Pasadena, CANCT06625177Now EnrollingIRB Ready

Vitiligo Clinical Trial in Pasadena, CA

Access cutting-edge vitiligo treatment through this phase 1 clinical trial at a research site in Pasadena. Study-provided care at no cost to qualified participants.

Sponsored by Teva Branded Pharmaceutical Products R&D LLC

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Expert Care in Pasadena

Access vitiligo specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related vitiligo treatment provided free

Apply for This Pasadena Location

Check if you qualify for this vitiligo clinical trial in Pasadena, CA

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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 Pasadena

    Convenient for CA 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 Pasadena site if eligible
  4. 4Begin participation

About This Vitiligo Study in Pasadena

The purpose of the trial is to evaluate the safety of TEV-53408 when given as an under the skin injection to adults with vitiligo. Vitiligo is a condition where patches of skin lose color (pigment) and turn white.

Sponsor: Teva Branded Pharmaceutical Products R&D LLC

Who Can Participate

Inclusion Criteria

The participant has a diagnosis of active or stable vitiligo for at least 3 months.
The participant has a body mass index (BMI) within the range of 18.5 to 40.0 kg/m2
A female participant is eligible if she is not pregnant or breastfeeding AND is a woman of nonchildbearing potential OR is a women of childbearing potential using a contraceptive method that is highly effective AND agrees not to donate eggs for the purpose of reproduction for the required period
A male participant is eligible if he agrees to refrain from donating sperm PLUS remain abstinent from heterosexual intercourse OR use a male condom with a female partner for the required period
The participant is capable of giving signed, informed consent
The participant agrees to discontinue all agents and procedures used to treat vitiligo during the treatment period in the trial
If receiving permitted concomitant medications for any reason other than vitiligo, the participant must be on a stable regimen,
The participant must agree to avoid prolonged exposure to the sun, must use sunscreen, and must not use tanning booths, sun lamps, or other ultraviolet light sources NOTE - Additional criteria apply, please contact the investigator for more information

Exclusion Criteria

The participant suffers from vitiligo induced by exposure to chemicals or immunotherapy known to induce vitiligo
The participant has other autoimmune diseases for which systemic immunotherapy is or may be warranted
The participant has current or history of malignancy or treatment of malignancy in the last 5 years, excluding fully-treated basal cell carcinoma
Infectious disease
The participant has used skin bleaching treatments for past treatment of vitiligo or other pigmented areas
The participant has a history of melanocyte-keratinocyte transplantation procedure or other surgical treatment for vitiligo. After 2 or more years since last melanocyte-keratinocyte transplantation procedure, the participants may be included in the trial.
The participant has donated or received any blood or blood products (white blood cells, platelets, etc) within the 60 days prior to screening or has donated blood or blood products on 2 or more occasions within the 6 months prior to IMP administration, or has donated plasma within 7 days before the screening visit, or has planned donations during the trial
The participant has current or history of alcohol or other substance abuse NOTE- Additional criteria apply, please contact the investigator for more information

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 Pasadena?

Yes, this clinical trial (NCT06625177) has an active research site in Pasadena, CA 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.

Vitiligo Treatment Options in Pasadena, CA

If you're searching for vitiligo treatment options in Pasadena, CA, this clinical trial (NCT06625177) 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 Pasadena research site is actively enrolling participants for this phase 1 clinical trial. You'll receive care from experienced vitiligo 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 vitiligo clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Pasadena, CA