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Clinical Trial ● Currently Recruiting Phase I NCT07295951

A Study of 14C-Bleximenib (Radiolabeled) in Participants With Acute Leukemia

A Study of 14C-Bleximenib (Radiolabeled) in Participants With Acute Leukemia — Recruiting • Phase I • Oncology • NCT07295951.

📅 08 May 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase I
NCT ID
NCT07295951
Sponsor
Janssen Research & Development, LLC
Start
2025-11-18
ClinicaliQ Trial Snapshot
  • A Study of 14C-Bleximenib (Radiolabeled) in Participants With Acute Leukemia — Recruiting • Phase I • Oncology • NCT07295951.
  • What is being tested: Pharmacokinetic and metabolic profiling of radiolabeled bleximenib using radioactive carbon-14 tracing to determine absorption, metabolism, and excretion pathways in acute leukemia patients.
  • Patient eligibility overview: The trial enrolls adult participants with confirmed acute leukemia diagnoses who meet specific safety and organ function criteria, with detailed screening to ensure suitability for radioactive compound administration.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The purpose of this study is to assess how the body absorbs, breaks down (metabolism), and removes (excretes) radiolabeled bleximenib (a drug molecule that has been chemically bonded with a radioactive isotope which emits radiation making it easier to track in the body) in participants with acute leukemia (highly aggressive blood cancer typically characterized by large numbers of immature white blood cells in the bone marrow).

Eligibility Snapshot
  • : * Body weight greater than or equal to (>=) 40 kilograms (kg) * Relapsed or refractory (R/R) acute leukemia harboring histone-lysine N-methyltransferase 2A (KMT2A), nucleophosmin 1 (NPM1), nucleoporin 98 (NUP98) or nucleoporin 214 (NUP214) gene alterations, and has exhausted, or is ineligible for available therapeutic options * Eastern cooperative oncology group (ECOG) performance status grade of 0 or 1 * Regular bowel movements (that is [i.e.], average production of at least one stool every 2 days) * A woman of childbearing potential must have a negative highly sensitive serum beta-human chorionic gonadotropin at screening and within 48 hours prior to the first dose of study treatment

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
View Trial ↗
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