Estudo de Segurança de Fase I Aberto de Pembrolizumab para Sequelas Neurológicas Pós-Agudas da SARS-CoV-2 (PD1-PASC I)
Estudo de Segurança Fase I, Aberto, de Pembrolizumab para Sequelas Neurológicas Pós-Agudas do SARS-CoV-2 (PD1-PASC I)
Background:
SARS-CoV-2 is the virus that causes COVID-19. Some people who recover from an acute COVID-19 infection may continue to have symptoms that persist for months or years. These can include neurological symptoms, such as headaches, loss of taste or smell, dizziness, or trouble walking. Pembrolizumab is a drug approved to treat certain cancers. Researchers think this drug might reduce long-term neurologic symptoms after a COVID-19 infection.
Objective:
To test pembrolizumab in people with ongoing neurologic symptoms of COVID-19.
Eligibility:
People aged 18 years or older who had COVID-19 at least 6 months ago and have ongoing neurologic symptoms.
Design:
Participants will have 7 clinic visits in 7 months.
Participants will be screened. They will have a physical exam with blood tests. Swabs will be used to collect cells from inside the mouth and nose. They may opt to have an imaging scan.
Participants will also have other tests before they are given the study drug. These include eye and skin exams; tests of their memory and thinking; and tests of involuntary body functions, such as heart rate, blood pressure, sweating, and digestion. Their grip strength and walking pace will be measured. They will wear a heart rate monitor for 24 hours. They will wear devices on a wrist and thigh to measure activity for 10 days.
Participants will have a lumbar puncture (spinal tap): A thin needle will be inserted into their lower back to draw out a sample of the fluid around their spinal cord.
Pembrolizumab is given through a needle inserted into a vein. Participants will receive 1 dose of the drug.
Participants will have 4 follow-up visits over 6 months. Tests may be repeated during these visits.
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Descrição detalhada
Study Description:
Despite clinical recovery from an acute SARS-CoV-2 infection, some individuals continue to experience ongoing symptoms for months to years afterwards, with many of these symptoms being neurologic. These neurologic post-acute sequelae of SARS-CoV-2 infection (Neuro-PASC) may be related to persisting viral antigen that leads to immune exhaustion. This study will primarily evaluate the safety of one dose of intravenous Pembrolizumab therapy in neuro-PASC participants with evidence of immune exhaustion. Pembrolizumab therapy may have positive clinical and laboratory effects on participants with persistent neurological symptoms, which will be measured as secondary outcomes.
Objectives:
Primary Objective:
-To determine the safety of a single dose of intravenous Pembrolizumab in participants with neurological postacute sequalae of SARS-CoV-2 infection.
Secondary objectives:
- To determine if one dose of intravenous Pembrolizumab can normalize markers of immune exhaustion in neuro-PASC.
- To determine if one dose of intravenous Pembrolizumab can lead to clinically relevant improvement in subjective and objective measures of ability.
Exploratory objectives:
- To determine if one dose of intravenous Pembrolizumab can change measures of SARS-CoV-2 antigen.
- To determine if one dose of intravenous Pembrolizumab can change measures of cytokines.
- To determine if one dose of intravenous Pembrolizumab can lead to improvement in subjective measures of symptoms.
Endpoints:
Primary endpoint:
- Number of adverse events and serious adverse events.
Secondary endpoints:
-
Number of participants with normalization of PD-1 expression on CD3 T cells.
-
Number of participants achieving a minimal clinically important difference in measures of function:
- Work Disability Functional Assessment Battery (WDFAB)
- PROMIS Global Health
- Short Form - 36 (SF-36)
- PROMIS Cognitive Function
- Montreal Cognitive Assessment (MoCA)
- Incremental shuttle walk test
Exploratory endpoints:
-
Detection of viral antigen
-
Change in cytokine profile
-
Statistically significant positive change from baseline:
- PROMIS Depression score
- PROMIS Anxiety
- PROMIS Fatigue
- PROMIS Sleep Disturbance
- WHO post COVID-19 functional scale
- Patient Post-COVID-19 Functional Status (PCFS) scale (0-4).
- Provider Post-COVID-19 Functional Status (PCFS) scale (0-4).
- FUNCAP55
- Multidimensional Fatigue Inventory (MFI)
- Pittsburgh Sleep Quality Index (PSQI)
- Modified Depaul Symptom Questionnaire-Post Exertional Malaise (DSQ-PEM)
- Post Exertional Malaise Visual Analogue Scale
- Patient Global Impression of Change
- Physician Global Impression of Change
- Brief tablet-based neurocognitive testing
- Near Infrared Spectroscopy of muscle
- Actigraphy
- Hand grip strength
- Holter monitoring for 24 hrs
- Orthostatic Intolerance Questionnaire/Orthostatic Intolerance Daily Activities Scale (OIQ/OIDAS)
- Dysautonomia measures in response to the QSART, Valsalva maneuver or head-up tilt table testing.
- Ophthalmology Examination
Tipo de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: Avindra Nath, M.D.
- Número de telefone: (301) 496-1561
- E-mail: natha@mail.nih.gov
Estude backup de contato
- Nome: Ladifatou N Fouanta, R.N.
- Número de telefone: (301) 529-6340
- E-mail: ladifatou.fouanta@nih.gov
Locais de estudo
-
-
Maryland
-
Bethesda, Maryland, Estados Unidos, 20892
- National Institutes of Health Clinical Center
-
Contato:
- NIH Clinical Center Office of Patient Recruitment (OPR)
- Número de telefone: TTY dial 711 800-411-1222
- E-mail: ccopr@nih.gov
-
Contato:
- Ladifatou Fouanta
- Número de telefone: (301) 529-6340
- E-mail: ladifatou.fouanta@nih.gov
-
-
Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
- INCLUSION CRITERIA:
To be eligible to participate in this study, an individual must meet all the following criteria:
-
Stated willingness to comply with all study procedures and availability for the duration of the study.
-
Male or female, aged at least 18 or older.
--Documentation of the SARS-CoV-2 infection that led to development of PASC confirmed either by a positive testing by a commercial laboratory or a positive home test followed by confirmatory nucleocapsid antibody testing.
-
Previously diagnosed with mild-moderate COVID-19 (WHO Clinical Progression Scale between 2-5. Participants who had severe acute COVID-19 requiring hospitalization or ICU care are excluded.
-
If participants had multiple SARS-CoV-2 infections, they would need to be at least 6 months after the last infection.
-
All participants would need to have a negative SARS-CoV-2 nasal swab at the time of enrollment.
-
Exhibiting persistent neurologic symptoms evidenced by a self-reported illness narrative of the development of persistent PASC symptoms after recovering from a SARS-CoV-2 infection. These include symptoms such as fatigue, cognitive difficulties, sleep disturbances, orthostatic intolerance, and any ongoing issues with gait instability, vision, speech, swallowing, sensation, or strength. Symptoms must persist for at least 6 months after the diagnosis of acute COVID-19.
-
At screening or within 3 months prior to screening, all participants will have PD-1 expression on CD3 T cells that is at or above the 75th percentile of normal controls as established in the SINS Lab and published previously.
-
Moderate to severe PASC symptom severity, as determined using PCFS (minimal score of 3) at screening time point.
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Ability of participant to understand and sign a written informed consent document.
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Prior completion of a clinical brain MRI after the diagnosis of COVID-19, or willingness to complete a brain MRI.
-
Agrees not to have vaccinations over the course of the study.
-
Participants of childbearing potential must agree to use a combination of contraception (defined as two forms of effective birth control) or have had surgical sterilization, from the time of enrollment until 4 months after the dose of study drug.
-
Participants capable of sperm donation must agree to not donate sperm from the time of enrollment until 4 months after the dose of study drug.
EXCLUSION CRITERIA:
An individual who meets any of the following criteria will be excluded from participation in this study:
-
For participants who have not completed a brain MRI since onset of symptoms: inability to complete brain MRI with gadolinium including contraindicated metal in the body, prior allergic reaction to gadolinium, eGFR <45 mmol/L, or claustrophobia that is unable to be adequately treated with a low dose oral benzodiazepine.
-
Contraindication to a research lumbar puncture, including use of anticoagulant medication, platelets < 50,000/uL, PT or PTT >1.5 x ULN for the NIH Clinical Center, if risk of lumbar puncture is increased for other reasons such as space occupying lesion, skin infection at site of the puncture or otherwise inability to complete the procedure.
-
A condition that would significantly confound interpretation of the clinical and research tests as determined by the study investigators. This could include traumatic brain injury, substance use disorder, active malignancy, systemic immunologic disorders, current or previous long-term immune suppressive therapy.
-
Any premorbid medical condition that would potentially cause fatigue and exercise intolerance. This includes many chronic medical diseases, such as congestive heart failure, coronary artery disease, chronic obstructive pulmonary disease, severe arthritis, uncontrolled asthma, renal failure, fibromyalgia, and ME/CFS.
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Symptom severity that makes it impossible for the participant to travel to NIH.
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Received a SARS-CoV-2 vaccine dose within less than 4 weeks of enrollment or is planning for any additional vaccines during the study.
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Prior treatment for PASC with immunomodulatory therapies such as check point inhibitors which in the opinion of the investigators could impact the outcome of this study.
-
Current medications include oral steroids or other immunosuppressive medications which in the opinion of the investigators could impact the outcome of this study.
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Active participation in a clinical protocol which includes any intervention that may affect the results of the current study.
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Abnormal anti-thyroid panel (anti-TPO and anti-TG) test at screening visit.
-
ANA titer of 1:80 or greater, positive anti-CCP.
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Abnormal screening blood tests exceeding any of the limits defined below or as deemed exclusionary by the investigators on review at baseline:
- Aspartate aminotransferase and alanine aminotransferase values >2x upper limit of normal precluding the use of acetaminophen
- Fasting triglyceride > 300 mg/dL.
- Total bilirubin >2x upper limit of normal (unless participant has Gilbert syndrome)
- Creatinine Clearance or eGFR <60 ml/minute (adjusted for race)
- Hemoglobin < 10 g/dL
- Absolute neutrophil count < 1000/microliter
- Platelet count <130,000/mm3 (if platelet clumping is present on hematology slide review, platelet count <100,000/mm3 is considered exclusionary to study)
- Hemoglobin A1c >= 6%
- Thyroid-stimulating hormone (TSH) and adrenocorticotropic hormone (ACTH) within normal limits. If TSH is not within normal limits then the participant may be eligible if thyroxine (T4) is within normal limits. Participants are not excluded if they are on a stable dose of replacement thyroid medication; dose may be adjusted as needed.
-
Previously documented anaphylaxis or severe systemic reaction to check point inhibitors, acetaminophen, or diphenhydramine.
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A severe psychiatric condition, which based on the assessment of the study investigators, will impact the ability to complete the study.
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Pregnancy or planning to get pregnant.
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Currently lactating/breastfeeding.
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Current or previous malignancy. A history of malignancy that has fully resolved with surgical resection only (e.g. no chemotherapy, radiation therapy, or immunotherapy) will be allowed.
-
Current or past substance use disorder within last five years. Marijuana use within the past five years will not be an exclusion.
-
Infection with HIV, tuberculosis, hepatitis B or C.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
|---|---|
|
Experimental: Open Label
Single dose of Pembrolizumab 200 mg IV |
Single dose of Pembrolizumab 200 mg IV |
O que o estudo está medindo?
Medidas de resultados primários
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
O resultado primário deste estudo é determinar a segurança de uma dose única intravenosa de Pembrolizumab em participantes com sequelas neurológicas pós-agudas da infeção por SARS-CoV-2.
Prazo: Desde a triagem até ao Dia 180.
|
Desde a triagem até ao Dia 180.
|
Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
To determine if one dose of intravenous Pembrolizumab can lead to clinically relevant improvement in subjective and objective measures of ability.
Prazo: Comparison between baseline, day 14, day 60 , and day 180 visits.
|
Comparison between baseline, day 14, day 60 , and day 180 visits.
|
|
To determine if one dose of intravenous Pembrolizumab can normalize markers of immune exhaustion in neuro-PASC.
Prazo: Comparison between baseline, day 14, day 60 , and day 180 visits.
|
Comparison between baseline, day 14, day 60 , and day 180 visits.
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: Avindra Nath, M.D., National Institute of Neurological Disorders and Stroke (NINDS)
Publicações e links úteis
Links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Início do estudo
Conclusão Primária (Estimado)
Conclusão Primária
Conclusão do estudo (Estimado)
Conclusão do estudo
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Primeira postagem
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última Atualização Postada
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Distúrbios pós-infecciosos
- Processos Patológicos
- Doença crônica
- Atributos da doença
- Infecções do Trato Respiratório
- Infecções
- Infecções por vírus de RNA
- Doenças Virais
- Doenças Respiratórias
- Doenças pulmonares
- Pneumonia Viral
- Pneumonia
- Infecções por coronavírus
- Infecções por Coronaviridae
- Infecções por Nidovírus
- Condições Patológicas, Sinais e Sintomas
- COVID-19
- Síndrome Pós-Aguda de COVID-19
- Pembrolizumab
Outros números de identificação do estudo
Outros números de identificação do estudo
- 10002294
- 002294-N
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
De-identified subject data, harmonized to a common standard, are available to qualified researchers. Summary data are available to all. Data will be made available as soon as possible or at the time of associated publication. All data will be deposited in MapME/CFS (RTI).
Prazo de Compartilhamento de IPD
Data will be made available as soon as possible or at the time of associated publication.
Critérios de acesso de compartilhamento IPD
Request for data access will need to adhere to the standard processes per each repository. These repositories allow for querying and access to shared datasets.
Tipo de informação de suporte de compartilhamento de IPD
- CIF
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