Summary

Eligibility
for people ages 18-70 (full criteria)
Location
at San Francisco, California and other locations
Dates
study started
estimated completion
Principal Investigator
by Cameron Dietiker

Description

Summary

The primary objective of this study is to evaluate the safety and tolerability of multiple ascending doses of BIIB132 administered via intrathecal (IT) injection to participants with spinocerebellar ataxia type 3 (SCA3). The secondary objective of this study is to characterize the multiple-dose pharmacokinetics (PK) of BIIB132 administered via IT injection to participants with SCA3.

Official Title

A Phase 1, Blinded, Randomized, Placebo-controlled Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Multiple Ascending Doses of BIIB132 Administered Intrathecally to Adults With Spinocerebellar Ataxia 3

Details

BIIB132 is an investigational anti-sense oligonucleotide developed to target ataxin-3 (ATXN3) pre-messenger ribonucleic acid (pre-mRNA). Preclinical studies have shown that lowering of ATXN3 protein is associated with decreased progression of SCA3-like disease. This trial consists of a blinded 12 week study period with a 26 week follow up period to evaluate the safety and tolerability of intrathecal BIIB132 and to assess the effect on treatment response biomarkers in symptomatic SCA3 participants.

Keywords

Spinocerebellar Ataxia Type 3 Ataxia Cerebellar Ataxia Spinocerebellar Ataxias Spinocerebellar Degenerations Machado-Joseph Disease BIIB132

Eligibility

You can join if…

Open to people ages 18-70

  • Diagnosis of SCA3 with CAG repeats ≥60 in ATXN3 gene.
  • Symptomatic ataxia with a screening Scale for Assessment and Rating of Ataxia (SARA) score 3 to 15 (still ambulatory) and a minimum SARA gait subscore of 1.
  • Able to ambulate 8 m independently without any assistive device.
  • Treatment naïve or on a stable dose of symptomatic therapy for a minimum of 4 weeks prior to screening.

You CAN'T join if...

  • Unstable psychiatric illness or untreated major depression within 90 days before screening.
  • History or screening magnetic resonance imaging (MRI) results show evidence of structural abnormalities that could contribute to the participant's clinical state other than findings typical of SCA3 or any finding that might pose a risk to the participant.
  • MRI brain findings of prior cerebellar stroke or clinical stroke within 12 months before screening.
  • History of brain surgery regardless of purpose.
  • Any contraindications to undergoing brain MRI.
  • History of, or ongoing, malignant disease, (with the exception of basal cell carcinomas and squamous cell carcinomas that have been completely excised and considered cured at least 12 months prior to screening). Participants with cancers in remission for longer than 5 years may be included.
  • History of epilepsy or the occurrence of seizures within 3 years prior to screening.
  • Evidence of untreated/unstable thyroid disease.
  • Poorly controlled diabetes mellitus.
  • History of alcohol or substance abuse within the past year prior to screening.
  • Use of off-label drugs for ataxia within 4 weeks prior to screening.
  • Prior enrollment in any interventional clinical study in which an investigational treatment or approved therapy for investigational use is administered within 5 half-lives or 3 months, whichever is longer, prior to the screening visit.
  • Any antiplatelet [except for aspirin up to 100 milligrams per day (mg/day)] or anticoagulant medication that cannot be safely interrupted for an lumbar puncture (LP) procedure.
  • Any contraindications to LP procedures.
  • Participants who are pregnant or currently breastfeeding and those intending to become pregnant during the study.
  • Prior enrollment in any interventional clinical study in which an investigational treatment or approved therapy for investigational use is administered within 3 months prior to screening visit.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

Locations

  • University of California San Francisco accepting new patients
    San Francisco California 94143 United States
  • University of California - Los Angeles accepting new patients
    Los Angeles California 90035 United States

Lead Scientist at UCSF

  • Cameron Dietiker
    Cameron Dietiker, M.D. is an Assistant Clinical Professor in the UCSF Department of Neurology where she treats people with movement disorders in the Movement Disorders and Neuromodulation Center at the Mt. Zion campus as well as the Memory and Aging Center at the Mission Bay campus. She is a graduate of UCSD where she obtained a degree in psychology and a minor in organic chemistry.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Biogen
ID
NCT05160558
Phase
Phase 1 Spinocerebellar Ataxia Research Study
Study Type
Interventional
Participants
Expecting 48 study participants
Last Updated