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Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (HaploHCT) Following Reduced Intensity Conditioning (RIC) for Selected High Risk Non-Malignant Diseases

Primary Purpose

Sickle Cell Disease, Thalassemia, High Risk Hematologic Disorders

Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Blood and Marrow Transplant
Sponsored by
Masonic Cancer Center, University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sickle Cell Disease focused on measuring SCD, cALD

Eligibility Criteria

0 Years - 25 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Sickle Cell Disease (SCD)

    * If diagnosis of SCD must meet one or more of the following disease characteristics:

    • Stroke, CNS hemorrhage or a neurologic event lasting longer than 24 hours, or abnormal cerebral MRI or cerebral arteriogram or MRI angiographic study and impaired neuropsychological testing
    • Acute chest syndrome with a history of recurrent hospitalizations or exchange transfusions
    • Recurrent vaso-occlusive pain 3 or more episodes per year for 3 years or more years or recurrent priapism,
    • Impaired neuropsychological function and abnormal cerebral MRI scan
    • Stage I or II sickle lung disease,
    • Sickle nephropathy (moderate or severe proteinuria or a glomerular filtration rate [GFR] 30-50% of the predicted normal value)
    • Bilateral proliferative retinopathy and major visual impairment in at least one eye
    • Osteonecrosis of multiple joints with documented destructive changes
    • Requirement for chronic transfusions
    • RBC alloimmunization
  • Transfusion Dependent Alpha- or Beta-Thalassemia
  • Other Non-Malignant Hematologic Disorders:

Transfusion dependent or involve other potential life-threatening cytopenias, including but not limited to Paroxysmal Nocturnal Hemoglobinuria, Glanzmann's Thrombasthenia, Severe Congenital Neutropenia and Shwachman-Diamond Syndrome

  • cALD

    • Diagnosis of ALD by abnormal plasma very long chain fatty acid (VLCFA) profile or ABCD1 gene mutation
    • Cerebral disease on MRI
    • Absence of a Major Functional Disability (cortical blindness, loss of communication, wheelchair dependence) on the ALD Neurologic Function Scale
  • Other inherited metabolic disorders:

Any other inherited metabolic disorder for which alloHCT is indicated and for whom, in the opinion of the treating physician, the patient's best treatment option is with a haploidentical donor following non-myeloablatve conditioning.

  • Age, Performance Status, Consent

    • Age: 0-55 years
    • Performance Status: Karnofsky ≥ 70%, Lansky play score ≥ 70
    • Consent: voluntary written consent (adult or parental/guardian)
  • Adequate Organ Function

    • Renal: Creatinine <2.0 mg/dl for adults or glomerular filtration rate > 50 ml/min for children
    • Hepatic: Bilirubin and ALT <3 times the upper limit of institutional normal
    • Cardiac: Absence of decompensated congestive heart failure, or uncontrolled arrhythmia and left ventricular ejection fraction > 40%.

Exclusion Criteria:

  • Availability of a suitable HLA-matched related donor
  • Uncontrolled infection
  • Pregnant or breastfeeding
  • HIV positive

Sites / Locations

  • Masonic Caner Center at University of Minnesota

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

rATG, FLU/CY/TBI, & Thiotepa

Arm Description

Anti-Thymocyte Globulin - Rabbit (rATG), Fludarabine (Fludara), Cyclophosphamide (Cytoxan, Neosar), Total Body Irradiation (TBI), & Thiotepa

Outcomes

Primary Outcome Measures

Neutrophil Recovery
Incidence of neutrophil recovery by day +42

Secondary Outcome Measures

Overall Survival (OS)
Incidence of overall survival at 1 year
Primary Graft Failure (neutropenic and non-neutropenic)
Incidence of primary graft failure (neutropenic and non-neutropenic) by day +42

Full Information

First Posted
December 5, 2017
Last Updated
June 2, 2023
Sponsor
Masonic Cancer Center, University of Minnesota
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1. Study Identification

Unique Protocol Identification Number
NCT03367546
Brief Title
Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (HaploHCT) Following Reduced Intensity Conditioning (RIC) for Selected High Risk Non-Malignant Diseases
Official Title
Haploidentical Donor T-cell Replete Allogeneic Hematopoietic Cell Transplant Following Reducing Intensity Conditioning for Patients With Selected High Risk Non-Malignant Disease
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 2, 2018 (Actual)
Primary Completion Date
December 19, 2022 (Actual)
Study Completion Date
November 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Masonic Cancer Center, University of Minnesota

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This is a Phase II study for the use of T-cell replete reduced intensity conditioning (RIC) haploidentical donor allogeneic hematopoietic cell transplantation (HaploHCT) for individuals with high-risk non-malignant diseases who lack a suitable HLA-matched sibling donor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle Cell Disease, Thalassemia, High Risk Hematologic Disorders, Cerebral Adrenoleukodystrophy, Inherited Metabolic Disorders
Keywords
SCD, cALD

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
rATG, FLU/CY/TBI, & Thiotepa
Arm Type
Experimental
Arm Description
Anti-Thymocyte Globulin - Rabbit (rATG), Fludarabine (Fludara), Cyclophosphamide (Cytoxan, Neosar), Total Body Irradiation (TBI), & Thiotepa
Intervention Type
Procedure
Intervention Name(s)
Blood and Marrow Transplant
Intervention Description
Reduced intensity conditioning (RIC) with rabbit ATG, fludarabine, cyclophosphamide, thiotepa and low dose (2 Gy) total body irradiation followed by T-cell replete, unmanipulated, haploidentical related donor stem cell transplant (HaploHCT) and post-transplant cyclophosphamide (PTCy)
Primary Outcome Measure Information:
Title
Neutrophil Recovery
Description
Incidence of neutrophil recovery by day +42
Time Frame
Day 42
Secondary Outcome Measure Information:
Title
Overall Survival (OS)
Description
Incidence of overall survival at 1 year
Time Frame
1 year
Title
Primary Graft Failure (neutropenic and non-neutropenic)
Description
Incidence of primary graft failure (neutropenic and non-neutropenic) by day +42
Time Frame
Day 42

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sickle Cell Disease (SCD) * If diagnosis of SCD must meet one or more of the following disease characteristics: Stroke, CNS hemorrhage or a neurologic event lasting longer than 24 hours, or abnormal cerebral MRI or cerebral arteriogram or MRI angiographic study and impaired neuropsychological testing Acute chest syndrome with a history of recurrent hospitalizations or exchange transfusions Recurrent vaso-occlusive pain 3 or more episodes per year for 3 years or more years or recurrent priapism, Impaired neuropsychological function and abnormal cerebral MRI scan Stage I or II sickle lung disease, Sickle nephropathy (moderate or severe proteinuria or a glomerular filtration rate [GFR] 30-50% of the predicted normal value) Bilateral proliferative retinopathy and major visual impairment in at least one eye Osteonecrosis of multiple joints with documented destructive changes Requirement for chronic transfusions RBC alloimmunization Transfusion Dependent Alpha- or Beta-Thalassemia Other Non-Malignant Hematologic Disorders: Transfusion dependent or involve other potential life-threatening cytopenias, including but not limited to Paroxysmal Nocturnal Hemoglobinuria, Glanzmann's Thrombasthenia, Severe Congenital Neutropenia and Shwachman-Diamond Syndrome cALD Diagnosis of ALD by abnormal plasma very long chain fatty acid (VLCFA) profile or ABCD1 gene mutation Cerebral disease on MRI Absence of a Major Functional Disability (cortical blindness, loss of communication, wheelchair dependence) on the ALD Neurologic Function Scale Other inherited metabolic disorders: Any other inherited metabolic disorder for which alloHCT is indicated and for whom, in the opinion of the treating physician, the patient's best treatment option is with a haploidentical donor following non-myeloablatve conditioning. Age, Performance Status, Consent Age: 0-55 years Performance Status: Karnofsky ≥ 70%, Lansky play score ≥ 70 Consent: voluntary written consent (adult or parental/guardian) Adequate Organ Function Renal: Creatinine <2.0 mg/dl for adults or glomerular filtration rate > 50 ml/min for children Hepatic: Bilirubin and ALT <3 times the upper limit of institutional normal Cardiac: Absence of decompensated congestive heart failure, or uncontrolled arrhythmia and left ventricular ejection fraction > 40%. Exclusion Criteria: Availability of a suitable HLA-matched related donor Uncontrolled infection Pregnant or breastfeeding HIV positive
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christen L Ebens, MD, MPH
Organizational Affiliation
University of Minnesota - Pediatrics Blood and Marrow Transplant
Official's Role
Principal Investigator
Facility Information:
Facility Name
Masonic Caner Center at University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States

12. IPD Sharing Statement

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Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (HaploHCT) Following Reduced Intensity Conditioning (RIC) for Selected High Risk Non-Malignant Diseases

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