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NCT07464951 · ClinicalTrials.gov registry record · Phase 1

CART123 Cells With or Without Ruxolitinib in Relapsed/Refractory Acute Myeloid Leukemia

A Phase 1 study, sponsored by Stephan Grupp MD PhD.

Recruiting
Registry status
Phase 1
Development phase
30
Enrollment target

NCT07464951: Recruiting Phase 1 study, sponsored by Stephan Grupp MD PhD.

NCT07464951 is a Phase 1 study that is actively recruiting participants, run by Stephan Grupp MD PhD. The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07464951, a Phase 1 study, is actively recruiting participants, sponsored by Stephan Grupp MD PhD.

RECRUITING
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

This study is designed to evaluate the safety and effectiveness of CART123 cells either alone or when combined with ruxolitinib in pediatric and young adult subjects with relapsed or refractory AML. Subjects will be enrolled into one of two treatment cohorts: subjects who will receive CART123 alone (Cohort A) or subjects who will receive CART123 in combination with ruxolitinib (Cohort B).

Primary Outcome

Frequency of Adverse events will be measured by evaluating the frequency and severity of treatment related adverse events following administration of CART123

Interventions

  • BIOLOGICAL Anti-CD123 LV redirected T cells (CART123)
  • DRUG Ruxolitinib (JAKAVI®)

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2026-05-14
Est. Completion 2030-05-14
Phase Phase 1
Stephan Grupp MD PhD

8 total trials

What NCT07464951 shows while recruiting

NCT07464951 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 2 interventions - of which Anti-CD123 LV redirected T cells (CART123) is the first listed.

NCT07464951 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07464951 about?

NCT07464951 is a clinical study titled "CART123 Cells With or Without Ruxolitinib in Relapsed/Refractory Acute Myeloid Leukemia". This study is designed to evaluate the safety and effectiveness of CART123 cells either alone or when combined with ruxolitinib in pediatric and young adult subjects with relapsed or refractory AML. Subjects will be enrolled into one of two treatment cohorts: subjects who will receive CART123 alone ...

What is the current status of trial NCT07464951?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2026-05-14. Estimated completion is 2030-05-14.

What interventions are being tested in trial NCT07464951?

The interventions under investigation include: Anti-CD123 LV redirected T cells (CART123) (BIOLOGICAL), Ruxolitinib (JAKAVI®) (DRUG).

Who is sponsoring clinical trial NCT07464951?

This trial is sponsored by Stephan Grupp MD PhD, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07464951's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07464951, the US trial registry maintained by the National Library of Medicine. NCT07464951 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.