death protein 1 ligand 1)AKT1 (Proto-oncogene serine/threonine-protein kinase Akt1)TUBB (Tubulin (alpha and beta subunits))

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