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A Study of ARV-393 in Relapsed/Refractory Non-Hodgkin Lymphoma.

StatusRecruiting
PhasePhase 1
Started
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Record History

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  1. Minor Study sites: 19 to 21v18
  2. Minor Enrollment increased: 255 → 329 participants
    • Study sites: 17 to 19
    • Eligibility criteria expanded, about 51 words
    v17
  3. Notable Enrollment target: 112 to 255v16 Show 7 more changesShow less
    • Primary and study completion dates: Dec 2025 to Mar 2028
    • Primary endpoints revised (4)
    • Interventions: ARV-393 (Drug) to ARV-393 (Drug), Glofitamab (Drug)
    • Eligibility criteria expanded, about 173 words
    • Secondary endpoints: 9 to 10
    • Study description expanded, about 64 words
    • Study arms: 1 to 4
  4. Minor Study sites: 16 to 17v15
  5. Minor Study sites: 15 to 16v14
Show 12 earlier versionsHide 12 earlier versions
  1. Minor Site details revised at 1 of 15 sitesv13
  2. Minor Site details revised at 3 of 15 sitesv12
  3. Minor Study sites: 14 to 15v11
  4. Minor Site details revised at 1 of 14 sitesv10
  5. Minor Site details revised at 1 of 14 sitesv9
  6. Minor Site details revised at 3 of 14 sitesv8
  7. Minor Site details revised at 1 of 14 sitesv7
  8. Minor Study sites: 12 to 14v6
  9. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date: Aug 12, 2024 to Sep 5, 2024
    • Site details revised at 12 of 12 sites
    v5
  10. Minor Re-verified, no change to tracked fieldsv4
  11. Minor Study sites: 1 to 12v3
  12. Notable Start date: Apr 30, 2024 to Aug 12, 2024
    • Trial status: Recruiting to Not Yet Recruiting
    • Study sites: 8 to 1
    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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This clinical trial is studying the safety and potential anti-tumor activity of an investigational drug called ARV-393 in patients diagnosed with advanced Relapsed/Refractory non-Hodgkin's lymphoma (R/R NHL) to determine if ARV-393 may be a possible treatment option. ARV-393 is thought to work by breaking down a protein present in many types of non-Hodgkins lymphomas, which may prevent, slow or stop tumor growth. This is the first time ARV-393 will be used by people. The investigational drug will be given as an oral tablet.
Trial Details
NCT Number NCT06393738
Lead Sponsor Arvinas Inc.
Conditions
(from sponsor)
Relapsed/Refractory (R/R) Mature B Cell Non Hodgkin Lymphoma (NHL), Relapsed/Refractory (R/R) Angioimmunoblastic T-cell Lymphoma (AITL)
Related terms Immunoblastic Lymphadenopathy, Lymphoma, B-Cell, Lymphoma, Non-Hodgkin, Recurrence
Enrollment 329 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov