Minneapolis, MNNCT06308978Now EnrollingIRB Ready

Antineutrophilic Cytoplasmic Antibody (ANCA)- Associated Vasculitis (AAV) Clinical Trial in Minneapolis, MN

Access cutting-edge antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) treatment through this clinical trial at a research site in Minneapolis. Study-provided care at no cost to qualified participants.

Sponsored by Fate Therapeutics

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Expert Care in Minneapolis

Access antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) treatment provided free

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Check if you qualify for this antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) clinical trial in Minneapolis, MN

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Why Participate?

  • No-Cost Study Care

  • Local to Minneapolis

    Convenient for MN residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Minneapolis site if eligible
  4. 4Begin participation

About This Antineutrophilic Cytoplasmic Antibody (ANCA)- Associated Vasculitis (AAV) Study in Minneapolis

This is a phase 1 study designed to evaluate the safety, pharmacokinetics (PK), and anti-B-cell activity of FT819 following treatment with or without auxiliary medicinal product (AMP) in participants with moderate-to-severe active systemic lupus erythematosus (SLE) with or without nephritis, antineutrophilic cytoplasmic antibody (ANCA)-associated vasculitis (AAV), idiopathic inflammatory myositis (IIM), and systemic sclerosis (SSc). The study will consist of a dose-escalation stage, followed by an expansion stage to further evaluate the safety and activity of FT819.

Sponsor: Fate Therapeutics

Who Can Participate

Inclusion Criteria

Age: 12 to 70 years old.
Diagnosis: Must have active B-cell mediated autoimmune disease (SLE, AAV, IIM, or SSc) confirmed by standard criteria.
Disease Severity: Moderate to severe, requiring at least two prior treatments that were ineffective.
Health Status: Adequate organ function to tolerate treatment.
Consent: Able to provide informed consent or assent/obtain parental consent and comply with study procedures. Key

Exclusion Criteria

Pregnancy/Breastfeeding: Women must not be pregnant or nursing.
Severe Organ Dysfunction: Significant heart, lung, liver, or kidney impairment.
Active Infections: No recent or ongoing serious infections.
Recent Cancer or Prior Cell Therapy: No active/recent malignancies, prior CAR T-cell therapy, or organ transplant.
Allergies: No known allergies to study treatments.
Weight Restriction: Must weigh at least 50 kg (110 lbs).

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Minneapolis?

Yes, this clinical trial (NCT06308978) has an active research site in Minneapolis, MN that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Antineutrophilic Cytoplasmic Antibody (ANCA)- Associated Vasculitis (AAV) Treatment Options in Minneapolis, MN

If you're searching for antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) treatment options in Minneapolis, MN, this clinical trial (NCT06308978) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Minneapolis research site is actively enrolling participants for this clinical trial. You'll receive care from experienced antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all antineutrophilic cytoplasmic antibody (anca)- associated vasculitis (aav) clinical trials near you to find additional studies recruiting in your area.

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