PET-Based Imaging of Radiolabeled CIT-013

Study acronym: Cityview
StatusCompleted
PhasePhase 2
SponsorCitryll BV
Started

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Record History

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  1. Minor Trial completed Show 5 more changesShow less
    • Final enrollment: 7 participants (planned 12)
    • Primary completion date changed from estimate of Oct 1, 2026 to Jul 15, 2026
    • Study completion date changed from estimate of Dec 1, 2026 to Aug 15, 2026
    • Site details revised
    • Eligibility criteria expanded, about 4 words
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Dec 1, 2025 to Jan 15, 2026
    • Site details revised
    v3
  3. Minor Study sites: 0 to 1
    • Eligibility criteria revised
    v2
  4. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Inflammatory mediated immune diseases (IMIDs), such as rheumatoid arthritis (RA) and hidradenitis suppurativa (HS), are characterized by chronic inflammation resulting from an aberrant immune response. Recent studies have identified neutrophil extracellular traps (NETs) as key contributors to the pathology of these diseases. CIT-013 is a novel humanized monoclonal antibody designed to inhibit NET release and enhance phagocytosis, offering a new potential therapeutic strategy for RA and HS. Previous clinical trials have demonstrated that CIT-013 is well tolerated in both healthy volunteers and patients with RA, with evidence of reduced NET formation and positive effects in active RA cases. Since NET-related inflammation primarily occurs in local tissues, understanding CIT-013's distribution beyond blood measurements is crucial for evaluating its therapeutic potential. This trial therefore uses radiolabeled CIT-013 and Positron Emission Tomography-Computed Tomography (PET-CT) imaging, along with lymph node biopsies, to evaluate the distribution of CIT-013 and target engagement in patients with IMIDs.
Trial Details
NCT Number NCT07147959
Lead Sponsor Citryll BV
Conditions
(from sponsor)
RA
Enrollment 7 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov