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WVE-HDSNP2-002

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Sponsored by WAVE Life Sciences.

WVE-HDSNP2-002 was discontinued on March 29, 2021. For more information please click here.

WVE-HDSNP2-002 is an open-label extension (OLE) study to evaluate the safety, tolerability, PK, PD, and clinical effects of WVE-120102 in adult patients with early manifest HD who carry a targeted single nucleotide polymorphism, rs362331 (SNP2). To participate in the study, patients must have completed the Phase 1b/2a clinical study WVE-HDSNP2-001.

Status
Study Closed – Not Recruiting

Formal Name 

A Multicenter, Open-label Extension Study to Evaluate the Safety, Pharmacodynamics, and Clinical Effects of WVE-120102 in Patients With Huntington’s Disease

Study Type
Interventional (Clinical Trial)

Purpose
WVE-HDSNP2-002 is an open-label extension (OLE) study to evaluate the safety, tolerability, PK, PD, and clinical effects of WVE-120102 in adult patients with early manifest HD who carry a targeted single nucleotide polymorphism, rs362331 (SNP2). To participate in the study, patients must have completed the Phase 1b/2a clinical study WVE-HDSNP2-001.

Canadian Locations:

Edmonton, AB

Location: University of Alberta
Edmonton, Alberta, Canada, T6G 2B7
Status: By invitation only

Toronto, ON

Location: Centre For Movement Disorders
Toronto, Ontario, Canada, M3B 2S7
Status: By invitation only

Montréal, QC

Location: Centre Hospitalier de l’Universite de Montreal
Montreal, Quebec, Canada, H2X019
Status: By invitation only

Ages Eligible for Study: Child, Adult, Older Adult

Sexes Eligible for Study: All

Accepts Healthy Volunteers: No

Inclusion Criteria

  • Patient successfully completed the Phase 1b/2a study with WVE-120101, WVE-HDSNP1-001.

Exclusion Criteria  (eligibility that would exclude you from this study)

  • Received an investigational drug other than WVE-120101, including an investigational oligonucleotide, within the past 1 year or 5 half-lives of the drug, whichever is longer.
  • Inability to undergo brain MRI (with or without sedation).
  • Clinically significant medical finding on the physical examination other than HD that, in the judgment of the Investigator, will make the patient unsuitable for participation in and/or completion of the study procedures.

Source

ClinicalTrials.gov

For more detailed information on this study and others and for the most recent updates, please go to clinicaltrials.gov. ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world.

 

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