Expanded Access for Use of ExoFlo in Abdominal Solid Organ Transplant Patients

Solid Organ Transplant Rejection Clinical Trial

Official title:

Intermediate Size Expanded Access for the Use of ExoFlo in the Treatment of Abdominal Solid Organ Transplant Patients Who Are at Risk of Worsening Allograft Function With Conventional Immunosuppressive Therapy Alone

Clinical Trial Details — Status: Available

Administrative data

• NCT number: NCT05215288
• Other study ID #: DB-EF-TP_ASO-1a
• Status: Available

Study information

• Verified date: February 2024
• Source: Direct Biologics, LLC
• Contact: Bill Arana
• Phone: 1-800-791-1021
• Email: clinicalaffairs[@]directbiologics.com
• Is FDA regulated: No
• Study type: Expanded Access

Clinical Trial Summary

This Expanded Access Protocol will provide access to the IMP ExoFlo for patients who have severe or life-threatening abdominal solid organ transplant rejection or who are evaluated and determined to be at high risk of progression to severe or life-threatening condition related to rejection of an abdominal solid organ transplant, at risk of worsening allograft function, or at risk of complications from current immunosuppressive therapeutic regimens.

Description:

Objectives:

The primary objective of this expanded access program is to evaluate safety and tolerability of ExoFlo in patients with graft inflammation, or worsening graft function, or evidence of rejection of an abdominal solid organ transplant despite conventional therapies. The secondary objective is to characterize the improvement seen in serum inflammatory markers and inflammation of solid abdominal organ.

Endpoints:

Primary Endpoint:

Incidence of AEs or SAEs.

Secondary Endpoint:

Improvement seen in serum inflammatory markers and inflammation of solid abdominal organ. This could include improvements seen in the following transplant types:

• Liver transplant: overall improved liver function, as seen by reduction in liver function test and improved albumin.

• Small bowel transplant: decreased inflammation on biopsy

• Pancreas: decreased amylase and lipase

• Multivisceral: any of the above criteria

Number of subjects: 20

Phase: Expanded Access Protocol

Recruitment information / eligibility

• Status: Available
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Provision of signed and dated informed consent form.

2. Stated willingness to comply with all study procedures and availability for the duration of the study.

3. Male or female, ages 18 to 75.

4. Previous abdominal solid organ transplant, including intestinal transplant.

5. Diagnosis of acute or chronic rejection / inflammation based on clinical observations, laboratory analysis, histological evaluation.

6. Diagnosis of worsening allograft function based on clinical observations, laboratory analysis, histological evaluation.

7. Failed primary and alternate standard of care therapies.

8. Serious or life-threatening condition or progressing to serious or life-threatening condition if not treated as evaluated by the treating physician.

9. In otherwise good general health as evidenced by medical history.

10. Male or female of reproductive potential must utilize a medically effective birth control method during from time of enrollment to 6 months after last dose of IMP.

Exclusion Criteria:

1. Pregnant or breastfeeding.

2. Treatment with another investigational drug or other intervention within 30 days of enrollment.

Related Conditions & MeSH terms

• Solid Organ Transplant Rejection

Intervention

Biological:
• ExoFlo
Intravenous administration of bone marrow mesenchymal stem cell derived extracellular vesicles

Locations

Country	Name	City	State
United States	Direct Biologics Investigational Site	Palo Alto	California
United States	Direct Biologics Investigational Site	San Francisco	California

Sponsors (1)

Lead Sponsor	Collaborator
Direct Biologics, LLC

Country where clinical trial is conducted

United States, 

External Links

•   Direct Biologics, LLC