Neurogenetic Pharmaceuticals (NGP) 555 in Healthy Young Volunteers (Single-ascending Dose)

Completed · Phase 1

Conditions studied: Alzheimer's Disease

In brief

NGP 555 is a small molecule preventative therapy aimed at reducing Alzheimer's disease amyloid buildup by targeting Abeta 42 production.

Key facts

Study ID

NCT02534480

Run by

NeuroGenetic Pharmaceuticals Inc

People needed

40

Starts

2015-03-01

Expected to finish

2015-11-01

Last updated by the study team

2016-01-13

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male and female volunteers aged 18-55 yrs and in good health as determined by medical history, physical examination, clinical laboratory studies, electrocardiograms (ECGs), vital signs, and investigator judgment
• Volunteer voluntarily agrees to participate in this study and signs an Institutional Review Board (IRB)-approved informed consent prior to performing any of the screening procedures
• Female volunteers who are of child-bearing potential must agree to use a medically acceptable method of contraception (e.g., abstinence, an intrauterine device.
• Male healthy volunteers willing to use barrier contraception.
• Body mass index (BMI) of ≥ 18.0 kg/m2 and ≤ 32.0 kg/m2

You may not qualify if…

• History of seizure disorder, symptomatic seizures (not including a history of simple febrile seizures in childhood) or any past or present medical condition which, in the opinion of the investigator has the potential to reduce seizure threshold (e.g., history of head trauma or concussion, previous alcohol abuse, substance abuse)
• Any concurrent disease or condition that, in the opinion of the Investigator, would make the volunteer unsuitable for participation in the clinical study
• History of alcohol and/or illicit drug abuse within two years of entry
• Any psychiatric diagnosis or symptoms (e.g., hallucinations, major depression, anxiety or delusions)
• History of cerebrovascular events or non-vasovagal related loss of consciousness
• History of cardiac arrhythmias, ischemic heart disease or cerebrovascular disease
• Hepatic impairment as defined by >1.3 times the upper limit of normal ranges of serum liver enzymes
• Renal impairment as defined by abnormal ranges of serum creatinine.
• Presence of clinically significant orthostatic hypotension (fall in systolic blood pressure of >20 mmHg or fall diastolic blood pressure of > 10 mmHg; and increase in heart rate by > 20 beats per minute [bpm])
• Corrected QT interval (QTc) values of > 450 ms for males and > 470 ms for females.
• Volunteers with abnormally low serum B12, folate or abnormal thyroid function tests
• Positive Screening test for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody, or human immunodeficiency virus (HIV) antibody
• Positive urine test for alcohol or drugs
• Suicidal ideation
• Female volunteers that are breastfeeding or female volunteers with a positive urine pregnancy test
• Clinically significant deviation from normal in physical examination, vital signs or clinical laboratory tests
• Volunteer is unable to understand the protocol requirements, instructions and study-related restrictions, the nature, scope and possible consequences of the clinical study

Where it is running

• WCCT — Cypress, California, United States

Full record on ClinicalTrials.gov

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