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This is an open-label, multicenter, Phase 1/2 study evaluating the safety and efficacy of CTX112â„¢ in subjects with relapsed or refractory B-cell malignancies.
This is an open-label, multi-center Phase 1/2 study of CTX112 in subjects with relapsed/refractory B cell malignancies. CTX112 is an is allogeneic CD19-directed chimeric antigen receptor (CAR) T cell immunotherapy comprised of allogeneic T cells that are genetically modified ex vivo using CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats/ CRISPR associated protein 9) gene editing components (single guide RNA and Cas9 nuclease).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CTX112 | Experimental | Administered by IV infusion following lymphodepleting chemotherapy. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CTX112 | Biological | CTX112 (CD19-directed T-cell immunotherapy comprised of allogeneic T cells genetically modified ex vivo using CRISPR-Cas9 gene editing components) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Phase 1 (Dose Escalation): Incidence of adverse events, defined as dose-limiting toxicities | From CTX112 infusion up to 28 days post-infusion | |
| Phase 2 (Cohort Expansion): Objective response rate | From CTX112 infusion up to 60 months post-infusion |
| Measure | Description | Time Frame |
|---|---|---|
| Duration of Response | Duration of Response (DOR) will only be reported for subjects who have had CR/PR events | From date of first objective response of complete response (CR)/partial response (PR) until date of disease progression or death due to any cause, assessed up to 60 months |
| Duration of Clinical Benefit (DOCB) |
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Key Inclusion Criteria:
Key Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Clinical Trials | Contact | +1 (877) 214-4634 | MedicalAffairs@crisprtx.com |
| Name | Affiliation | Role |
|---|---|---|
| Melanie Allen, M.Sc. | CRISPR Therapeutics | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Kansas | Recruiting | Westwood | Kansas | 66205 | United States | |
| Washington University |
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| From date of first objective response of CR/PR until the relapse or death that followed the last response, assessed up to 60 months |
| Progression Free Survival | From date of CTX112 infusion until date of disease progression or death due to any cause, assessed up to 60 months |
| Overall Survival | From date of CTX112 infusion until date of death due to any cause, assessed up to 60 months |
| Recruiting |
| St Louis |
| Missouri |
| 63110 |
| United States |
| SCRI | Recruiting | San Antonio | Texas | 78229 | United States |
| University of Utah | Recruiting | Salt Lake City | Utah | 84112 | United States |
| Royal Prince Alfred | Recruiting | Camperdown | New South Wales | 2050 | Australia |
| Alfred Health | Recruiting | Melbourne | Victoria | 3004 | Australia |
| Sir Charles Gairdner Hospital | Recruiting | Nedlands | Western Australia | 6009 | Australia |
| ID | Term |
|---|---|
| D016393 | Lymphoma, B-Cell |
| D008228 | Lymphoma, Non-Hodgkin |
| D015451 | Leukemia, Lymphocytic, Chronic, B-Cell |
| D008224 | Lymphoma, Follicular |
| D020522 | Lymphoma, Mantle-Cell |
| D018442 | Lymphoma, B-Cell, Marginal Zone |
| D008223 | Lymphoma |
| ID | Term |
|---|---|
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D015448 | Leukemia, B-Cell |
| D007945 | Leukemia, Lymphoid |
| D007938 | Leukemia |
| D006402 | Hematologic Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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