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CompletedNCT02331706Updated Apr 21, 2020

IFN-DLI for Relapsed Acute Leukemia After Allo-SCT

An Early Phase 1 interventional study of Interferon alpha-2B (IFN-α) 3 million units (MU) subcutaneous daily in Leukemia, sponsored by Abramson Cancer Center at Penn Medicine. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-04-21.

Sponsored by Abramson Cancer Center at Penn Medicine · Early Phase 1, Interventional, and Treatment

Phase
Early Phase 1
Study type
Interventional
Enrollment
16
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

This trial is designed to determine the feasibility of conventional induction chemotherapy, IFNand G-CSF mobilized DLI (IFN-DLI) in subjects with relapsed AML and ALL after allo-SCT.

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Conditions studied

  • Leukemia

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03

In context

Leukemia

5,441 studies on the registry are indexed under Leukemia; 636 are open to participants now.

This study's enrollment of 16 is below the median of 38 across 4,247 interventional studies indexed under Leukemia.

Browse Leukemia studies →

Lead sponsor

Abramson Cancer Center at Penn Medicine is the lead sponsor of 446 studies on the registry; 86 are open to participants now.

Of its 32 completed or terminated interventional studies of FDA-regulated products, 14 (44%) have results posted.

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

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Who can participate

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

Inclusion criteria

DLI Recipient

  • Relapsed AML or ALL ≥ 60 days after allogeneic SCT.
  • Evidence of residual donor chimerism on most recent analysis (within 4 weeks of enrollment).
  • Age ≥ 18 years of age,
  • Karnofsky performance status ≥ 60%.
  • Absence of active GVHD and off immunosuppression. Subjects on tapering prednisone will be eligible if their dose is 0.25 mg/kg or less and being actively tapered. We suggest a 28 day waiting period off of immunosuppression but some subjects with rapidly progressive disease may need to be treated before 30 days and will still be eligible.
  • Adequate organ function: Cr ≤ 2 mg/dL; ALT/AST \< 3x ULN, direct bili \<3x ULN.
  • Matched sibling or un-related donor (A, B, C, and DR) available to undergo leukopheresis.
  • Subjects must be able to sign consent and be willing and able to comply with scheduled visits, treatment plan and laboratory testing.
  • Willing to provide blood samples for research purposes.
  • Willing to adhere to medically accepted form of birth control to prevent pregnancy (includes: complete abstention from intercourse, condoms, diaphragms, cervical cap, intra-uterine device, history of surgical sterility - tubal ligation or vasectomy in patient or partner, or oral contraceptive).

DLI Donor

  1. HLA identical to recipient subject.
  2. Considered medically eligible for leukopheresis procedure by independent donor physician (University of Pennsylvania physician who is not the recipient's primary transplant physician for related donors; physician designated by National Marrow Donor Program for unrelated donors).
  3. Considered medically eligible to receive G-CSF (filgrastim) by independent donor physician.

Exclusion criteria

Exclusion Criteria

Recipient

  • Prior cell therapy for relapse within the past 90 days.
  • Requirement for active immunosuppression to treat GVHD.
  • Pregnant or lactating women. The safety of this therapy on unborn children and effects on breast milk are not known.
  • Uncontrolled active infection
  • Any uncontrolled active medical disorder that would preclude participation as outlined.

Donor

  • Unable to participate in a leukopheresis procedure or receive G-CSF (filgrastim).
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Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    Subject Recipients

    Drug: Interferon alpha-2B (IFN-α) 3 million units (MU) subcutaneous daily

  • Experimental
    Subject Donors

    Drug: Interferon alpha-2B (IFN-α) 3 million units (MU) subcutaneous daily

Interventions

  • DrugInterferon alpha-2B (IFN-α) 3 million units (MU) subcutaneous daily
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What researchers measure

Primary outcomes

  1. Number of Adverse Events

    Time frame: 2 years

Secondary outcomes

  1. overall survival

    Time frame: 2 years

  2. disease-free survival

    Time frame: 2 years

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Study locations

1 site
  • Abramson Cancer Center of the University of Pennsylvania
    Philadelphia, Pennsylvania 19104, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 21, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02331706
Lead sponsor
Abramson Cancer Center at Penn Medicine
Responsible party
Sponsor
First posted
Jan 6, 2015
Start date
Dec 2014
Primary completion
Nov 11, 2016
Completion
Nov 11, 2017
Last update
Apr 21, 2020

Study contacts

David Porter, MD
principal investigator · Abramson Cancer Center at Penn Medicine

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2020. You cannot join it, but the record below documents what was studied.

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