Biologics and Clinical Immunology Cohort At Sinai

NCT ID: NCT04784364

Last Updated: 2024-11-06

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 800 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-03-03
• Study Completion Date: 2028-11-30

Brief Summary

The study team plans to establish a bioregistry of patients receiving biologic therapy as part of their standard treatment at the Mount Sinai Therapeutic Infusion Center and affiliated practices. The study team will to apply state-of-the-art approaches to assessing and predicting immunological and clinical responses associated with these standards and prescribed treatments. The approach is twofold. The first component is to establish a robust and flexible biorepository and database that includes demographic, immunologic, exposure and clinical records, and can facilitate research across disciplines, and across other registries affiliated with Mount Sinai. The second component is to address specific key research questions focused on using novel diagnostics to increase the effectiveness of biologic treatment. Most patients will be recruited from the Mount Sinai Therapeutic Infusion Center (TIC), although others receiving infusions elsewhere or at home will be recruited from outpatient Sinai affiliated clinical practices.

Detailed Description

The study team proposes a twofold approach to determine how immunophenotype may affect the course of clinical immunological disease for patients receiving biologic therapy. First, the team intends to establish a biorepository and database that includes demographic, immunologic, exposure and clinical records. The registry will be set up to facilitate research across disease disciplines, and across other registries affiliated with ISMMS. Second, over time, the team aims to address specific and an increasing number of research questions focused on using novel diagnostics to increase the effectiveness of biologic treatment as outlined below. Most subjects will be recruited from the Mount Sinai Therapeutic Infusion Center (TIC), although others receiving infusions elsewhere or at home will be recruited from outpatient affiliated clinical practices during scheduled medical visits.

Specific Aims:

1. (Overarching) Build a repository of biological specimens, questionnaire data, and apply state-of-the-art assessment tools to assess the current immunological and clinical condition, and changes over time. Specimens and data will be collected in a manner that can readily incorporate new technology, new research questions, link to intelligent analytics, and provide a resource for future consortia across disciplines. An infrastructure will be created that includes a multi-disciplinary Steering Committee to facilitate spinoff research studies and harmonize protocols within the TIC and across the Sinai system, resolve procedural questions, and communicate updated policies to referring physicians.

Additional initial specific scientific aims related to responses to biologics prescribed as part of standard practice that will be considered in this proposal are to determine:

2 . Effects of anti-IgE therapy on IgE phenotypes, maturation and production, and clinical outcomes.

3. Effects of anti-IgE and anti-IL-5 therapies on dopaminergeric pathways and clinical outcomes.

4. Effects of anti-TNF, anti-CD20, and other biologic therapies on immunological and clinical outcomes.

5. Effects of IVIG therapy on immunological and clinical course in Common Variable Immune Deficiency.

Futures studies will focus on Clinical Decision Support (CDS), Artificial Intelligence, and use of technology to inform and educate current TIC patients. Future studies also will feature studies related to immunological and clinical responses to additional biological therapies.

Background The prescription of biological agents and immune modulators to treat chronic immunological-based diseases continues to expand. This trend is predicted to continue. Applying data-driven and immunophenotype-driven approaches to their use could reveal additional pharmacologic targets and signal disease presence or relapse prior to the onset of clinical symptoms. These advances in precision medicine also may reduce adverse drug reactions and help control overall cost of healthcare associated with inefficient and 'trial and error' prescribing. They also may provide information on susceptible individuals and their appropriate care during healthcare crises, such as the current COVID-19 pandemic.

Despite these developments, prospective studies and clinical trials that feature immunophenotyping to facilitate 'real world' therapeutic decision-making are limited. More comprehensive immunophenotyping has predicted clinical responses to cancer immunotherapy, suggesting that this approach may translate to immunologically-mediated nonmalignant diseases. But widespread application to multiple chronic diseases is limited by several research gaps. These include determination of: 1) new biomarkers (discovery, validation) that may inform clinicians of drug responsive endotypes, 2) biomarkers that predict disease course over time in replicate studies, 3) optimal methods to link immunophenotype with analytic diagnostic and clinical decision-making tools to predict disease course, 4) factors that mediate treatment responses, some of which may be modifiable (eg environmental exposures, viruses, disease phenotypes).

The Mount Sinai Therapeutic Infusion Center is an ideal location where investigators have the potential to fill in many of these research gaps. The volume is large, with currently 1803 individuals actively (in 2019) receiving anti-cytokine or anti-CD20 biological treatment for their immunological, dermatological and neurological disorders, largely prescribed by members of the Divisions of Clinical Immunology, Rheumatology, Pulmonary, Inflammatory Bowel Disease (IBD), Neurology and Dermatology. Further, investigators across Divisions (Clinical Immunology, Rheumatology, IBD) and Departments (Medicine, Neurology, Dermatology) have created a research working group to discuss collaborations and standardized approaches to assessing immunological responses to biologics. This registry also intends to coordinate with other registries at ISMMS to ensure that it utilizes common approaches to biomonitoring and common data elements as much as feasible to facilitate comparisons across cohorts.

Primary and Secondary Study Endpoints

The initial scientific hypotheses focus on these endpoints:

Aim 1 An expanded repository of biological specimens and questionnaire data.

Aim 2 Measures of IgE phenotypes and associated clinical airway outcomes.

Aim 3 Measures of changes in the dopaminergic pathway and clinical airway outcomes.

Aim 4 Measures of anti-TNF, anti-CD20, and other biologic therapies on immunological and clinical outcomes.

Aim 5 Measures of IVIG-induced immunological and clinical outcomes.

Conditions

Immunological Disease; Autoimmune Diseases; Primary Immune Deficiency

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Age 12 years and up.
• Able to provide informed consent.
• Medical care at Mount Sinai.
• Receiving a biologic medication or immune modulator at Mount Sinai, or considered an appropriate negative control or comparison participant by the study team.

• Minimum Eligible Age: 12 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Icahn School of Medicine at Mount Sinai

OTHER

Sponsor Role: lead

Responsible Party

Rachel Miller

Chief, Division of Clinical Immunology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Rachel Miller

Role: PRINCIPAL_INVESTIGATOR

Icahn School of Medicine

Locations

Mount Sinai

New York, New York, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Sarah Alvi

Role: CONTACT

Sarah.Alvi@mssm.edu

212-659-9416

Sonia Parmar

Role: CONTACT

sonia.parmar@mssm.edu

973-944-8221

Facility Contacts

Sarah Alvi

Role: primary

Sarah.Alvi@mssm.edu

Rachel Miller

Role: backup

rachel.miller2@mssm.edu

2126599436

Rachel Miller

Role: backup

Other Identifiers

HSM 20-01252

Identifier Type: -

Identifier Source: org_study_id