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COMPLETED Phase 2

Efficacy and Safety of ETX-018810 for the Treatment of Diabetic Peripheral Neuropathic Pain

NCT04688671 · View on ClinicalTrials.gov ↗

Study Summary

A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-Group Study to Evaluate the Efficacy and Safety of ETX 018810 in Subjects with Diabetic Peripheral Neuropathic Pain.

Interventions

  • DRUG Placebo
  • DRUG ETX-018810

Study Locations (20)

California

  • Neuro-Pain Medical Cneter — Fresno
  • Encompass Clinical Research — Spring Valley
  • Diabetes Research Center — Tustin

Florida

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

New York

  • IMA Clinical Research — New York
  • Upstate Clinical Research Associates — Williamsville

Utah

  • Alpine Research Organization — Clinton
  • Jean Brown Research — Salt Lake City

Alabama

  • Delta Clinical Research — Mobile

Arizona

  • Arizona Research Center — Phoenix

Connecticut

  • Chase Medical Research LLC — Hamden

Georgia

  • Better Health Clinical Reseach — Newnan

Trial Details

FieldValue
Enrollment Target 167 participants
Start Date 2020-11-09
Est. Completion 2022-02-18
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 NCT04688671

The ClinicalTrials.gov registry entry for NCT04688671 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 167 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 2 conditions, with Diabetic Peripheral Neuropathy 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: NCT04688671 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, Florida, 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 NCT04688671 about?

NCT04688671 is a clinical study titled "Efficacy and Safety of ETX-018810 for the Treatment of Diabetic Peripheral Neuropathic Pain". A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-Group Study to Evaluate the Efficacy and Safety of ETX 018810 in Subjects with Diabetic Peripheral Neuropathic Pain.

What is the current status of trial NCT04688671?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 167 participants. The study started on 2020-11-09. Estimated completion is 2022-02-18.

What conditions does trial NCT04688671 study?

This clinical trial studies the following conditions: Diabetic Peripheral Neuropathy, Diabetic Peripheral Neuropathic Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04688671?

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 NCT04688671?

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 NCT04688671 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Connecticut, Florida. 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