Phase
Condition
Osteomyelitis
Diabetes And Hypertension
Treatment
Placebo
Phage Therapy
Clinical Study ID
Ages 18-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female ≥18 to <85 years of age.
- Ongoing diagnosis of diabetes.
- Have undergone or are scheduled to undergo surgical debridement for DFO as part ofSoC, with the associated bone culture positive for S. aureus
- Availability of at least 1 matching phage for S. aureus cultured from the bone culture
- Receiving SoC treatment for DFO, including antibiotics after debridement and beforerandomization
- Meet defined study ulcer requirements as defined in the protocol
- Adequate circulation to the affected extremity demonstrated within 3 months prior torandomization and no revascularization procedure anticipated
- History of compliance with prior appointments and treatments in the investigator'sopinion and willingness to receive and comply with SOC antimicrobial and clinicaltreatments for the study ulcer, including offloading
Exclusion
Exclusion Criteria:
- Healing of the ulcer by more than 30% between screening and randomization.
- Treated with hyperbaric oxygen or cellular/tissue products with 30 days of screening
- Suspicion of neoplasm associated with the study ulcer or any non-study diabetic ulcerindependent of biopsy result.
- Presence of any cellulitis not localized to the study ulcer.
- Indwelling hardware at the site of the DFO.
- Body weight <50 kg.
- Presence of above ankle ulcer, with >50% above medial malleolus
- Hemoglobin < 7g/dL
- Abnormal liver function tests
- History of underlying liver disease at screening or within last 3 months
- Positive test for HIV-1 and /or HIV-2
- Any other clinically significant or severe disease that in the judgment of theinvestigator makes the patient unfit for the study or likely to withdraw prematurelyfrom the study, or that could jeopardize the safety of the patient or confound theresults of the study.
- Known allergy to phage products.
- Pregnant and/or breastfeeding.
- Immunocompromised at screening in the judgment of the investigator.
- Taking any systemic or topical antibacterial antibiotic within 2 weeks prior to thestart of study treatment, for a condition other than Diabetic Foot Infection and DFO.
- Taking any antiviral medication within 2 weeks prior to the start of study treatmentand up through the last administration of study treatment.
- Taking and/or receiving any therapies for the study ulcer that are not considered tobe SOC.
- More than 30 days has elapsed between screening and randomization (start of treatment)
- Participating in another clinical trial within 4 weeks prior to screening.
- Inability to obtain or provide informed consent or adhere to the protocol in thejudgment of the investigator.
- Once approximately 30% of subjects are enrolled with DFO involving digits, additionalsubjects will be excluded.
Study Design
Study Description
Connect with a study center
Compass Medical Research
Tucson, Arizona 85715
United StatesActive - Recruiting
Southern Arizona VA Health Care System
Tucson, Arizona 85723
United StatesActive - Recruiting
Central Arkansas Veteran's Healthcare System
Little Rock, Arkansas 72205
United StatesSite Not Available
NorthBay Healthcare
Fairfield, California 94534
United StatesActive - Recruiting
BioSolutions Clinical Research Center
La Mesa, California 91942
United StatesActive - Recruiting
Harbor Hospital / UCLA
Torrance, California 90502
United StatesActive - Recruiting
Rocky Mountain VA
Aurora, Colorado 80045
United StatesActive - Recruiting
MedStar Washington Hospital Center
Washington, District of Columbia 20010
United StatesActive - Recruiting
South Lake Pain Institute
Clermont, Florida 34711
United StatesActive - Recruiting
Midland Florida Clinical Research Center
DeLand, Florida 32720
United StatesActive - Recruiting
Holy Cross Health
Fort Lauderdale, Florida 33308
United StatesActive - Recruiting
University of Florida Health - Jacksonville
Jacksonville, Florida 32209
United StatesSite Not Available
LCC Medical Research
Miami, Florida 33126
United StatesSite Not Available
Floridian Clinical Research
Miami Lakes, Florida 33016
United StatesSite Not Available
Infectious Disease Consultants od the Treasure Coast
Sebastian, Florida 32958
United StatesActive - Recruiting
Advanced Specialty Research
Boise, Idaho 83702
United StatesSite Not Available
Podiatry 1st / Gateway Clinical Trials
O'Fallon, Illinois 62269
United StatesActive - Recruiting
Foot & Ankle Center of Illinois
Springfield, Illinois 62704
United StatesActive - Recruiting
Henry Ford Health
Detroit, Michigan 48202
United StatesActive - Recruiting
Jersey Shore University Medical Center
Neptune, New Jersey 07753
United StatesActive - Recruiting
Holy Name Medical Center
Teaneck, New Jersey 07666
United StatesActive - Recruiting
CurAlta Foot and Ankle
Westwood, New Jersey 07675
United StatesActive - Recruiting
James J. Peters VA
Bronx, New York 10468
United StatesSite Not Available
Nextstage Tulsa
Tulsa, Oklahoma 74104
United StatesSite Not Available
Martin Foot and Ankle
York, Pennsylvania 17402
United StatesSite Not Available
Cardio Voyage / Texoma Health
Denison, Texas 75020
United StatesActive - Recruiting
Futuro Clinical Trials, LLC
McAllen, Texas 78501
United StatesActive - Recruiting
Bio X Cell Research LLC
San Antonio, Texas 78224
United StatesActive - Recruiting
Foot and Ankle Specialists of the Mid-Atlantic
Salem, Virginia 24153
United StatesActive - Recruiting
Salem VA
Salem, Virginia 24153
United StatesActive - Recruiting
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