For Healthcare Professionals

Study of SGR-1505 in Mature B-Cell Neoplasms

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About the study

The purpose of this study is to evaluate safety and tolerability and to determine the maximum tolerated dose (MTD) or maximum administered dose (MAD) and/or recommended dose (RD) of SGR-1505.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

  1. Subject must have a history of histologically or cytologically confirmed mature B-cell malignancy.
  2. Subject must have measurable or detectable disease according to the applicable disease-specific classification system and meet criteria for initiation of treatment.
  3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  4. Life expectancy ≥ 12 weeks.

EXCLUSION CRITERIA

Exclusion Criteria:

  1. The subject is in need of immediate cytoreductive therapy (unless the patient has no remaining treatment choice with potential benefit).
  2. Subject has previous invasive malignancy in the last 2 years.
  3. Subject has a known allergy to SGR-1505 or excipients of SGR-1505.
  4. Subject has symptomatic or active CNS involvement of disease.
  5. 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.
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall +15032991150Email iconEmail Study Center

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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