Safety, Tolerability and Pharmacokinetics of CMS121, a Drug Candidate for Alzheimer's Disease, in Healthy Subjects

Inclusion Criteria: To qualify for enrollment, subjects must meet all of the following inclusion criteria: All Subjects:

• Capable of understanding the written informed consent document; willingly providesvalid, signed written informed consent; willing and able to comply with the studyschedule, requirements, and restrictions.
• Continuous non smoker who has not used nicotine containing products for at least 3months prior to the first dosing.
• Body mass index (BMI) ≥ 18.0 and ≤ 32.0 kg/m2 at the screening visit.
• In good general health, free from clinically significant medical or psychiatricillness, based on medical/surgical history, physical examination, and clinicallaboratory tests.
• All laboratory parameters (serum chemistry, hematology, coagulation, and urinalysis)are within the reference range or considered not clinically significant by the PI, atthe screening visit.
• Negative results for human immunodeficiency virus (HIV), Hepatitis B virus (HBV), andHepatitis C virus (HCV) tests (as outlined in protocol) at the screening visit.
• Female subjects must have negative results for pregnancy test at the screening visitand the first check-in and must not be lactating.
• Able to swallow multiple capsules.
• Adequate venous access in the left or right arm to allow collection of the requiredblood samples. Parts 1 (SAD) and 2 (MAD):
• Healthy, adult, male or female, 19-60 years of age, inclusive, at the screening visit.
• Females of childbearing potential .
• Females of non-childbearing potential are defined as follows:
• Individuals who have undergone one of the following sterilization proceduresat least 6 months prior to the first dosing:
• hysteroscopic sterilization;
• bilateral tubal ligation or bilateral salpingectomy;
• hysterectomy;
• bilateral oophorectomy. or
• Individuals who are postmenopausal (PMP) with amenorrhea for at least 1 yearprior to the first dosing and follicle stimulating hormone (FSH) serumlevels consistent with PMP status.
• Females of childbearing potential and male subjects must follow protocol-specifiedcontraception guidance.
• Vital signs must be within the protocol-specified ranges.
• No presence of a clinically significant ECG abnormality as judged by the PI orqualified designee and as per protocol-specified ranges. Part 3 (Elderly):
• Healthy, adult, male or female, 65-85 years of age, inclusive, at the screening visit.
• Females of childbearing potential.
• Females of non-childbearing potential are defined as follows:
• Individuals who have undergone one of the following sterilization proceduresat least 6 months prior to the first dosing:
• hysteroscopic sterilization;
• bilateral tubal ligation or bilateral salpingectomy;
• hysterectomy;
• bilateral oophorectomy. or
• Individuals who are postmenopausal (PMP) with amenorrhea for at least 1 yearprior to the first dosing and follicle stimulating hormone (FSH) serumlevels consistent with PMP status. or
• Individuals who are PMP with amenorrhea for at least 1 year prior to the first dosingand FSH serum levels consistent with PMP status.
• Females of childbearing potential and male subjects must follow protocolspecified contraception guidance.
• Vital signs must be within the protocol-specified ranges.
• QTcF interval is ≤450 msec (males) or ≤470 msec (females) and has ECG findingsconsidered normal or not clinically significant by the PI or designee at thescreening visit and prior to the first dosing. Part 4 (Food Effect):
• Healthy, adult, male or female, 19-60 years of age, inclusive, at the screening visit.
• Females of childbearing potential.
• Females of non-childbearing potential are defined as follows:
• Individuals who have undergone one of the following sterilization proceduresat least 6 months prior to the first dosing:
• hysteroscopic sterilization;
• bilateral tubal ligation or bilateral salpingectomy;
• hysterectomy;
• bilateral oophorectomy. or
• Individuals who are PMP with amenorrhea for at least 1 year prior to thefirst dosing and FSH serum levels consistent with PMP status.
• Females of childbearing potential and male subjects must follow protocol specifiedcontraception guidance.
• Vital signs must be within the protocol-specified ranges.
• QTcF interval is ≤450 msec (males) or ≤470 msec (females) and has ECG findingsconsidered normal or not clinically significant by the PI or designee at the screeningvisit and prior to the first dosing.
• Able to completely consume a standardized high-fat/high-calorie breakfast as requiredby the study protocol.

Exclusion Criteria:

• Subjects who meet any of the following criteria must be excluded from the study: All Subjects:
• Is mentally or legally incapacitated or has significant emotional problems at the timeof the screening visit or expected during the conduct of the study.
• History or presence of malignancy within the past 2 years, with the exception ofadequately treated localized skin cancer (basal cell or squamous cell carcinoma) orcarcinoma in-situ of the cervix.
• History of any illness that, in the opinion of the PI or designee, might confound theresults of the study or poses an additional risk to the subject by their participationin the study in the opinion of the PI or designee.
• Evidence of clinically relevant medical illness including cardiovascular,hematological, psychiatric, gastrointestinal, hepatic, renal, rheumatologic,autoimmune, endocrine, pulmonary, neurologic or dermatologic disorder in the opinionof the PI or designee.
• History of skin rash(es) associated with the use of any medication(s).
• Any condition (e.g., chronic diarrhea) or prior surgery (e.g., gastric bypass) thatcould interfere with drug absorption, distribution, metabolism, or excretion.
• Clinically significant surgical procedure within 90 days prior to the screening visit.
• Clinically significant acute illness or infection within 14 days prior to the firstdosing.
• History of significant drug allergies including a history of anaphylactic reaction.
• Family history of sudden death in an otherwise healthy individual.
• Positive urine cotinine at the screening visit or at first check-in.
• Excessive use of alcohol, defined as weekly intake in excess of 14 units of alcohol (1unit = 12 fluid ounces of beer, 5 fluid ounces of wine, or 1.5 fluid ounces [1 shot]of distilled spirits or liquor), within 6 months prior to the screening visit.
• Positive test result for alcohol or drugs of abuse at the screening visit or firstcheck-in, or history of alcohol and/or drug abuse within the past 2 years prior to thescreening visit.
• Heavy caffeine drinker (defined as consumption of >5 servings of caffeinated beverages [e.g., coffee, tea, cola, energy drinks] per day).
• Refusal to refrain from strenuous physical activity from screening until firstcheck-in.
• Unwillingness to avoid sun and/or phototherapy exposure for 72 hours after the lastdose of study drug.
• Has been on a diet incompatible with the on study diet, in the opinion of the PI ordesignee, within the 30 days prior to the first dosing.
• Use of any investigational drug or device within 30 days or biologics for 90 days (or 5 half-lives of the drug, whichever is the longer) prior to the first dosing, orcurrently participating in another study of an investigational drug or biologics, or amedical device.
• Loss or donation of >500 mL blood within 56 days prior to study drug administration,or donation of plasma within 30 days prior to the first dosing.
• Employee or family member of the PI, study site personnel, or Sponsor.
• Any other reason that, in the opinion of the PI, would render the subject unsuitablefor study enrollment. Parts 1 (SAD):
• History or presence of:
• risk factors for Torsade de Pointes (e.g., heart failure, cardiomyopathy, orfamily history of Long QT Syndrome or sudden unexpected cardiac death at a youngage);
• sick sinus syndrome, second or third degree atrioventricular block, myocardialinfarction, pulmonary congestion, symptomatic or significant cardiac arrhythmia,prolonged QTcF interval, or conduction abnormalities;
• ischemic heart disease, symptomatic arrhythmias, or poorly controlledhypertension.
• conditions predisposing to QT prolongation including pathological Q-wave.
• Unable to refrain from or anticipates the use of:
• any drugs, including prescription and non prescription medications, herbalremedies, or vitamin supplements beginning 14 days prior to the first dosing;
• any drugs known to be significant inducers of CYP enzymes and/or P gp, includingSt. John's Wort, for 28 days prior to the first dosing. Appropriate sources (e.g., Flockhart Table™) will be consulted to confirm lack of PK/pharmacodynamic (PD) interaction with study drug;
• any drugs that prolong the QT/QTc interval within 14 days (or 5 half-lives,whichever is longer) prior to the first dosing.
• Allergy to band aids, adhesive dressing, or medical tape.
• Glomerular filtration rate (GFR) ≤ 80 mL/min/1.73 m2, as estimated by the ChronicKidney Disease Epidemiology Collaboration (CKD-EPI) equation. Part 2 (MAD):
• History or presence of:
• risk factors for Torsade de Pointes (e.g., heart failure, cardiomyopathy, orfamily history of Long QT Syndrome or sudden unexpected cardiac death at a youngage);
• sick sinus syndrome, second or third degree atrioventricular block, myocardialinfarction, pulmonary congestion, symptomatic or significant cardiac arrhythmia,prolonged QTcF interval, or conduction abnormalities;
• ischemic heart disease, symptomatic arrhythmias, or poorly controlledhypertension.
• conditions predisposing to QT prolongation including pathological Q-wave.
• Unable to refrain from or anticipates the use of:
• any drugs, including prescription and non prescription medications, herbalremedies, or vitamin supplements beginning 14 days prior to the first dosing;
• any drugs known to be significant inducers of CYP enzymes and/or P gp, includingSt. John's Wort, for 28 days prior to the first dosing. Appropriate sources (e.g., Flockhart Table™) will be consulted to confirm lack of PK/PD interactionwith study drug;
• any drugs that prolong the QT/QTc interval within 14 days (or 5 half-lives,whichever is longer) prior to the first dosing.
• Is at risk of suicide. Has attempted suicide in the past 12 months or Is at risk ofsuicide, as determined by the PI, psychiatric interview and/or the baseline C-SSRS.
• Allergy to band aids, adhesive dressing, or medical tape.
• GFR ≤ 80 mL/min/1.73 m2, as estimated by the CKD-EPI equation. Part 3 (Elderly):
• Is at risk of suicide. Has attempted suicide in the past 12 months or Is at risk ofsuicide, as determined by the PI, psychiatric interview and/or the baseline C-SSRS.
• Unable to refrain from or anticipates the use of:
• any drugs, including prescription and non prescription medications, herbalremedies, or vitamin supplements beginning 14 days prior to the first dosing.Thyroid hormone replacement medication (refer to protocol) will be allowed;
• any drugs known to be significant inducers of CYP enzymes and/or P gp, includingSt. John's Wort, for 28 days prior to the first dosing. Appropriate sources (e.g., Flockhart Table™) will be consulted to confirm lack of PK/PD interactionwith study drug.
• GFR ≤ 70 mL/min/1.73 m2, as estimated by the CKD-EPI equation. Part 4 (Food Effect):
• Is lactose intolerant.
• Unable to refrain from or anticipates the use of:
• any drugs, including prescription and non prescription medications, herbalremedies, or vitamin supplements beginning 14 days prior to the first dosing;
• any drugs known to be significant inducers of CYP enzymes and/or P gp, includingSt. John's Wort, for 28 days prior to the first dosing. Appropriate sources (e.g., Flockhart Table™) will be consulted to confirm lack of PK/PD interactionwith study drug.
• GFR ≤ 80 mL/min/1.73 m2, as estimated by the CKD-EPI equation.