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Adipose Derived Mesenchymal Cell Treatment in Lungtransplantation

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Rigshospitalet

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Lung Transplant Rejection

Treatments

Drug: Saline
Drug: adipose derived mesenchymal stromal cells

Study type

Interventional

Funder types

Other

Identifiers

NCT04714801
ASC Lungtransplantation

Details and patient eligibility

About

To investigate safety of treatment with allogeneic adipose tissue-derived mesenchymal stromal cells (ASCs) in patients undergoing lung transplantation, to evaluate whether the treatment can reduce host immunological reaction towards the graft, and to reduce the ischemic reperfusion-injury after transplantation.

Full description

The emerging field of stem cell therapy holds promise of treating a variety of diseases. Especially the mesenchymal stromal cells from bone marrow (BMSCs) or adipose tissue (ASCs) have proven their potential for regenerative therapy in patients with ischemic heart disease. Both of these cell types have putative immunomodulatory properties, as they have demonstrated to actively suppress the immune system and hereby evade recognition.

This knowledge will be transferred into studies in the ischemic reperfusion-injury/primary lung graft dysfunction in lung transplantation, and in suppressing the initial host immunological response towards the transplanted lung where a high degree of immunological and inflammatory activity is involved.

We will conduct a clinical trial in which patients receiving lung transplantation will be randomized to either placebo or treatment with allogeneic MSCs from adipose tissue. The aim is to assess the impact of MSCs on primary graft dysfunction.

The perspective is that this new information can be of pivotal importance and potentially be a paradigm shift for the clinical problems seen in the first period after lung transplantation and reduce the long-term graft rejection and dysfunction.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female lung recipients 18-70 years of age undergoing primary double (including size reduction) lung transplantation.
  • Patient willing and capable of giving written informed consent for study participation and anticipated to be able to participate in the study for 3 months.

Exclusion criteria

  • Recipients of multi-organ transplant, and or previously transplanted with any solid organ, including previous lung transplantation.
  • Patients scheduled for single lung transplantation.
  • Patients in need of acute transplantation e.g. patients on urgent call for transplantation and patients on respirator or on extra corporal membrane oxygenation (ECMO) treatment at time of transplantation.
  • Patients that based on crossmatch prior to transplantation have need for additional immunosuppressive treatment
  • Donor lung cold ischemic time > 12 hours.
  • Patients with platelet count < 50,000/mm3 at the evaluation before transplantation.
  • Patients who are unlikely to comply with the study requirements.
  • Patient unable to participate in the study for the full study period
  • Patients with any past (within the past 3-5 years) or present malignancy (other than excised basal cell carcinoma).
  • Females capable of becoming pregnant must have a negative pregnancy test prior to transplantation. After inclusion, they must use contraceptives for 2 months following the given stem cell treatment. The pill, spiral, depot injection of progesterone, sub-dermal implantation, hormonal vaginal ring and transdermal patch regarded as safe contraceptives.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

30 participants in 3 patient groups, including a placebo group

Infusion of 100 million ASC
Active Comparator group
Description:
Infusion of 100 million adipose derived mesenchymal stromal cells from healthy donors
Treatment:
Drug: adipose derived mesenchymal stromal cells
Infusion of 200 million ASC
Active Comparator group
Description:
Infusion of 200 million adipose derived mesenchymal stromal cells from healthy donors
Treatment:
Drug: adipose derived mesenchymal stromal cells
Infusion of placebo
Placebo Comparator group
Description:
Infusion of saline
Treatment:
Drug: Saline

Trial contacts and locations

1

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Central trial contact

Jens Kastrup, MD Professor; Abbas A Qayuum, MD

Data sourced from clinicaltrials.gov

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