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ABBVAbbVieSigning up patients

A Study to Assess Adverse Events and Change in Disease Activity of Oral Surzetoclax Alone or in Combination With Subcutaneous and/or Oral Antimyeloma Agents in Adult Participants With Multiple Myeloma (MM)

Multiple Myeloma

0Calmworry score, out of 100

No strong warning signs right now. The score counts warning signs; it is not a prediction.

Why this score

No warning signs right now. That's why the score is 0.

Score over time

Stage
Phase 1/2
Patients
325 (planned)
Started
Jul 23, 2025
Main results expected
Dec 2030
Fully finished
Dec 2030
Results posted
not yet

What counts as success

The trial's main goal(s), called the “primary outcome.”

  • Dose-Limiting Toxicities (DLT)s of ABBV-453

    Measured over: Up to Approximately 45 Months

  • Number of Participants with Adverse Events (AE)s

    Measured over: Up to Approximately 4.5 Years

Changes Tremor has spotted

No changes since Tremor started watching this trial.
Show details (technical version)

Score inputs

  • none

Raw record changes

  • none yet

Trial ID NCT06953960 · record last updated 2026-10-27 · checked 2026-11-09 15:47 UTC

See the official record on ClinicalTrials.gov (NCT06953960) ↗