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Autologous Transplant Targeted Against Crohn's (ATTAC)

Primary Purpose

Crohn's Disease

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Fludarabine
Cyclophosphamide
Mesna
Alemtuzumab
G-CSF
Rifaximin
Tacrolimus
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn's Disease focused on measuring Autologous Stem Cell Transplantation, Hematopoietic Stem Cell Transplant

Eligibility Criteria

18 Years - 49 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 18 years and less than age 50 years at the time of pre-transplant evaluation
  2. Ability to give informed consent
  3. An established clinical diagnosis of severe Crohn's Disease* that has failed therapy with prednisone or budesonide (Entocort) and either a or b below:

    1. At least two anti-tumor necrosis factor (TNF) drugs (e.g., infliximab (Remicade), adalimumab (Humira), or certolizumab pegol (Cimzia))
    2. One anti-TNF drug as above and either vedolizumab (Entyvio) or ustekinumab (Stelara)

      • Severe Crohn's Disease is defined as a CDAI (see Appendix A) of 250 to 400 or a Craig's Crohn's Severity Index (CCSI, see Appendix B) that is > 17.

Exclusion Criteria:

  1. Uncontrolled diabetes mellitus or any other illness that in the opinion of the investigators would jeopardize the ability of the patient to tolerate aggressive treatment
  2. Prior history of malignancy (except localized basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix). Other malignancies for which the patient is judged to be cured by local surgical therapy, such as head and neck cancer, or stage I breast cancer will be considered on an individual basis
  3. Positive pregnancy test, inability to pursue effective means of birth control, or failure to willingly accept or comprehend irreversible sterility as a side effect of therapy
  4. HIV positive
  5. Hepatitis B or C positive
  6. Psychiatric illness or mental deficiency making compliance with treatment or informed consent impossible
  7. Untreated life-threatening cardiac arrhythmia on EKG or 24-hour holter or history of coronary artery disease or congestive heart failure
  8. Left ventricular ejection fraction (LVEF) <50%
  9. Forced vital capacity (FVC) <60% of predicted after bronchodilator therapy (if necessary) or diffusing capacity of the lungs for carbon monoxide (DLCO) hemoglobin corrected <60 % predicted
  10. Serum creatinine >2 mg/dl
  11. 24-hour urine creatinine clearance <90
  12. Liver transaminases >2x of normal limits, or bilirubin >2 mg/dl unless due to Crohn's Disease
  13. Major hematological abnormalities such as platelet count < 100,000/ul or absolute neutrophil count (ANC) < 1500/ul
  14. Failure to collect at least 2 x10^6 cluster of differentiation 34 (CD34+) cells/kg
  15. Any active infection
  16. Known hypersensitivity to mouse, rabbit, or E. coli derived proteins
  17. Short Bowel Syndrome defined as intestinal dysfunction with the presence of significant malabsorption of both macronutrients and micronutrients or when gastrointestinal function is inadequate to maintain nutrient and hydration status without intravenous or enteral supplementation.
  18. History of anorexia nervosa (serum albumin ≤ 20 g/L, body mass index ≤ 18)
  19. Patients presenting with intestinal perforation or toxic megacolon or a problem that will require urgent surgery. The presence of intestinal stomas, strictures, or fistulae does not exclude the patient from study.
  20. Unable or unwilling to stop using and/or smoking tobacco products
  21. Abnormal peripheral blood cytogenetics

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Hematopoietic Stem Cell Transplantation

Arm Description

Hematopoietic Stem Cell Therapy will be performed as follows: Autologous stem cells will be infused after conditioning with fludarabine, cyclophosphamide, mesna, and alemtuzumab. Granulocyte-colony stimulating factor (G-CSF) will be administered post-transplant until engraftment. Rifaximin and tacrolimus will be administered for 6 and 12 months, respectively, beginning one day before the infusion of stem cells.

Outcomes

Primary Outcome Measures

Treatment-related mortality
Treatment-related mortality
Overall survival
Survival of participants
Clinical remission
Change of Crohn's Disease Activity Index CDAI ≤ 150, Harvey-Bradshaw Index (HBI) ≤4, may be on immune suppressive drugs
Complete remission
Change of Clinical, endoscopic, and histologic remission on no immune modulating drugs

Secondary Outcome Measures

Craig's Crohn's Severity Index
Improvement in the severity of Crohn's Disease according to the Craig's Crohn's Severity Index (CDAI)
Endoscopic severity scales
Improvement on the Simple Endoscopic Score for Crohn's Disease (SES-CD)
Histologic remission on colonoscopy with biopsy
No evidence of disease on biopsy
Endoscopic remission
No evidence of disease on colonoscopy
Drug-free clinical remission
Crohn's Disease Activity Index (CDAI ≤ 150),Harvey Bradshaw Index HBI ≤4, no immune suppressive drugs
Relapse-free survival
Relapse is defined as Crohn's Disease Activity Index CDAI >150, Harvey Bradshaw Index HBI >4, and restarting or increasing immune based medication(s)
Stool markers
Improvement in fecal calprotectin and fecal lactoferrin
Quality of life short form Survey (SF-36)
Improvement in quality of life, measured by 36-Item Short Form Survey (SF-36) The evaluation of the results was done by attributing scores to each question, which were then transformed into a scale ranging from 0 to 100, where 0 corresponds to the worst quality of life and 100 to the best.
Inflammatory Bowel Disease Questionnaire
Improvement on the Inflammatory Bowel Disease Questionnaire (IBDQ) Total IBDQ score ranges from 32 to 224. A higher score indicates better quality of life.
Crohn's Disease Endoscopic Index of Severity (CDEIS)
Improvement on the Crohn's Disease Endoscopic Index of Severity (CDEIS)

Full Information

First Posted
March 8, 2019
Last Updated
November 6, 2019
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT04154735
Brief Title
Autologous Transplant Targeted Against Crohn's
Acronym
ATTAC
Official Title
Autologous Hematopoietic Stem Cell Transplant for Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Withdrawn
Why Stopped
Discontinued by Investigator
Study Start Date
November 2019 (Anticipated)
Primary Completion Date
March 2023 (Anticipated)
Study Completion Date
March 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a new Phase II trial to assess the toxicity and efficacy of autologous hematopoietic stem cell transplantation (HSCT) utilizing a new non-myeloablative conditioning regimen in patients with high-risk Crohn's disease (CD). The regimen will include low-dose immunosuppressive therapy and a targeted antibiotic for six to twelve months post-HSCT.
Detailed Description
The autologous hematopoietic stem cell transplantation (HSCT) in this study utilizes a new non-myeloablative conditioning regimen in patients with high-risk Crohn's disease (CD). The regimen includes two types of chemotherapy (cyclophosphamide and fludarabine) as well as alemtuzumab. The regimen will include low-dose immunosuppressive therapy with tacrolimus (Prograf) for one year post-HSCT in attempt to prevent relapse and improve long-term remission. Patients will also receive rifaximin (Xifaxan) for six months post-HSCT to target abnormal intestinal microbiota that may trigger intestinal inflammation. The ability of these experimental treatments to stop relapses and progression (worsening) of Crohn's disease will be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease
Keywords
Autologous Stem Cell Transplantation, Hematopoietic Stem Cell Transplant

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Hematopoietic Stem Cell Transplantation
Arm Type
Experimental
Arm Description
Hematopoietic Stem Cell Therapy will be performed as follows: Autologous stem cells will be infused after conditioning with fludarabine, cyclophosphamide, mesna, and alemtuzumab. Granulocyte-colony stimulating factor (G-CSF) will be administered post-transplant until engraftment. Rifaximin and tacrolimus will be administered for 6 and 12 months, respectively, beginning one day before the infusion of stem cells.
Intervention Type
Drug
Intervention Name(s)
Fludarabine
Intervention Description
A chemotherapy medication commonly used in the treatment of leukemia and lymphoma
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Other Intervention Name(s)
Cytoxan
Intervention Description
A medication used as chemotherapy and to suppress the immune system
Intervention Type
Drug
Intervention Name(s)
Mesna
Other Intervention Name(s)
Mesnex
Intervention Description
A medication used in those taking cyclophosphamide or ifosfamide to decrease the risk of bleeding from the bladder
Intervention Type
Drug
Intervention Name(s)
Alemtuzumab
Other Intervention Name(s)
Lemtrada, Campath
Intervention Description
A protein that kills the immune cells that are thought to be causing Crohn's; it is commonly used in the treatment of leukemia and lymphoma
Intervention Type
Drug
Intervention Name(s)
G-CSF
Other Intervention Name(s)
Neupogen, Filgrastim, Granix, Zarxio
Intervention Description
A glycoprotein that stimulates the bone marrow to produce granulocytes and stem cells and release them into the bloodstream
Intervention Type
Drug
Intervention Name(s)
Rifaximin
Other Intervention Name(s)
Xifaxan
Intervention Description
An antibiotic used to treat irritable bowel syndrome and relapsing C. difficile infection; it inhibits DNA-dependent RNA polymerase
Intervention Type
Drug
Intervention Name(s)
Tacrolimus
Other Intervention Name(s)
Prograf, Envarsus XR, Stargraf XL
Intervention Description
A medication which suppresses the immune system and inhibits T-lymphocytes; commonly used to lower the risk of organ rejection following transplant
Primary Outcome Measure Information:
Title
Treatment-related mortality
Description
Treatment-related mortality
Time Frame
3 years
Title
Overall survival
Description
Survival of participants
Time Frame
3 years
Title
Clinical remission
Description
Change of Crohn's Disease Activity Index CDAI ≤ 150, Harvey-Bradshaw Index (HBI) ≤4, may be on immune suppressive drugs
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Complete remission
Description
Change of Clinical, endoscopic, and histologic remission on no immune modulating drugs
Time Frame
1 year, 2 years, 3 years
Secondary Outcome Measure Information:
Title
Craig's Crohn's Severity Index
Description
Improvement in the severity of Crohn's Disease according to the Craig's Crohn's Severity Index (CDAI)
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Endoscopic severity scales
Description
Improvement on the Simple Endoscopic Score for Crohn's Disease (SES-CD)
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Histologic remission on colonoscopy with biopsy
Description
No evidence of disease on biopsy
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Endoscopic remission
Description
No evidence of disease on colonoscopy
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Drug-free clinical remission
Description
Crohn's Disease Activity Index (CDAI ≤ 150),Harvey Bradshaw Index HBI ≤4, no immune suppressive drugs
Time Frame
1 year, 2 years, 3 years
Title
Relapse-free survival
Description
Relapse is defined as Crohn's Disease Activity Index CDAI >150, Harvey Bradshaw Index HBI >4, and restarting or increasing immune based medication(s)
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Stool markers
Description
Improvement in fecal calprotectin and fecal lactoferrin
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Quality of life short form Survey (SF-36)
Description
Improvement in quality of life, measured by 36-Item Short Form Survey (SF-36) The evaluation of the results was done by attributing scores to each question, which were then transformed into a scale ranging from 0 to 100, where 0 corresponds to the worst quality of life and 100 to the best.
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Inflammatory Bowel Disease Questionnaire
Description
Improvement on the Inflammatory Bowel Disease Questionnaire (IBDQ) Total IBDQ score ranges from 32 to 224. A higher score indicates better quality of life.
Time Frame
6 months, 1 year, 2 years, 3 years
Title
Crohn's Disease Endoscopic Index of Severity (CDEIS)
Description
Improvement on the Crohn's Disease Endoscopic Index of Severity (CDEIS)
Time Frame
6 months, 1 year, 2 years, 3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years and less than age 50 years at the time of pre-transplant evaluation Ability to give informed consent An established clinical diagnosis of severe Crohn's Disease* that has failed therapy with prednisone or budesonide (Entocort) and either a or b below: At least two anti-tumor necrosis factor (TNF) drugs (e.g., infliximab (Remicade), adalimumab (Humira), or certolizumab pegol (Cimzia)) One anti-TNF drug as above and either vedolizumab (Entyvio) or ustekinumab (Stelara) Severe Crohn's Disease is defined as a CDAI (see Appendix A) of 250 to 400 or a Craig's Crohn's Severity Index (CCSI, see Appendix B) that is > 17. Exclusion Criteria: Uncontrolled diabetes mellitus or any other illness that in the opinion of the investigators would jeopardize the ability of the patient to tolerate aggressive treatment Prior history of malignancy (except localized basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix). Other malignancies for which the patient is judged to be cured by local surgical therapy, such as head and neck cancer, or stage I breast cancer will be considered on an individual basis Positive pregnancy test, inability to pursue effective means of birth control, or failure to willingly accept or comprehend irreversible sterility as a side effect of therapy HIV positive Hepatitis B or C positive Psychiatric illness or mental deficiency making compliance with treatment or informed consent impossible Untreated life-threatening cardiac arrhythmia on EKG or 24-hour holter or history of coronary artery disease or congestive heart failure Left ventricular ejection fraction (LVEF) <50% Forced vital capacity (FVC) <60% of predicted after bronchodilator therapy (if necessary) or diffusing capacity of the lungs for carbon monoxide (DLCO) hemoglobin corrected <60 % predicted Serum creatinine >2 mg/dl 24-hour urine creatinine clearance <90 Liver transaminases >2x of normal limits, or bilirubin >2 mg/dl unless due to Crohn's Disease Major hematological abnormalities such as platelet count < 100,000/ul or absolute neutrophil count (ANC) < 1500/ul Failure to collect at least 2 x10^6 cluster of differentiation 34 (CD34+) cells/kg Any active infection Known hypersensitivity to mouse, rabbit, or E. coli derived proteins Short Bowel Syndrome defined as intestinal dysfunction with the presence of significant malabsorption of both macronutrients and micronutrients or when gastrointestinal function is inadequate to maintain nutrient and hydration status without intravenous or enteral supplementation. History of anorexia nervosa (serum albumin ≤ 20 g/L, body mass index ≤ 18) Patients presenting with intestinal perforation or toxic megacolon or a problem that will require urgent surgery. The presence of intestinal stomas, strictures, or fistulae does not exclude the patient from study. Unable or unwilling to stop using and/or smoking tobacco products Abnormal peripheral blood cytogenetics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Burt, MD
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Autologous Transplant Targeted Against Crohn's

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