A Long-term Follow-up Study of Subjects Who Received CRISPR CAR T Cellular Therapies

Part of paid clinical trials in Duarte, California.

Sponsor
CRISPR Therapeutics AG
Study ID
NCT06208878
Status
Enrolling By Invitation

Conditions

  • Hematologic Malignancy
  • Solid Malignancy

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Non Interventional — OTHER
    Safety and Efficacy Assessment

Study Details

This study will evaluate the long-term safety and efficacy of CRISPR CAR T cellular therapies

Key Dates

Start date
Nov 22, 2023
Status verified
Aug 2025
Primary completion
Aug 31, 2038
Completion
Aug 31, 2038

Study Design

Enrollment
70 participants (estimated)

Arms

  • Arm: Non Interventional
    All subjects with hematological and solid malignancies who are enrolled in a parent study and were exposed to allogeneic CRISPR CAR T cellular therapy will be asked to participate in this long-term follow-up (LTFU) study.

Primary Outcome Measure

The incidence of adverse events, serious adverse events and adverse events of special interest related to CRISPR CAR T cellular therapy treatment. [ Time Frame: 15 years ]

Locations (17)

FacilityCityStateZIPSite coordinators
City of HopeDuarteCalifornia91010-
Cedars SinaiLos AngelesCalifornia90048-
StanfordStanfordCalifornia94305-
Yale New Haven HospitalNew HavenConnecticut06510-
EmoryAtlantaGeorgia30322-
University of ChicagoChicagoIllinois60637-
University of KansasWestwoodKansas66205-
University of MinnesotaMinneapolisMinnesota55455-
Washington University Saint LouisSt LouisMissouri63110-
MSKCCNew YorkNew York10065-
Montefiore Medical CenterThe BronxNew York10467-
Oregon Health and Science UniversityPortlandOregon97239-
University of PennsylvaniaPhiladelphiaPennsylvania19104-
UT SouthwesternDallasTexas75390-
MD Anderson Cancer CenterHoustonTexas77030-
Methodist Hospital-Sarah CannonSan AntonioTexas78229-
University of Utah-Huntsman Cancer InstituteSalt Lake CityUtah84112-

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