Personalized Immunotherapeutic for Antibiotic-resistant Infection
Primary Purpose
Infection, Immune Deficiency, Hypogammaglobulinemia
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
anti-mycoplasma hominis antibodies
Sponsored by
About this trial
This is an interventional treatment trial for Infection
Eligibility Criteria
Inclusion Criteria:
- Adult with decision making capacity afflicted with chronic mycoplasma hominis septic arthritis despite standard treatments.
Exclusion Criteria:
- None
Sites / Locations
- Brigham and Women's Hosptial
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Intervention
Arm Description
This is a single patient treatment IND
Outcomes
Primary Outcome Measures
Presence or absence of mycoplasma hominis cultured from joint and wound fluid
see publication below
Patency of fistula as assessed by clinical exam
see publication below
Pain reduction as measured by pain scale and amount of pain medication required
see publication below
Secondary Outcome Measures
Full Information
NCT ID
NCT02508584
First Posted
July 9, 2015
Last Updated
January 13, 2020
Sponsor
Brigham and Women's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02508584
Brief Title
Personalized Immunotherapeutic for Antibiotic-resistant Infection
Official Title
Personalized Immunotherapeutic for Antibiotic-resistant Infection
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
April 12, 2016 (Actual)
Primary Completion Date
June 12, 2019 (Actual)
Study Completion Date
June 12, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
M. A. suffers from hypogammaglobulinemia that has been complicated by refractory Mycoplasma hominis septic arthritis. He has been receiving the antibiotic valnemulin under Emergency Investigational New Drug (eIND) 114686 following many prior treatments with standard antibiotics. M.A. has also been receiving intravenous immunoglobulin (IVIG) replacement. The antibiotic and IVIG have been helpful, but not sufficient for cure. Antibodies have been shown to be critical for defense against mycoplasma. Hyperimmune serum against mycoplasma isolated from rabbit or goat has been effective in cases of chronic erosive arthritis in the setting of immune deficiency, and in some cases resulted in cures. The investigators propose to use M. hominis isolated from M. A. to vaccinate one transgenic cow (developed by SAB Biotherapeutics), purify human antibody after vaccination, test the purified antibody in killing assays to confirm potency, and then administer the purified human IgG to M. A. after FDA compassionate use IND application and local Institutional Review Board (IRB) approval.
Detailed Description
M. A. suffers from hypogammaglobulinemia that has been complicated by refractory Mycoplasma hominis septic arthritis. He has been receiving the antibiotic valnemulin under Emergency Investigational New Drug (eIND) 114686 following many prior treatments with standard antibiotics. M.A. has also been receiving intravenous immunoglobulin (IVIG) replacement. The antibiotic and IVIG have been helpful, but not sufficient for cure.
Antibodies have been shown to be critical for defense against mycoplasma. Hyperimmune serum against mycoplasma isolated from rabbit or goat has been effective in cases of chronic erosive arthritis in the setting of immune deficiency, and in some cases resulted in cures.
SAB Biotherapeutics, Inc. (formerly Sanford Applied Biosciences, LLC) located in Sioux Falls, SD, have developed transchromosomic (Tc) cows containing human immunoglobulin (Ig) heavy (IgH) and light (IgL) chain loci in the setting of inactivated bovine IgH and Ig lambda loci. To date, SAB Biotherapeutics (SAB) has several products in development that have been tested in animal models, but to date no human trials.
Investigators propose to use M. hominis isolated from M. A. to vaccinate one transgenic cow, purify antibody after vaccination, test the purified antibody in killing assays to confirm potency, and then administer the purified human IgG to M. A. after FDA compassionate use IND application and local Institutional Review Board (IRB) approval.
M. A. is a highly educated person with full decision making capacity and is well aware of the uncertainties and risks associated with this treatment. This proposal is designed to offer this patient an alternative and perhaps curative approach to his disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infection, Immune Deficiency, Hypogammaglobulinemia, Septic Arthritis, Mycoplasma Hominis
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
This is a single patient treatment IND
Intervention Type
Biological
Intervention Name(s)
anti-mycoplasma hominis antibodies
Intervention Description
provision of customized anti-mycoplasma hominis antibodies in the context of a treatment IND.
Primary Outcome Measure Information:
Title
Presence or absence of mycoplasma hominis cultured from joint and wound fluid
Description
see publication below
Time Frame
from date of initiation of therapy up to 1 year
Title
Patency of fistula as assessed by clinical exam
Description
see publication below
Time Frame
from date of initiation of therapy up to 1 year
Title
Pain reduction as measured by pain scale and amount of pain medication required
Description
see publication below
Time Frame
from date of initiation of therapy up to 1 year
10. Eligibility
Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult with decision making capacity afflicted with chronic mycoplasma hominis septic arthritis despite standard treatments.
Exclusion Criteria:
None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Duane R. Wesemann, MD, PhD
Organizational Affiliation
Brigham and Women's Hosptial
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hosptial
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
29272362
Citation
Silver JN, Ashbaugh CD, Miles JJ, Wu H, Marecki GT, Hwang JK, Jiao JA, Abrams M, Sullivan EJ, Wesemann DR. Deployment of Transchromosomal Bovine for Personalized Antimicrobial Therapy. Clin Infect Dis. 2018 Mar 19;66(7):1116-1119. doi: 10.1093/cid/cix977.
Results Reference
result
Links:
URL
https://academic.oup.com/cid/article/66/7/1116/4739430
Description
Deployment of Transchromosomal Bovine for Personalized Antimicrobial Therapy
Learn more about this trial
Personalized Immunotherapeutic for Antibiotic-resistant Infection
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