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Completed Phase 2Phase 3 Interventional Results available

Oral Sodium Fusidate (CEM-102) for the Treatment of Staphylococcal Bone or Joint Infections

ClinicalTrials.gov ID: NCT02569541

Public ClinicalTrials.gov record NCT02569541. 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 22, 2026, 1:11 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

An Open-Label, Non-Randomized, Single-Arm, Multi-Center Study to Evaluate Oral Sodium Fusidate (CEM-102) for the Treatment of Staphylococcal Bone or Joint Infections in Subjects for Whom Chronic Antibiotic Suppressive Therapy is Indicated

Brief summary

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

To evaluate the safety and effectiveness of oral sodium fusidate (CEM-102) as chronic antibiotic for the treatment of bone or joint infections.

Study identification

NCT ID
NCT02569541
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Arrevus Inc.
Industry
Enrollment
30 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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 2015 (Type not available)
Primary completion
Oct 17, 2017 (Actual)
Completion
Feb 21, 2019 (Actual)
Last update posted
Jan 30, 2020

2015 – 2019

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Not listed Fountain Valley California 92708 —
Not listed San Dimas California 91773 —
Not listed Sylmar California 91432 —
Not listed Torrance California 90502 —
Not listed Tamarac Florida 33321 —
Not listed Springfield Illinois 62703 —
Not listed Louisville Kentucky 40202 —
Not listed Baltimore Maryland 21218 —
Not listed Boston Massachusetts 02111 —
Not listed Detroit Michigan 48202 —
Not listed Butte Montana 59701 —
Not listed Somers Point New Jersey 08244 —
Not listed Charlotte North Carolina 28207 —
Not listed Cincinnati Ohio 45219 —
Not listed Cleveland Ohio 44195 —
Not listed Haverford Pennsylvania 19041 —
Not listed Malvern Pennsylvania 19355 —
Not listed Philadelphia Pennsylvania 19107 —
Not listed Houston Texas 77030 —

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 NCT02569541, 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 Jan 30, 2020 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02569541 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →