Port Orange, FLNCT07610837Now EnrollingIRB Ready

Liver Fibrosis Clinical Trial in Port Orange, FL

Access cutting-edge liver fibrosis treatment through this clinical trial at a research site in Port Orange. Study-provided care at no cost to qualified participants.

Sponsored by AstraZeneca

Quick Self-Assessment

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Expert Care in Port Orange

Access liver fibrosis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related liver fibrosis treatment provided free

Apply for This Port Orange Location

Check if you qualify for this liver fibrosis clinical trial in Port Orange, FL

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

Why Participate?

  • No-Cost Study Care

  • Local to Port Orange

    Convenient for FL 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 Port Orange site if eligible
  4. 4Begin participation

About This Liver Fibrosis Study in Port Orange

The purpose of this study is to evaluate the safety, tolerability, and pharmacodynamic effects of AZD2389 in adult participants with steatotic liver disease (SLD) and advanced fibrosis.

Sponsor: AstraZeneca

Who Can Participate

Inclusion Criteria

Males/females aged 18 or over
A diagnosis of SLD with advanced fibrosis
No significant change in weight over the last 6 months
Contraceptive us by participants or participants partners
Capable of giving informed consent
Judged by the investigator to be suitable for study Key

Exclusion Criteria

Portal hypertension (LSM \>25 kPa or 20-25 kPa with platelets \<150×10⁹/L), decompensated liver disease, Child-Pugh \>A6, MELD \>12, other chronic liver diseases, prior/planned liver transplant, or malignant liver tumors.
Positive viral infections, including HIV or hepatitis B, or hepatitis C unless HCV RNA-negative ≥12 weeks after treatment.
Alcohol intake above protocol thresholds, or positive screen for drugs of abuse.
Significant metabolic, cardiovascular, or GI disorders, including T1DM or insulin-treated T2DM, uncontrolled hypertension, recent major cardiac/cerebrovascular events, severe heart failure, serious arrhythmias, significant pancreatic disease, or major GI surgery.
History of psychosis, bipolar disorder, recent major depression, or suicide attempt/ideation within 1 year.
Bleeding risk or wound-healing concerns, including coagulation disorders, major bleeding history, active wounds or recent major surgery, or severe dermatologic immune conditions.
Prohibited medications or hypersensitivities, including moderate/strong CYP3A4 or BCRP/OAT3 inhibitors/inducers, anticoagulants/antiplatelets (except aspirin ≤81 mg/day), or hypersensitivity to DPP4 inhibitors.
Other protocol-defined exclusions, including significant abnormal labs (e.g., worsening ALT/AST), recent participation in another IMP study, or investigator judgment of unsuitability.

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 Port Orange?

Yes, this clinical trial (NCT07610837) has an active research site in Port Orange, FL 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.

Liver Fibrosis Treatment Options in Port Orange, FL

If you're searching for liver fibrosis treatment options in Port Orange, FL, this clinical trial (NCT07610837) 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 Port Orange research site is actively enrolling participants for this clinical trial. You'll receive care from experienced liver fibrosis 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 liver fibrosis clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Port Orange, FL