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NCT06680037 · TG Therapeutics, Inc.

A Study to Assess the Safety and Clinical Activity of Azer-cel in Participants With B-cell Mediated Autoimmune Disorders

What this study is about

The main objective of the study is to determine the recommended phase 2 dose (RP2D) of Azercabtagene zapreleucel (azer-cel).

View original scientific description

The main objective of the study is to determine the recommended phase 2 dose (RP2D) of Azercabtagene zapreleucel (azer-cel).

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • PMS and RMS inclusion criteria:
  • Age 18 years to ≤60 years (inclusive) at screening.
  • Expanded Disability Status Scale (EDSS) score 3.0 - 6.5 (inclusive) at screening.
  • Diagnosis of primary progressive multiple sclerosis (PPMS), secondary progressive multiple sclerosis (non-active or active), or Relapsing MS (RMS).
  • Documented evidence of disability progression independent of relapse (PIRA) at any point over the 12 months prior to the screening visit. NMOSD inclusion criteria:
  • Between age 18 and 65 years, inclusive at the time of signing the informed consent.
  • EDSS score between 2.0 and 7.0 at screening, inclusive (for higher EDSS, the Investigator must assess that the participant is reasonably able to participate in the study).
  • Diagnosis of anti-aquaporin-4 immunoglobulin G (AQP4-IgG) seropositive at screening (verified by the allocated central laboratory) and Neuromyelitis Optica Spectrum Disorder (NMOSD).
  • Must meet the appropriate NMOSD treatment washout criteria prior to receiving lymphodepletion. MG Inclusion criteria:
  • Age ≥18 and ≤70 years of age at the time of signing the informed consent.
  • Diagnosed with gMG at least 1 year prior to the date of signing the informed consent.
  • Confirmation of MG Diagnosis:
  • Positive serologic test for anti-acetylcholine receptor (AChR) antibodies or anti-muscle-specific kinase (MuSK) antibodies confirmed at screening AND
  • One of the following (either historical or during screening):
  • Abnormal neuromuscular transmission test demonstrated by single-fiber electromyography or repetitive nerve stimulation.
  • Positive anticholinesterase test (e.g., edrophonium chloride test).
  • Demonstrated improvement in MG signs on oral cholinesterase inhibitors, as assessed by the treating physician.
  • MG activities of daily living (MG-ADL) score ≥6 at screening. CIDP Inclusion criteria
  • Age ≥18 and ≤70 years of age at the time of signing the informed consent.
  • Participant must have either typical CIDP, or one of the following two CIDP variants: motor CIDP, multifocal CIDP (also known as Lewis Sumner Syndrome).
  • CIDP Disease Activity Status (CDAS): CDAS score ≥3 at screening.
  • INCAT Disability Score: INCAT disability score ≥4 to ≤9 score at screening. General

Exclusion criteria

  • History of malignancy that has not been in remission for at least 2 years.
  • Viral Screening
  • Evidence of chronic active or history of hepatitis B virus (HBV).
  • Seropositive for human immunodeficiency virus (HIV) antibody.
  • History of bone marrow/hematopoietic stem cell or solid organ transplantation.
  • Prior treatment with adoptive T-cell therapy or any gene therapy product directed at any target (e.g. CAR T-cell therapy). Note: Other protocol-specified Inclusion/Exclusion criteria may apply.

Where

  • La Jolla, California
  • Ann Arbor, Michigan
  • Omaha, Nebraska
  • New York, New York
  • Rochester, New York
  • Cleveland, Ohio
  • Columbus, Ohio
  • Milwaukee, Wisconsin

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Jun 18, 2026 · Source of record for eligibility and locations

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1 of 100 participants interested
1% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

La Jolla

California

Location available
RECRUITING

Ann Arbor

Michigan

Location available
RECRUITING

Omaha

Nebraska

Location available
View Omaha location page
RECRUITING

New York

New York

Location available
RECRUITING

Rochester

New York

Location available
RECRUITING

Cleveland

Ohio

Location available
RECRUITING

Columbus

Ohio

Location available
RECRUITING

Milwaukee

Wisconsin

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for B-cell Mediated Autoimmune Disorders Treatment in La Jolla?

Join others in California exploring innovative treatment options through clinical research

B-cell Mediated Autoimmune Disorders Treatment Options in La Jolla, California

If you're searching for B-cell Mediated Autoimmune Disorders treatment in La Jolla, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in La Jolla, Ann Arbor, Omaha and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with B-cell Mediated Autoimmune Disorders. All study-related care is provided at no cost to participants.

Local Sites
3 locations in California
Now Enrolling
Up to 100 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for B-cell Mediated Autoimmune Disorders?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for B-cell Mediated Autoimmune Disorders

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This B-cell Mediated Autoimmune Disorders Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT06680037. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.