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    HP:0001369: Arthritis

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (49)


    Name (Synonyms) Correlation
    drug637 Breath Biopsy face masks with removable filters and fitted PVA strip Wiki 0.32
    drug656 Bromhexine 8 MG Wiki 0.23
    drug1996 Intra-articular corticosteroid injection Wiki 0.23
    Name (Synonyms) Correlation
    drug4637 oropharyngeal swabs Wiki 0.23
    drug65 40ml blood sample Wiki 0.23
    drug673 C21 Wiki 0.23
    drug3195 Questionnaire by phone call Wiki 0.23
    drug636 Breath Biopsy Analysis Wiki 0.23
    drug1324 EU-approved RoActemra Wiki 0.23
    drug671 Butterfly iQ Wiki 0.23
    drug639 Breath biopsy sampling using the ReCIVA Breath Sampler Wiki 0.23
    drug655 Brief informational infographic Wiki 0.23
    drug3672 Sofusa DoseConnect Wiki 0.23
    drug1502 Face-to-face medical visits Wiki 0.23
    drug675 C3+ Holter Monitor Wiki 0.23
    drug680 CAP-1002 Allogeneic Cardiosphere-Derived Cells Wiki 0.23
    drug3099 Project ECHO Wiki 0.23
    drug4050 Traditional antirheumatic drugs Wiki 0.23
    drug771 COVID-19 infection Wiki 0.23
    drug2250 MSB11456 Wiki 0.23
    drug2959 Placebo control (non-behavioral infographic) Wiki 0.23
    drug1826 Hydroxychloroquine/Chloroquine Wiki 0.23
    drug640 Breath sample Wiki 0.23
    drug695 CETA Short Session (CSS) Wiki 0.23
    drug3787 Stools Wiki 0.23
    drug687 CD24 Extracellular Domain-IgG1 Fc Domain Recombinant Fusion Protein CD24Fc Wiki 0.23
    drug3586 Serological analyses to be lead on a pre-existing biobank Wiki 0.23
    drug3058 Pravastatin Wiki 0.23
    drug1533 Filgotinib Wiki 0.23
    drug3136 Psychoeducation and Safety Wiki 0.23
    drug635 Breath Biopsy Wiki 0.23
    drug262 Alternating face-to-face medical visits and video medical consultations Wiki 0.23
    drug690 CDC training Wiki 0.23
    drug688 CD24Fc Wiki 0.23
    drug4410 blood tests Wiki 0.23
    drug1381 Enbrel Wiki 0.23
    drug685 CCP Wiki 0.23
    drug645 Brequinar Wiki 0.16
    drug386 Atorvastatin Wiki 0.16
    drug2514 Nasopharyngeal swabs Wiki 0.16
    drug1597 GLPG3970 Wiki 0.16
    drug663 Bucillamine Wiki 0.16
    drug2933 Placebo Administration Wiki 0.11
    drug3392 Rosuvastatin Wiki 0.11
    drug4689 questionnaire assesment Wiki 0.10
    drug2512 Nasopharyngeal swab Wiki 0.08
    drug1795 Hydroxychloroquine Sulfate Wiki 0.07
    drug2916 Placebo Wiki 0.04
    drug1775 Hydroxychloroquine Wiki 0.02

    Correlated MeSH Terms (17)


    Name (Synonyms) Correlation
    D001168 Arthritis NIH 1.00
    D001172 Arthritis, Rheumatoid NIH 0.86
    D015535 Arthritis, Psoriatic NIH 0.46
    Name (Synonyms) Correlation
    D025241 Spondylarthritis NIH 0.40
    D001167 Arteritis NIH 0.32
    D008180 Lupus Erythematosus, Systemic NIH 0.28
    D011111 Polymyalgia Rheumatica NIH 0.26
    D013700 Giant Cell Arteritis NIH 0.26
    D001171 Arthritis, Juvenile NIH 0.23
    D012859 Sjogren's Syndrome NIH 0.23
    D001327 Autoimmune Diseases NIH 0.21
    D003095 Collagen Diseases NIH 0.16
    D012216 Rheumatic Diseases NIH 0.15
    D020370 Osteoarthritis, Knee NIH 0.10
    D059350 Chronic Pain NIH 0.06
    D003141 Communicable Diseases NIH 0.02
    D007239 Infection NIH 0.01

    Correlated HPO Terms (6)


    Name (Synonyms) Correlation
    HP:0001370 Rheumatoid arthritis HPO 0.86
    HP:0012089 Arteritis HPO 0.32
    HP:0002725 Systemic lupus erythematosus HPO 0.28
    Name (Synonyms) Correlation
    HP:0002960 Autoimmunity HPO 0.21
    HP:0005086 Knee osteoarthritis HPO 0.10
    HP:0012532 Chronic pain HPO 0.06

    Clinical Trials

    Navigate: Correlations   HPO

    There are 19 clinical trials


    1 Early Biomarkers for ARthritic PAIN to Guide Improved Treatments for Arthritis (ARPAIN) Study

    Osteoarthritis (OA) is a condition affecting the whole joint and is a major cause of pain and disability worldwide. Although OA is very common, the initial steps which lead to the development of pain and tissue damage are not fully understood. In this study participants will be investigated for markers in the blood, joint and urine in people who have a diagnosis of osteoarthritis or inflammatory arthritis and are receiving a steroid injection for their condition. Markers will be evaluated in participants with osteoarthritis compared with other types of arthritis, including rheumatoid arthritis and spondyloarthritis.

    NCT03533569
    Conditions
    1. Osteoarthritis, Knee
    2. Rheumatoid Arthritis
    3. Spondyloarthritis
    4. Psoriatic Arthritis
    Interventions
    1. Procedure: Intra-articular corticosteroid injection
    MeSH:Arthritis Arthritis, Psoriatic Osteoarthritis, Knee Spondylarthritis
    HPO:Arthritis Knee osteoarthritis Polyarticular arthritis

    Primary Outcomes

    Description: Pain outcome measure. The Numerical Rating Scale for pain has a range of 0 - 10, with the lowest score being 0 and the highest rating at 10.The pain rating will be reported by the participants for their symptomatic knee

    Measure: Change from Baseline Numerical Rating Scale (NRS) for pain in target knee after 3 months

    Time: Baseline (Visit 1) and 3 months after treatment (Visit 2)

    Secondary Outcomes

    Description: Protein measurements in serum, urine and synovial fluid for type II collagen degradation products in the samples. The levels of type II collagen degradation products may range from 0 to greater than 500 ng/mmol, depending on the stage and severity of the condition

    Measure: Change in Biomarkers 3 months following treatment

    Time: Baseline (Visit 1) and 3 months after treatment (Visit 2)
    2 COVID-19 Infection in Vulnerable Patients With Inflammatory Rheumatic Diseases

    The trial is a prospective, observational study aiming to identify risk factors for serious COVID-19 infection by evaluating clinical measures and biomarkers of inflammation in patients with inflammatory rheumatic disease hospitalized with COVID-19 compared with control groups.

    NCT04335747
    Conditions
    1. Rheumatoid Arthritis
    2. Psoriatic Arthritis
    3. Axial Spondyloarthritis
    4. Systemic Lupus Erythematosus
    5. Giant Cell Arteritis
    Interventions
    1. Other: COVID-19 infection
    MeSH:Arthritis Arthritis, Psoriatic Rheumatic Diseases Polymyalgia Rheumatica Giant Cell Arteritis Arteritis Lupus Erythematosus, Systemic Collagen Diseases
    HPO:Arteritis Arthritis Polyarticular arthritis Systemic lupus erythematosus

    Primary Outcomes

    Description: The objective is to examine whether increased disease activity leads to increased risk of hospitalization due to COVID-19 in patients with inflammatory rheumatic disease

    Measure: Disease activity

    Time: Last registration of disease activity in the medical journal before admission/inclusion

    Secondary Outcomes

    Description: Examine whether immune modulating treatments protect or leads to increased risk of hospitalization due to COVID-19 in patients with inflammatory rheumatic disease.

    Measure: Immune modulating treatments

    Time: Current immune modulating treatments at admission/inclusion

    Description: Identify prognostic biomarkers by comparing serology of patients with inflammatory rheumatic disease hospitalized with COVID-19 and comparing them with the two control groups

    Measure: Biomarkers

    Time: Blood sample 1 is taken 0-3 days after inclusion and blood sample 2 is taken 2-6 weeks after blood sample 1
    3 Association Between Long-term Hydroxychloroquine Treatment and Outcome of a History of Symptoms Suggestive of COVID-19 Infection During the Epidemic Period in France in Patients With Autoimmune Disease

    This epidemiological, transversal, cohort study aims to determine the potential influence of an active long-term hydroxychloroquine intake over the prevalence of a history of symptoms evocative of a COVID-19 infection in patients with a history of systemic lupus erythematosus, rheumatoid arthritis, Sjogren's syndrome or psoriatic arthritis, during the epidemic period in France. The information is gathered using a standardized questionnaire, by phone call.

    NCT04345159
    Conditions
    1. SARS-CoV-2
    2. Systemic Lupus Erythematosus
    3. Rheumatoid Arthritis
    4. Sjogren's Syndrome
    5. Psoriatic Arthritis
    Interventions
    1. Other: Questionnaire by phone call
    MeSH:Arthritis Arthritis, Psoriatic Sjogren's Syndrome Lupus Erythematosus, Systemic Autoimmune Diseases
    HPO:Arthritis Autoimmunity Polyarticular arthritis Systemic lupus erythematosus

    Primary Outcomes

    Description: Adjusted Odds Ratio measuring the association between an exposure to long-term hydroxychloroquine intake and a history of symptoms compatible with a COVID-19 infection.

    Measure: Adjusted Odds Ratio

    Time: 4 months after inclusion
    4 IMPACT RAPPORT: IMPact of Antimalarials on Covid Infections: a Case Control sTudy of RAPPORT

    This study aims to evaluate the experience of Alberta patients with inflammatory arthritis who participate in the the RAPPORT-ONTRAAC registry during the COVID-19 pandemic, specifically comparing the experience of those taking anti-malarial medications compared to those who do not. This registry includes approximately 2500 northern Alberta patients with inflammatory arthritis who receive highly complex therapies which may be associated with side effects. This program of data collection and research has been evaluating the effectiveness and safety as well as associated health care costs of rheumatoid and psoriatic arthritis patients since 2004. The principle investigators are based at the University of Alberta while the co-investigators are academic rheumatologists at the University of Alberta. The registry has approximately 900 patients taking anti-malarials combined with their complex therapies and ~ 1500 not on anti-malarials in combination with their complex therapies. We aim to perform a case control study evaluating the impact of anti-malarial drugs (eg. hydroxychloroquine and chloroquine) on the development of COVID-19 compared to those patients who are not on anti-malarial drugs over the next 6-12 months. In addition to frequent e-mail surveys screening for the clinical symptoms of COVID-19 and understanding their concomitant arthritis medication use, we will compare the healthcare outcomes of both groups of arthritis patients with and without COVID-19 for the duration of the pandemic. This information will provide critical information beyond an anecdotal level on whether or not anti-malarials truly provide a protective benefit against COVID-19 or reduce the severity of infection. A blood sample from all participants (Covid-19 positive and negative) will be drawn approximately six months into the study for measurement of antibodies to Covid-19 and possible blood types and HLA alleles. Additionally, this study will be linked to another study "Persistence of SARS-Cov2 in immunocompromised patients" which will specifically evaluate COVID-19 serology and nasopharyngeal swab findings in the subset of patients who develop COVID-19.

    NCT04347798
    Conditions
    1. Covid-19 Infection
    2. Rheumatoid Arthritis
    3. Psoriatic Arthritis
    4. Hydroxychloroquine
    Interventions
    1. Other: Hydroxychloroquine/Chloroquine
    MeSH:Infection Communicable Diseases Arthritis Arthritis, Rheumatoid Arthritis, Psoriatic
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Number of patients developing signs and symptoms of Covid-19 or other infections

    Measure: Impact of anti-malarials on the development and severity of Covid-19 in the anti-malarial group compared to the non-anti-malarial group

    Time: 12 months

    Secondary Outcomes

    Description: Number of patients developing Covid-19 infection

    Measure: Incidence of Covid-19 infection in the anti-malarial group compared to the non-anti-malarial group

    Time: 12 months

    Description: Incidence of Covid-19 infection in the sub-groups of patients on biologic agents with different mechanisms of action

    Measure: Incidence of Covid-19 infection in the sub-groups of patients on biologic agents with different mechanisms of action

    Time: 12 months

    Other Outcomes

    Description: Quantitative measurement of Covid-19 serology to understand possible differences in degree of immune response adjusted for anti-malarial and/or biologic exposure

    Measure: Quantification of Covid-19 antibodies in anti-malarial vs non-anti-malarial groups of inflammatory arthritis patients

    Time: 6 months
    5 Psychological Impact of Quarantine in Rheumatoid Arthritis Patient During COVID-19 Outbreak

    Clinical data about psychological impact of quarantine are well studied in transient event or more prolonged situation like jail incarceration. In recent metaanalysis, psychological impact of quarantine was well documented in a specific population during first SARS epidemy. Even after the end of quarantine several patients were still with symptom of avoiding mainly agoraphobia, frequent hand washing and a carefull return to normal life COVID-19 infection is already associated with psychological symptom like anxiety, depression, sleep disorders and symptoms of acute stress However psychological impact of quarantine is on none in chronic painful inflammatory rheumatism in France. The prevalence of rheumatoid arthritis is 0.5% of the population with frequent comorbidity such as anxiety and depression. During the quarantine secondary to COVID-19 pandemic it's possible to evaluated the psychological impact of adult RA patients. The present study is an "emergency" being realize before the end of the quarantine.

    NCT04351399
    Conditions
    1. Sars-CoV2
    2. Rheumatic Diseases
    3. Rheumatoid Arthritis
    4. Chronic Pain
    Interventions
    1. Other: questionnaire assesment
    MeSH:Arthritis Arthritis, Rheumatoid Rheumatic Diseases Collagen Diseases Chronic Pain
    HPO:Arthritis Chronic pain Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Measure: Frequency of RA patients with emotional impact (feeling of isolation)

    Time: maximum 1 week from baseline on

    Secondary Outcomes

    Description: Self reported questionnaire with questions to assess the characteristic,intensity of pain on quality of life, and consumption of analgesic.

    Measure: self-reported questionnaire for painful

    Time: maximum 1 week from baseline on
    6 Immune Cells and the Coronavirus for Inflammatory Arthritis

    A team at the University of Manchester are developing a test that tcould be helpful in detecting immunity to the Coronavirus (which causes the COVID-19 disease) in participants with inflammatory arthritis. It is based on a flu assay has already developed; the team will replace the flu antigen with a Coronavirus antigen to see if it is effective. This project aims to develop a test to see if people who have had the virus have developed immunity to it. This could help to predict who might or might not get the disease a second time, who should stay at home to be protected from potential infection or who will not develop any symptoms, even if exposed to the virus. When vaccination trials against the Coronavirus will be launched, this test could also help to see if the vaccine is effective.

    NCT04363047
    Conditions
    1. SARS Virus
    Interventions
    1. Other: 40ml blood sample
    MeSH:Arthritis
    HPO:Arthritis Polyarticular arthritis

    Primary Outcomes

    Description: the prevalence and abundance of CD4+ T lymphocytes specifically recognizing SARS-CoV-2 in COVID-19 patients with inflammatory arthritis, in pre- and post-infection samples; in patients without COVID-19 and in healthy volunteers with or without COVID-19. Correlation of these cells with COVID-19 severity.

    Measure: Prevalence and abundance of CD4+ T lymphocytes

    Time: 2 years
    7 Antimalarial and Covid 19 in Rheumatoid Arthritis

    The antimalarial agent hydroxychloroquine(HCQ) have been used widely used for the treatment of rheumatoid arthritis and systemic lupus erythematosus. These compounds lead to improvement of clinical and laboratory parameters, but their slow onset of action differ them from glucocorticoids and nonsteroidal antiinflammatory agents. Among rheumatic diseases, the primary role of HCQ is in the management of articular and skin manifestations of systemic lupus erythematosus (SLE) and the treatment of mild to moderately active rheumatoid arthritis (RA).

    NCT04389320
    Conditions
    1. Rheumatoid Arthritis
    Interventions
    1. Drug: Hydroxychloroquine
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: serum level

    Measure: immunoglobulin mesurement

    Time: 1 month
    8 Drug Management of Rheumatoid Arthritis in Covid-19 Context : Impact on Therapeutic De-escalation

    The current situation of Sars-Cov-2 pandemic generates fears in the general population. Among patients receiving long-term immunomodulatory drugs, especially in the context of auto-immune diseases, there may be legitimates interrogations about the appropriateness of continuing treatment, without modification, in the current context. Most patients with Juvenile Rheumatoid Arthritis benefit from long-term immunmodulatory therapy (DMARD - disease modifying anti-rheumatic drug), more or less combined with regular use of non-steroidal anti-inflammatory drugs (NSAIDs) or corticosteroids.The present study will characterize this issue by defining the proportion of patients whose usual treatment of Rheumatoid Arthritis has been modified in relation to the actual sanitary crisis.

    NCT04393233
    Conditions
    1. Rheumatoid Arthritis
    2. COVID
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Reduction or discontinuation of treatment with sDMARD, bDMARD or tsDMARD

    Measure: Reduction or discontinuation of the DMARD therapy in relation to the Covid-19 sanitary crisis

    Time: 1 Day
    9 Prevalence, Seroconversion and Impact of COVID-19 in Autoimmune Diseases in Europe

    The coronavirus disease 2019 (COVID-19) pandemic is a potentially fatal disease that represents a great global public health concern. In European countries such as Spain, Italy, Germany, Portugal, England and France, the pandemic has been of utmost importance. To date, no treatment has been robustly validated, and two theoretically opposite therapeutic strategies are proposed, based either on antiretroviral therapy or on immunomodulating agents. In this complex context, people living with immune-mediated inflammatory diseases (IMID) raise specific concerns due to their potentially increased risk of infections or of severe infections. Among IMID, Sjögren's syndrome, systemic lupus erythematosus, rheumatoid arthritis, spondyloarthritis and giant cell arteritis are some key diseases. In this cross-sectional, observational, multi-centric study, the investigators aim to assess both clinical and serological prevalence of COVID-19 among samples of IMID patients in Europe. In parallel, the investigators aim to compare the prevalence of COVID-19 seroconversion across these five IMIDs, their penetration across different 6 European countries (France, Italy, Spain, Germany, United Kingdom and Portugal), and to assess the severity of COVID-19 in these patients. Moreover, changes in treatment will be assessed, including immunomodulatory tapering or discontinuation, its causes over the outbreak period, as well as the incidence of IMID flares and their severity over this same period. Finally, patient's perceptions towards the pandemic will be evaluated and compared to medication beliefs. Data will be collected through questionnaires during medical visit or phone consultation and serological tests will be performed within routine blood collection. As so, all study procedures are comprised within usual care. Through this study the investigators expect to have a better knowledge of the clinical and serological prevalence of COVID-19 in IMID across Europe, along with the psychological, clinical, and therapeutic impact of COVID-19 in this particular patient population.

    NCT04397237
    Conditions
    1. COVID-19
    2. Systemic Lupus Erythematosus
    3. Sjogren's Syndrome
    4. Axial Spondyloarthritis
    5. Rheumatoid Arthritis
    6. Giant Cell Arteritis
    MeSH:Arthritis Arthritis, Rheumatoid Sjogren's Syndrome Spondylarthritis Polymyalgia Rheumatica Giant Cell Arteritis Arteritis Lupus Erythematosus, Systemic Autoimmune Diseases
    HPO:Arteritis Arthritis Autoimmunity Polyarticular arthritis Rheumatoid arthritis Systemic lupus erythematosus

    Primary Outcomes

    Description: ELISA tests for COVID-19 antibodies

    Measure: COVID-19 seroconversion

    Time: 1 day, during routine blood collection

    Description: Case report form filled by the health professional

    Measure: COVID-19 infection

    Time: During medical visit or phone consultation, up to 2 hours

    Secondary Outcomes

    Description: Descriptive analysis for each disease's rate

    Measure: Seroconversion rate by disease

    Time: 1 day, during routine blood collection

    Description: Descriptive analysis for each country's rate

    Measure: Penetration across Europe

    Time: 1 day, during routine blood collection

    Description: World Health Organization ordinal scale for clinical improvement at any given point of the infection, going from 0 to 8, where higher scores means worse outcome.

    Measure: COVID-19 severity

    Time: During medical visit, up to 1 hour

    Description: Descriptive analysis for overall and COVID-19-linked mortality rates

    Measure: COVID-19 mortality rate

    Time: During contact with family members, up to 1 hour

    Description: Case report form filled by the health professional

    Measure: COVID-19 impact on immunomodulatory treatment

    Time: During medical visit, up to 1 hour

    Description: Case report form filled by the patient

    Measure: Patient-reported flares

    Time: During medical visit, up to 1 hour

    Description: Fear of COVID-19 scale, going from 7 to 35, where higher scores means worse outcome.

    Measure: Patient's fears towards COVID-19

    Time: During medical visit, up to 1 hour

    Description: Beliefs about Medicines Questionnaire, going from 11 to 55, with higher scores indicating stronger beliefs regarding medicine.

    Measure: Patient's beliefs in their medicines towards COVID-19

    Time: During medical visit, up to 1 hour
    10 Impact of the Rheumatoid Factor on Serological Testing Performance for Covid-19 in Rheumatoid Arthritis Patients

    Due to the Covid-19 worldwide outbreak, fragile patients with immune diseases, notably rheumatoid arthritis (RA), have to be even more specifically and carefully followed-up. However, it has been shown that false postive serological results often occured while detecting antibodies directed against SARS-CoV-2 in patients with positive rheumatodoid factor (RF). The investigators propose here to investigated this issue. Therefore, the investigators will test three different immunoassays on this specific population. The investigators aim to establish these assays specificity and the levels of RF for which there is a risk of anti-SARS-CoV-2 false positivity and thus ensure a better follow-up of RA patients. The RF isotype will be analysed to determine whether there is a correlation and the impact of the presence of anti-CCP (citrullinated cyclic antipeptide antibodies) will be studied and assessed.

    NCT04407559
    Conditions
    1. COVID-19
    2. Rheumatoid Arthritis
    Interventions
    1. Other: Serological analyses to be lead on a pre-existing biobank
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Evaluate the false positive results rate when using each one of the three SARS-CoV-2 serology tests in patients with rheumatoid factor plasma levels, so as to define the specificity of these tests in this RA population. all serum samples will be tested by the 3 different immunoassays. The RF plasma levels have already been measured (routine exam) and are written in the patients files. The results will be analysed, the data proceeded and hopefully we will be able to answer the question.

    Measure: Evaluate the false positive results rate

    Time: 4 months

    Secondary Outcomes

    Description: Characterize the RF isotype (IgG, IgM or IgA) associated with the false positivity of the test.all serum samples will be tested by the 3 different immunoassays. The RF isotype will be established using the routine method and the results of anti-CCP and RF plasma levels are already known and this information is available in the patients files. The results will be analysed, the data proceeded and hopefully we will be able to answer the questions

    Measure: Characterize the RF isotype (IgG, IgM or IgA) associated

    Time: 4 months

    Description: Determine the influence of RA on the false positivity rate in subjects with negative RF titer. All serum samples will be tested by the 3 different immunoassays. The RF isotype will be established using the routine method and the results of anti-CCP and RF plasma levels are already known and this information is available in the patients files. The results will be analysed, the data proceeded and hopefully we will be able to answer the questions

    Measure: Determine the influence of RA on the false positivity rate in subjects

    Time: 4 months

    Description: Assess the influence of the presence of anti-CCP on the false positivity of the SARS-CoV-2 test : all serum samples will be tested by the 3 different immunoassays. The RF isotype will be established using the routine method and the results of anti-CCP and RF plasma levels are already known and this information is available in the patients files. The results will be analysed, the data proceeded and hopefully we will be able to answer the questions.

    Measure: Assess the influence of the presence of anti-CCP on the false positivity of the SARS-CoV-2 test

    Time: 4 months

    Description: Assess the relation between the RF plasma levels and the false positivity of the SARS-CoV-2 test : all serum samples will be tested by the 3 different immunoassays. The RF isotype will be established using the routine method and the results of anti-CCP and RF plasma levels are already known and this information is available in the patients files. The results will be analysed, the data proceeded and hopefully we will be able to answer the questions.

    Measure: Assess the relation between the RF plasma levels and the false positivity of the SARS-CoV-2 test

    Time: 4 months
    11 Drug Management of Juvenile Idiopathic Arthritis in Covid-19 Context

    The current situation of Sars-Cov-2 pandemic generates fears in the general population. Among patients receiving long-term immunomodulatory drugs, especially in the context of auto-immune diseases, there may be legitimates interrogations about the appropriateness of continuing treatment, without modification, in the current context. Juvenile Idiopathic Arthritis is concerns by these fears (the patient and their parents). Patients are treated by several classes of immunomodulatory drugs, including non-steroidal anti-inflammatory drugs, corticosteroids and disease modifying anti-rheumatic drugs. The present study will characterize this issue by defining the proportion of patients whose usual treatment of Juvenile Idiopathic Arthritis has been modified in relation to the actual sanitary crisis, and also to return to school.

    NCT04407923
    Conditions
    1. Juvenile Idiopathic Arthritis
    2. COVID 19
    3. Treatment
    MeSH:Arthritis Arthritis, Juvenile
    HPO:Arthritis Polyarticular arthritis

    Primary Outcomes

    Description: Reduction or discontinuation of treatment with sDMARD, bDMARD or tsDMARD

    Measure: Reduction or discontinuation of the DMARD therapy in relation to the Covid-19 sanitary crisis

    Time: 1 Day
    12 Anti-rheumatic Drug Use and Risk of COVID-19 Infection in Rheumatoid Arthritis Patients: A Retrospective, Case-control Study

    Rheumatoid arthritis (RA) patients have an underlying immune deficiency and typically treated with immunosuppressive drugs, which may increase the risk of COVID-19 infection. Hydroxychloroquine (HCQ) has been found to possess antiviral activity against COVID-19. Thus, the aim of this study to investigate the ability of HCQ to reduce the risk of COVID-19 among RA patients.

    NCT04434118
    Conditions
    1. Rheumatoid Arthritis
    2. COVID
    Interventions
    1. Drug: Traditional antirheumatic drugs
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Realtion between hydroxychloroquine use and COVID-19 infection

    Measure: The risk of COVID-19 infection among RA patients

    Time: 12 week

    Secondary Outcomes

    Description: Number of cases and number of hospitalization days

    Measure: The incidence of hospitalization for Covid-19 patients.

    Time: 12 week
    13 A Randomized, Double-Blind, Multiple-Dose, Parallel-Group, Two-Arm Study to Evaluate the Efficacy, Safety and Immunogenicity of MSB11456 Compared to European Union-approved RoActemra® in Patients With Moderately to Severely Active Rheumatoid Arthritis (APTURA I Study)

    The purpose of the study is to compare the efficacy, safety and immunogenicity of MSB11456 and EU approved RoActemra® in participants with moderately to severely active rheumatoid arthritis. Participants will be randomized at the beginning of the Core Treatment Period (Baseline to Week 24) to receive either MSB11456 or EU approved RoActemra® once a week (QW). At the beginning of the Extended Treatment Period (Week 24 to Week 52), participants who received RoActemra® will be re-randomized to either continue receiving RoActemra® QW or switch to receive MSB11456 QW.

    NCT04512001
    Conditions
    1. Rheumatoid Arthritis
    Interventions
    1. Drug: MSB11456
    2. Drug: EU-approved RoActemra
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Measure: Change from Baseline in Disease Activity Score 28-Erythrocyte Sedimentation Rate (DAS28-ESR)

    Time: Baseline; Week 24

    Secondary Outcomes

    Measure: Change from Baseline in Disease Activity Score 28-Erythrocyte Sedimentation Rate (DAS28-ESR)

    Time: Baseline; Week 52

    Measure: Number of Participants with 20% Improvement in American College of Rheumatology (ACR20) Response

    Time: Week 24

    Measure: Number of Participants who Experienced One or More Treatment-Emergent Adverse Event (TEAE)

    Time: Baseline to end of study, up to Week 63

    Measure: Number of Participants who Experienced One or More Serious Adverse Event (SAE)

    Time: Baseline to end of study, up to Week 63

    Measure: Number of Participants with Positive Anti-Drug Antibodies (ADAs)

    Time: Week 2; Week 55

    Measure: Anti-Drug Antibodies (ADAs) Titer Levels

    Time: Week 2; Week 55

    Measure: Number of Participants with Confirmed Neutralizing Antibodies (NAb)

    Time: Week 2; Week 55
    14 Seroprevalence and Clinical Expression of SARS-CoV-2 Infection in Patients With Chronic Inflammatory Rheumatisms and Impact of Immuno-suppressive Drugs on the Persistence of Anti-SARS-CoV2 Antibodies During Two Years of Follow-up

    A better understanding of the different phenotypes of COVID 19 in patients with inflammatory rheumatisms, and the persitence of antibodies against SARS CoV-2 in these patients under immunosuppressive drugs are required to propose appropriated recommendations for these patients in order to guide the strategy of vaccination in this immune-depressed population who is not immunized.

    NCT04530682
    Conditions
    1. Rheumatoid Arthritis
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Variation of anti-SARS-CoV2 antibodies titers between baseline

    Measure: Seroprevalence of COVID-19 in patients with inflammatory rheumatisms

    Time: 6 months

    Description: Variation of anti-SARS-CoV2 antibodies titers between baseline

    Measure: Seroprevalence of COVID-19 in patients with inflammatory rheumatisms

    Time: 12 months

    Secondary Outcomes

    Description: Coagulation factors in patients with inflammatory rheumatisms compared to health professionals

    Measure: Clinical expression of COVID-19 compared to health professionals : phenotypes, thrombo-embolic events and stress repercussion

    Time: 6 months

    Description: Coagulation factors in patients with inflammatory rheumatisms compared to health professionals

    Measure: Clinical expression of COVID-19 compared to health professionals : phenotypes, thrombo-embolic events and stress repercussion

    Time: 12 months

    Description: Coagulation factors in patients with inflammatory rheumatisms compared to health professionals

    Measure: Clinical expression of COVID-19 compared to health professionals : phenotypes, thrombo-embolic events and stress repercussion

    Time: 24 months
    15 Impact of a Hybrid Medical Care Model (Face-to-face Medical Visits Alternating With Video Medical Consultations) in the Rheumatoid Arthritis Patient-reported-outcomes Measures: A Non-inferiority Study

    The COVID-19 outbreak has affected health care of patients with rheumatic diseases; telemedicine might help to assist patients. The primary objective is to determine if a hybrid medical care model, which consists of alternating face-to-face medical visits and video medical consultations, is not inferior, in terms of the Patient Reported Outcomes measures (PROMs), to the face-to-face medical care model, among rheumatoid arthritis (RA) outpatients. We also aim to investigate if adherence to RA-related treatment (considered a surrogate of patient´s education) might be improved when patients are re-integrated to the health care system, irrespective of the health care model. In Mexico, COVID-19 pandemic still uncontrolled. Our Institution provides health care to 1500 RA patients/year and up to August 2020, it is estimated that 500 RA patients might be affected, which is our target audience. Reinstalling institutional health care provision is challenging. This a non-inferiority, cross-over study, with 2 intervention arms. Patients will be randomized to 1. Six months of usual medical care model, followed by 4 months of a control period, and 6 months of hybrid medical care model, or 2. Six months of hybrid medical care model, followed by 4 months of a control period, and 6 months of usual medical care model. The following PROMs will be assessed at specific time points: disease activity/disease severity (RAPID-3), disability (HAQ-DI), quality of life (WHOQOL-BREF), patient satisfaction with the medical care model (questionnaire locally developed), patient´s adherence to medical care (missed scheduled visits) and patient´s adherence to RA-related treatment (the Compliance-Questionnaire).

    NCT04558905
    Conditions
    1. Rheumatoid Arthritis
    2. Telehealth
    Interventions
    1. Other: Face-to-face medical visits
    2. Other: Alternating face-to-face medical visits and video medical consultations
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: The disease activity measured by a RAPID-3 instrument

    Measure: Rheumatoid arthritis patient´s disease activity

    Time: During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)

    Description: Quality of life measured by a WHOQOL-BREF instrument

    Measure: Rheumatoid arthritis patient´s quality of life

    Time: During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)

    Description: Disability measured by a HAQ-DI instrument

    Measure: Rheumatoid arthritis patient's disability

    Time: During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)

    Secondary Outcomes

    Description: Questionnaire locally developed

    Measure: Satisfaction with medical care

    Time: During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)

    Description: Number of missed scheduled visits

    Measure: Patient´s adherence to medical care

    Time: During the 16 months of follow up, the evaluations will be in each medical visits (in both medical care models)
    16 Phase 1b Proof-of-concept, Open-label Study to Assess the Safety and Pilot Efficacy of Enbrel® Administered by the Sofusa® DoseConnect™ Delivery System for the Treatment of Rheumatoid Arthritis

    This is an open-label pilot study in patients with rheumatoid arthritis (RA). All patients will receive SOFUSA Enbrel 25 mg once weekly. The dose will be increased to 50 mg if the dose escalation criteria are met during the dose escalation phase of the study.

    NCT04559412
    Conditions
    1. Rheumatoid Arthritis
    Interventions
    1. Device: Sofusa DoseConnect
    2. Drug: Enbrel
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Incidence and severity of adverse events and their relationships to SOFUSA administration

    Measure: Incidence and severity of adverse events and their relationships to SOFUSA administration

    Time: Baseline through Week 12

    Secondary Outcomes

    Description: Change from Baseline in DAS28(CRP) score at Week 12

    Measure: Change in Disease Activity Score 28-joint count C reactive protein (DAS28(CRP))

    Time: Baseline to Week 12

    Description: Change from Baseline in DAS28(CRP) score over time

    Measure: Change in DAS28(CRP) score over time

    Time: Baseline through Week 12

    Description: Change from Baseline in DAS28(ESR) score over time

    Measure: Change in Disease Activity Score 28-joint count erythrocyte sedimentation rate (DAS28(ESR)) over time

    Time: Baseline through Week 12

    Description: Change from Baseline in SDAI score over time

    Measure: Change in Simplified Disease Activity Index (SDAI) score over time

    Time: Baseline through Week 12

    Description: Change from Baseline in CDAI score over time

    Measure: Change in Clinical Disease Activity Index (CDAI) score over time

    Time: Baseline through Week 12

    Description: Proportion of patients with DAS28(CRP) score < 2.9 over time

    Measure: Proportion of patients with low disease activity (LDA) over time as assessed by the DAS28(CRP)

    Time: Baseline through Week 12

    Description: Proportion of patients with DAS28(ESR) score ≤ 3.2 over time

    Measure: Proportion of patients with LDA over time as assessed by the DAS28(ESR)

    Time: Baseline through Week 12

    Description: Proportion of patients with SDAI score ≤ 11.0 over time

    Measure: Proportion of patients with LDA over time as assessed by the SDAI

    Time: Baseline through Week 12

    Description: Proportion of patients with CDAI score ≤ 10 over time

    Measure: Proportion of patients with LDA over time as assessed by the CDAI

    Time: Baseline through Week 12

    Description: Proportion of patients achieving ACR20/50/70 response over time

    Measure: Proportion of patients achieving ACR20/50/70 response over time

    Time: Baseline through Week 12

    Description: Proportion of patients achieving moderate or good EULAR response over time

    Measure: Proportion of patients achieving moderate or good EULAR response over time

    Time: Baseline through Week 12

    Description: Proportion of patients achieving a MCID of 0.22 in HAQ-DI over time

    Measure: Proportion of patients achieving a minimally clinically important difference (MCID) of 0.22 in the Health Assessment Questionnaire-Disability Index (HAQ-DI) over time

    Time: Baseline through Week 12
    17 A Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of GLPG3970, Administered Orally for 6 Weeks in Adult Subjects With Moderately to Severely Active Rheumatoid Arthritis and an Inadequate Response to Methotrexate

    The primary objective of this study is to evaluate the effect of GLPG3970 compared to placebo on the signs and symptoms of Rheumatoid Arthritis (RA) in participants with moderately to severely active RA and an inadequate response to methotrexate (MTX).

    NCT04577781
    Conditions
    1. Arthritis, Rheumatoid
    Interventions
    1. Drug: GLPG3970
    2. Drug: Placebo
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Measure: Change From Baseline in Disease Activity Score Based on 28 Joints (DAS28) (C-reactive protein [CRP]) at Week 6

    Time: Baseline and Week 6

    Secondary Outcomes

    Measure: Incidence of Treatment-emergent Adverse Events (TEAEs) by Severity

    Time: Screening up to Follow-up (Week 11)

    Measure: Observed Plasma Trough Concentration (Ctrough) of GLPG3970

    Time: Predose (within 30 minutes prior to dosing) on Days 15, 29 and 43
    18 Study of the Viral Load and Humoral and Cellular B and T Responses in Patients With Rheumatoid Arthritis and Spondyloarthritis Under Immunosuppressive Treatments

    The purpose of this study is to assess whether immunosuppressive therapies used by patients with chronic inflammatory rheumatic diseases have an impact on the viral load and the humoral and cellular responses during viral infection with SarSCoV2, compared to members of their family cluster infected with the same viral strain.

    NCT04584541
    Conditions
    1. Spondyloarthritis
    2. Rheumatoid Arthritis
    3. Covid19
    Interventions
    1. Biological: blood tests
    2. Biological: Nasopharyngeal swabs
    3. Biological: Stools
    MeSH:Arthritis Arthritis, Rheumatoid Spondylarthritis
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Description: Nasopharyngeal swabs : Detection of SarS-Cov-2 RNA

    Measure: Detection of SarS-Cov-2 RNA in feces and nasopharyngeal swabs

    Time: up to Day 30

    Description: Nasopharyngeal swabs : Detection of SarS-Cov-2 RNA

    Measure: Detection of SarS-Cov-2 RNA in feces and nasopharyngeal swabs

    Time: between Day 30 and Day 90

    Measure: Detection and quantification of IgG, IgM and IgA specific for SarS-Cov-2 N and S proteins in blood

    Time: up to Day 30

    Measure: Detection and quantification of IgG, IgM and IgA specific for SarS-Cov-2 N and S proteins in blood

    Time: between Day 30 and Day 90

    Measure: Detection and quantification of IgG, IgM and IgA specific for SarS-Cov-2 N and S proteins in blood

    Time: 6 Months

    Measure: Detection and quantification of IgG, IgM and IgA specific for SarS-Cov-2 N and S proteins in blood

    Time: 12 Months

    Measure: Detection and quantification of IgG, IgM and IgA specific for SarS-Cov-2 N and S proteins in blood

    Time: 24 Months

    Measure: Isolation and characterization of B and T lymphocytes in blood

    Time: up to Day 30

    Measure: Isolation and characterization of B and T lymphocytes in blood

    Time: between Day 30 and Day 90

    Measure: Isolation and characterization of B and T lymphocytes in blood

    Time: 6 Months

    Measure: Isolation and characterization of B and T lymphocytes in blood

    Time: 12 Months

    Measure: Isolation and characterization of B and T lymphocytes in blood

    Time: 24 Months
    19 A Phase 1 Study to Evaluate OATP Transporter-Mediated Drug-Drug Interactions Between Filgotinib and Statins as Probe Drugs in Healthy Participants

    The primary objective of this study is to evaluate the effect of filgotinib on a mixed organic anion transporting polypeptide/cytochrome P450 3A (OATP/CYP3A), OATP/ breast cancer resistance protein (BCRP), and OATP substrates using phenotypic probes.

    NCT04608344
    Conditions
    1. Rheumatoid Arthritis
    Interventions
    1. Drug: Atorvastatin
    2. Drug: Pravastatin
    3. Drug: Rosuvastatin
    4. Drug: Filgotinib
    MeSH:Arthritis Arthritis, Rheumatoid
    HPO:Arthritis Polyarticular arthritis Rheumatoid arthritis

    Primary Outcomes

    Measure: Area Under the Concentration Versus Time Curve From Time Zero to the Last Quantifiable Concentration (AUClast) of ATV, PRA, and ROS

    Time: Pre-dose, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 16, 24, 36, 48 and 72 hours post dose (Sequence AB: Days 1 and 12 up to 48 hours; Days 3 and 14 up to 72 hours. Sequence BA: Days 6 and 18 up to 48 hours; Days 8 and 20 up to 72 hours)

    Measure: Area Under the Concentration Versus Time Curve Extrapolated to Infinite Time (AUCinf) of ATV, PRA, and ROS

    Time: Pre-dose, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 16, 24, 36, 48 and 72 hours post dose (Sequence AB: Days 1 and 12 up to 48 hours; Days 3 and 14 up to 72 hours. Sequence BA: Days 6 and 18 up to 48 hours; Days 8 and 20 up to 72 hours)

    Measure: Maximum Observed Plasma Concentration (Cmax) for ATV, PRA, and ROS

    Time: Pre-dose, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 16, 24, 36, 48 and 72 hours post dose (Sequence AB: Days 1 and 12 up to 48 hours; Days 3 and 14 up to 72 hours. Sequence BA: Days 6 and 18 up to 48 hours; Days 8 and 20 up to 72 hours)

    Secondary Outcomes

    Measure: Percentage of Participants Experiencing Treatment-Emergent Adverse Events

    Time: Up to 26 days for sequence AB and up to 29 days for sequence BA

    Measure: Percentage of Participants Experiencing Laboratory Abnormalities

    Time: Up to 26 days for sequence AB and up to 29 days for sequence BA

    HPO Nodes


    HP:0001369: Arthritis
    Genes 269
    PADI4 AEBP1 KLRC4 IL12A-AS1 NLRP3 COL5A1 HLA-DRB1 TGFB3 NTRK1 NLRP3 FCGR2B GBA GJB2 GP1BB TRPV4 PTPN22 NLRP12 SCARB2 LEMD3 SLC37A4 ABCG8 SEC61A1 IL2RB HPRT1 SEC24C TRAPPC2 HLA-B MVK TF STAT4 FGFR3 NLRP3 RREB1 MMP2 COL2A1 FBN1 MMP14 EXT1 CFI APOE HJV ARVCF MLX STAT4 GCH1 ANKH HLA-C COL2A1 TBX1 HGD F9 ACAN HPRT1 LRBA IL2RA UMOD COMP PRPS1 MYH14 GJB6 PRG4 OCRL ADAR UFSP2 MMP13 JMJD1C UFD1 CCR6 ANKH IL6 LMX1B RAG1 HPRT1 PSTPIP1 HNF1B DNASE1L3 MATN3 KIF7 SPP1 G6PC PHEX SPTB PTPN2 LRRC8A COL9A2 PTPN22 CD244 IGHM NLRP3 CD79A IGLL1 MATN3 CD79B PRKCD HOXD10 COMP ACP5 MTHFD1 MIR140 BLNK HLA-DRB1 SLCO2A1 RASGRP1 ANKRD55 CAV1 HLA-B COL5A2 PFKM NLRP3 BTK IL10 PIK3CD GLA COL9A1 SLC4A1 MEFV FCGR2A RNF168 RAG2 COL11A1 PTPN2 GDF5 AIP COL1A1 COL5A1 SLC12A3 SLC22A4 FASLG MEFV CD247 SH3KBP1 EXT2 COL2A1 F8 CLCNKB DNASE1 MEFV STAT3 IL2RA TRPS1 HPGD CLCN7 IFIH1 BTK HLA-DRB1 KIF22 ANKRD55 NOD2 TRAPPC2 WIPF1 ACAN MATN3 HNF4A FAS HGD ASPN RNASEH2A COMT TBX1 HPGD ASAH1 LACC1 DNAJB11 PSMB9 MEFV FAS FAS COL2A1 UBAC2 LMNA LBR FRZB MUC1 SLC40A1 STAT4 STAT4 ADA2 TRPV4 SMAD3 CD247 HLA-B ACAN PHEX RNASEH2C SLC37A4 VPS13A SPTA1 ASAH1 MYD88 MIF ACP5 PSMB4 TLR4 TNFRSF11B IRAK1 CCN2 MMP13 CLCN7 CCN6 COPA ZNF687 ERAP1 TREX1 IL2RB TNFRSF1A COMP CTLA4 C4A COL2A1 TREX1 BTK UFSP2 IL12B AGA RNASEH2B DCLRE1C ATP7B LRP6 ANK1 FOXP3 HNF1B COL1A1 WAS KNSTRN PTPN22 COL11A2 ZMPSTE24 MVK COL9A1 TCF3 IL12A COL11A2 PSTPIP1 GNAS NOD2 COMP SAMHD1 IRF5 COL9A3 IL10 CCR1 SLC26A2 HIRA GHR PIK3R1 COL9A2 HPRT1 EPCAM TFR2 COL9A3 IL36RN COL2A1 EPB42 COL11A2 GPR101 COL3A1 CCN6 ATP7B IL23R NFKBIL1 SMAD3 CTLA4 PTPN22 UMOD CIITA HPGD CASP10 PTPN22 CANT1
    Protein Mutations 4
    A147T N363S R620W V600E

    HPO

    Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials


    HPO Nodes


    HP:0001369: Arthritis
    Genes 269
    PADI4 AEBP1 KLRC4 IL12A-AS1 NLRP3 COL5A1 HLA-DRB1 TGFB3 NTRK1 NLRP3 FCGR2B GBA GJB2 GP1BB TRPV4 PTPN22 NLRP12 SCARB2 LEMD3 SLC37A4 ABCG8 SEC61A1 IL2RB HPRT1 SEC24C TRAPPC2 HLA-B MVK TF STAT4 FGFR3 NLRP3 RREB1 MMP2 COL2A1 FBN1 MMP14 EXT1 CFI APOE HJV ARVCF MLX STAT4 GCH1 ANKH HLA-C COL2A1 TBX1 HGD F9 ACAN HPRT1 LRBA IL2RA UMOD COMP PRPS1 MYH14 GJB6 PRG4 OCRL ADAR UFSP2 MMP13 JMJD1C UFD1 CCR6 ANKH IL6 LMX1B RAG1 HPRT1 PSTPIP1 HNF1B DNASE1L3 MATN3 KIF7 SPP1 G6PC PHEX SPTB PTPN2 LRRC8A COL9A2 PTPN22 CD244 IGHM NLRP3 CD79A IGLL1 MATN3 CD79B PRKCD HOXD10 COMP ACP5 MTHFD1 MIR140 BLNK HLA-DRB1 SLCO2A1 RASGRP1 ANKRD55 CAV1 HLA-B COL5A2 PFKM NLRP3 BTK IL10 PIK3CD GLA COL9A1 SLC4A1 MEFV FCGR2A RNF168 RAG2 COL11A1 PTPN2 GDF5 AIP COL1A1 COL5A1 SLC12A3 SLC22A4 FASLG MEFV CD247 SH3KBP1 EXT2 COL2A1 F8 CLCNKB DNASE1 MEFV STAT3 IL2RA TRPS1 HPGD CLCN7 IFIH1 BTK HLA-DRB1 KIF22 ANKRD55 NOD2 TRAPPC2 WIPF1 ACAN MATN3 HNF4A FAS HGD ASPN RNASEH2A COMT TBX1 HPGD ASAH1 LACC1 DNAJB11 PSMB9 MEFV FAS FAS COL2A1 UBAC2 LMNA LBR FRZB MUC1 SLC40A1 STAT4 STAT4 ADA2 TRPV4 SMAD3 CD247 HLA-B ACAN PHEX RNASEH2C SLC37A4 VPS13A SPTA1 ASAH1 MYD88 MIF ACP5 PSMB4 TLR4 TNFRSF11B IRAK1 CCN2 MMP13 CLCN7 CCN6 COPA ZNF687 ERAP1 TREX1 IL2RB TNFRSF1A COMP CTLA4 C4A COL2A1 TREX1 BTK UFSP2 IL12B AGA RNASEH2B DCLRE1C ATP7B LRP6 ANK1 FOXP3 HNF1B COL1A1 WAS KNSTRN PTPN22 COL11A2 ZMPSTE24 MVK COL9A1 TCF3 IL12A COL11A2 PSTPIP1 GNAS NOD2 COMP SAMHD1 IRF5 COL9A3 IL10 CCR1 SLC26A2 HIRA GHR PIK3R1 COL9A2 HPRT1 EPCAM TFR2 COL9A3 IL36RN COL2A1 EPB42 COL11A2 GPR101 COL3A1 CCN6 ATP7B IL23R NFKBIL1 SMAD3 CTLA4 PTPN22 UMOD CIITA HPGD CASP10 PTPN22 CANT1
    Protein Mutations 4
    A147T N363S R620W V600E

    Reports

    Data processed on September 26, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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    4,180 reports on interventions/drugs

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    691 reports on MeSH terms

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