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WithdrawnNCT05293509Updated Sep 21, 2023

Pharmacologic Pretransplant Immunosuppression (PTIS) + Reduced Toxicity Conditioning (RTC) Allogeneic Stem Cell Transplantation in Inherited Hematologic Disorders

A Phase 2 interventional study of Fludarabine and Dexamethasone in Stem Cell Transplantation, sponsored by M.D. Anderson Cancer Center. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-09-21.

Sponsored by M.D. Anderson Cancer Center · Phase 2, Interventional, and Treatment

Why this study was withdrawn
0 accrual
Phase
Phase 2
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

To assess the outcomes of NRM when administering pharmacologic pretransplant immunosuppression (PTIS) followed by pretransplant reduced toxicity conditioning (RTC) and an allogeneic stem cell transplant (allo-SCT) and post-transplant graft-versus-host disease prophylaxis based on post-transplant cyclophosphamide (PT-Cy) in patients with inherited blood disorders.

Read the detailed description

Objectives

Primary:

To estimate the 100-day non-relapse mortality (NRM) rate when administering pharmacologic pretransplant immunosuppression (PTIS) followed by pretransplant reduced toxicity conditioning (RTC) and an allogeneic stem cell transplant (allo-SCT) and post-transplant graft-versus-host disease prophylaxis based on post-transplant cyclophosphamide (PT-Cy) in patients with inherited blood disorders.

Secondary outcomes include the following:

i. Immune reconstitution ii. Infectious complications iii. Quality of life (QOL) at 3 months,100 days, and 1 year post-transplant iv. OS, EFS, and GRFS v. Incidence of aGVHD at day 100. vi. Rate of chronic GVHD within the first-year post transplantation. vii. Rate of Graft failure

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Conditions studied

  • Stem Cell Transplantation

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03

In context

Hematologic Diseases

460 studies on the registry are indexed under Hematologic Diseases; 105 are open to participants now.

Browse Hematologic Diseases studies →

Lead sponsor

M.D. Anderson Cancer Center is the lead sponsor of 2,999 studies on the registry; 581 are open to participants now.

Of its 599 completed or terminated interventional studies of FDA-regulated products, 402 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. The first six patients will be ages >12 years old and \<35 years old. Thereafter in a second stage, patients ages 2 to 50 years old will be included.
  2. Patient with a matched related donor or who has a related haploidentical donor identified.
  3. Performance score of at least 70 by Karnofsky or 0 to 1 by ECOG (age > 12 years), or Zubrod or Lansky Play Performance Scale of at least 70 (age \<12 years).
  4. Adequate major organ system function as demonstrated by:

    1. Serum creatinine clearance equal or more than 50 ml/min (calculated with Cockroft-Gault formula).
    2. Bilirubin equal or less than 1.5 mg/dl except for Gilbert's disease. ALT and/or AST equal or less than 3x institutional ULN. Conjugated (direct) bilirubin less than 2x upper limit of normal.
    3. Left ventricular ejection fraction equal or greater than 50%.
    4. Diffusing capacity for carbon monoxide (DLCO) equal or greater than 50%
    5. Predicted, corrected for hemoglobin. For children \< 7 years of age who are unable to perform PFT, oxygen saturation > 92% on room air by pulse oximetry.
  5. Patient or the patient's legal representative, parent(s) or guardian should be able to provide written informed consent. Assent of a minor if participant's age is at least seven and less than eighteen years.
  6. Sexually active males and females of childbearing potential must agree to use a form of contraception considered effective and medically acceptable by the Investigator.

Exclusion criteria

Exclusion Criteria:

  1. HIV positive; active hepatitis B or C.
  2. Uncontrolled infections.
  3. Liver cirrhosis. However mild fibrosis will be allowed i.e. fine reticulin or Grade 1, with bridging fibrosis.
  4. CNS involvement within 3 months.
  5. Positive pregnancy test in a woman with child bearing potential defined as not post-menopausal for 12 months or no previous surgical sterilization.
  6. Inability to comply with medical therapy or follow-up.
  7. Will restrict eligibility to a maximum BMI of ≤40
  8. Patient with a known history of allergic reactions to any constituents of the cell product, including a known history of allergic reactions to DMSO.
  9. Prior allo-SCT
  10. Other active malignancy/cancer diagnosis in remission for at least 2yrs. Malignancies not being excluded are as follows: Ductal carcinoma in situ (DCIS), Basal cell carcinoma (BCC), Cervical intraepithelial neoplasia (CIN)
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Phase I: Sequential Pharmacological PTIS

    Drug: Fludarabine · Drug: Dexamethasone · Drug: Cyclophosphamide · Drug: Bortezomib · Drug: Rituximab · Drug: Busulfan · Drug: Cyclophosphamide (Cy) · Drug: Tacrolimus (or cyclosporine)

  • Experimental
    Phase II: RTC Regimen and GVHD Prophylaxis Based on Post-Cy

    Drug: Fludarabine · Drug: Cyclophosphamide · Drug: Busulfan · Drug: Cyclophosphamide (Cy) · Drug: Tacrolimus (or cyclosporine) · Drug: Mycophenolate mofetil (MMF) · Drug: Rabbit ATG

Interventions

  • DrugFludarabine

    40 mg/m2/day i.v.- by vein

    Also known as: Fludara™

  • DrugDexamethasone

    25 mg/m2/day i.v.-by vein

  • DrugCyclophosphamide

    100 mg/m2 IV-by vein

    Also known as: Cytoxan™

  • DrugBortezomib

    Four doses of bortezomib at a dose of 1.3 mg/m2 -injection under the skin

    Also known as: Velcade®

  • DrugRituximab

    Four doses of rituximab at a dose of 375 mg/m2- by vein

    Also known as: Rituxan®

  • DrugBusulfan

    110 mg/m2 i.v-by vein

    Also known as: Busulfex™

  • DrugCyclophosphamide (Cy)

    by vein

    Also known as: Cytoxan™

  • DrugTacrolimus (or cyclosporine)

    by vein

  • DrugMycophenolate mofetil (MMF)

    given by PO

  • DrugRabbit ATG

    by vein

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What researchers measure

Primary outcomes

  1. To determine the 100-day non-relapse mortality (NRM) rate when administering pharmacologic pretransplant immunosuppression (PTIS) followed by pretransplant reduced toxicity conditioning (RTC

    Time frame: through study completion, an average of 1 year

07

Study locations

1 site
  • M D Anderson Cancer Center
    Houston, Texas 77030, United States
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05293509
Lead sponsor
M.D. Anderson Cancer Center
Responsible party
Sponsor
First posted
Mar 24, 2022
Start date
Mar 2, 2022
Primary completion
Sep 18, 2023
Completion
Sep 18, 2023
Last update
Sep 21, 2023

Study contacts

Jeremy Ramdial, Ramdial
principal investigator · M.D. Anderson Cancer Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is withdrawn, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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