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

NCT06326476 · ClinicalTrials.gov registry record · Early Phase 1

An Open-label, Time-lagged, Dose-escalation Study to Evalaute the Safety and Efficacy of Subcutaneous Siplizumab in the Treatment of Hidradenitis Suppurativa.

A Early Phase 1 study of Hidradenitis Suppurativa, sponsored by University of Alabama at Birmingham.

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

NCT06326476: Recruiting Early Phase 1 study of Hidradenitis Suppurativa, sponsored by University of Alabama at Birmingham.

NCT06326476 is a Early Phase 1 study of Hidradenitis Suppurativa that is actively recruiting participants, run by University of Alabama at Birmingham. The registered enrollment target is 12 participants, below the 598-participant average among 52 other Hidradenitis Suppurativa trials with a reported enrollment target (98% 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

NCT06326476, a Early Phase 1 study of Hidradenitis Suppurativa, is actively recruiting participants, sponsored by University of Alabama at Birmingham.

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

Study Summary

This study is to investigate the efficacy of siplizumab in the treatment of Hidradenitis Suppurativa.

Primary Outcome

Inflammatory lesions are defined as inflammatory nodules or abscesses. These will be counted at screening, baseline, weeks 1-4, then at week 6 and 8. We will then asses the average change in inflammatory lesion count per subjects at weeks 4, 8 and 12.

Conditions Studied

Interventions

  • DRUG Siplizumab

Study Locations (1)

Alabama

  • University of Alabama at Birmingham - Birmingham

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2025-05-09
Est. Completion 2027-07-31
Phase Early Phase 1
University of Alabama at Birmingham

1,160 total trials

What NCT06326476 shows while recruiting

NCT06326476 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 598-participant average among 52 other Hidradenitis Suppurativa trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Hidradenitis Suppurativa appearing as the primary indexed condition, and to 1 intervention - of which Siplizumab is the first listed.

NCT06326476 reports a single indexed study location in Alabama.

Frequently Asked Questions

What is clinical trial NCT06326476 about?

NCT06326476 is a clinical study titled "An Open-label, Time-lagged, Dose-escalation Study to Evalaute the Safety and Efficacy of Subcutaneous Siplizumab in the Treatment of Hidradenitis Suppurativa.". This study is to investigate the efficacy of siplizumab in the treatment of Hidradenitis Suppurativa.

What is the current status of trial NCT06326476?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 12 participants. The study started on 2025-05-09. Estimated completion is 2027-07-31.

What conditions does trial NCT06326476 study?

This clinical trial studies the following conditions: Hidradenitis Suppurativa.

What interventions are being tested in trial NCT06326476?

The interventions under investigation include: Siplizumab (DRUG).

Who is sponsoring clinical trial NCT06326476?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06326476 being conducted?

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

Similar trials for Hidradenitis Suppurativa

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 NCT06326476's enrollment target sits among peer trials

12 49th of 52 higher than 4 of 52 other Hidradenitis Suppurativa trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Hidradenitis Suppurativa 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 NCT06326476, the US trial registry maintained by the National Library of Medicine. NCT06326476 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.