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COMPLETED Phase 2

Efficacy and Safety of ETX-018810 in Subjects With Lumbosacral Radicular Pain

NCT04778592 · View on ClinicalTrials.gov ↗

Study Summary

Efficacy and Safety of ETX 018810 in Subjects with Lumbosacral Radicular Pain

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG ETX-018810

Study Locations (20)

Florida

  • Charter Research — Lady Lake
  • Cordova Research Institute — Miami
  • Advanced Medical Research Institute — Miami
  • Coral Research Clinic Corp — Miami

Georgia

  • Drug Studies America — Marietta
  • Better Health Clinical Research — Newnan

New York

  • Drug Trials America — Hartsdale
  • University of Rochester Translational Pain Research — Rochester

Alabama

  • Delta Clinical Research — Mobile

Arizona

  • Arizona Research Center — Phoenix

Colorado

  • DBPS Research LLC — Greenwood Village

Idaho

  • Injury Care Research — Boise

Illinois

  • Chicago Anesthesia Research Specialist — Chicago

Trial Details

FieldValue
Enrollment Target 149 participants
Start Date 2021-01-19
Est. Completion 2022-05-25
Phase Phase 2

Sponsor

Eliem Therapeutics (UK)

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04778592

The ClinicalTrials.gov registry entry for NCT04778592 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 149 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eliem Therapeutics (UK), which has 2 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 Lumbosacral Radiculopathy 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: NCT04778592 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Florida, Georgia, New York. 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 NCT04778592 about?

NCT04778592 is a clinical study titled "Efficacy and Safety of ETX-018810 in Subjects With Lumbosacral Radicular Pain". Efficacy and Safety of ETX 018810 in Subjects with Lumbosacral Radicular Pain

What is the current status of trial NCT04778592?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 149 participants. The study started on 2021-01-19. Estimated completion is 2022-05-25.

What conditions does trial NCT04778592 study?

This clinical trial studies the following conditions: Lumbosacral Radiculopathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04778592?

The interventions under investigation include: Placebo (DRUG), ETX-018810 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04778592?

This trial is sponsored by Eliem Therapeutics (UK), which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04778592 being conducted?

This trial has 20 study locations across Alabama, Arizona, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial