Phase III Study of Capivasertib + Paclitaxel versus Placebo + Paclitaxel as First line Treatment for Patients with Locally Advanced or Metastatic Triple-negative Breast Cancer

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• Prior treatment with any of the following treatments listed below. Patients are not eligible to enter the study if they have received any of the medications specified below or are unable to meet the cautions and restrictions : - Chemotherapy in the (neo)adjuvant setting within 6 months from the end of chemotherapy to the date of randomization; taxane chemotherapy in the (neo)adjuvant setting within 12 months from the end of chemotherapy to the start of randomization - Prior systematic therapy for inoperable locally advanced or metastatic disease - - AKT, PI3K, and/or mTOR inhibitors - Capivasertib in the present study (ie, any dosing with capivasertib due to previous participation in this study) - Any other immunotherapy, immunosuppressant medication (other than corticosteroids) or anticancer agents within 3 weeks of the first dose of study treatment. A longer washout may be required for drugs with a long half-life (eg, biologics) as agreed by the sponsor - Potent inhibitors or inducers of CYP3A4 within 2 weeks prior to the first dose of study treatment (3 weeks for St John's wort), or drug that are sensitive to CYP3A4, within 1 week prior to the first dose of study treatment
• Radiotherapy with a wide field of radiation within 4 weeks before the first dose of study treatment (capivasertib/placebo)
• Pre-existing sensory or motor polyneuropathy ≥grade 2 according to NCI CTCAE v5 4. With the exception of alopecia, any unresolved toxicities from prior therapy greater than CTCAE grade 1 at the time of starting study treatment
• With the exception of alopecia, any unresolved toxicities from prior therapy greater than CTCAE grade 1 at the time of starting study treatment
• Any of the following cardiac criteria at screening: -Mean resting corrected QT interval (QTc) >470 msec obtained from 3 consecutive ECGs -Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG (eg, complete left bundle branch block, third degree heart block) - Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalaemia, potential for Torsades de Pointes, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years of age or any concomitant medication known to prolong the QT interval - Experience of any of the following procedures or conditions in the preceding 6 months: coronary artery bypass graft, angioplasty, vascular stent, myocardial infarction, angina pectoris, congestive heart failure New York Heart Association (NYHA) grade ≥2 -Uncontrolled hypotension – SBP <90 mmHg and/or DBP <50 mmHg - Cardiac ejection fraction outside institutional range of normal or <50% (whichever is higher) as measured by echocardiogram (or multiplegated acquisition [MUGA] scan if an echocardiogram cannot be performed or is inconclusive).
• Clinically significant abnormalities of glucose metabolism as defined by any of the following at screening: -Patients with diabetes mellitus type I or diabetes mellitus type II requiring insulin treatment -HbA1c ≥8.0% (63.9 mmol/mol)