Charleston, SCNCT05334368Now EnrollingIRB Ready

Hypereosinophilic Syndrome Clinical Trial in Charleston, SC

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

Sponsored by GlaxoSmithKline

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Expert Care in Charleston

Access hypereosinophilic syndrome specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hypereosinophilic syndrome treatment provided free

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Check if you qualify for this hypereosinophilic syndrome clinical trial in Charleston, SC

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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 Charleston

    Convenient for SC 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 Charleston site if eligible
  4. 4Begin participation

About This Hypereosinophilic Syndrome Study in Charleston

This is a 52-week, randomized, placebo-controlled, double-blind, parallel group, multicenter study of depemokimab in adults with uncontrolled HES receiving standard of care (SoC) therapy. The study will recruit patients with a confirmed diagnosis of HES and who are on stable HES therapy for at least 4 weeks prior to randomization (Visit 2). Eligible participants must have uncontrolled HES with a history of repeated flare (≥2 flares in the previous 12 months) and blood eosinophil count of ≥1,000

Sponsor: GlaxoSmithKline

Who Can Participate

Inclusion Criteria

Participants who are greater than or equal (\>=) 40 kilogram (kg) at Screening Visit 1.
Participants who have a documented diagnosis of HES prior to Visit 2.
A history of 2 or more HES flares within the past 12 months prior to Visit 1.
A female participant is eligible to participate if she is not pregnant or breastfeeding, and one of the following conditions applies: a) woman of non-childbearing potential (WONCBP) Or b) woman of childbearing potential (WOCBP) and using a contraceptive method that is highly effective, with a failure rate of less than (\<) 1 percentage (%).
Capable of giving signed informed consent.

Exclusion Criteria

Participants with HES disease manifestations which in the opinion of the investigator may put the participant at unacceptable risk from study participation or confound interpretation of efficacy or safety data.
Participants with chronic or ongoing active infections requiring systemic treatment or a pre-existing parasiti

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 Charleston?

Yes, this clinical trial (NCT05334368) has an active research site in Charleston, SC 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.

Hypereosinophilic Syndrome Treatment Options in Charleston, SC

If you're searching for hypereosinophilic syndrome treatment options in Charleston, SC, this clinical trial (NCT05334368) 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 Charleston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hypereosinophilic syndrome 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 hypereosinophilic syndrome clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Charleston, SC