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NCT06215859 · ClinicalTrials.gov registry record · Phase 3

Study of MR-107A-02 for the Treatment of Acute Postoperative Pain Following Herniorrhaphy

A Phase 3 study of Pain and Post Operative Pain, sponsored by Viatris Specialty.

Completed
Registry status
Phase 3
Development phase
579
Enrollment target
18
Study locations

NCT06215859 is a Phase 3 study of Pain and Post Operative Pain that has completed, run by Viatris Specialty. The registered enrollment target is 579 participants, above the 303-participant average among 374 other Pain trials with a reported enrollment target (91% higher). The trial reports 18 study locations across 9 states.

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The verdict

NCT06215859, a Phase 3 study of Pain and Post Operative Pain, has completed, sponsored by Viatris Specialty.

COMPLETED
Registry status
Phase 3
Development phase
579 participants
Enrollment target
18
Study locations

Study Summary

MR-107A-02 is being studied to investigate its efficacy and safety for treatment of acute pain after herniorrhaphy.

Interventions

  • DRUG Placebo
  • DRUG Tramadol
  • DRUG MR-107A-02
  • PROCEDURE Herniorrhaphy

Study Locations (18)

Texas

  • Investigator site 212 - Bellaire
  • Investigator site 215 - Carrollton
  • Investigator site 204 - Houston
  • Investigator site 216 - McAllen
  • Investigator site 219 - San Antonio
  • Investigator site 203 - San Antonio
  • Investigator site 214 - San Antonio

California

  • Investigator site 202 - Anaheim
  • Investigator site 222 - Bakersfield
  • Investigator site 208 - Riverside

Florida

  • Investigator site 211 - Miami
  • Investigator site 206 - Tampa

Alabama

  • Investigator site 210 - Sheffield

Arizona

  • Investigator site 213 - Phoenix

Georgia

  • Investigator site 207 - Atlanta

Kansas

  • Investigator site 205 - Wichita

Utah

  • Investigator site 201 - Salt Lake City

Trial Details

FieldValue
Enrollment Target 579 participants
Start Date 2023-12-29
Est. Completion 2025-03-12
Phase Phase 3

Sponsor

Viatris Specialty

5 total trials

What the Registry Record Tells You About NCT06215859

The ClinicalTrials.gov registry entry for NCT06215859 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 579 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 303-participant average among 374 other Pain trials with a reported enrollment target (91% higher). The listed sponsor is Viatris Specialty, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Pain appearing as the primary indexed condition, and to 4 interventions - of which Placebo is the first listed.

NCT06215859 reports 18 study locations spanning 9 distinct geographic areas - top geographies include Texas, California, Florida.

Frequently Asked Questions

What is clinical trial NCT06215859 about?

NCT06215859 is a clinical study titled "Study of MR-107A-02 for the Treatment of Acute Postoperative Pain Following Herniorrhaphy". MR-107A-02 is being studied to investigate its efficacy and safety for treatment of acute pain after herniorrhaphy.

What is the current status of trial NCT06215859?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 579 participants. The study started on 2023-12-29. Estimated completion is 2025-03-12.

What conditions does trial NCT06215859 study?

This clinical trial studies the following conditions: Pain, Post Operative Pain, Acute Pain.

What interventions are being tested in trial NCT06215859?

The interventions under investigation include: Placebo (DRUG), Tramadol (DRUG), MR-107A-02 (DRUG), Herniorrhaphy (PROCEDURE).

Who is sponsoring clinical trial NCT06215859?

This trial is sponsored by Viatris Specialty, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06215859 being conducted?

This trial has 18 study locations across Alabama, Arizona, California, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.