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Completed Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT06215820

Public ClinicalTrials.gov record NCT06215820. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 1:18 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Double-Blind, Placebo- (Double-Dummy) and Active-Controlled, Parallel-Group Study of MR-107A-02 for the Treatment of Acute Postoperative Pain Following Bunionectomy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT06215820
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Viatris Specialty LLC
Industry
Enrollment
410 participants

Conditions and interventions

Interventions

Drug · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 29, 2023 (Actual)
Primary completion
Aug 24, 2024 (Actual)
Completion
Sep 30, 2024 (Actual)
Last update posted
Oct 14, 2025

2023 – 2024

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Investigator site 114 Sheffield Alabama 35660 —
Investigator site 115 Phoenix Arizona 85053 —
Investigator site 103 Anaheim California 92801 —
Investigator site 110 Riverside California 92501 —
Investigator site 112 Miami Florida 35660 —
Investigator site 108 Tampa Florida 33613 —
Investigator site 109 Atlanta Georgia 30331 —
Investigator site 104 O'Fallon Illinois 62269 —
Investigator site 102 Pasadena Maryland 21122 —
Investigator site 113 Bellaire Texas 77401 —
Investigator site 107 Carrollton Texas 75007 —
Investigator site 106 Houston Texas 77008 —
Investigator site 111 McAllen Texas 78501 —
Investigator site 105 San Antonio Texas 62269 —
Investigator site 101 Salt Lake City Utah 84107 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06215820, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 14, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06215820 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →