Asthma Clinical Trial
— ASTECOfficial title:
A Phase I, Trial to Evaluate the Safety, Tolerability, and Potential Efficacy of Allogeneic Human Mesenchymal Stem Cell Infusion in Patients With Mild Asthma
| Verified date | May 2020 |
| Source | University of Miami |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
A Phase 1 investigation will be performed to test the safety of two doses of bone marrow-derived MSCs (20,000,000 and 100,000,000) administered via peripheral intravenous infusion.
| Status | Terminated |
| Enrollment | 3 |
| Est. completion date | April 29, 2020 |
| Est. primary completion date | March 3, 2020 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Provide written informed consent - be between 18 and 65 years at the time of signing the Informed Consent - have a clinical diagnosis of asthma prior to screening in accordance with the guidelines of the American Thoracic Society/European Respiratory Society - ACQ over 1.25 - have a smoking history of less than 10 pack-years total and have not been smoking for at least the last 12 months - Perform a positive methacholine challenge at screening and repeat positive methacholine challenge at baseline visit (14 days later) - Have normal or mild obstructive spirometry - Have normal right heart function as documented by Doppler echo or right heart catheterization - If female, be surgically sterile, post-menopausal (more than 1 year), or practice double barrier methods of birth control - Subjects may receive non-drug therapies including oxygen supplementation no greater than 2L/minute, and pulmonary rehabilitation - Subjects may be on standard of care asthma medications including inhaled corticosteroids-long acting beta agonist at a dose not greater than 1 mg of a fluticasone equivalent Exclusion Criteria: - Have any active infection that is not treated - Be unable to perform any of the assessments required for endpoint analysis. - currently receive (or have received within four weeks of screening) experimental agents for the treatment of asthma - be actively listed (or expecting to be listed in the near future) for transplant of any organ - Have clinically important abnormal screening laboratory values : blood screening tests (Hematology, Chemistry, CBC including Eosinophil count) results that are not within normal limits (according to UMHC Laboratory Reference Ranges) Have a serious comorbid illness that, in the opinion of the investigator, may compromise the safety or compliance of the patient or preclude successful completion of the study - Have known allergies to penicillin or streptomycin - Be an organ transplant recipient - Have a clinical history of malignancy within 5 years (i.e., patients with prior malignancy must be disease free for 5 years), except curatively-treated basal cell carcinoma - Have a non-pulmonary condition that limits lifespan to less than a year. - Have a history of drug or alcohol abuse within the past 24 months. - Be serum positive for HIV, hepatitis BsAg or Viremia hepatitis C - Be currently participating (or have participated within the previous 30 days) in an investigational therapeutic or device trial. - Have hypersensitivity to dimethyl sulfoxide (DMSO) - Have a resting oxygen saturation (SpO2) on room air of more than 93% at sea level or more than 88% at an altitude above 5,000 feet above sea level (1524 meters) |
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Miami Miller School of Medicine | Miami | Florida |
| Lead Sponsor | Collaborator |
|---|---|
| Marilyn Glassberg | The Marcus Foundation |
United States,
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Number of Participant with treatment emergent serious adverse events | as defined as the incidence of any treatment-emergent serious adverse events; these are a composite of death, non-fatal pulmonary embolism, stroke, hospitalization for worsening dyspnea and clinically significant laboratory test abnormalities | Week 4 post infusion | |
| Secondary | Difference in lung function | Difference in FEV1 Variability in morning peak expiratory flow measurements Difference in frequency of acute exacerbations defined as: hospitalizations, missed work days, and/or oral steroids for more than 3 days Decrease in fractional excretion of inhaled NO (FENO; less than 50 ppb) |
Participants will be followed from 1 week to an expected average of 48 weeks following infusion | |
| Secondary | Decrease in peripheral eosinophilia | Decrease in number of peripheral eosinophils | Participants will be followed from 1 week to an expected average of 48 weeks following infusion | |
| Secondary | Difference in subject reported dyspnea and quality of life assessments | Difference in subject reported dyspnea and quality of life assessments: Asthma Control Test (ACT) and Asthma Control Questionnaire (ACQ) |
Participants will be followed from 1 week to an expected average of 48 weeks following infusion | |
| Secondary | Death from any cause | Death from any cause | Participants will be followed from 1 week to an expected average of 48 weeks following infusion |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04624425 -
Additional Effects of Segmental Breathing In Asthma
|
N/A | |
| Terminated |
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Study of Efficacy and Safety of CSJ117 in Patients With Severe Uncontrolled Asthma
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Phase 2 | |
| Active, not recruiting |
NCT03927820 -
A Pharmacist-Led Intervention to Increase Inhaler Access and Reduce Hospital Readmissions (PILLAR)
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N/A | |
| Completed |
NCT04617015 -
Defining and Treating Depression-related Asthma
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Early Phase 1 | |
| Recruiting |
NCT03694158 -
Investigating Dupilumab's Effect in Asthma by Genotype
|
Phase 4 | |
| Terminated |
NCT04946318 -
Study of Safety of CSJ117 in Participants With Moderate to Severe Uncontrolled Asthma
|
Phase 2 | |
| Completed |
NCT04450108 -
Vivatmo Pro™ for Fractional Exhaled Nitric Oxide (FeNO) Monitoring in U.S. Asthmatic Patients
|
N/A | |
| Completed |
NCT03086460 -
A Dose Ranging Study With CHF 1531 in Subjects With Asthma (FLASH)
|
Phase 2 | |
| Completed |
NCT01160224 -
Oral GW766944 (Oral CCR3 Antagonist)
|
Phase 2 | |
| Completed |
NCT03186209 -
Efficacy and Safety Study of Benralizumab in Patients With Uncontrolled Asthma on Medium to High Dose Inhaled Corticosteroid Plus LABA (MIRACLE)
|
Phase 3 | |
| Completed |
NCT02502734 -
Effect of Inhaled Fluticasone Furoate on Short-term Growth in Paediatric Subjects With Asthma
|
Phase 3 | |
| Completed |
NCT01715844 -
L-Citrulline Supplementation Pilot Study for Overweight Late Onset Asthmatics
|
Phase 1 | |
| Terminated |
NCT04993443 -
First-In-Human Study to Evaluate the Safety, Tolerability, Immunogenicity, and Pharmacokinetics of LQ036
|
Phase 1 | |
| Completed |
NCT02787863 -
Clinical and Immunological Efficiency of Bacterial Vaccines at Adult Patients With Bronchopulmonary Pathology
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Phase 4 | |
| Recruiting |
NCT06033833 -
Long-term Safety and Efficacy Evaluation of Subcutaneous Amlitelimab in Adult Participants With Moderate-to-severe Asthma Who Completed Treatment Period of Previous Amlitelimab Asthma Clinical Study
|
Phase 2 | |
| Completed |
NCT03257995 -
Pharmacodynamics, Safety, Tolerability, and Pharmacokinetics of Two Orally Inhaled Indacaterol Salts in Adult Subjects With Asthma.
|
Phase 2 | |
| Completed |
NCT02212483 -
Clinical Effectiveness and Economical Impact of Medical Indoor Environment Counselors Visiting Homes of Asthma Patients
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N/A | |
| Recruiting |
NCT04872309 -
MUlti-nuclear MR Imaging Investigation of Respiratory Disease-associated CHanges in Lung Physiology
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||
| Withdrawn |
NCT01468805 -
Childhood Asthma Reduction Study
|
N/A | |
| Recruiting |
NCT05145894 -
Differentiation of Asthma/COPD Exacerbation and Stable State Using Automated Lung Sound Analysis With LungPass Device
|