Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07029204 · ClinicalTrials.gov registry record · Early Phase 1

Intralesional Cyclosporine for Alopecia Areata

A Early Phase 1 study of Alopecia Areata, sponsored by University of California, Davis.

Recruiting
Registry status
Early Phase 1
Development phase
12
Enrollment target
1
Study location

NCT07029204: Recruiting Early Phase 1 study of Alopecia Areata, sponsored by University of California, Davis.

NCT07029204 is a Early Phase 1 study of Alopecia Areata that is actively recruiting participants, run by University of California, Davis. The registered enrollment target is 12 participants, below the 1,955-participant average among 26 other Alopecia Areata trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07029204, a Early Phase 1 study of Alopecia Areata, is actively recruiting participants, sponsored by University of California, Davis.

RECRUITING
Registry status
Early Phase 1
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

Alopecia areata (AA) is a chronic autoimmune disease that causes non-scarring, focal areas of hair loss. Due to its resulting disfigurement and unpredictable course, it is recognized as a serious medical condition with severe emotional and psychosocial distress, including a high prevalence of depression and anxiety.1-4 Treatment options for alopecia areata are limited. Cyclosporine has been used as an effective therapeutic option in the treatment of psoriasis. Additionally, the use of oral cyclosporine, alone or in combination with other agents, has been used in the management of a multitude of dermatologic conditions, including alopecia areata, pyoderma gangrenosum, chronic idiopathic purpura, atopic dermatitis, dyshidrotic eczema, Behcet disease, dermatomyositis, among others.8 Although cyclosporine has demonstrated efficacy in the management of these diseases, systemic side effects of oral cyclosporine often limit its long-term use. However, intralesional injections of cyclosporine have not been investigated. Through this randomized double-blind placebo-controlled clinical study, the study team aims to evaluate the safety, dosing, and efficacy of intralesional cyclosporine for use in the treatment of alopecia areata. The study team expects about 12 people at UC Davis to take part in this research. The study itself includes 11 visits and will last about 12 weeks.

Primary Outcome

Using the Severity of Alopecia Tool (SALT), study team will track and monitor the percentage of scalp hair loss throughout participant's duration in the trial.

Conditions Studied

Interventions

  • DRUG CycloSPORINE Injectable Product
  • DRUG Saline Solution

Study Locations (1)

California

  • University of California, Davis - Dermatology Department - Sacramento

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2025-08-19
Est. Completion 2026-10-01
Phase Early Phase 1
University of California, Davis

657 total trials

What NCT07029204 shows while recruiting

NCT07029204 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,955-participant average among 26 other Alopecia Areata trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Alopecia Areata appearing as the primary indexed condition, and to 2 interventions - of which CycloSPORINE Injectable Product is the first listed.

NCT07029204 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT07029204 about?

NCT07029204 is a clinical study titled "Intralesional Cyclosporine for Alopecia Areata". Alopecia areata (AA) is a chronic autoimmune disease that causes non-scarring, focal areas of hair loss. Due to its resulting disfigurement and unpredictable course, it is recognized as a serious medical condition with severe emotional and psychosocial distress, including a high prevalence of depres...

What is the current status of trial NCT07029204?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 12 participants. The study started on 2025-08-19. Estimated completion is 2026-10-01.

What conditions does trial NCT07029204 study?

This clinical trial studies the following conditions: Alopecia Areata.

What interventions are being tested in trial NCT07029204?

The interventions under investigation include: CycloSPORINE Injectable Product (DRUG), Saline Solution (DRUG).

Who is sponsoring clinical trial NCT07029204?

This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07029204 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Alopecia Areata

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07029204's enrollment target sits among peer trials

12 23rd of 26 higher than 2 of 26 other Alopecia Areata trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Alopecia Areata trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02602769 · 12 participants

    Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome

  • NCT02605421 · 12 participants · Phase 2

    Myeloablative Consolidation Therapy and Tandem Autologous Stem Cell Rescue in Patients With High-Risk Neuroblastoma

  • NCT02619448 · 12 participants · Early Phase 1

    Concurrent Chemotherapy Plus HFR Radiation Therapy in Inoperable NSCLC

  • NCT03311503 · 12 participants · Phase 1

    Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07029204, the US trial registry maintained by the National Library of Medicine. NCT07029204 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.