Study to Assess Safety and Clinical Activity of Local MBN-101 in Treatment of Infected Bone Sites

Bacterial Infection Clinical Trial

Official title:

Phase 2a Randomized, Single-Blind, Placebo-Controlled, 12-week Escalating Dose Study to Assess the Safety, Tolerability and Clinical Activity of 3 Concentrations of Locally Applied MBN-101 to Infected Bone Sites

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02436876
• Other study ID #: MBN-101-201
• Secondary ID: W81XWH-12-2-0100
• Status: Completed
• Phase: Phase 2
• Start date: May 24, 2016
• Est. completion date: July 26, 2018

Study information

• Verified date: September 2021
• Source: Microbion Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study evaluates the safety and clinical benefit of MBN-101 administered intraoperatively to osteosynthesis or osteomyelitis sites for patients diagnosed with an orthopedic infection, with or without orthopaedic hardware. Three quarters of the patients will receive MBN-101, while the other one quarter will receive placebo.

Description:

Postoperative orthopaedic infections, particularly antibiotic-resistant infections, present a serious clinical challenge to surgeons and other treating physicians. These infections frequently involve implanted foreign materials (stabilizing orthopaedic hardware), making infection of these sites much more likely than if foreign materials were not involved. MBN-101 has broad spectrum antimicrobial activity against orthopaedic wound pathogens.

This is a randomized, single-blind, placebo-controlled, multi-center study to assess the safety and tolerability of escalating doses of MBN-101 to treat orthopaedic infections during revision surgery, (a) with or without orthopaedic hardware, and (b) with or without removal and replacement of orthopaedic hardware.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 29
• Est. completion date: July 26, 2018
• Est. primary completion date: October 27, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• To be eligible for this study, each of the following criteria must be satisfied with a "YES" answer (unless not applicable):

Patients who:

• have had operative fracture fixation of the upper extremity (AO/OTA class 15, 11-13, 21-23), lower extremity (AO/OTA class 31-34, 41 44, 81, 82) or pelvis (61, 62), or have undergone arthrodesis, and have subsequently been diagnosed with an apparent fracture site infection or are diagnosed with chronic or acute-on-chronic osteomyelitis of the long bone extremities (including residual amputated limbs)

• have at least one of the following:

• require surgical debridement of infected soft tissue and/or bone, with or without removal and/or placement/replacement of hardware

• male or female between the ages of 18 and 75 at the time the ICF is reviewed and signed

• patients receiving or anticipated to receive systemic antibiotic therapy as per institution's standard of care

• patients requiring postoperative hospitalization for at least 48 hours after revision surgery

• have read and signed the Informed Consent Form (ICF) after the nature of the study has been fully explained

• be willing and able to provide authorization for use and disclosure of personal health information in accordance with the Health Insurance Portability and Accountability Act (HIPAA)

Exclusion Criteria:

• To be eligible for this study, each of the following criteria must be satisfied with a "NO" answer (unless not applicable):

• Patients who are no longer hardware dependent or are definitively treated for their infection by hardware removal without replacement

• Patients with multiple, non-contiguous sites of infection

• Pathologic fracture (not including osteoporosis)

• Patient requires immunosuppressive therapy (Topical or inhaled corticosteroids are permitted)

• Serum creatinine, ALT, AST or Alkaline Phosphatase >2.0 times the upper limit of the normal range of the local testing laboratory

• Absolute neutrophil count <1000

• Patients without definitive soft-tissue coverage over the surgical site at time of study product administration

• Any condition that has required treatment with any other bismuth containing compound within the last 2 weeks (i.e., Kaopectate or Pepto Bismol)

• Participation in an investigational trial to evaluate pharmaceuticals or biologics within the past 3 months

• Individuals undergoing surgical treatment for more than one infected site

• Patients who are pregnant, lactating, or female patients who have a positive serum hCG (human Chorionic Gonadotropin) as determined by laboratory testing

• Immunocompromised due to illness or organ transplant

• History of chronic or recurrent infections (= 3 infections at the same site within 12 months)

• History of any type of cancer (excluding non-melanomatous localized skin cancer or completely excised and cured carcinoma-in-situ of uterine cervix)

• Poorly controlled diabetes mellitus

• History of medical noncompliance

• Other medical conditions which, in the opinion of the Principal Investigator, would jeopardize the safety of the study subject or impact the validity of the study results.

• Current incarceration

Related Conditions & MeSH terms

• Bacterial Infection
• Bacterial Infections

Intervention

Drug:
• MBN-101
MBN-101 is a locally administered, anti-infective drug product

Other:
• Placebo
The placebo is comprised of the vehicle/excipients used to formulate MBN-101, but does not contain the active pharmaceutical ingredient

Locations

Country	Name	City	State
United States	LifeBridge Health, Inc.	Baltimore	Maryland
United States	OhioHealth Research Institute	Columbus	Ohio
United States	The University of Texas - Health Science Center & Medical School at Houston	Houston	Texas
United States	University of Pennsylvania	Philadelphia	Pennsylvania
United States	Orthopedic Trauma Institute, University of California San Francisco	San Francisco	California
United States	UCSF - Parnassus	San Francisco	California

Sponsors (5)

Lead Sponsor	Collaborator
Microbion Corporation	Congressionally Directed Medical Research Programs, Medpace, Inc., University of California, San Francisco, University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Adverse Events	This study evaluates the safety and tolerability of single escalating doses of locally administered MBN-101 or placebo, as adjunct to standard of care antimicrobial and surgical therapy.	12 weeks
Secondary	Number of Treatment Failures	Treatment failure is defined as clinical course requiring additional infection-related interventions including rehospitalization, additional surgery, or additional courses of systemic antibiotics.	12 weeks
Secondary	Treatment Failure in Subjects With Antibiotic-resistant Infections	Treatment failure in subjects with baseline infections resistant to one or more antibiotics based on Central Laboratory Microbiological data	Up to 12weeks