Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Study of CD388 for the Prevention of Influenza in Subjects Not at Risk for Influenza Complications
NCT06609460 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the effectiveness of CD388 in preventing symptomatic laboratory-confirmed influenza infections, as compared to placebo, and to select a dose of CD388 that is effective in preventing the same, when administered as a single dose via 3 subcutaneous (SQ) injections to adult participants in stable health, and to evaluate the safety and tolerability of CD388, as compared to placebo.
Conditions Studied
Interventions
- COMBINATION_PRODUCT Placebo
- COMBINATION_PRODUCT CD388 Injection
Study Locations (20)
Florida
- Alliance for Multispecialty Research, LLC — Fort Myers
- Nature Coast Clinical Research — Inverness
- Health Awareness, LLC — Jupiter
- South Florida Research Center, Inc. — Miami
- Clinical Site Partners, LLC dba Flourish Research — Miami
- Floridian Clinical Research — Miami Lakes
- Healthcare Clinical Data, Inc. — North Miami
California
- Velocity Clinical Research - Huntington Park — Huntington Park
- Velocity Clinical Research - San Diego — La Mesa
- Catalina Research Institute, LLC — Montclair
- Profound Research LLC — Oceanside
- Acclaim Clinical Research — San Diego
Alabama
- Pinnacle Research Group, LLC — Anniston
- Cullman Clinical Trials — Cullman
Arizona
- Fiel Family and Sports Medicine/CCT Research — Tempe
- Del Sol Research Management, LLC — Tucson
Colorado
- Lynn Institute of the Rockies — Colorado Springs
- Critical Care, Pulmonary & Sleep Associates, PLLP/CCT Research — Lakewood
Arkansas
- Baptist Health Center for Clinical Research — Little Rock
Georgia
- DelRicht Research — Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5,071 participants |
| Start Date | 2024-09-20 |
| Est. Completion | 2025-09-19 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06609460
The ClinicalTrials.gov registry entry for NCT06609460 describes a study currently listed as completed. 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 5,071 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cidara Therapeutics, which has 5 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 Influenza appearing as the primary indexed condition, and to 2 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: NCT06609460 reports 20 study locations spanning 7 distinct geographic areas — top geographies include Florida, California, Alabama. 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 NCT06609460 about?
NCT06609460 is a clinical study titled "Study of CD388 for the Prevention of Influenza in Subjects Not at Risk for Influenza Complications". The purpose of this study is to evaluate the effectiveness of CD388 in preventing symptomatic laboratory-confirmed influenza infections, as compared to placebo, and to select a dose of CD388 that is effective in preventing the same, when administered as a single dose via 3 subcutaneous (SQ) injectio...
What is the current status of trial NCT06609460?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 5,071 participants. The study started on 2024-09-20. Estimated completion is 2025-09-19.
What conditions does trial NCT06609460 study?
This clinical trial studies the following conditions: Influenza. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06609460?
The interventions under investigation include: Placebo (COMBINATION_PRODUCT), CD388 Injection (COMBINATION_PRODUCT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06609460?
This trial is sponsored by Cidara Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06609460 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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