Dalbavancin vs Comparator in Pediatric Subjects With Acute Hematogenous Osteomyelitis (AHOM)
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|ClinicalTrials.gov Identifier: NCT02344511|
Recruitment Status : Withdrawn
First Posted : January 26, 2015
Last Update Posted : September 23, 2016
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|Condition or disease||Intervention/treatment||Phase|
|Osteomyelitis||Drug: Dalbavancin Drug: cefazolin, nafcillin, oxacillin or vancomycin||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||A Phase 3, Multicenter, Double-Blind, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin Versus Active Comparator in Pediatric Subjects With Acute Hematogenous Osteomyelitis of the Long Bones Known or Suspected to be Due to Gram-Positive Organisms|
|Study Start Date :||March 2016|
|Estimated Primary Completion Date :||October 2018|
|Estimated Study Completion Date :||April 2019|
Patients with Creatine Clearance (CrCl) greater than 30 mL/min and patients receiving regular hemodialysis or peritoneal dialysis will receive 15 mg/kg Intravenous (IV) dalbavancin over 30 (+/- 5) minutes on Day 1 and on Day 8, not to exceed 1500 mg per administration in children at least 12 years and not to exceed 1000 mg per administration in children less than 12 years of age.
• Patients with CrCl < 30 mL/min who are not receiving regular hemodialysis or peritoneal dialysis will receive 10 mg/kg IV dalbavancin over 30 (+/- 5) minutes on Day 1 and on Day 8, not to exceed 1000 mg per administration in children at least 12 years and not to exceed 750 mg per administration in children less than 12 years of age.
Additionally, subjects randomized to the dalbavancin group will receive an IV placebo infusion at times corresponding to comparator group dosage times for the first eight days.
Other Name: Dalvance
Active Comparator: 4 Comparators
cefazolin, oxacillin, nafcillin or vancomycin according to the commercial label
Patients with normal renal function will receive either vancomycin 15 mg/kg/dose, infused over 60 (+/- 10) minutes, every 6 hours (+/- 1 hour) not to exceed a daily total dose of 4000 mg, with dose adjustment based on local standard of care to achieve serum trough concentrations of 10 μg/mL to 20 μg/mL; or cefazolin 25 mg/kg/dose, infused over 60 (+/- 10) minutes, every 6 hours (+/- 1 hour); or nafcillin or oxacillin 50 mg/kg/dose, infused over 60 (+/- 10) minutes, every 6 hours (+/- 1 hour).
Drug: cefazolin, nafcillin, oxacillin or vancomycin
Standard of Care
- Number of patients with clinical improvement at Day 8 [ Time Frame: Day 8 ]
- Number of clinical responders [ Time Frame: Day 8 ]
- Average reduction in C-reactive Protein (CRP) relative to the highest value [ Time Frame: Day 8 ]
- Number of clinical responders by pathogen [ Time Frame: Day 8 ]
- Number of Participants with Adverse Events [ Time Frame: 6 months ]
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|Ages Eligible for Study:||2 Years to 16 Years (Child)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Male or female 2-16 yrs
- diagnosis of Acute Hematogenous Osteomyelitis (AHOM) of the long bones (ulna, radius, femur, tibia) defined by the following clinical signs and symptoms (< 2 weeks in duration; multiple sites of infection within long bones):
- Limb abnormality: Pain, point tenderness upon palpation, motion restriction, loss of function
- Magnetic resonance imaging (MRI) -OR- Gram-positive cocci documented on a Gram-stain from a bone specimen or from blood cultures.
- Elevated C-Reactive Protein (CRP)
- informed consent
- willing and able to comply with the study protocol
- Life Expectancy with appropriate antibiotic therapy and thru study duration
- Treatment with an investigational drug within 30 days preceding the first dose of study medication.
- Receipt of > 24 hours of potentially effective intravenous antibacterial therapy for AHOM within 96 hours before randomization, unless the pathogen isolated was documented to be Methicillin resistant Staphylococcus aureus (MRSA) that was resistant to the administered antibiotic.
- Evidence of subacute or chronic osteomyelitis including: symptoms > 2 weeks in duration
- AHOM of non-long bones (e.g., pelvis or spine).
- Extraosseous findings such as: subperiosteal abscess, pyomyositis, venous thrombosis, or pulmonary embolism.
- Previous history of septic arthritis or osteomyelitis.
- Major trauma, open-fracture, puncture wound of the foot, post-operative osteomyelitis, foreign body in or adjacent to affected bone or joint, or other iatrogenic bone or joint infections present at the site of infection.
- Septic arthritis that is non-contiguous to osteomyelitis
- Immunosuppression/immune deficiency
- Evidence of Gram-negative bacteria by gram stain in the absence of Gram-positive organisms; fungus or mycobacteria at baseline.
- Gram-negative bacteremia, even in the presence of gram-positive infection or gram-positive bacteremia.
- A history of oral ulcers preceding the onset of musculoskeletal findings, recent gastrointestinal surgery (within 2 months)
- Infection due to an organism known prior to study entry to be not susceptible to dalbavancin (dalbavancin mean inhibitory concentration > 0.12 µg/mL) or vancomycin (vancomycin mean inhibitory concentration (MIC) > 2 μg/mL).
- Concomitant systemic antibacterial therapy for Gram-positive infections (eg. Rifampin, gentamicin).
- Concomitant condition requiring any antibiotic therapy that would interfere with the assessment of study drug for the condition under study.
- Sickle cell anemia.
- Cystic fibrosis.
- hypersensitivity to glycopeptide antibiotics.
- not expected to survive for 3 months.
- Positive urine (or serum) pregnancy test
- Women of Child Bearing Potential who are unwilling or unable to use adequate contraceptive precautions.
- Other severe acute or chronic medical or psychiatric condition would make the patient inappropriate for entry into this study.
- Unwilling or unable to follow study procedures.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02344511
|Study Director:||Alena Jamdourek, MD||Durata Therapeutics Inc., an affiliate of Allergan plc|
|Responsible Party:||Durata Therapeutics International BV (an Affiliate of Actavis, Inc.)|
|Other Study ID Numbers:||
|First Posted:||January 26, 2015 Key Record Dates|
|Last Update Posted:||September 23, 2016|
|Last Verified:||September 2016|
Bone Diseases, Infectious