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Tirzepatide for Treatment of CCCA
Plain-language guide to NCT07734870: phase 2 interventional trial of Tirzepatide, 20 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT07734870
- Phase
- phase 2
- Status
- recruiting participants
- Start
- 2026-09-15
- Completion (planned or actual)
- 2028-05-25
- Participants
- 20 (estimated)
- Design
- na, open label (everyone knows who gets what), treatment
- Conditions studied
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
In this phase 2 trial, researchers set out to test Tirzepatide.
The goal of this pilot clinical trial is to learn if tirzepatide can treat active central centrifugal cicatricial alopecia (CCCA), a type of permanent scarring hair loss, in adults.
Participants will: * Inject tirzepatide once a week for 12 months. * Visit the clinic for scalp examinations, photographs, and other health assessments. * Have scalp biopsies at the beginning of the study and after 6 months of treatment. * Have blood tests and other safety monitoring during the study.
It had 1 arm (groups): Tirzepatide Treatment (experimental).
The registry classes the interventions as drug.
Who Took Part
20 planned participants were the target.
It was open to people of any sex aged from 18 years up to 80 years.
Healthy volunteers were not accepted; participants needed the condition being studied.
Examples of who could join: Age 18 to 80 years. Clinical and/or biopsy-confirmed diagnosis of central centrifugal cicatricial alopecia (CCCA). Active CCCA, defined as a C-CAT disease activity score greater than 1. No treatment for CCCA during the 6 weeks before enrollment. Able and willing to complete the study and follow all study procedures.
The full record lists 6 inclusion and 21 exclusion criteria; among the exclusions: currently taking an oral or systemic blood glucose-lowering medication; currently taking another medication for weight loss; homeostatic model assessment for insulin resistance (homa-ir) score below 2.
How the Study Was Run
The set-up was single-group and open-label.
Everyone knew when Tirzepatide was being given (open label), which is simpler to run but leaves more room for expectations to affect what is reported.
Everyone received the same intervention, so there was no separate comparison group inside the trial.
It started in 2026-09-15 with completion listed for 2028-05-25.
It ran at 2 sites in United States (2).
Its stated primary purpose is treatment.
What Was Measured
Researchers chose this as the main measure: Change in Central Centrifugal Cicatricial Alopecia Clinical Activity Tool Score (time frame: Baseline, 3 months, 6 months). Change in Scalp Gene-Expression Profiles (time frame: Baseline, 6 months).
It also tracked 2 secondary outcomes, for example Change in Central Hair Loss Grade and Physician Global Assessment of Change in Hair Loss.
What This Means in Plain Language
Put simply, this is a phase 2 trial of Tirzepatide in 20 people.
Its size is small, so on its own it can only give an early look.
It is still recruiting; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the Tirzepatide compound page, all human trials.
Our Notes on the Compound
Tirzepatide: A prescription peptide medicine that acts on both the GIP and GLP-1 receptors; Mounjaro and Zepbound contain the same active ingredient.
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.