Tempe, AZNCT06989840Now EnrollingIRB Ready

Acne Clinical Trial in Tempe, AZ

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

Sponsored by Sagimet Biosciences Inc.

Quick Self-Assessment

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Expert Care in Tempe

Access acne specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related acne treatment provided free

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Check if you qualify for this acne clinical trial in Tempe, AZ

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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 Tempe

    Convenient for AZ 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 Tempe site if eligible
  4. 4Begin participation

About This Acne Study in Tempe

This is a 4-part study. Part A will be a randomized, double-blind, placebo-controlled investigation of single ascending doses (SAD) to assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamic (PD) biomarkers of TVB-3567 administered orally in healthy participants. Part B will be a randomized, open-label, 2-way crossover investigation to assess the effect of food on a single dose TVB-3567 administered orally in healthy participants. Parts C and D will be randomized, double-blind, placebo-controlled investigations of multiple ascending doses (MAD) to assess the safety, tolerability, PK, and PD/biomarkers of TVB-3567 administered orally in healthy participants without and with moderate to severe acne, respectively.

Sponsor: Sagimet Biosciences Inc.

Who Can Participate

Inclusion Criteria

Healthy Participants (Parts A, B and C)
Healthy, adult, male or female 18-55 years of age
Body mass index (BMI) ≥18.0 and ≤32.0 kg/m2
Medically healthy with no clinically significant medical history
Understands the study procedures in the informed consent form (ICF) and willing and able to comply with the protocol Healthy Participants with Acne (Part D only) Participants must meet all of the above criteria, as well as the following inclusion criteria to be eligible for participation in the study:
BMI ≥18.0 and ≤37.0 kg/m2.
Must be diagnosed with moderate to severe acne vulgaris

Exclusion Criteria

Healthy Participants (Parts A, B and C)
History or presence of clinically significant medical or psychiatric condition or disease
History or presence of hypersensitivity or idiosyncratic reaction to the study drug or related compounds including over the counter acne products.
Has a clinically significant ophthalmic examination finding
Female participant of childbearing potential
Unable to refrain from or anticipates the use of:
Any drugs, including prescription and non-prescription medications, herbal remedies, or vitamin supplements
Any topical anti-acne treatment on the face
Any drugs known to be moderate or strong inducers of CYP3A4 enzymes, BCRP, and/or P gp, including St. John's Wort, beginning 28 days prior to the first dosing.
Part C only: Any previous tretinoin treatments, including tazarotene, adapalene, isotretinoin, and all-trans retinoic acid. Healthy Participants with Acne (Part D only) Participants must not be enrolled if they do not meet any of the above criteria, as well as the following exclusion criteria:
Unable to refrain from or anticipates the use of:
Any previous tretinoin treatments, including tazarotene, adapalene, isotretinoin, and all trans retinoic acid.
Photoelectric therapy, dermabrasion, or chemical peeling
Intra-articular and systemic corticosteroid therapy
Significant skin diseases

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 Tempe?

Yes, this clinical trial (NCT06989840) has an active research site in Tempe, AZ 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.

Acne Treatment Options in Tempe, AZ

If you're searching for acne treatment options in Tempe, AZ, this clinical trial (NCT06989840) 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 Tempe research site is actively enrolling participants for this clinical trial. You'll receive care from experienced acne 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 acne clinical trials near you to find additional studies recruiting in your area.

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