Temelimab 54mg/kg
DrugTemelimab 54mg/kg will be given as monthly (every 4 weeks) intravenous (IV) infusion over 24 weeks (6 infusions in total)
NCT Number: NCT05497089
This study is a Phase 2, 24-week, randomized, prospective, double-blind, multicenter study in patients experiencing neuropsychiatric symptoms and functional impairment in the course of PASC. The purpose of the study is to evaluate the efficacy and safety of Temelimab as a treatment for PASC neuropsychiatric symptoms in patients who had severe acute respiratory syndrome coronavirus - type 2 (SARS-CoV-2) infection but did not undergo intensive care treatment during the acute period. Patients meeting eligibility criteria will be randomized to Temelimab or placebo in a 1:1 ratio via interactive voice/web response system to obtain 182 protocol completers. The randomization will be stratified by age (≤65 years versus >65 years).
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Clinica Metabolica dell'Università di Modena e Reggio Emilia, Modena, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
Temelimab 54mg/kg will be given as monthly (every 4 weeks) intravenous (IV) infusion over 24 weeks (6 infusions in total)
Placebo will be given as monthly (every 4 weeks) intravenous (IV) infusion over 24 weeks (6 infusions in total)
Time frame: 24 weeks
Occurrence of an improvement in fatigue, measured by a decrease of ≥3 points in the Patient-Reported Outcomes Measurement Information System Fatigue Short Form 7a (PROMIS Fatigue SF 7a) score, at Week 24 as compared to baseline.
Time frame: 24 weeks
Change from baseline to Week 24 in the Severity of fatigue as measured by the PROMIS Fatigue SF 7a score
Time frame: 24 weeks
Change from baseline to Week 24 in 5 domain scores (verbal memory test, digit sequencing test, Token Motor Test, verbal semantic and letter fluency, and Tower of London) as measured by BAC tests
Time frame: 24 weeks
Change from baseline to Week 24 in Symbol Digit Modalities Test (SDMT) score
Time frame: 24 weeks
Change from baseline to Week 24 in Cognitive function as measured by the composite score of the BAC excluding symbol coding test
Time frame: 24 weeks
Change from baseline to Week 24 in Cognitive function as measured by the Perceived Deficits Questionnaire, 20 items (PDQ-20)
Time frame: 24 weeks
Change from baseline to Week 24 in Severity of anxiety as measured by the Generalized Anxiety Disorder, 7 Items (GAD 7)
Time frame: 24 weeks
Change from baseline to Week 24 in Severity of depression as measured by the Patient Health Questionnaire, 9 Items (PHQ-9)
Time frame: 24 weeks
Change from baseline to Week 24 in Overall quality of life as measured by the European Quality of Life 5 Dimensions, 5 Levels (EQ5D-5L)
Time frame: 24 weeks
Change from baseline to Week 24 in Level of functional impairment as measured by the Sheehan Disability Scale (SDS)
Time frame: 24 weeks
Change from baseline to Week 24 in Post-COVID-19 Functional Status Scale (PCFS)
Time frame: 24 weeks
Incidence of serious AEs [SAEs], AEs and analysis of physical examination findings, clinical laboratory values results
GeNeuro SA
Industry
Temelimab as a Disease Modifying Therapy in Patients With Neurological, Neuropsychological, and Psychiatric (=Neuropsychiatric) Symptoms in Post-COVID 19 or Postacute Sequelae of COVID-19 (PASC) Syndrome
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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