Single-Ascending-Dose Study of BIIB076 in Healthy Volunteers and Participants With Alzheimer's Disease
A Phase 1, Randomized, Blinded, Placebo-Controlled, Single-Ascending-Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BIIB076 in Healthy Volunteers and Subjects With Alzheimer's Disease
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
Florida
-
Hallandale Beach, Florida, United States, 33009
- MD Clinical
-
Orlando, Florida, United States, 32806
- Bioclinica Research
-
Port Orange, Florida, United States, 32127
- Progressive Medical Research
-
-
Hawaii
-
Honolulu, Hawaii, United States, 96817
- Hawaii Pacific Neuroscience
-
-
Indiana
-
Indianapolis, Indiana, United States, 46202
- Indiana University
-
-
Missouri
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Saint Louis, Missouri, United States, 63141
- St Louis Clinical Trial
-
-
Texas
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Dallas, Texas, United States, 75247
- Covance Dallas CRU
-
-
Wisconsin
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Madison, Wisconsin, United States, 53704
- Covance CRU
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Key Inclusion Criteria - Healthy Participants
- Must be in good health as determined by the Investigator, based on medical history and Screening evaluations.
Key Inclusion Criteria - Participants with Alzheimer's Disease (AD)
- Must meet all of the clinical criteria for mild cognitive impairment (MCI) due to AD or mild AD according to the National Institutes of Aging-Alzheimer's Association [McKhann 2011], and in addition must have the following:
- Clinical Dementia Rating (CDR) global score of 0.5 for MCI due to AD or 0.5 or 1 for mild AD.
- CDR Memory Box Score of ≥0.5.
- Mini-Mental State Examination score between 18 and 30 (inclusive) at Screening.
- Must have amyloid beta positivity confirmed at Screening
Key Exclusion Criteria - Healthy Participants
- Brain MRI findings that might pose a risk to the participant, or might prevent a satisfactory MRI assessment for safety monitoring.
- History of any clinically significant cardiac, endocrine, gastrointestinal, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, or renal disease, or other major disease, as determined by the Investigator.
- Current enrollment in any other drug, biologic, device, or clinical study or treatment with an investigational drug or approved therapy for investigational use within 30 days (6 months for biologics) or 5 half-lives, whichever is longer, prior to Day-1.
- Contraindications to having a brain MRI (e.g., pacemaker; MRI-incompatible aneurysm clips, artificial heart valves, or other metal foreign body; claustrophobia that cannot be medically managed).
- Contraindications to having an Lumbar Puncture (LP).
Key Exclusion Criteria - Participants with Alzheimer's Disease (AD)
- Any medical or neurologic/neurodegenerative condition (other than AD) that, in the opinion of the Investigator, might be a contributing cause to the participant's cognitive impairment (e.g.,current history of substance abuse, uncontrolled vitamin B12 deficiency or uncontrolled thyroid disease, stroke or other cerebrovascular condition, Parkinson's disease, Lewy body dementia, or frontotemporal dementia or head trauma), or could lead to discontinuation, noncompliance with study assessments, or safety concerns.
- Diagnosis within 1 year prior to Screening and/or evidence of clinically significant (in the opinion of the Investigator) psychiatric illness including uncontrolled major depression, bipolar affective disorder, other psychiatric illness, and suicidal ideation.
- Any documented prior history of chronic schizophrenia.
- History of any clinically significant cardiac, endocrine, gastrointestinal, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary (including chronic obstructive pulmonary disease), neurologic, dermatologic, or renal disease, or other major disease, as determined by the Investigator.
- Use of any medications for the treatment of comorbid conditions that have not been stable for at least 8 weeks prior to Day -1 and/or that are not expected to remain stable for the duration of the study.
- Current enrollment or plan to enroll in any other drug, biologic, device, or clinical study or treatment with an investigational drug or approved therapy for investigational use within 30 days (6 months for biologics) or 5 half-lives, whichever is longer, prior to Day-1.
- Contraindications to having a brain MRI (e.g., pacemaker; MRI-incompatible aneurysm clips, artificial heart valves, or other metal foreign body; claustrophobia that cannot be medically managed).
- Brain MRI findings that might be a contributing cause of the participant's dementia, might pose a risk to the participant, or might prevent a satisfactory MRI assessment for safety monitoring.
- Contraindications to having an LP.
- History of, or ongoing chronic uncontrolled hypertension
- History of unstable angina, myocardial infarction, chronic heart failure (New York Heart Association Class 3 or 4), or clinically significant conduction abnormalities (e.g., unstable atrial fibrillation) within 1 year prior to Day -1.
- Medications with platelet anti-aggregant or anticoagulant properties, except the use of aspirin at a dose ≤325 mg per day.
- For participants whose eligibility for study entry will be based on cerebral Aβ positivityas determined by amyloid PET (positron emission tomography), contraindication to having a PET scan (e.g., inability to lie flat or still for the duration of the scan) or intolerance to previous PET scans (i.e. previous hypersensitivity reactions to any PET radioligand or imaging agent, failure to participate in and comply with previous PET scans).
NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Cohort HV1
|
Administered as single intravenous (IV) infusion
Administered as single IV infusion
|
|
Experimental: Cohort HV2
|
Administered as single intravenous (IV) infusion
Administered as single IV infusion
|
|
Experimental: Cohort HV3
|
Administered as single intravenous (IV) infusion
Administered as single IV infusion
|
|
Experimental: Cohort HV4
|
Administered as single intravenous (IV) infusion
Administered as single IV infusion
|
|
Experimental: Cohort HV5
|
Administered as single intravenous (IV) infusion
Administered as single IV infusion
|
|
Experimental: Cohort AD1
|
Administered as single intravenous (IV) infusion
Administered as single IV infusion
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of participants that experience Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time Frame: Baseline up to Week 20
|
Safety surveillance
|
Baseline up to Week 20
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
BIIB076 serum pharmacokinetics (PK) concentration levels
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Area under the concentration-time curve from time zero to infinity (AUCinf)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Area under the concentration-time curve from time zero to the time of the last measurable sample (AUClast)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Maximum observed concentration (Cmax)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Time to reach maximum observed concentration (Tmax)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Terminal elimination half-life (t1/2)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Clearance (CL)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
PK parameter of BIIB076: Volume of distribution (Vd)
Time Frame: Up to Week 20
|
Assessment of BIIB076 pharmacokinetics in blood
|
Up to Week 20
|
|
Number of participants with positive serum BIIB076 antibodies
Time Frame: Up to Week 20
|
Serological assessment (of anti-BIIB076 antibodies in blood)
|
Up to Week 20
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 243HV101
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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