A Clinical Trial to Demonstrate the Effectiveness and Safety of Liposomal Cyclosporine A Inhalation Solution in the Treatment of Bronchiolitis Obliterans Syndrome in Patients Post Single Lung Transplant
This is a Phase III randomized, controlled clinical trial of L-CsA for the treatment of bronchiolitis obliterans syndrome in adults diagnosed with BOS following single lung transplant. Patients will receive either L-CsA (5 mg) via the PARI Investigational eFlow® Device twice daily plus Standard of Care (SoC) treatment, or SoC alone, for a period of 48 weeks. All patients will be eligible to continue in an open-label extension trial of L-CsA following completion of BOSTON-1.
A Phase III, Prospective, Multicenter, Randomized, Controlled Clinical Trial to Demonstrate the Effectiveness and Safety of Liposomal Cyclosporine A (L-CsA) Inhalation Solution Delivered Via the PARI Investigational eFlow® Device Plus Standard of Care Versus Standard of Care Alone in the Treatment of Bronchiolitis Obliterans Syndrome in Patients Post Single Lung Transplantation
Regardless of treatment allocation, all patients will continue to receive their SoC regimen for maintenance of the lung allograft. Eligible patients for the clinical trial must have a tacrolimus-based triple-drug therapy in combination with mycophenolate mofetil or its equivalent and a corticosteroid.
A total of 11 visits will be performed during the clinical trial. After informed consent has been obtained, a Screening Visit will be carried out in order to check general eligibility for participation. At the Randomization Visit, inclusion and exclusion criteria will be re-checked and spirometry performed. During the 48-week treatment period, visits are scheduled every 4-8 weeks. If a patient has an event that meets one of the criteria for progression of BOS, he/she will return to the clinic within 2-weeks for an unscheduled visit to have spirometry and other procedures performed.
Bronchiolitis Obliterans Bronchiolitis Cyclosporins Cyclosporine Liposomal Cyclosporine A
You can join if…
Open to people ages 18 years and up
- Adult patients of ≥ 18 years.
- Patients with diagnosis of BOS Grade 0-p with screening FEV1 between 85-81% of personal best FEV1 value post-transplant plus risk factors as defined below, OR BOS Grade 1 with screening FEV1 between 80-66% of personal best FEV1 value post-transplant.
Patients with diagnosis of BOS Grade 0-p must have >/=2 of these risk factors for BOS:
- Primary graft dysfunction (PGD)
- Acute cellular rejection
- Lymphocytic bronchiolitis
- Humoral rejection (e.g. de novo anti-human leukocyte antigen antibodies)
- Gastro-oesophageal reflux and microaspiration
- Infection (Viral, Bacterial, Fungal)
- Persistent neutrophil influx and sequestration (bronchoalveolar lavage neutrophilia)
- Autoimmunity (collagen V sensitization)
- Patients with an FEV1/FVC ratio of < 0.8.
- Patients in whom the diagnosis of BOS has been confirmed by the elimination of other possible causes of obstructive lung disease.
- Patients with a diagnosis of BOS 0-p or BOS 1 made at least 1 year after transplant surgery and within 6 months prior to the Screening Visit.
- Patients receiving a tacrolimus-based basic immunosuppression regimen in combination with MMF (or equivalent) and corticosteroids. This basic immunosuppression regimen must be stable (without changes to doses) for at least 4-weeks prior to Randomization.
- Patients must consent to retrieve prespecified data from the historic medical record(e.g., information related to the transplant surgery; spirometry data; medication use).
- Patients must be receiving prophylaxis against Cytomegalovirus (CMV) and Pneumocystis pneumonia.
- Patients capable of understanding the purposes and risks of the clinical trial, who have given written informed consent and agree to comply with the clinical trial requirements/visit schedules, and who are capable of aerosol inhalation.
- . Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to randomization and must agree to use one of the methods of contraception listed in Appendix II of the protocol for their duration of clinical trial participation.
- . Patients have no concomitant diagnoses that are considered fatal wtihin one year (12 months).
You CAN'T join if...
- Patients with confirmed other causes for loss of lung function, such as infection,acute rejection, restrictive allograft syndrome (RAS), etc.
- Patients with Cystic Fibrosis.
- Patients with donor-specific antibody (DSA) positivity at the Screening Visit.
- Active bacterial, viral, or fungal infection not successfully resolved at least 4 weeks prior to the Screening Visit.
- Mechanical ventilation within 12 weeks prior to Randomization.
- Patient has baseline resting oxygen saturation of < 89% on room air or use of supplemental oxygen.
- History or presence of bronchial strictures or airway stents or airways requiring balloon dilatations to maintain patency.
- Known hypersensitivity to L-CsA or to cyclosporine A.
- Patients with chronic renal failure, defined as serum creatinine > 2.5 mg/dL, or requiring chronic dialysis.
- . Patients with liver disease and serum bilirubin > 3-fold upper normal value or transaminases > 2.5 upper normal value.
- . Patients with a history of malignancy, including post-transplant lymphoproliferative disorder, with the exception of treated, localized basal and squamous cell carcinomas.
- . Pregnant women or women who are unwilling to use appropriate birth control to avoid pregnancy over the course of the clinical trial.
- . Women who are currently breastfeeding.
- . Receipt of an investigational drug as part of a clinical trial within 4 weeks prior to the Screening Visit. This is defined as any treatment that is implemented under an Investigational New Drug (IND) or compassionate use.
- . Patients who have received extracorporeal photophoresis (ECP) for treatment of BOS within 2 months prior to Randomization.
- . Patients who are currently participating in an interventional clinical trial.
- . Psychiatric disorders or altered mental status precluding understanding of the informed consent process and/or completion of the necessary procedures.
- . Any co-existing medical condition that in the Investigator's judgment will substantially increase the risk associated with the patient's participation in the clinical trial.
- UC San Francisco not yet accepting patients
San Francisco California 94143 United States
- Stanford University Hospital not yet accepting patients
Palo Alto California 94305 United States
- not yet accepting patients
- Start Date
- Completion Date
- Breath Therapeutics Inc.
- Phase 3
- Study Type
- Last Updated
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study. Submitting your contact information does not obligate you to participate in research.
The study team should get back to you in a few business days.
You will also receive an email with next steps. Check your junk/spam folder if needed.
If you do not hear from the study team, please call 888-689-8273 and tell them you’re interested in study number NCT03657342.