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Study of SGR-1505 in Mature B-Cell Neoplasms

StatusRecruiting
PhasePhase 1
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Enrollment target: 52 to 98
    • Primary and study completion dates: Mar 2026 to Nov 2027
    v19
  2. Minor Re-verified, no change to tracked fieldsv18
  3. Minor Study sites: 17 to 36v17
  4. Minor Re-verified, no change to tracked fieldsv16
  5. Minor Study sites: 16 to 17v15
Show 13 earlier versionsHide 13 earlier versions
  1. Minor Study sites: 15 to 16v14
  2. Notable Primary and study completion dates: Mar 2025 to Mar 2026v13 Show 4 more changesShow less
    • Eligibility criteria shortened, about 8 words
    • Secondary endpoints: 12 to 6
    • Study description shortened, about 6 words
    • Study arms: 2 to 1
  3. Minor Study sites: 14 to 15v12
  4. Minor Study sites: 13 to 14v11
  5. Minor Study sites: 8 to 13v10
  6. Minor Study sites: 7 to 8v9
  7. Minor Study sites: 5 to 7v8
  8. Minor Study sites: 4 to 5v7
  9. Minor Study sites: 3 to 4v6
  10. Minor Study description expanded, about 5 wordsv5
  11. Notable Primary and study completion dates: Mar 2024 to Mar 2025
    • Start date changed from estimate of Jun 2023 to Apr 10, 2023
    v4
  12. Notable Start date: Oct 2022 to Jun 2023
    • Study sites: 1 to 3
    v3
  13. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date: Sep 2022 to Oct 2022
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
2,948 trials monitored
See 180 trials at risk
703 trials monitored
See 44 trials at risk
and 3 more diseases
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.
Trial Details
NCT Number NCT05544019
Lead Sponsor Schrödinger, Inc.
Conditions
(from sponsor)
Mature B-Cell Neoplasm, Non Hodgkin Lymphoma, DLBCL, Waldenstrom Macroglobulinemia, MALT Lymphoma, Follicular Lymphoma, Pediatric-Type Follicular Lymphoma, IRF4 Gene Rearrangement +18 more
Related terms Burkitt Lymphoma, Leukemia, Lymphocytic, Chronic, B-Cell, Lymphoma, B-Cell, Marginal Zone, Lymphoma, Follicular, Lymphoma, Mantle-Cell, Lymphoma, Non-Hodgkin, Lymphoma, Primary Effusion, Plasmablastic Lymphoma, Pyloric Stenosis, Hypertrophic, Waldenstrom Macroglobulinemia
Enrollment 98 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov