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NCT05497089CompletedPhase 2

Temelimab as a Disease Modifying Therapy in Patients With Neuropsychiatric Symptoms in Post-COVID 19 or PASC Syndrome

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

Source: ClinicalTrials.gov · Last updated 17 May 2024

Brief summary (registry, in English)

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).

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
203 (actual)
First submitted
3 Aug 2022
Start date
29 Aug 2022
Primary completion date
10 May 2024
Lead sponsor
GeNeuro SA
NCT number
NCT05497089
EudraCT number
2022-000618-32

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 203
  • From 29 Aug 2022 to the primary completion date, 10 May 2024
  • 14 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Main Inclusion Criteria:
  • PASC Syndrome in accordance with NICE criteria with neuropsychiatric symptoms still occurring \>12 weeks after their first appearance.
  • Has had a SARS-CoV-2-positive diagnostic test (using a validated SARS-CoV-2 antigen, reverse transcription polymerase chain reaction \[RT-PCR\], or other molecular diagnostic assay, and an appropriate sample such as nasopharyngeal \[NP\], nasal, oropharyngeal \[OP\], or saliva). In case that the local standard of care did not foresee the previously mentioned tests, a confirmed SARS-CoV-2 nucleocapsid or membrane antibody test associated to a medical report documenting the date of COVID-19 clinical diagnostic, will be accepted.
  • PROMIS Fatigue SF 7a total raw score ≥21 with onset of fatigue post coronavirus disease 2019 (COVID-19) infection.
  • Patients affected with at least one of the following measures of objective impairment of cognitive function or of quality of life as defined by: i. Token Motor Test ≥1 z-score below the age/sex-adjusted mean ii. EQ5D-5L: Presence of at least 1 score ≥3 in any of the 5 variables of EQ5D-5L questionnaire (mobility; self-care; usual activities; pain/discomfort; anxiety/depression) iii. PQD-20 ≥27
  • HERV-W ENV positive as defined by automated capillary western system, specific signal level over background noise (S/N) \>1.
    • Main Exclusion Criteria:
  • Intubation and mechanical ventilation in the course of COVID19 or reception of convalescent COVID19 plasma treatment at any time prior to study entry
  • Major psychiatric conditions including but not restricted to (e.g. attention deficit/hyperactivity disorder, substance use disorder, schizophrenia documented in patient history or diagnosed using M.I.N.I), at the discretion of the site investigator, these do not refer to patients with typical mild to moderate symptoms of depression and anxiety associated with PASC
  • Neurological signs and symptoms including change in level of consciousness, seizures, movement disorders or focal neurological deficits, disorders of the central nervous system with tissue damage or a pre-COVID-19 diagnosis of Chronic Fatigue Syndrome documented in the patient history or diagnosed during the neurological examination
  • Current immunosuppressive//immunomodulating medication (e.g., azathioprine, tacrolimus, cyclosporine, methotrexate, hydroxychloroquine, cytotoxic chemotherapy, or neutralizing antibodies against SARS-CoV-2 epitopes) or therapy with HIV protease inhibitors

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (14)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
REHAB Clinic for Neurorehabilitation and Paraplegiology
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BaselSwitzerlandUnknown status
Inselspital Bern University Hospital Bern
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BernSwitzerlandUnknown status
Kantonsspital Graubunden
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ChurSwitzerlandUnknown status
Geneva University Hospital
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GenevaSwitzerlandUnknown status
Centre hospitalier du Valais Romand (CHVR) - Hôpital du Valais
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SionSwitzerlandUnknown status
Ace Alzheimer Center
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BarcelonaSpainUnknown status
Private clinic Blue Healthcare
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MadridSpainUnknown status
Hospital Universitario Quirónsalud Madrid
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MadridSpainUnknown status
Hospital General Universitario- Servicio de Medicina Interna
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ValenciaSpainUnknown status
Hospital Royo Villanova
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ZaragozaSpainUnknown status
Clinica Metabolica dell'Università di Modena e Reggio Emilia
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ModenaItalyUnknown status
U.O.C. Malattie Infettive Tor Vergata, Policlincio Tor Vergata
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RomaItalyUnknown status
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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RomaItalyUnknown status
Hospital of Vipiteno
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SterzingItalyUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.