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A Long-term Follow-up Study in Participants Who Received CS-101

C

CorrectSequence Therapeutics

Status

Invitation-only

Conditions

Beta-Thalassemia

Treatments

Other: Safety and efficacy assessments

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT06685536
CS-101-13

Details and patient eligibility

About

This is a study to evaluate the long-term safety and efficacy of CS-101 in participants who received CS-101 in study CS -101-06 (NCT06024876),No investigational drug product will be administered in the study.

Full description

This is a study to evaluate the long-term safety and efficacy of CS-101 in participants who received CS-101 in study CS -101-06 (NCT06024876). Subjects in the CS-101-06 study will be entered into long-term follow-up of this study up to 15 years post-infusion at the completion of the last (12-month) followup visit after treatment with CS-101 Injection.

Enrollment

5 estimated patients

Sex

All

Ages

6 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants (or his or her legally appointed and authorized representative or guardian) must sign and date informed consent form (ICF) and, where applicable, an assent form
  • Participants must have received CS-101 infusion in last study

Exclusion criteria

  • There are no exclusion criteria

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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