CLBR001 and SWI019 in Patients With Relapsed / Refractory B-cell Malignancies
Public ClinicalTrials.gov record NCT04450069. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 1, Open-label, Dose Escalating Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the Combination of CLBR001 and SWI019 in Patients With Relapsed/Refractory B-cell Malignancies
Study identification
- NCT ID
- NCT04450069
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 1
- Lead sponsor
- Calibr, a division of Scripps Research
- Other
- Enrollment
- 18 participants
Conditions and interventions
Conditions
- Burkitt Lymphoma
- Chronic Lymphocytic Leukemia (CLL)
- Diffuse Large B Cell Lymphoma (DLBCL)
- Follicular Lymphoma (FL)
- Lymphoplasmacytic Lymphoma
- Mantle Cell Lymphoma
- Marginal Zone Lymphoma (MZL)
- Primary Mediastinal Large B Cell Lymphoma
- Relapsed/Refractory B-cell Lymphomas
- Small Lymphocytic Lymphoma (SLL)
- Transformed Follicular Lymphoma
- Waldenstrom Macroglobulinemia
Interventions
- CLBR001 and SWI019 Combination Product
Combination Product
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 13, 2020
- Primary completion
- May 5, 2024
- Completion
- May 5, 2024
- Last update posted
- Aug 19, 2024
2020 – 2024
United States locations
- U.S. sites
- 8
- U.S. states
- 7
- U.S. cities
- 8
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| City of Hope National Medical Center | Duarte | California | 91010 | — |
| University of California at San Diego | San Diego | California | 92093 | — |
| University of Chicago | Chicago | Illinois | 60637 | — |
| Masonic Cancer Center, University of Minnesota | Minneapolis | Minnesota | 55455 | — |
| Weill Cornell Medical College - New York Presbyterian Hospital | New York | New York | 10065 | — |
| Wake Forest Baptist Health | Winston-Salem | North Carolina | 27157 | — |
| Sarah Cannon Research Institute - Tennessee Oncology | Nashville | Tennessee | 37203 | — |
| Sarah Cannon Research Institute - Texas Transplant Institute | San Antonio | Texas | 78229 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT04450069, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 19, 2024 · Synced May 11, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT04450069 live on ClinicalTrials.gov.