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

C

Cartesian Therapeutics

Status and phase

Terminated
Phase 2

Conditions

Myeloma Multiple

Treatments

Biological: Descartes 08

Study type

Interventional

Funder types

Industry

Identifiers

NCT04816526
DC-08-B

Details and patient eligibility

About

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.

Enrollment

13 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients must be 18 years of age or older at the time of enrollment
  • High-risk multiple myeloma patients who complete pre-transplant induction treatment anti- myeloma drug combination (minimum 2 drugs).

Exclusion criteria

  • Patients who are pregnant or lactating.
  • Patients who have any active and uncontrolled infection. No blood cultures are necessary unless clinically indicated.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

13 participants in 1 patient group

Descartes 08
Experimental group
Treatment:
Biological: Descartes 08

Trial documents
1

Trial contacts and locations

2

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Central trial contact

Adam Chowdhury, MD, MBA

Data sourced from clinicaltrials.gov

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