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Clinical Trial Details — Status: Available

Administrative data

NCT number NCT05930223
Other study ID # VAL1221-LEAP-01
Secondary ID
Status Available
Phase
First received
Last updated

Study information

Verified date June 2023
Source Parasail, LLC
Contact Dustin Armstrong, PhD
Phone (617) 462-3084
Email dustin.armstrong@parasailllc.com
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

Only qualified physicians treating a Lafora Disease patient may request VAL-1221 Expanded Access treatment under the Parasail Lafora Expanded Access Protocol (LEAP). According to FDA guidance, this protocol can enroll up to 10 patients. However, individual patient inclusion will ultimately be dependent on protocol eligibility, site geography, treatment requirements, and available supply of the investigational therapy. Inquiring physicians can submit a request by contacting the Central Contact personnel listed below in Contacts/Locations.


Recruitment information / eligibility

Status Available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 12 Years to 28 Years
Eligibility Inclusion Criteria: - Documented genetic diagnosis of Lafora Disease (LD) based on likely pathogenic or pathogenic variants in both alleles of either the EPM2A or the EPM2B gene - Mid-stage in evolution of LD between 12 and 28 years of age - Able and willing to comply with the protocol, including travel to Protocol Center, procedures, measurements and visits, including: - Adequately supportive psychosocial circumstances, in the opinion of the Investigator - Caregiver/trial partner committed to facilitate patient's involvement in the study who is reliable, competent, at least 18 years of age Exclusion Criteria: - Have any other conditions, which, in the opinion of the Investigator or Sponsor would make the participant unsafe for inclusion or could interfere with the participant participating in or completing the protocol

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
VAL-1221
VAL-1221 20mg/kg intravenous (IV) infusion every other week

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Parasail, LLC
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