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NCT03665155 · ClinicalTrials.gov registry record · Phase 1

First-in- Human Imaging of Multiple Myeloma Using 89Zr-DFO-daratumumab, a CD38-targeting Monoclonal Antibody

A Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
11
Enrollment target

NCT03665155: Completed Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT03665155 is a Phase 1 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 11 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03665155, a Phase 1 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
11 participants
Enrollment target

Study Summary

The purpose of this study is to test 89Zr-DFO-daratumumab, a new imaging agent, to demonstrate its safety and ability to take pictures of the myeloma.

Primary Outcome

Standardized uptake value (SUV) in various organs will be estimated from VOI analysis of clinical images and converted to activity-time curves. The areas under the activity-time curves will be derived by integration, converted to residence times, and used as input to the OLINDA/EXM dosimetry program to obtain absorbed dose estimates for normal tissues for all Phase I participants, regardless of study dose. Each participant underwent four PET/CT scans over the next 8 days, as well as blood chemis

Interventions

  • OTHER Blood draws
  • DRUG 89Zr-daratumumab
  • DEVICE PET/CT scans

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2018-09-05
Est. Completion 2020-04-20
Phase Phase 1
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT03665155 record still lists

NCT03665155 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 3 interventions - of which Blood draws is the first listed.

NCT03665155 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03665155 about?

NCT03665155 is a clinical study titled "First-in- Human Imaging of Multiple Myeloma Using 89Zr-DFO-daratumumab, a CD38-targeting Monoclonal Antibody". The purpose of this study is to test 89Zr-DFO-daratumumab, a new imaging agent, to demonstrate its safety and ability to take pictures of the myeloma.

What is the current status of trial NCT03665155?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 11 participants. The study started on 2018-09-05. Estimated completion is 2020-04-20.

What interventions are being tested in trial NCT03665155?

The interventions under investigation include: Blood draws (OTHER), 89Zr-daratumumab (DRUG), PET/CT scans (DEVICE).

Who is sponsoring clinical trial NCT03665155?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03665155's enrollment target sits among peer trials

11 1911th of 2000 higher than 88 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 NCT03665155, the US trial registry maintained by the National Library of Medicine. NCT03665155 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.