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Long-Term Follow-up of Subjects Who Were Treated With ST-920

S

Sangamo Therapeutics

Status

Invitation-only

Conditions

Fabry Disease
Fabry Disease, Cardiac Variant

Treatments

Biological: ST-920

Study type

Observational

Funder types

Industry

Identifiers

NCT05039866
ST-920-LT01

Details and patient eligibility

About

Long-term follow-up of subjects who received ST-920 in a previous trial (ST-920-201) and completed at least 52 weeks post-infusion follow-up in their primary protocol. Enrolled subjects will be followed for a total of up to 5 years following ST-920 infusion.

Full description

Non-interventional, multi-center, long-term follow-up (LTFU) study of subjects dosed with ST-920 in the clinical study ST-920-201. All subjects dosed in the study who completed at least 52 weeks post-infusion follow-up in their primary protocol will be offered to participate. Subjects who enroll will be monitored for a total of up to 5 years following ST-920 infusion.

Enrollment

48 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects who received ST-920 therapy in a separate parent trial
  • Subjects who have consented to participate in this LTFU study.

Exclusion criteria

-This study has no exclusion criteria

Trial design

48 participants in 1 patient group

Subjects who received ST-920
Description:
Subjects who received ST-920 in a separate parent trial
Treatment:
Biological: ST-920

Trial contacts and locations

13

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Data sourced from clinicaltrials.gov

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