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TER-2013 is an investigational drug currently undergoing a Phase 1/2, open-label, multicenter clinical trial. This first-in-human study is evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and anti-tumor activity of TER-2013 in patients with advanced solid tumors that harbor alterations in the AKT/PI3K/PTEN pathway. The drug is being assessed both as a monotherapy and in combination with fulvestrant, with the trial structured into a dose escalation part and a dose expansion part to determine the maximum tolerated/administered dose and preliminary clinical activity.
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