A Phase 1, Randomized, Placebo-controlled Study With a Double Blind Period With Open-label Extension Period to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ALN-5288 in Adult Patients With Alzheimer
What is this Study about?
The purpose of this study is to:Evaluate the safety and tolerability of intrathecal (IT) ALN-5288 in patients with Alzheimer's Disease (AD) and Evaluate the pharmacodynamic (PD) and pharmacokinetic (PK) effects of ALN-5288 after dose administration
What Will Happen in This Study?
Study drug or placebo will be administered intrathecally.
Planned duration of treatment is 32 months.
Who is Eligible to Participate in this Study?
Male or female participants aged 40 to 80 years of age
Has mild cognitive impairment (MCI) or dementia due to AD
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