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Status unknownNCT05203952CURE RAUpdated Feb 1, 2022

Purify Antigen-specific B Cells From Patients With Rheumatoid Arthritis

An observational study in Rheumatoid Arthritis, sponsored by University Hospital, Montpellier. Status unknown at 1 site in France. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2022-02-01.

Sponsored by University Hospital, Montpellier · Observational

The sponsor has not verified this record recently (last verified Jan 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
10
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Rheumatoid arthritis (RA) is an autoimmune disease characterized by the presence of autoantibodies directed against citrullinated proteins, called ACPAs. These antibodies are very specific to RA, and the severity of the disease is closely correlated with the level of these ACPAs, even though they appear much earlier than the clinical signs. Current treatments by biotherapies are effective but only treat the inflammatory symptoms of the disease or, on the contrary, induce a global immunosuppression with a depletion of all B lymphocytes.

Contrary to the current approaches, the CURE RA project proposes a double innovative character:

  • The project aims at specifically destroying B lymphocytes expressing / or secreting ACPAs for a more specific approach to RA, without inducing immunosuppression.
  • The new therapeutic molecule is entirely original and has no equivalent at present, it uses the target antigens of autoantibodies, the citrullinated peptides, as tools to destroy the pathogenic B cells that express/produce these autoantibodies.
02

Conditions studied

  • Rheumatoid Arthritis

Keywords

  • B cells
  • Rheumatoid arthritis
  • ACPA
03

In context

Arthritis

3,554 studies on the registry are indexed under Arthritis; 317 are open to participants now.

This study's planned enrollment of 10 is below the median of 155 across 1,057 observational studies indexed under Arthritis.

Browse Arthritis studies →

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients are selected based on the presence of high serum ACPA levels (medical record analyses). Patients treated with Rituximab resulting in total B cell depletion are not selected for this study

Inclusion criteria

  • Antibodies anti-CCP + (ACPA +) > 250 IU/mL

Exclusion criteria

Exclusion criteria:

  • Current or past Rituximab (Mabthera) treatment past (\< 9 months)
  • Abatacept treatment
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
10 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Establishment of B cell line

    Establishment of B cell line From first COVID-19 symtpoms, or first positive SARS-COV2 PCR result, to recovery.

    Time frame: 1 day

Secondary outcomes

  1. Validation of new therapeutic molecules

    Validation of new therapeutic molecules

    Time frame: 1 day

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — NC

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 1, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05203952
Lead sponsor
University Hospital, Montpellier
Responsible party
Sponsor
First posted
Jan 24, 2022
Start date
Dec 1, 2021
Primary completion
Dec 30, 2023 (estimated)
Completion
Jan 1, 2024 (estimated)
Last update
Feb 1, 2022

Study contacts

Yves-Marie PERS, MCU-PH
Contact
ym-pers@chu-montpellier.fr
0467337231 ext. 33
Christian Jorgensen, PU PH
Contact
christian.jorgensen@inserm.fr
0467337231 ext. 33
Yves-Marie PERS, MCU-PH
study director · University Hospitals of Montpellier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2022. You cannot join it, but the record below documents what was studied.

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