Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Study to Evaluate Solrikitug in Participants With COPD (ZION)
NCT06496620 · View on ClinicalTrials.gov ↗
Study Summary
A Randomized, Double-blind, Placebo-controlled, Multiple Dose-Ranging Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Solrikitug in Participants with Chronic Obstructive Pulmonary Disease (COPD).
Conditions Studied
Interventions
- OTHER Placebo
- BIOLOGICAL Biological: Solrikitug low dose
- BIOLOGICAL Biological: Solrikitug high dose
Study Locations (20)
California
- Antelope Valley Clinical Trials — Lancaster
- Ark Clinical Research - Ballinger — Long Beach
- Downtown LA Research Center, Inc. — Los Angeles
- Newport Native MD, Inc. — Newport Beach
- OM Research — Oxnard
- Prospective Research Innovations, Inc. — Rancho Cucamonga
Florida
- Access Research Institute — Brooksville
- Innovative Research of West Florida, Inc. — Clearwater
- Clinical Research of West Florida - Clearwater — Clearwater
- JY Research Institute — Cutler Bay
- Hillcrest Medical Research, LLC — DeLand
- North Florida Foundation for Research and Education — Gainesville
Arizona
- Phoenix Medical Group — Peoria
- Epic Medical Research-Surprise — Sun City
- Alliance for Multispecialty Research — Tempe
- Novak Clinical Research — Tucson
Alabama
- University of Alabama at Birmingham Hospital — Birmingham
- Syed Research Consultants — Sheffield
Colorado
- Velocity Clinical Research - Denver — Englewood
Connecticut
- Yale University School of Medicine — New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 171 participants |
| Start Date | 2024-08-14 |
| Est. Completion | 2026-10-31 |
| Phase | Phase 2 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06496620
The ClinicalTrials.gov registry entry for NCT06496620 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 171 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Uniquity One (UNI), which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with COPD appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06496620 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06496620 about?
NCT06496620 is a clinical study titled "A Study to Evaluate Solrikitug in Participants With COPD (ZION)". A Randomized, Double-blind, Placebo-controlled, Multiple Dose-Ranging Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Solrikitug in Participants with Chronic Obstructive Pulmonary Disease (COPD).
What is the current status of trial NCT06496620?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 171 participants. The study started on 2024-08-14. Estimated completion is 2026-10-31.
What conditions does trial NCT06496620 study?
This clinical trial studies the following conditions: COPD. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06496620?
The interventions under investigation include: Placebo (OTHER), Biological: Solrikitug low dose (BIOLOGICAL), Biological: Solrikitug high dose (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06496620?
This trial is sponsored by Uniquity One (UNI), which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06496620 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.