Multicenter Trial of the Effect of AAT on Islet Transplant Engraftment and Durability After Renal Transplant

NCT ID: NCT02464878

Last Updated: 2023-12-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 2 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-01-31
• Study Completion Date: 2022-12-31

Brief Summary

Patients meeting the study entry criteria will receive 1-3 infusion(s) of in vitro cultured islets. Patients will receive three times a week AAT infusions in the peri-transplant period for three weeks.

Conditions

Kidney Transplant; Type 1 Diabetes

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Main study treatment

Group Type: OTHER

Alpha 1-Antitrypsin

Intervention Type: DRUG

Patients will receive three times a week AAT infusions in the peri-transplant period for three weeks.

Islet Transplantation

Intervention Type: PROCEDURE

Thymoglobulin

Intervention Type: DRUG

Patients will receive a total of 5 doses between Day -2 and Day +2

Basiliximab

Intervention Type: DRUG

Basiliximab will be used for subsequent transplants.

Etanercept

Intervention Type: DRUG

Etanercept will be given on the day of transplant and on Days 3, 7, and 10 post-transplant.

Interventions

Alpha 1-Antitrypsin

Patients will receive three times a week AAT infusions in the peri-transplant period for three weeks.

Intervention Type: DRUG

Islet Transplantation

Intervention Type: PROCEDURE

Thymoglobulin

Patients will receive a total of 5 doses between Day -2 and Day +2

Intervention Type: DRUG

Basiliximab

Basiliximab will be used for subsequent transplants.

Intervention Type: DRUG

Etanercept

Etanercept will be given on the day of transplant and on Days 3, 7, and 10 post-transplant.

Intervention Type: DRUG

Other Intervention Names

Glassia; Antithymocyte Globulin; Enbrel

Eligibility Criteria

Inclusion Criteria

• Male and female subjects age 18 to 70 years.
• Subjects who are able to provide written informed consent and to comply with the procedures of the study protocol.
• Subjects must have one of the following payment mechanisms in place:

1. Medicare,

2. A third-party insurer who agrees, via pre-authorization, to pay for participation in the study, or

3. Another mechanism of payment (self-pay, hospital, university, donations, etc.) for participation in the study.

• Clinical history compatible with T1D with disease onset < 40 years of age and insulin-dependence for ≥ 5 years at the time of enrollment.
• Absent stimulated c-peptide (< 0.3 ng/mL) in response to a MMTT [Boost® 6 mL/kg body weight (BW) to a maximum of 360 mL; another product with equivalent caloric and nutrient content may be substituted for Boost®] measured at 60 and 90 min after start of consumption.
• Subjects who are ≥ 3 months post-renal transplant who are taking appropriate calcineurin inhibitor (CNI) based maintenance immunosuppression ([tacrolimus alone or in conjunction with sirolimus, mycophenolate mofetil, myfortic, or azathioprine; or cyclosporine in conjunction with sirolimus, mycophenolate mofetil, or myfortic] ± Prednisone ≤ 10 mg/day).
• Stable renal function as defined by a creatinine of no more than one third greater than the average creatinine determination performed in the 3 previous months prior to islet transplantation, until rejection, obstruction or infection is ruled out.
• Subjects who meet one of the options in the following criterion are eligible for transplantation:

• Reduced awareness of hypoglycemia manifested by a Clarke score of 4 or more measured upon study enrollment and at least one episode of severe hypoglycemia in the 12 months prior to study enrollment.
• A subject must have a reduced awareness of hypoglycemia manifested by a Clarke score of 4 or more and at least 1 episode of severe hypoglycemia;
• Any subject not meeting the hypoglycemia option must have an HbA1c > 7.5%.

Exclusion Criteria

• Weight more than 100 kg or body mass index (BMI) > 33 kg/m2.
• Insulin requirement of >1.0 U/kg/day or, > 60 U/day total, or <15 U/day.
• Other (non-kidney) organ transplants except prior failed pancreatic graft where graft failure is attributed to thrombosis within the first 4 weeks or to other technical reasons that require graft pancreatectomy; with the graft pancreatectomy occurring more than 6 months ago.
• Untreated or unstable proliferative diabetic retinopathy.
• Blood Pressure: SBP > 160 mmHg or DBP >100 mmHg despite treatment with antihypertensive agents.
• Calculated GFR of ≤ 40 mL/min/1.73 m2 using the subject's measured serum creatinine and the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation1. Strict vegetarians (vegans) will be excluded only if their estimated GFR is ≤ 35 mL/min/1.73 m2.

7. Proteinuria (albumin/creatinine ratio or ACr > 300mg/g) of new onset since kidney transplantation.

• Calculated panel-reactive anti-HLA antibodies > 50%. Subjects with calculated panel reactive anti-HLA antibodies ≤ 50% will be excluded if any of the following are detected:

• Positive cross-match,
• Islet donor-directed anti-HLA antibodies detected by Luminex Single Antigen/specificity bead assay including weakly reactive antibodies that would not be detected by a flow cross-match, or
• Antibodies to the renal donor (i.e. presumed de novo).
• For female subjects: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of the study and 4 months after discontinuation. For male subjects: intent to procreate during the duration of the study or within 4 months after discontinuation or unwillingness to use effective measures of contraception. Oral contraceptives, Norplant®, Depo-Provera®, and barrier devices with spermicide are acceptable contraceptive methods; condoms used alone are not acceptable.
• Presence or history of active infection including hepatitis B, hepatitis C, HIV, or tuberculosis (TB). Subjects with laboratory evidence of active infection are excluded even in the absence of clinical evidence of active infection.
• Negative screen for Epstein-Barr virus (EBV) by IgG determination at time of screening or previous kidney transplant.
• Invasive aspergillus, histoplasmosis, and coccidoidomycosis infection within the last year.
• Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin.
• Known active alcohol or substance abuse.
• Any coagulopathy or medical condition requiring long-term anticoagulant therapy (e.g. warfarin) after islet transplantation (low-dose aspirin treatment [325 mg PO] is allowed) or subjects with international normalized ratio (INR) > 1.5. The use of Plavix is allowed only in conjunction with mini- laparotomy procedure at the time of islet transplant.
• Severe co-existing cardiac disease, characterized by any one of these conditions:

• Recent MI (within past 6 months);
• Evidence of ischemia on functional cardiac exam within the last year;
• Left ventricular ejection fraction < 30%; or
• Valvular disease requiring replacement with prosthetic valve.
• Persistent serum glutamic-oxaloacetic transaminase (SGOT [AST]), serum glutamate pyruvate transaminase (SGPT [ALT],) alkaline phosphatase or total bilirubin, with values > 1.5 times normal upper limits will exclude a subject.
• Active infections (except mild skin and nail fungal infections).
• Acute or chronic pancreatitis.
• Active peptic ulcer disease, symptomatic gallstones, or portal hypertension.
• Use of any investigational agents within 4 weeks of enrollment.
• Administration of live attenuated vaccine(s) within 2 months of enrollment.
• Any medical condition that, in the opinion of the investigator, will interfere with the safe participation in the trial. (Cancer screenings should be performed per current American Cancer Society guidelines).
• Positive screen for BK virus by polymerase chain reaction (PCR) performed at time of screening.
• A kidney transplant patient with type 1 diabetes who has an HbA1c < 7.5 and no history of severe hypoglycemia.
• Selective or severe IgA deficiency (levels < 5-7 mg/dL)
• AAT deficiency (defined as < 1.0ng/mg AAT)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

Sponsor Role: collaborator

University of Iowa

OTHER

Sponsor Role: collaborator

Massachusetts General Hospital

OTHER

Sponsor Role: lead

Responsible Party

James F. Markmann, MD, PhD

Chief, Division of Transplant Surgery

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jim Markmann, M.D. Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

Massachusetts General Hospital

Boston, Massachusetts, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

Islet after Kidney - AAT

Identifier Type: -

Identifier Source: org_study_id