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Completed Phase 2 Interventional Results available

Efficacy and Safety of MM-II for Treatment of Knee Pain in Subjects With Symptomatic Knee Osteoarthritis

ClinicalTrials.gov ID: NCT04506463

Public ClinicalTrials.gov record NCT04506463. 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 Sep 25, 2026, 9:09 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 Phase IIb, Randomized, Double-Blind, Placebo-Controlled, Single-administration, Multiple-Dose Study to Demonstrate the Efficacy and Safety of MM-II for Treatment of Knee Pain in Subjects With Symptomatic Knee Osteoarthritis

Brief summary

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

This is a phase IIb, randomized, double-blind, placebo-controlled study to determine the efficacy and safety of MM-II in subjects with symptomatic knee OA as compared to matching placebo.

Study identification

NCT ID
NCT04506463
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
397 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 99 Years
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 21, 2020
Primary completion
May 3, 2022
Completion
Aug 9, 2022
Last update posted
Aug 28, 2024

2020 – 2022

United States locations

U.S. sites
21
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
Sunpharma site no. 20 Birmingham Alabama 35209 —
Sunpharma site no. 11 Tempe Arizona 85283 —
Sunpharma site no. 25 Riverside California 92503 —
Sunpharma site no. 26 San Diego California 92103 —
Sunpharma site no. 06 Stamford Connecticut 06905 —
Sunpharma site no. 10 Lady Lake Florida 32159 —
Sunpharma site no. 08 Lake Worth Florida 33461 —
Sunpharma site no. 13 Maitland Florida 32751 —
Sunpharma site no. 22 Miami Florida 33145 —
Sunpharma Site no 27 Miami Florida 33155 —
Sunpharma site no. 12 Miami Florida 33155 —
SunPharma Site no 23 Miami Florida 33176 —
Sunpharma site no. 05 Sunrise Florida 33351 —
Sunpharma site no. 04 The Villages Florida 32159 —
Sunpharma site no. 18 Flossmoor Illinois 60422 —
Sunpharma site no. 07 Hazelwood Missouri 63042 —
Sunpharma site no. 17 Williamsville New York 14221 —
Sunpharma site no. 19 Edmond Oklahoma 73013 —
Sunpharma site no. 09 Charleston South Carolina 29406 —
SunPharma Site No 24 Columbia South Carolina 29206 —
Sunpharma site no. 21 Fort Mill South Carolina 29707 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04506463, 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 Aug 28, 2024 · Synced Sep 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04506463 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →