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NCT03856216Leállítva2. fázis

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

Addition of Inotuzumab Ozogamicin Pre- and Post-Allogeneic Transplantation

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. ápr. 15.

Megadott ok: \<75% participation

Rövid összefoglaló (regiszter, angolul)

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.

Állapot (regiszter)
Leállítva
Fázis (regiszter)
2. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
15 (tényleges)
Első benyújtás
2019. febr. 21.
Kezdés
2019. okt. 28.
Elsődleges befejezés
2025. okt. 13.
Fő szponzor
M.D. Anderson Cancer Center
NCT-szám
NCT03856216

Ki nem vehet részt

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Korábbi kezelés

  • Prior autologous transplant less than 1 year prior to consent.
  • Recent systemic chemotherapy or radiation within 3 weeks of study entry (intrathecal therapy is allowed).
    • Standard biological agents such as rituximab, TKIs such as ibrutinib and venetoclax are allowed to be given within 3 days prior to receiving inotuzumab ozogamicin. Blinatumomab is allowed to be given until 1 week prior to Day -13 inotuzumab ozogamicin on study.
  • Prior inotuzumab ozogamicin within 3 weeks of study entry.

Más betegség

  • Human immunodeficiency virus (HIV) positive.
  • Active and uncontrolled disease/infection.
  • Current active hepatic or biliary disease (with exception of Gilbert's syndrome).
  • Active hepatitis B or C.
  • Participants with cognitive impairments and/or any serious unstable pre-existing medical condition or psychiatric disorder that can interfere with safety or with obtaining informed consent or compliance with study procedures.

Laborértékek

  • Peripheral blast count of greater than 10 K/mL.

Egyéb

  • Unable or unwilling to sign consent.
  • QTcF interval > 470 ms.

Kiket keres a vizsgálat

  • Participants age 12 to 75.
  • English and non-English speaking participants are eligible.
  • CD22+ lymphoid malignancies including B-ALL
  • Eligible to receive a reduced-intensity alloSCT
    • Participants with:
  • Indolent lymphoma participants who failed conventional treatment; or,
  • Acute lymphoblastic leukemia (ALL), aggressive lymphoma, indolent lymphoma in transformation, or those who have failed ≥ three small molecule inhibitors
  • Donor: HLA compatible (8/8 match) related or matched unrelated donor (HLA-A, B, C, DRB1) or mismatched MUD (7/8 match) or haploidentical
  • Performance status of 0 to 2, Lansky ≥ 80 for < 16 years and Karnofsky ≥ 80 for ≥ 16 years of age.
  • Adequate organ function at time of study entry
    • Creatinine less than or equal to 1.6 mg/dL
    • Bilirubin less than 1.6 mg/dL
    • SGPT < 2 x UL
    • Ejection fraction >/= 40%
    • FEV1, FVC and cDLCO >/= 40%
  • Negative Beta HCG test in a woman with child bearing potential defined as not post-menopausal for 12 months or no previous surgical sterilization) or currently breast-feeding. Pregnancy testing is not required for post-menopausal or surgically sterilized women.

Életkor a regiszterben: 12 év – 75 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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HelyszínVárosOrszágHelyszín állapota
M D Anderson Cancer CenterHoustonEgyesült ÁllamokIsmeretlen állapot

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