Clinical Trials for Advanced Infusion Treatments in New Jersey

Clinical Research at a High-Volume Outpatient Infusion Center Serving South Jersey & the Philadelphia REgion

Idyllic Infusion Treatment Center is an outpatient infusion practice operated under Arthritis, Rheumatic & Back Disease Associates, P.A., and one of New Jersey’s most active settings for biologic infusion therapy. In just one year, we've completed 29,000+ infusions for over 8,000 patients with complex autoimmune, inflammatory, neurological, and bone disease conditions. That volume, combined with our board-certified ARBDA healthcare practitioners, makes us a strong option for patients considering clinical trial participation.

For patients in South Jersey and across the Philadelphia region who haven’t found adequate relief through standard therapies, a clinical trial can open access to emerging treatments before they’re widely available. We’re a preferred referral destination for complex inflammatory and autoimmune cases among local referring providers, a status earned through 15+ years of innovative, patient-focused care. Our outpatient setting also means trial participation happens in a comfortable, cost-conscious environment rather than a hospital infusion department.

To ask about clinical trial enrollment or find out whether you qualify for a current study, call us at (856) 267-3966.

What Are Clinical Trials for Advanced Infusion Treatments?

Clinical trials assess the safety and effectiveness of new drugs, therapies, or medical devices designed to target autoimmune diseases, inflammatory conditions, and other complex health concerns. 

These studies generally fall into two categories:

• Interventional studies: Participants may be randomly assigned to receive one of two or more treatments.
• Observational studies: Participants are monitored over time without changing their standard treatment plans.

These trials collect data to determine whether a new treatment offers benefits over existing options. Researchers also track adverse events, such as side effects or complications. 

What Does PArticipating in a Clinical Trial Involve?

Understanding where a trial sits in its development phase helps set expectations about what participation involves:

• Phase I: Tests a new treatment in a small group primarily to assess safety and determine appropriate dosage.
• Phase II: Expands testing to evaluate how effective the treatment is for a specific disease or condition.
• Phase III: Compares the new treatment to existing standard-of-care options using a larger patient population.
• Phase IV: Conducted after FDA approval to monitor long-term safety and effectiveness in a broad patient population.

Most infusion-based clinical trials for autoimmune and inflammatory conditions fall into Phase II or Phase III, where the focus shifts from initial safety to how the treatment compares with existing biologic medications.

Once enrolled, participation typically involves: 

• Medication administration
• Symptom tracking
• Regular follow-up visits

Taking part in clinical research studies may also provide access to new biologic medications that aren’t yet available to the public. Beyond the potential personal benefit, data collected through these trials helps shape future care guidelines and support the development of safer, more effective therapies for a wide range of autoimmune and inflammatory conditions.

Who Can Participate?

Each clinical trial has a study protocol that outlines eligibility requirements, and participants go through a thorough screening process before enrollment. Screening typically includes a physical exam, a review of medical records, and sometimes imaging studies. Patients with chronic autoimmune conditions who haven’t responded adequately to conventional therapies are often strong candidates for trial enrollment.

Before joining a clinical research trial, you’ll receive an informed consent document outlining the study’s purpose, risks, potential benefits, and any procedures involved. This is a formal part of the process, not a formality: you should read it carefully and ask our team any questions before agreeing to participate. Participation is entirely voluntary, and you can withdraw at any point without penalty or impact on your future care.