Ann Arbor, MINCT06430528Now EnrollingIRB Ready

Endogenous Cushing Syndrome Clinical Trial in Ann Arbor, MI

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

Sponsored by University of Michigan

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Expert Care in Ann Arbor

Access endogenous cushing syndrome specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related endogenous cushing syndrome treatment provided free

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Check if you qualify for this endogenous cushing syndrome clinical trial in Ann Arbor, MI

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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 Ann Arbor

    Convenient for MI 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 Ann Arbor site if eligible
  4. 4Begin participation

About This Endogenous Cushing Syndrome Study in Ann Arbor

The major goal of this study is to determine the incidence of adrenal insufficiency in patients with endogenous Cushing syndrome receiving osilodrostat treatment combined with a replacement of glucocorticoid (block-and-replace approach). The investigators are also evaluating new biomarker steroids to reflect adequate osilodrostat dosing, the durability and safety, and clinical improvement during treatment.

Sponsor: University of Michigan

Who Can Participate

Inclusion Criteria

Endogenous Cushing syndrome, either following surgery or not candidates for surgery
Under consideration to receive osilodrostat as part of their clinical care
Able to provide informed consent.

Exclusion Criteria

Treatment with other investigational drugs within 30 days or five half-lives (whichever is longer).
A history of hypersensitivity to osilodrostat or therapies of a similar chemical class.

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 Ann Arbor?

Yes, this clinical trial (NCT06430528) has an active research site in Ann Arbor, MI 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.

Endogenous Cushing Syndrome Treatment Options in Ann Arbor, MI

If you're searching for endogenous cushing syndrome treatment options in Ann Arbor, MI, this clinical trial (NCT06430528) 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 Ann Arbor research site is actively enrolling participants for this clinical trial. You'll receive care from experienced endogenous cushing 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 endogenous cushing syndrome clinical trials near you to find additional studies recruiting in your area.

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