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NCT06547112 · ClinicalTrials.gov registry record · Phase 1

A Pharmacodynamic Study of the Apheresis Product of Multiple Myeloma Patients Undergoing Quad-induction Followed by Motixafortide + G-CSF Mobilization

A Phase 1 study, sponsored by Washington University School of Medicine.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT06547112: Completed Phase 1 study, sponsored by Washington University School of Medicine.

NCT06547112 is a Phase 1 study that has completed, run by Washington University School of Medicine. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06547112, a Phase 1 study, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

This study includes extended CD34+ profiling on the apheresis product of multiple myeloma patients undergoing standard-of-care quad-induction followed by motixafortide + G-CSF mobilization, and in addition, assesses the pharmacodynamics (PD) of motixafortide following "standard" (\~12 hours) vs "early" (\~16 hours) dosing. The investigators hypothesize that quad-induction may alter the stem cell subsets within the mobilized graft. The investigators further hypothesize that standard and early dosing strategies will result in comparable mobilization and stem cell collection rates.

Interventions

  • DRUG G-CSF
  • DRUG Motixafortide

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-10-31
Est. Completion 2025-08-19
Phase Phase 1

What the finished NCT06547112 record still lists

NCT06547112 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 2 interventions - of which G-CSF is the first listed.

NCT06547112 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06547112 about?

NCT06547112 is a clinical study titled "A Pharmacodynamic Study of the Apheresis Product of Multiple Myeloma Patients Undergoing Quad-induction Followed by Motixafortide + G-CSF Mobilization". This study includes extended CD34+ profiling on the apheresis product of multiple myeloma patients undergoing standard-of-care quad-induction followed by motixafortide + G-CSF mobilization, and in addition, assesses the pharmacodynamics (PD) of motixafortide following "standard" (\~12 hours) vs "ear...

What is the current status of trial NCT06547112?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2024-10-31. Estimated completion is 2025-08-19.

What interventions are being tested in trial NCT06547112?

The interventions under investigation include: G-CSF (DRUG), Motixafortide (DRUG).

Who is sponsoring clinical trial NCT06547112?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06547112's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 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 NCT06547112, the US trial registry maintained by the National Library of Medicine. NCT06547112 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.