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NCT04816526 · ClinicalTrials.gov registry record · Phase 2

Descartes-08 Consolidation Treatment in Patients With High-Risk Multiple Myeloma High-Risk Multiple Myeloma Who Have Residual Disease After Induction Therapy

A Phase 2 study, sponsored by Cartesian Therapeutics.

Terminated
Registry status
Phase 2
Development phase
13
Enrollment target

NCT04816526: Clinical Trial Phase 2 study, sponsored by Cartesian Therapeutics.

NCT04816526 is a Phase 2 study that was terminated before completion, run by Cartesian Therapeutics. The registered enrollment target is 13 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04816526, a Phase 2 study, was terminated before completion, sponsored by Cartesian Therapeutics.

TERMINATED
Registry status
Phase 2
Development phase
13 participants
Enrollment target

Study Summary

To assess Minimal Residual Disease (MRD)-negative Complete Response (sCR) rate after consolidation treatment with Descartes-08 in patients with high-risk myeloma who have residual disease following induction therapy.

Primary Outcome

Per IMWG 2016 Response Criteria Summary sCR: Complete response (CR) plus a normal free light chain ratio and no clonal cells in bone marrow (by immunohistochemistry). The FLC ratio must be Kappa/Lambda ≤ 4:1 or ≥ 1:2 after counting at least 100 plasma cells. CR: Negative immunofixation in serum and urine, disappearance of any soft tissue plasmacytomas, and \<5% plasma cells in bone marrow. VGPR: Serum M-protein detectable by immunofixation (not on electrophoresis) or a ≥ 90% reduction in M-prote

Interventions

  • BIOLOGICAL Descartes 08

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2021-12-01
Est. Completion 2022-11-03
Phase Phase 2
Cartesian Therapeutics

12 total trials

Why NCT04816526 stopped before completion

NCT04816526 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which Descartes 08 is the first listed.

NCT04816526 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04816526 about?

NCT04816526 is a clinical study titled "Descartes-08 Consolidation Treatment in Patients With High-Risk Multiple Myeloma High-Risk Multiple Myeloma Who Have Residual Disease After Induction Therapy". To assess Minimal Residual Disease (MRD)-negative Complete Response (sCR) rate after consolidation treatment with Descartes-08 in patients with high-risk myeloma who have residual disease following induction therapy.

What is the current status of trial NCT04816526?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 13 participants. The study started on 2021-12-01. Estimated completion is 2022-11-03.

What interventions are being tested in trial NCT04816526?

The interventions under investigation include: Descartes 08 (BIOLOGICAL).

Who is sponsoring clinical trial NCT04816526?

This trial is sponsored by Cartesian Therapeutics, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04816526's enrollment target sits among peer trials

13 1947th of 2000 higher than 53 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT04816526, the US trial registry maintained by the National Library of Medicine. NCT04816526 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.