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Monoclonal Antibodies
ANX005 for Huntington's Disease
Phase 2
Waitlist Available
Led By Rajeev Kumar, MD
Research Sponsored by Annexon, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to week 36
Awards & highlights
Study Summary
This study is evaluating whether a drug may help reduce symptoms of Huntington's disease.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to week 36
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to week 36
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pharmacodynamics (PD) effects of ANX005
Pharmacokinetics (PK) of ANX005
Safety and tolerability of intravenous ANX005 administered for up to 22 weeks in subjects with, or at risk for, manifest Huntington's Disease
Other outcome measures
Exploratory effects of ANX005 on measures of efficacy
Trial Design
1Treatment groups
Experimental Treatment
Group I: ANX005Experimental Treatment1 Intervention
IV
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
ANX005
2020
Completed Phase 2
~50
Find a Location
Who is running the clinical trial?
Annexon, Inc.Lead Sponsor
12 Previous Clinical Trials
770 Total Patients Enrolled
Rajeev Kumar, MDPrincipal InvestigatorRocky Mountain Movement Disorders Center, Englewood, CO
2 Previous Clinical Trials
118 Total Patients Enrolled
Benjamin Hoehn, MDStudy DirectorAnnexon, Inc.
2 Previous Clinical Trials
127 Total Patients Enrolled
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