Syk Inhibition in MItigating Lung Allograft Rejection (SIMILAR): A Trial to Evaluate the Safety and Tolerability of Fostamatinib in Lung Transplant Patients With Donor-Specific Antibodies

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-99
SponsorNational Heart, Lung, and Blood Institute (NHLBI)

About this trial

Background:

People who have lung transplants often survive 6 or 7 years. But some people develop donor-specific antibodies (DSA) after their transplants; antibodies are proteins that attack foreign invaders in the body. Antibodies typically kill viruses and other agents that can cause disease. But when the antibodies attack a transplanted organ, they can cause the body to reject the new tissues. People who develop DSA after a transplant have a higher risk of death within 1 year.

Objective:

To test a drug called fostamatinib in people who develop DSA after a lung transplant.

Eligibility:

Adults aged 18 and older who developed DSA after a lung transplant.

Design:

Participants will continue with their standard care after a transplant.

Fostamatinib is a pill taken by mouth. Some participants will take the study drug along with their standard care; others will take a placebo. A placebo is a pill that looks just like the real drug but contains no medicine. All participants will take 1 pill per day for 2 weeks. Then they will take 2 pills per day for the next 6 weeks.

Participants will have clinic visits every 2 weeks while taking their pills. They will have a physical exam, with blood and urine tests, during each visit.

If participants have fluid samples collected from their airways during their standard treatment, some extra fluid may be collected for this study.

Participants will have a follow-up visit 4 weeks after they stop taking their pills.

Eligibility criteria

Qualifiers

First time LT recipients

Have provided signed written informed consent, prior to performing any study procedure, including screening procedures.

Age greater than or equal to 18 years

Patients who are positive for de novo DSA that is first reported on or after day 21 post-transplantation in a recipient with no prior history of the same DSA specificity, and who sign informed consent within 30 days of positive test results.

Disqualifiers

History of neutropenia (benign ethnic neutropenia and/or acquired neutropenia) within 90 days of screening.

History of posterior reversible encephalopathy syndrome (PRES)

History of poorly controlled hypertension or hypertensive crises (defined as systolic blood pressure >=180 mmHg or average diastolic blood pressure >=120 mmHg based on an average of 3 blood pressure readings despite adequate antihypertensive therapy) unless controlled for >90 days prior to enrollment

History of positive post-transplant active hepatitis C and/or hepatitis B viral infection.

Trial design

Treatments tested in this trial

  • fostamatinib
  • Placebo

Treatment groups

30 Participants
are divided into 2 treatment groups