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This is a Phase 1b/2, single-arm, open-label, multi-center, clinical study of AZD0120, a CD19/BCMA dual CAR T cell therapy, to evaluate the safety, tolerability, and efficacy in adult participants with refractory Systemic Lupus Erythematosus.
The study will enrol adult participants with refractory Systemic Lupus Erythematosus (SLE) The study will be run in 2 parts;
First part is Phase 1b during which the study aims to assess safety and tolerability of AZD0120 in patients in refractory SLE cohorts
Second part is Phase 2, during which the study aims to assess safety, tolerability and efficacy of the selected dose, following Phase 1b completion, in patients with refractory SLE
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AZD0120 | Experimental | Single dose of AZD0120 |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AZD0120 | Biological | Single infusion of AZD0120 on visit DAY 1 after completing required lymphodepleting chemotherapy.. |
|
| Measure | Description | Time Frame |
|---|---|---|
| PHASE 1B: To evaluate the safety and tolerability of AZD0120 in participants with refractory systemic lupus erythematosus (SLE) | The incidence and severity of adverse events (AEs) | 2 years |
| PHASE 1B: Recommended Phase 2 Dose (RP2D) of AZD0120 in for Phase 2 | To determine the recommended phase 2 dose (RP2D) of AZD0120 | 2 years |
| PHASE 2: To evaluate the efficacy of AZD0120 in participants with refractory SLE | Proportion of participants achieving SRI-4 response | 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| PHASE 1B & 2: To evaluate the efficacy of AZD0120 in participants with refractory SLE | Proportion of participants achieving SLE Responder Index 4 (SRI-4) response over time | 2 years |
| PHASE 1B & 2: To evaluate the efficacy of AZD0120 in participants with refractory SLE |
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INCLUSION:
EXCLUSION:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| AstraZeneca Clinical Study Information Center | Contact | 1-877-240-9479 | information.center@astrazeneca.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research Site | Not yet recruiting | San Francisco | California | 94143 | United States | |
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Drug: AZD0120 Single infusion of AZD0120
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| Cyclophosphamide | Drug | Lymphodepletion - specified dose prior to receiving AZD0120 |
|
| Fludarabine | Drug | Lymphodepletion - specified dose prior to receiving AZD0120 |
|
Proportion of participants achieving remission in SLE (DORIS) remission over time |
| 2 years |
| PHASE 1B & 2: To evaluate the efficacy of AZD0120 in participants with refractory SLE | Proportion of participants achieving Lupus Low Disease Activity State (LLDAS) over time | 2 years |
| PHASE 1B & 2: To evaluate the efficacy of AZD0120 in participants with refractory SLE | Proportion of participants achieving British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) response over time | 2 years |
| PHASE 1B & 2: To evaluate the efficacy of AZD0120 in participants with refractory SLE | Time from AZD0120 infusion and time from response to first disease flare | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | The area under the concentration-time curve (AUC) from time zero (T0) to the last measurable concentration time point (AUClast) | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | Area under the blood concentration-time curve from time zero to 28 days after dosing (AUC(0-28D)) | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | The last measurable concentration of AZD0120 (Clast) | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | Maximum observed blood concentration (Cmax) | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | Terminal half-life of a drug during its elimination phase in pharmacokinetics (t1/2λz) | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | Time of the last measurable (quantifiable) concentration of a AZD0120 (Tlast) | 2 years |
| PHASE 1B & 2: To characterize the cellular kinetics of AZD0120 in participants with refractory SLE | Time of maximum observed blood concentration (Tmax) | 2 years |
| PHASE 1B & 2: To assess immunogenicity of AZD0120 | Presence of AZD0120 antibodies | 2 years |
| PHASE 1B & 2: To determine whether replication-competent lentivirus is present in participants that receive AZD0120 | Presence of replication-competent lentivirus (RCL) | 2 years |
| PHASE 2: To further characterize the safety of AZD0120 in participants with refractory SLE | Further characterization of the safety of AZD0120 by measuring the incidence and severity of Treatment Emergent Adverse Events (TEAEs) | 2 years |
| PHASE 2: To assess changes from baseline for reported health-related quality of life, overall health status | To assess changes from baseline for Changes in Lupus Quality of life (LupusQoL) | 2 years |
| PHASE 2: To assess changes from baseline for reported health-related quality of life, overall health status | To assess changes from baseline for FUNCTIONAL ASSESSMENT OF CHRONIC ILLNESS THERAPY (FACIT) | 2 years |
| Research Site |
| Not yet recruiting |
| Stanford |
| California |
| 94304-2201 |
| United States |
| Research Site | Suspended | Tampa | Florida | 33612 | United States |
| Research Site | Not yet recruiting | Atlanta | Georgia | 30322 | United States |
| Research Site | Not yet recruiting | Chicago | Illinois | 60611 | United States |
| Research Site | Withdrawn | Bethesda | Maryland | 20892 | United States |
| Research Site | Recruiting | Boston | Massachusetts | 02115 | United States |
| Research Site | Recruiting | St Louis | Missouri | 63110 | United States |
| Research Site | Recruiting | New York | New York | 10032 | United States |
| Research Site | Recruiting | Syracuse | New York | 13202-2240 | United States |
| Research Site | Recruiting | Chapel Hill | North Carolina | 27599-7280 | United States |
| Research Site | Recruiting | Charlotte | North Carolina | 28204 | United States |
| Research Site | Not yet recruiting | Richmond | Virginia | 23298 | United States |
| Research Site | Recruiting | Seattle | Washington | 98104 | United States |
| Research Site | Recruiting | Seattle | Washington | 98195 | United States |
| Research Site | Recruiting | Darlinghurst | 2010 | Australia |
| Research Site | Not yet recruiting | Melbourne | 3000 | Australia |
| Research Site | Not yet recruiting | Toronto | M5T 2S8 | Canada |
| ID | Term |
|---|---|
| D008180 | Lupus Erythematosus, Systemic |
| D008181 | Lupus Nephritis |
| ID | Term |
|---|---|
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
| D005921 | Glomerulonephritis |
| D009393 | Nephritis |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
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| ID | Term |
|---|---|
| D003520 | Cyclophosphamide |
| C024352 | fludarabine |
| ID | Term |
|---|---|
| D010752 | Phosphoramide Mustards |
| D009588 | Nitrogen Mustard Compounds |
| D009150 | Mustard Compounds |
| D006846 | Hydrocarbons, Halogenated |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D063088 | Phosphoramides |
| D009943 | Organophosphorus Compounds |
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