Could a simple capsule beat chemo fatigue? new trial aims to find out

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Female patients aged ≥ 18 years and ≤ 65 years who are willing to voluntarily provide consent for participation in the study. * Patients with confirmed triple negative metastatic breast cancer who are planned or scheduled to receive standard chemotherapy treatment for at least 4 to 6 cycles respectively. * Patients must have a confirmed diagnosis of triple negative metastatic breast cancer as per standard guidelines. * Patients must have at least one tumour lesion with ≥ 1cm in one dimension that is radiographically apparent on computed tomography (CT) or magnetic resonance imaging (MRI). * Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 at screening. * The patient has stable haemoglobin (≥ 9 g/dL) throughout the screening. * Life expectancy ≥ 6 months, as per the investigator's judgment. * Patients with co-morbidities or medical conditions including Type 2 diabetes mellitus (DM) and hypertension who are deemed stable by the investigator can be included in the study. * At screening, patients with stable fatigue, newly developed fatigue, or worsening fatigue scores as assessed by the Brief Fatigue Inventory (BFI) should be included. Exclusion Criteria: * Patients who have any untreated reversible medical condition which may cause fatigue (e.g. major metabolic or electrolyte disturbance, active infection, endocrine abnormalities) as per the investigator's clinical judgment. * Patients with an inability to understand local language(s) for scales used for evaluations i.e. VAFS, BFI AND SF-36. * Patients who have received concurrent stimulant medication (e.g. dextroamphetamine or methylphenidate) during the screening period or any medication which may interfere with the study drug. * Patients with any delay in chemotherapy treatment such that the screening period extends beyond 21 days. * Patients with known central nervous system (CNS) involvement. * Patients with any serious, uncontrolled, non-malignant medical or psychiatric disorder, or any other medical condition which in the opinion of the investigator, may affect the patient's safety or study participation and conduct. * Female patients who are pregnant or breastfeeding. * Patients with known hepatitis C virus, hepatitis B virus, HIV infection. * Patients who have nausea and vomiting or any gastrointestinal disorder that is severe enough to interfere with study drug absorption in the opinion of the investigator. * Patients with uncontrolled pain, who in the opinion of the investigator are not eligible for the study. * Patients with known hypersensitivity or intolerance of rosmarinic acid, caffeic acid, and other related phenolic compounds as well as excipients in the Nuvastatic® 300 mg or placebo treatment. * Patients with planned therapy or treatment with another investigational agent. * Previous exposure to any investigational agent within 4 weeks prior to screening, or planned administration of an investigational agent, other than as specified by this protocol, during the study period.