Louisville, KYNCT07604974Now EnrollingIRB Ready

Hypertriglyceridemia Clinical Trial in Louisville, KY

Access cutting-edge hypertriglyceridemia treatment through this clinical trial at a research site in Louisville. Study-provided care at no cost to qualified participants.

Sponsored by Ionis Pharmaceuticals, Inc.

Quick Self-Assessment

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Expert Care in Louisville

Access hypertriglyceridemia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hypertriglyceridemia treatment provided free

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Check if you qualify for this hypertriglyceridemia clinical trial in Louisville, KY

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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 Louisville

    Convenient for KY 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 Louisville site if eligible
  4. 4Begin participation

About This Hypertriglyceridemia Study in Louisville

The main objective of this study is to evaluate the effect of ION775 on fasting triglyceride (TG) levels in participants with hypertriglyceridemia (HTG) and severe hypertriglyceridemia (sHTG).

Sponsor: Ionis Pharmaceuticals, Inc.

Who Can Participate

Inclusion Criteria

Adult males and females with HTG (fasting TG more than or equal to (≥) 350 milligrams per deciliter (mg/dL) \[3.95 millimoles per liter (mmol/L)\] or with sHTG (fasting TG ≥ 500 mg/dL \[5.65 mmol/L\]).
Participants should be on standard of care lipid-lowering medications per local guidelines. Key

Exclusion Criteria

Hemoglobin A1c (HbA1c) ≥ 8.5% at Screening.
Alanine aminotransferase or aspartate aminotransferase \> 2.0 × upper limit of normal.
Total bilirubin \> 1.5 upper limit of normal unless due to Gilbert's syndrome.
Estimated GFR \< 30 mL/min/1.73 m\^2. Note: Other protocol pre-specified inclusion/exclusion criteria may apply.

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 Louisville?

Yes, this clinical trial (NCT07604974) has an active research site in Louisville, KY 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.

Hypertriglyceridemia Treatment Options in Louisville, KY

If you're searching for hypertriglyceridemia treatment options in Louisville, KY, this clinical trial (NCT07604974) 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 Louisville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hypertriglyceridemia 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 hypertriglyceridemia clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Louisville, KY