A randomised, double blind, parallel, placebo controlled, drug-drug interaction study to investigate the safety, tolerability and pharmacokinetics of multiple doses of HTL0018318 given alone and in combination with donepezil at steady state in elderly volunteers.

Completed

• Conditions: Schizophrenia; Alzheimer's disease; dementia & schizophrenia; 10012272

• Registration Number: NL-OMON43229
• Lead Sponsor: Heptares Therapeutics Ltd.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 36

Inclusion Criteria

1. Elderly male or female subjects aged between 65 and 80 (inclusive) years old;
2. Healthy subjects as defined by the absence of evidence of any active or chronic disease following detailed medical and surgical history review and a complete physical examination including vital signs, 12-lead ECG, haematology, blood chemistry, and urinalysis;
3. BMI between 18 and 34 kg/m2, inclusive;
4. Able to understand the commitments of the study and to communicate effectively with the investigator and site staff;
5. If a woman of childbearing potential; must consent to and consistently and correctly use (from screening, during the entire study, and for at least 90 days after last study drug intake) double barrier contraception (a condom combined with a method of contraception with a failure rate of < 1% per year), be sexually inactive, or have a vasectomised partner; otherwise women not of childbearing potential who are defined as postmenopausal (i.e., amenorrhea for at least 1 year without an alternative medical cause), or surgically or naturally sterile;
6. If a male subject; must consent to and must consistently and correctly use (from screening, during the entire study, and for at least 90 days after last study drug intake) double barrier contraception (a condom combined with spermicide), be sexually inactive, or have a sterilised partner;
7. Able to participate and willing to give written informed consent and to comply with the study restrictions.

Exclusion Criteria

1. Legal incapacity or inability to understand or comply with the requirements of the study.
2. Clinically relevant history of abnormal physical or mental health interfering with the study as determined from the medical history review and the physical examinations obtained during the screening visit and/or at the start of the first study day for each period as judged by the investigator (including (but not limited to), neurological, psychiatric, endocrine, cardiovascular, respiratory, gastrointestinal (including history of ulcer disease or gastrointestinal bleeding), hepatic, or renal disorder).
3. A recent (<5 years) history of any chronic respiratory problems such as asthma, recurrent chest infections, chronic obstructive pulmonary disease (COPD).
4. Any disease associated with cognitive impairment, including but not limited to schizophrenia and dementia.
5. A history of epilepsy or seizures of any kind at any time (except uncomplicated infantile febrile seizures).
6. History of severe allergies, or history of an anaphylactic reaction to prescription or non-prescription drugs or food (non-active hay-fever is acceptable).
7. History of hypersensitivity to donepezil, piperidine derivatives or to the excipients used in the donepezil formulation (lactose monohydrate, maize starch, microcrystalline cellulose, hyprolose, magnesium stearate, talc, macrogol, hypromellose, titanium dioxide and yellow iron oxide).
8. History or clinical evidence of any disease and/or existence of any surgical or medical condition which might interfere with the absorption, distribution, metabolism or excretion of the study drugs.
9. Systolic blood pressure (SBP) greater than 150 or less than 90 mm Hg, and/or diastolic blood pressure (DBP) greater than 90 or less than 50 mm Hg at screening and baseline or a history of a significant period of hypertension as judged by the principal investigator.
10. Notable resting bradycardia (HR < 45 bpm) or tachycardia (HR > 100 bpm) at screening or baseline visit.
11. A QTcF > 450 (for males) or >460 (for females) or < 300 msec at resting ECG at screening and baseline visit.
12. Personal or family history of congenital long QT syndrome, *sick sinus syndrome* or other supraventricular cardiac conduction conditions such as sinoatrial or atrioventricular block or sudden death.
13. Based on the results of the 24 hour period ECG Holter monitoring during screening, potential subjects can be excluded based on the following exclusion criteria: more than 200 ventricular ectopics in 24 hours. Ventricular tachycardia (defined as being three or more successive ventricular ectopic beats at a rate of at least 120 beats per min). Second degree heart block. Sustained cardiac arrhythmias (atrial fibrillation, SVT, complete heart block). Any symptomatic arrhythmia (except isolated extra systoles).
14. Clinically relevant abnormal laboratory results (including hepatic and renal panels, complete blood count, chemistry panel and urinalysis), electrocardiogram (ECG) and vital signs, or physical findings at screening and/or at the start of the first study day for each period (as judged by the investigator). In case of uncertain or questionable results, tests performed during screening may be repeated before randomization to confirm eligibility or judged to be clinically irrelevant for healthy subjects.
15. Positive test for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody (HCV Ab),

Study & Design

• Study Type: Interventional
• Study Design: Not specified