Frequency of GBA and PSAP Gene Variants in Patients with MM or MGUS
Official title: Determine the Frequency of Variants in the GBA/PSAP Genes in Patients With Multiple Myeloma (MM) or Monoclonal Gammopathy of Undetermined Significance (MGUS)
Run by University Hospital, Rouen · NCT06559033 · Data updated 2026-11-12
This study tests whether people with multiple myeloma or MGUS have certain variants in the GBA and PSAP genes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 300 (estimated) |
| Sponsor | University Hospital, Rouen Academic / other |
| Locations | 2 sites (Rouen and 1 other locations) |
| Status | Recruiting |
| Started | October 7, 2025 |
| Main results expected | October 2, 2026 |
| Study ends | April 1, 2027 |
| Registry record updated | June 10, 2026 |
| Trial ID | NCT06559033 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with diagnosed multiple myeloma or MGUS who are members of a social security scheme and can provide informed consent.
✕Probably not a fit
Individuals without the specified GBA/PSAP variants or whose disease biology does not involve these pathways may not experience a direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study will evaluate the presence and number of mutated alleles in the GBA and PSAP genes among patients with multiple myeloma or MGUS. Researchers will analyze genetic data to explore potential links between these rare gene alterations and chronic plasma cell disorders. The aim is to better understand how metabolic network changes might relate to disease mechanisms and identify potential therapeutic targets. Participants are adults who meet the disease criteria and provide informed consent.
Why it matters
Potential benefit: Findings could clarify genetic contributors to MM and MGUS and point to new avenues for targeted therapies.
How similar studies have gone: Prior work has explored genetic variants in hematologic conditions, with mixed success; this study applies a targeted gene approach to a similar patient population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Major patients with multiple myeloma (MM) (defined by clonal proliferation of tumour plasma cells (\>10%), presence of a monoclonal peak in serum or urine (excluding non-secretory myeloma) and organ involvement secondary to bone marrow invasion) or with MGUS (defined as bone marrow plasmacytosis of less than 10%, associated with a monoclonal protein of less than 30g/L and no clinical involvement). * Membership of a social security scheme * Adult having read and understood the information letter and signed the consent form Exclusion Criteria: * Person deprived of liberty by an administrative or judicial decision or person placed under court protection / sub-guardianship or guardianship
Where it's running
-
University Rouen Hospital
Rouen, France Recruiting -
Centre Henri Becquerel
Rouen, France Not yet recruiting
Study contacts
- Study coordinator: Abdellah AB TEBANI, Pr
- Email: Abdellah.Tebani@chu-rouen.fr
- Phone: 02 32 88 81 24
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.