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Transcriptomics and Epigenetics Analysis in Drug-Resistance of Multiple Myeloma (TEDROMM)

R

Regina Elena Cancer Institute

Status

Enrolling

Conditions

Multiple Myeloma

Treatments

Other: ChIP-seq, NGS, ATAC-seq

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Multiple Myeloma (MM) is the more common hematological neoplastic disease second only to Hodgkin lymphoma. In MM patients, mutated genes are mainly KRAS (23%), NRAS (20%), FAM46C (11%), DIS3 (11%) e TP53 (8%). Epigenetics studies suggested that Changes in histone modifications and DNA methylation pattern, as well as non-coding RNAs (miRNAs) expression are involved in MM development. In particular, it has been shown that the aberrant expression of different miRNAs could discriminate healthy from ill patients. Unfortunately, the main critical issue for an effective treatment of MM is the intrinsic or acquired resistance to pharmacological treatments, due also to a plasmacellular clonal heterogeneity.

The prospective study will involve a patient cohort with MGUS, MM smouldering and MM, with the aim to characterize different transcriptional and epigenetic features, also including miRNAs, among MM cells susceptible or resistant to conventional therapies. The final goal is to identify new prognostic and predictive biomarkers that could be used as therapeutic tools to improve clinical targeted therapies.

Enrollment

200 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Compare Transcriptomics and epigenetic profile

Exclusion criteria

  • No exclusion criteria

Trial design

200 participants in 3 patient groups

MGUS
Treatment:
Other: ChIP-seq, NGS, ATAC-seq
MM smouldering
Treatment:
Other: ChIP-seq, NGS, ATAC-seq
Syntomatic MM
Treatment:
Other: ChIP-seq, NGS, ATAC-seq

Trial contacts and locations

2

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Central trial contact

Maurizio Fanciulli, PhD

Data sourced from clinicaltrials.gov

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