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D012859: Sjogren's Syndrome

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 (7)


Name (Synonyms) Correlation
drug576 C21 Wiki 0.50
drug3616 VIB4920 Wiki 0.50
drug683 CPI-006 Wiki 0.50
Name (Synonyms) Correlation
drug2744 Questionnaire by phone call Wiki 0.50
drug567 Bucillamine Wiki 0.35
drug3097 Serological test Wiki 0.29
drug2505 Placebo Wiki 0.07

Correlated MeSH Terms (15)


Name (Synonyms) Correlation
D008180 Lupus Erythematosus, Systemic NIH 0.61
D025241 Spondylarthritis NIH 0.50
D001327 Autoimmune Diseases NIH 0.45
Name (Synonyms) Correlation
D012507 Sarcoidosis NIH 0.35
D001167 Arteritis NIH 0.35
D009220 Myositis NIH 0.35
D001528 Behcet Syndrome NIH 0.35
D015535 Arthritis, Psoriatic NIH 0.29
D011111 Polymyalgia Rheumatica NIH 0.29
D013700 Giant Cell Arteritis NIH 0.29
D001168 Arthritis NIH 0.26
D001172 Arthritis, Rheumatoid NIH 0.15
D013577 Syndrome NIH 0.05
D045169 Severe Acute Respiratory Syndrome NIH 0.02
D018352 Coronavirus Infections NIH 0.02

Correlated HPO Terms (5)


Name (Synonyms) Correlation
HP:0002960 Autoimmunity HPO 0.50
HP:0002725 Systemic lupus erythematosus HPO 0.45
HP:0012089 Arteritis HPO 0.35
Name (Synonyms) Correlation
HP:0001369 Arthritis HPO 0.29
HP:0001370 Rheumatoid arthritis HPO 0.18

Clinical Trials

Navigate: Correlations   HPO

There are 4 clinical trials


1 A Phase 2 Randomized, Double-blind, Placebo-controlled, Proof of Concept Study to Evaluate the Efficacy and Safety of VIB4920 in Subjects With Sjögren's Syndrome (SS)

The purpose of the study is to evaluate the efficacy, safety, and tolerability of VIB4920 (formerly MEDI4920) in adult participants with Sjögren's Syndrome (SS).

NCT04129164
Conditions
  1. Sjögren's Syndrome
Interventions
  1. Drug: VIB4920
  2. Drug: Placebo
MeSH:Sjogren's Syndrome Syndrome

Primary Outcomes

Measure: Change From Baseline in European League Against Rheumatism (EULAR) Sjögren's Syndrome Disease Activity Index (ESSDAI) at Day 169 in Population 1

Time: Baseline (Day 1) and Day 169

Measure: Change From Baseline in EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI) at Day 169 in Population 2

Time: Baseline (Day 1) and Day 169

Secondary Outcomes

Measure: Change From Baseline in ESSPRI at Day 169 in Population 1

Time: Baseline (Day 1) and Day 169

Measure: Percentage of Participants achieving ESSDAI [3] and ESSDAI [4] response in Population 1

Time: Baseline (Day 1) to Day 169

Measure: Percentage of Participants achieving ESSPRI response in Population 2

Time: Baseline (Day 1) to Day 169

Measure: Change From Baseline in Functional Assessment of Chronic Illness Therapy (FACIT) - Fatigue Score at Day 169 in Populations 1 and 2

Time: Baseline (Day 1) and Day 169

Measure: Change From Baseline in Ocular Surface Disease Index (OSDI) at Day 169 in Populations 1 and 2

Time: Baseline (Day 1) and Day 169

Measure: Patient's Global Impression of Severity at Day 169 in Populations 1 and 2

Time: Day 169

Measure: Number of participants With Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Events (TESAEs) in Populations 1 and 2

Time: From Baseline (Day 1) up to Day 365

Measure: Number of participants With Adverse Events of Special Interest (AESIs) in Populations 1 and 2

Time: From Baseline (Day 1) up to Day 365

Measure: Number of Participants With Abnormal Laboratory Parameters, Vital Signs, and Electrocardiograms (ECGs) Reported as TEAEs in Populations 1 and 2

Time: From Baseline (Day 1) up to Day 365

Measure: Plasma Concentration of VIB4920

Time: Day 1 to Day 365

Measure: Percentage of Participants With Positive Antibody Titer to VIB4920 in Populations 1 and 2

Time: Day 1 to Day 365
2 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
3 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
4 Serologic Profile of SARS CoV2 in COVID-19 Patients With Systemic Diseases

An observational study aiming to assess the serological profile of SARS-Cov2 patients with systemic diseases such as systemic lupus erythematosus, Sjogren syndrome, sarcoidosis, inflammatory myopathies, Behçet's disease, Rheumatoid arthritis and Spondyloarthritis

NCT04530461
Conditions
  1. SARS-CoV Infection
  2. Systemic Disease
  3. Systemic Lupus Erythematosus
  4. Sjogren's Syndrome
  5. Sarcoidosis
  6. Inflammatory Myopathy
  7. Behçet Disease
  8. Rheumatoid Arthritis
  9. Spondyloarthritis
Interventions
  1. Diagnostic Test: Serological test
MeSH:Coronavirus Infections Severe Acute Respiratory Syndrome Sjogren's Syndrome Myositis Behcet Syndrome Sarcoidosis Lupus Erythematosus, Systemic
HPO:Inflammatory myopathy Myositis Systemic lupus erythematosus

Primary Outcomes

Description: Number of patients with positive serological test of SARS Cov2

Measure: Serological Profile

Time: Inclusion

HPO Nodes


HPO

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


HPO Nodes


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.

Drug Reports   MeSH Reports   HPO Reports  

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MeSH

691 reports on MeSH terms

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Alphabetical index of all Terms

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