Safety and Efficacy Evaluation of PNEUMOSTEM® Treatment in Premature Infants With Bronchopulmonary Dysplasia
Primary Purpose
Bronchopulmonary Dysplasia
Status
Completed
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Human Umbilical Cord Blood Derived-Mesenchymal Stem Cells
Sponsored by
About this trial
This is an interventional treatment trial for Bronchopulmonary Dysplasia focused on measuring Human Umbilical Cord Blood Derived Mesenchymal Stem Cells, Bronchopulmonary dysplasia, Premature infants
Eligibility Criteria
Inclusion Criteria:
- Birth weight range: 500g~1250g
- Fetal gestational age: 23 weeks to 29 weeks
- Premature infants who cannot do spontaneous breathing, which ventilation rate is less than 12 breaths per min of ventilation rate and 25% of oxygen demand
- Premature infants who does not improve the breathing or worse within 24 hours prior to enrollment of this study
- Written consent form signed by a legal representative or a parent
Exclusion Criteria:
- Cyanotic or acyanotic congenital heart diseases except patent ductus arteriosus
- Severe lung malformation (i.e. Pulmonary hypoplasia, congenital diaphragmatic hernia, congenital cystic lung disease)
- Severe lung malformation with chromosome anomalies (i.e. Edward syndrome, Patau syndrome, Down syndrome, etc) or severe congenital malformation (Hydrocephalus, Encephalocele, etc)
- Severe congenital infection (i.e. Herpes, Toxoplasmosis, Rubella, Syphilis, AIDS, etc)
- CRP > 30 mg/dL; Severe sepsis or shock
- Premature infants who is going to or expected to have surgery 72 hours before/after this study drug administration
- Surfactant administration within 24 hours prior to this study drug administration
- Severe intracranial hemorrhage ≥ grade 3 or 4
- Premature infants who have active pulmonary hemorrhage or active air leak syndrome at the time point of screening
- History of other clinical studies as a participant
- Premature infants who are allergic to Gentamicin
- Premature infants who is considered inappropriate by the investigators
Sites / Locations
- Samsung Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
PNEUMOSTEM®
Arm Description
Outcomes
Primary Outcome Measures
Number of participant with adverse reaction
Number of paitents with normal rage of vital signs and laboratory examination Chest x-ray result, Duration of ventilator dependence, Duration of CPAP treatment, Duration of intubation, Occurrence of pneumothorax, Occurrence of intraventricular hemorrhage, Postnatal steroid use (%), Dose of surfactant (%) Cumulative duration of oxygen use
Secondary Outcome Measures
Incidence of BPD at 36 Week's postmenstrual age
Incidence of BPD at 36 Week's postmenstrual age (PMA)and 28 week's PMA Survival rate at 28 days after birth and 36 week's PMA
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01297205
Brief Title
Safety and Efficacy Evaluation of PNEUMOSTEM® Treatment in Premature Infants With Bronchopulmonary Dysplasia
Official Title
Open Label, Single-Center, Phase 1 Clinical Study to Evaluate the Safety and the Efficacy of PNEUMOSTEM® Treatment in Premature Infants With Bronchopulmonary Dysplasia
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
December 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medipost Co Ltd.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
PNEUMOSTEM® is human umbilical cord blood derived mesenchymal stem cells and it is intended to treat premature infants with bronchopulmonary dysplasia. This study is to assess the safety and the efficacy of this study drug.
Detailed Description
Bronchopulmonary dysplasia (BPD) is most common cause of death of children who were born prematurely, with low birth weights. In addition, many children who were recovered from this disease are suffering from many side effects such as prolonged hospitalization, pulmonary hypertension, and failure to thrive.
The purpose of BPD treatment is to make a baby be able to do spontaneous breathing and to spontaneous breathing a baby needs much energy and because of this a baby may have difficulty to feed. For this reason, medication with steroid, diuretic and respiratory drugs are currently used. However, there is no effective cure so far.
It has been reported that bone marrow derived mesenchymal stem cells (BM-MSC) can differentiate to pulmonary epithelial and pulmonary endothelial cells. Some animal studies showed that BM-MSC differentiated to bronchial cells and type 2 pneumocytes in rats with pneumonia and improve the fibrosis that occur after administration of bleomycin. Based on the findings, it is considered that mesenchymal stem cell therapy can help regenerate the damaged lung as well as BPD that cause lung inflammation, fibrosis, deficiency of type 2 pneumocytes, and so on.
PNEUMOSTEM® is human umbilical cord blood derived mesenchymal stem cells and it is intended to treat premature infants with BPD. The main purpose of this study is to evaluate the safety and the tolerability of this study drug and to establish the maximum toxicity dose. The latent efficacy will also be assessed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchopulmonary Dysplasia
Keywords
Human Umbilical Cord Blood Derived Mesenchymal Stem Cells, Bronchopulmonary dysplasia, Premature infants
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PNEUMOSTEM®
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Human Umbilical Cord Blood Derived-Mesenchymal Stem Cells
Other Intervention Name(s)
PNEUMOSTEM®
Intervention Description
Dose A - 10 million cells per kg Dose B - 20 million cells per kg Single intratracheal administration
Primary Outcome Measure Information:
Title
Number of participant with adverse reaction
Description
Number of paitents with normal rage of vital signs and laboratory examination Chest x-ray result, Duration of ventilator dependence, Duration of CPAP treatment, Duration of intubation, Occurrence of pneumothorax, Occurrence of intraventricular hemorrhage, Postnatal steroid use (%), Dose of surfactant (%) Cumulative duration of oxygen use
Time Frame
12 weeks from the day of treatment
Secondary Outcome Measure Information:
Title
Incidence of BPD at 36 Week's postmenstrual age
Description
Incidence of BPD at 36 Week's postmenstrual age (PMA)and 28 week's PMA Survival rate at 28 days after birth and 36 week's PMA
Time Frame
36 week's postmenstrual age
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Days
Maximum Age & Unit of Time
14 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Birth weight range: 500g~1250g
Fetal gestational age: 23 weeks to 29 weeks
Premature infants who cannot do spontaneous breathing, which ventilation rate is less than 12 breaths per min of ventilation rate and 25% of oxygen demand
Premature infants who does not improve the breathing or worse within 24 hours prior to enrollment of this study
Written consent form signed by a legal representative or a parent
Exclusion Criteria:
Cyanotic or acyanotic congenital heart diseases except patent ductus arteriosus
Severe lung malformation (i.e. Pulmonary hypoplasia, congenital diaphragmatic hernia, congenital cystic lung disease)
Severe lung malformation with chromosome anomalies (i.e. Edward syndrome, Patau syndrome, Down syndrome, etc) or severe congenital malformation (Hydrocephalus, Encephalocele, etc)
Severe congenital infection (i.e. Herpes, Toxoplasmosis, Rubella, Syphilis, AIDS, etc)
CRP > 30 mg/dL; Severe sepsis or shock
Premature infants who is going to or expected to have surgery 72 hours before/after this study drug administration
Surfactant administration within 24 hours prior to this study drug administration
Severe intracranial hemorrhage ≥ grade 3 or 4
Premature infants who have active pulmonary hemorrhage or active air leak syndrome at the time point of screening
History of other clinical studies as a participant
Premature infants who are allergic to Gentamicin
Premature infants who is considered inappropriate by the investigators
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Won-Soon Park, M.D., PhD.
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
Country
Korea, Republic of
12. IPD Sharing Statement
Citations:
PubMed Identifier
24508444
Citation
Chang YS, Ahn SY, Yoo HS, Sung SI, Choi SJ, Oh WI, Park WS. Mesenchymal stem cells for bronchopulmonary dysplasia: phase 1 dose-escalation clinical trial. J Pediatr. 2014 May;164(5):966-972.e6. doi: 10.1016/j.jpeds.2013.12.011. Epub 2014 Feb 6.
Results Reference
derived
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Safety and Efficacy Evaluation of PNEUMOSTEM® Treatment in Premature Infants With Bronchopulmonary Dysplasia
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