RecruitingPhase 1NCT06435910

Engineered Dendritic Cell Vaccines for Multiple Myeloma

Engineered Dendritic Cell Vaccines for Remission Maintenance in Multiple Myeloma Patients


Sponsor

Shenzhen Geno-Immune Medical Institute

Enrollment

10 participants

Start Date

May 11, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine the feasibility, safety, and efficacy of dendritic cell (DC) vaccines in the treatment of multiple myeloma (MM) or plasmacytoma based on immune-modified DC vaccines (DCvac). This approach is aimed to achieve prolonged maintenance of remission in multiple myeloma or plasmacytoma patients.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria5

  • Male and female subjects with multiple myeloma or plasmacytoma
  • Very good partial or complete remission (CR) after prior combination therapies.
  • Expected survival \> 12 weeks
  • Adequate venous access for blood withdrawal or apheresis, and no other contraindications for blood withdrawal
  • Voluntary informed consent is given with willingness to continue follow up

Exclusion Criteria4

  • Pregnant or lactating women
  • Uncontrolled active infection
  • HIV or active hepatitis B or hepatitis C infection
  • Concurrent use of systemic steroids; the use of inhaled steroids is not exclusionary

Interventions

BIOLOGICALDC vaccines

Antigen-presenting and immune modifying DCvacs to treat MM


Locations(2)

Shenzhen Geno-immune Medical Institute

Shenzhen, Guangdong, China

The Regional Hematology Center in Clinical Hospital No. 2 of the Ministry of Health

Vladivostok, Russia

View Full Details on ClinicalTrials.gov

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NCT06435910