Study of SGR-1505 in Mature B-Cell Neoplasms
About the study
Who can take part
INCLUSION CRITERIA
Inclusion Criteria:
- Subject must have a history of histologically or cytologically confirmed mature B-cell malignancy.
- Subject must have measurable or detectable disease according to the applicable disease-specific classification system and meet criteria for initiation of treatment.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Life expectancy ≥ 12 weeks.
EXCLUSION CRITERIA
Exclusion Criteria:
- The subject is in need of immediate cytoreductive therapy (unless the patient has no remaining treatment choice with potential benefit).
- Subject has previous invasive malignancy in the last 2 years.
- Subject has a known allergy to SGR-1505 or excipients of SGR-1505.
- Subject has symptomatic or active CNS involvement of disease.
- Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding that would place the participant at increased risk to the use of an investigational drug.
Study Locations
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How to Apply
Study Details
Contition
Mature B-Cell Neoplasm,Non Hodgkin Lymphoma,DLBCL,Waldenstrom Macroglobulinemia,MALT Lymphoma,Follicular Lymphoma,Pediatric-Type Follicular Lymphoma,IRF4 Gene Rearrangement,EBV-Positive DLBCL, Nos,Burkitt Lymphoma,Plasmablastic Lymphoma,High-grade B-cell Lymphoma,Primary Cutaneous Follicle Center Lymphoma,Primary Effusion Lymphoma,Mantle Cell Lymphoma,DLBCL Germinal Center B-Cell Type,Primary Mediastinal Large B Cell Lymphoma,T-Cell/Histiocyte Rich Lymphoma,ALK-Positive Large B-Cell Lymphoma,Primary Cutaneous Diffuse Large B-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Chronic Lymphocytic Leukemia,Nodal Marginal Zone Lymphoma,HHV8-Positive DLBCL, Nos,Lymphoplasmacytic Lymphoma,Duodenal-Type Follicular Lymphoma
Age
18+
Phase
PHASE1
Participants Needed
52
Est. Completion Date
Mar 31, 2026
Treatment Type
INTERVENTIONAL
Sponsor
Schrödinger, Inc.
ClinicalTrials.gov NCT Identifier
NCT05544019
Study Number
SGR-1505-101
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