Rituximab at Low dosE for neuromyelitiS optiCa spectrUm disordEr (RESCUE)
What it found
We found no results in the registry or in papers.
This trial finished 6 years ago. We found no results in the registry or in any paper that cites it.
What was tested
Treatment tested
- Rituximab
B-lymphocyte antigen CD20 binding agent
What it measured
Main measures
Annualized relapse rate at last follow-up visit
12 months
Relapses
Other measures (5)
Expanded disability status scale (EDSS) score at last follow-up visit
12 months
Disability progressionRituximab-related adverse events
1 month, 3 months, 6 months, 9 months, 12 months
SafetyLesions in spinal cords
6 months, 12 months
MRI lesionsCirculating B cell monitoring
6 months, 12 months
Thinking and memoryImmune responseSwitch treatment
6 months, 12 months
Who could take part
NMOSD · 16 to 75
Inclusion Criteria: Age between 16 and 75 years old; Meet the 2007 or 2015 revised diagnostic criteria for NMOSD; At least two relapses in recent two years and/or at least one attack or relapse in recent one years; Expanded disability status scale (EDSS) score ≤7.0; Willingness to sample collection, imaging study and other disease-related examinations and assessments; Results of pregnancy tests for female patients with fertility during the screening period should be negative and effective contraception was used by the patient and her spouse during the study period; Patients with informed consent. Exclusion Criteria: Other immunosuppressive agents are being used or have been discontinued for less than 3 months; White blood cell count (WBC) \<3 ×109/L, neutrophil count \<1.5 ×109/L, hemoglobin (HGB) \< 85 g/L, and platelet count (PLT) \< 80×109/L; Concomitant active liver disease or persistent elevation of transaminases more than three times above the normal upper limit; Serious cardiovascular, kidney, blood and endocrine diseases, or history of malignant tumors, or severe infection; Other chronic active immune diseases or stable conditions but requiring immunosuppressants or glucocorticoids, such as rheumatoid arthritis, scleroderma, Sjögren's syndrome, ulcerative colitis, AIDS, genetic or drug-induced immune deficiency; Pregnant or lactating patients and those with family planning during the study period; Allergy to rituximab and other components; Inability to provide informed consent.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
In this research, a prospective, multicenter(Tangdu Hospital of Fourth Military Medical University, Xi'an Gaoxin Hospital of Xi'an Medical College, Xianyang Central Hospital, Baoji Central Hospital, Xi'an Central Hospital, The First Hospital of Xi'an, The Fourth Hospital of Xi'an) open-label, follow-up clinical trial will carry out to evaluate the efficacy and safety of low-dose rituximab in treating NMOSD in Northwest China.
Papers
Loading reviews and guidelines…
Related trials
- BEST-NMOSD
Phase 4 · Recruiting
Still running
- Inebilizumab and Rituximab in Neuromyelitis Optica Spectr…
Status unknown
No result found
- AQUARELLE
Phase 3 · Running, not recruiting
Still running
- Ofatumumab in AQP4-IgG Seropositive NMOSD
Phase 1 / Phase 2 · Recruiting
Still running
- ATTEND
Phase 2 / Phase 3 · Withdrawn
Stopped early
- Ublituximab for Acute Neuromyelitis Optica (NMO) Relapses
Phase 1 · Completed
Results posted, no main test reported
History
Started
Apr 2014
Main results due
Apr 2020
Finished
Jun 2020
Assembled by software from public sources and not checked by people. Each record links to its source. Report an error