Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 3

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

NCT06215859 · View on ClinicalTrials.gov ↗

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

1 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06215859

The ClinicalTrials.gov registry entry for NCT06215859 describes a study currently listed as completed. It is categorized as Phase 3, 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 579 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Viatris Specialty, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. 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: NCT06215859 reports 18 study locations spanning 9 distinct geographic areas — top geographies include Texas, California, Florida. 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 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, Acute Pain, Post Operative 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 NCT06215859?

The interventions under investigation include: Placebo (DRUG), Tramadol (DRUG), MR-107A-02 (DRUG), Herniorrhaphy (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06215859?

This trial is sponsored by Viatris Specialty, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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