deltatrials
Terminated INTERVENTIONAL NCT03856216

Inotuzumab Ozogamicin and Chemotherapy in Treating Patients With Leukemia or Lymphoma Undergoing Stem Cell Transplantation

Addition of Inotuzumab Ozogamicin Pre- and Post-Allogeneic Transplantation

Sponsor: M.D. Anderson Cancer Center

Updated 30 times since 2019 Last updated: Mar 27, 2026 Started: Oct 28, 2019 Primary completion: Oct 13, 2025 Completion: Oct 13, 2025
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

\<75% participation

A observational or N/A phase clinical study on Acute Lymphoblastic Leukemia and B Acute Lymphoblastic Leukemia, this trial is terminated or withdrawn. The trial is conducted by M.D. Anderson Cancer Center and has accumulated 30 data snapshots since 2019. Oncology trials at this stage typically focus on safety, tolerability, and early efficacy signals.

Study Description(click to expand)

PRIMARY OBJECTIVE: I. To assess the safety of the addition of inotuzumab ozogamicin (IO) pre- and post-allogeneic transplantation in patients with CD22-positive hematological malignancies. SECONDARY OBJECTIVES: I. Overall survival, progression-free survival and relapse rates. II. Treatment-related mortality. III. Cumulative incidence of acute and chronic graft-versus-host disease (GVHD). OUTLINE: Patients are assigned to 1 of 2 groups. GROUP I: Patients with acute lymphoblastic leukemia (ALL) and aggressive lymphoma receive inotuzumab ozogamicin intravenously (IV) over 1 hour on day -13, fludarabine IV over 1 hour on days -5 to -2, melphalan IV over 30 minutes on day -2, and tacrolimus IV continuously beginning on day -2 then orally (PO) once daily (QD) or twice daily (BID) for about 6 months. Patients also receive bone marrow or peripheral blood progenitor cells IV on day 0. Patients receive cylophosphamide IV over 3 hours and mesna IV on days +3 to +4 and filgrastim-sndz subcutaneously (SC) QD beginning 1 week after the transplant until blood cell levels return to normal. GROUP II: Patients with indolent lymphoma receive inotuzumab ozogamicin IV over 1 hour on day -13, fludarabine IV over 1 hour and bendamustine IV over 30 minutes to 1 hour on days -5 to -3,...

PRIMARY OBJECTIVE:

I. To assess the safety of the addition of inotuzumab ozogamicin (IO) pre- and post-allogeneic transplantation in patients with CD22-positive hematological malignancies.

SECONDARY OBJECTIVES:

I. Overall survival, progression-free survival and relapse rates. II. Treatment-related mortality. III. Cumulative incidence of acute and chronic graft-versus-host disease (GVHD).

OUTLINE: Patients are assigned to 1 of 2 groups.

GROUP I: Patients with acute lymphoblastic leukemia (ALL) and aggressive lymphoma receive inotuzumab ozogamicin intravenously (IV) over 1 hour on day -13, fludarabine IV over 1 hour on days -5 to -2, melphalan IV over 30 minutes on day -2, and tacrolimus IV continuously beginning on day -2 then orally (PO) once daily (QD) or twice daily (BID) for about 6 months. Patients also receive bone marrow or peripheral blood progenitor cells IV on day 0. Patients receive cylophosphamide IV over 3 hours and mesna IV on days +3 to +4 and filgrastim-sndz subcutaneously (SC) QD beginning 1 week after the transplant until blood cell levels return to normal.

GROUP II: Patients with indolent lymphoma receive inotuzumab ozogamicin IV over 1 hour on day -13, fludarabine IV over 1 hour and bendamustine IV over 30 minutes to 1 hour on days -5 to -3, and tacrolimus IV continuously beginning on day -2 then PO QD or BID for about 6 months. Patients also receive bone marrow or peripheral blood progenitor cells IV on day 0. Patients then receive rituximab IV over 4-6 hours on days 1 and 8, cyclophosphamide IC over 3 hours and mesna IV on days +3 to +4, and filgrastim-sndz SC once a day beginning 1 week after the transplant.

MAINTENANCE: Between 45 and 100 days after stem cell transplantation, all patients receive inotuzumab ozogamicin IV over 1 hour on days 1 and 2. Beginning 28 to 100 days after start of first cycle, patients receive inotuzumab ozogamicin IV over 1 hour on days 1 and 2 in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up periodically.

GROUP III: Recipients of haploidentical or mismatched unrelated stem cell transplant: Patients will receive inotuzumab ozogamicin intravenously (IV) over 1 hour on day -13, fludarabine IV over 1 hour on days -5 to -2, melphalan IV over 30 minutes on day -3 to -2, total body irradiation on day -1, and tacrolimus IV continuously beginning on day -2 then orally (PO) once daily (QD) or twice daily (BID) for about 6 months. Patients also receive bone marrow or peripheral blood progenitor cells IV on day 0. Patients receive cylophosphamide IV over 3 hours and mesna IV on days +3 to +4 and filgrastim-sndz subcutaneously (SC) QD beginning 1 week after the transplant until blood cell levels return to normal.

Status Flow

~Mar 2019 – ~Jul 2019 · 4 months · monthly snapshot~Jul 2019 – ~Oct 2019 · 3 months · monthly snapshot~Oct 2019 – ~Dec 2019 · 2 months · monthly snapshot~Dec 2019 – ~Jan 2020 · 31 days · monthly snapshot~Jan 2020 – ~Jun 2020 · 5 months · monthly snapshot~Jun 2020 – ~Aug 2020 · 2 months · monthly snapshot~Aug 2020 – ~Jan 2021 · 5 months · monthly snapshot~Jan 2021 – ~Apr 2021 · 3 months · monthly snapshot~Apr 2021 – ~Jun 2021 · 2 months · monthly snapshot~Jun 2021 – ~May 2022 · 11 months · monthly snapshot~May 2022 – ~Nov 2022 · 6 months · monthly snapshot~Nov 2022 – ~Mar 2023 · 4 months · monthly snapshot~Mar 2023 – ~Jul 2023 · 4 months · monthly snapshot~Jul 2023 – ~Sep 2023 · 2 months · monthly snapshot~Sep 2023 – ~Dec 2023 · 3 months · monthly snapshot~Dec 2023 – ~Feb 2024 · 2 months · monthly snapshot~Feb 2024 – ~Apr 2024 · 2 months · monthly snapshot~Apr 2024 – ~Jul 2024 · 3 months · monthly snapshot~Jul 2024 – ~Aug 2024 · 31 days · monthly snapshot~Aug 2024 – ~Sep 2024 · 31 days · monthly snapshot~Sep 2024 – ~Oct 2024 · 30 days · monthly snapshot~Oct 2024 – ~Nov 2024 · 31 days · monthly snapshot~Nov 2024 – ~Jan 2025 · 2 months · monthly snapshot~Jan 2025 – ~Mar 2025 · 59 days · monthly snapshot~Mar 2025 – ~Apr 2025 · 31 days · monthly snapshot~Apr 2025 – ~May 2025 · 30 days · monthly snapshot~May 2025 – ~Jul 2025 · 2 months · monthly snapshot~Jul 2025 – ~Nov 2025 · 4 months · monthly snapshot~Nov 2025 – ~Apr 2026 · 5 months · monthly snapshotApr 16, 2026 – present · 2 months · daily API

Change History

30 versions recorded
  1. Apr 16, 2026 — Present [daily]

    Terminated

    Phase: PHASE2None

  2. Nov 2025 — Apr 2026 [monthly]

    Terminated PHASE2

    Status: RecruitingTerminated

  3. Jul 2025 — Nov 2025 [monthly]

    Recruiting PHASE2

  4. May 2025 — Jul 2025 [monthly]

    Recruiting PHASE2

  5. Apr 2025 — May 2025 [monthly]

    Recruiting PHASE2

Show 25 earlier versions
  1. Mar 2025 — Apr 2025 [monthly]

    Recruiting PHASE2

  2. Jan 2025 — Mar 2025 [monthly]

    Recruiting PHASE2

  3. Nov 2024 — Jan 2025 [monthly]

    Recruiting PHASE2

  4. Oct 2024 — Nov 2024 [monthly]

    Recruiting PHASE2

  5. Sep 2024 — Oct 2024 [monthly]

    Recruiting PHASE2

  6. Aug 2024 — Sep 2024 [monthly]

    Recruiting PHASE2

  7. Jul 2024 — Aug 2024 [monthly]

    Recruiting PHASE2

  8. Apr 2024 — Jul 2024 [monthly]

    Recruiting PHASE2

  9. Feb 2024 — Apr 2024 [monthly]

    Recruiting PHASE2

  10. Dec 2023 — Feb 2024 [monthly]

    Recruiting PHASE2

  11. Sep 2023 — Dec 2023 [monthly]

    Recruiting PHASE2

  12. Jul 2023 — Sep 2023 [monthly]

    Recruiting PHASE2

  13. Mar 2023 — Jul 2023 [monthly]

    Recruiting PHASE2

  14. Nov 2022 — Mar 2023 [monthly]

    Recruiting PHASE2

  15. May 2022 — Nov 2022 [monthly]

    Recruiting PHASE2

  16. Jun 2021 — May 2022 [monthly]

    Recruiting PHASE2

  17. Apr 2021 — Jun 2021 [monthly]

    Recruiting PHASE2

  18. Jan 2021 — Apr 2021 [monthly]

    Recruiting PHASE2

  19. Aug 2020 — Jan 2021 [monthly]

    Recruiting PHASE2

  20. Jun 2020 — Aug 2020 [monthly]

    Recruiting PHASE2

  21. Jan 2020 — Jun 2020 [monthly]

    Recruiting PHASE2

  22. Dec 2019 — Jan 2020 [monthly]

    Recruiting PHASE2

    Status: Not Yet RecruitingRecruiting

  23. Oct 2019 — Dec 2019 [monthly]

    Not Yet Recruiting PHASE2

  24. Jul 2019 — Oct 2019 [monthly]

    Not Yet Recruiting PHASE2

  25. Mar 2019 — Jul 2019 [monthly]

    Not Yet Recruiting PHASE2

    First recorded

Eligibility Summary

The goal of this phase II clinical study is to learn about the safety of inotuzumab ozogamicin when given with fludarabine, with or without bendamustine, melphalan, and rituximab before and after a stem cell transplant. Researchers also want to learn if inotuzumab ozogamicin when given after a stem cell transplant can help control leukemia and lymphoma. Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a chemotherapy drug called ozogamicin. Inotuzumab attaches to CD22-positive cancer cells in a targeted way and delivers ozogamicin to kill them. Giving chemotherapy before a bone marrow or peripheral blood stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. Sometimes the transplanted cells from a donor attack the body's normal cells (called graft-versus-host disease). Giving tacrolimus and filgrastim before or after the transplant may stop this from happening. Fludarabine, bendamustine, melphalan, and rituximab are commonly given before stem cell transplants. Giving inotuzumab ozogamicin with chemotherapy may work better in treating patients with leukemia or lymphoma undergoing stem cell transplantation.

Contact Information

Sponsor contact:
  • M.D. Anderson Cancer Center
  • National Cancer Institute (NCI)
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations