PDE5 Inhibitor for Alzheimer's Disease

Prior treatment

• Any previous enrolment in clinical trials within the last 3 months.
• Current use of narcotic medications which could affect cognition.
• Patients who have been involved in a monoclonal antibody study are excluded unless it is known that they were receiving placebo in that trial.
• Patients who are taking nitrates (see detailed list of nitrate medications in section 7.5).
• Patients who take one or more of the following medications: PDE-5 inhibitors other than tadalafil, any other investigational drugs other than tadalafil, potent inhibitors of CYP3A4 (see detailed list of drugs and consumables in section 7.5), any anti-amyloid or anti-tau therapies, any other investigational therapies for Alzheimer's disease, and any therapy that may affect Alzheimer's disease, as per the judgement of the Investigator.

Other illness

• Significant neurological disease other than MCI due to AD that may affect cognition.
• MRI/CT showing unambiguous aetiological evidence of cerebrovascular disease.
• Current presence of a clinically significant major psychiatric disorder.
• Current clinically significant systemic illness that is likely to result in deterioration of the patient's condition or affect the patient's safety during the study.
• History of epilepsy, where seizures or treatment could have contributed to cognitive impairment.
• ST Elevation Myocardial infarction within the last 1 year.
• History of cancer within the last 5 years, except localised skin cancer.
• History of alcohol or drug dependence or abuse within the last 2 years.
• Any contraindications to MRI scanning, including contraindications for the use of contrast agents, such as renal failure with the estimated glomerular filtration rate of less than 30 ml/minute or known allergy to gadolinium-based contrast agents.
• Hypersensitivity to PDE-5 inhibitors.
• Severe cardiac diseases.
• Patients with unstable angina or angina occurring during exercise or patients with symptomatic coronary artery disease.
• Patients with New York Heart Association Class 2 or greater heart failure in the last 6 months.
• Patients with uncontrolled arrhythmias, hypotension (\< 90/50 mmHg), or uncontrolled hypertension.
• Patients with a stroke within the last 6 months.
• Patients with life-threatening arrhythmias.

Lab values

• Other clinically significant abnormality on physical, neurological or laboratory examination that could compromise the study or be detrimental to the patient.
• Patients with severe renal impairment, defined by eGFR \<30 mL/min/1.73 m² or the need for dialysis, and severe hepatic Impairment or any evidence of hepatic failure.
• \[Only applicable for those agreeing to undertake an optional lumbar puncture\] Any contraindications of lumbar puncture, including raised intracranial pressure (ICP) with suspected mass effect, skin infections at the puncture site, suspected spinal epidural abscesses, and cellulitis. Individuals with bleeding disorders that may increase the risk of bleeding (e.g. known bleeding diathesis, anticoagulant therapy, thrombocytopenia, abnormal coagulation parameters like prolonged Prothrombin Time (PT), prolonged activated Partial Thromboplastin Time (aPTT), and abnormal International Normalized Ratio (INR) will be excluded from having lumbar puncture.

Other

• Any contraindications to the use of tadalafil.
• Women of childbearing potential.
• Patients with pericardial constriction.
• Any other contraindication listed in SmPC.

• Capable of giving and capacity to give informed consent.
• An individual who can act as a reliable study partner with regular contact.
• Participants must meet the clinical criteria of MCI or AD.
• Age from 50 years.
• Mini-Mental State Examination (MMSE) score of 22-28.
• Rosen Modified Hachinski Ischemic score ≤4.
• Fluency in English and evidence of adequate premorbid intellectual functioning
• Likely to be able to participate in all scheduled evaluations and complete all required tests.