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A Study to Investigate Use of Off-the-shelf Natural Killer (NK) Cells (SAR445419) in Relapsed/Refractory Acute Myeloid Leukemia

A legfontosabb adatok

Ki végzi
Sanofi
Hol
Houston, Omaha és The Bronx (Egyesült Államok)Mind a 3 helyszín megnézése
Azonosító
Állapot
Leállítva
Fázis
1. fázis
Résztvevők
7 fő vett részt
Kezdés
2023. jún. 16.
Befejezés
2024. márc. 12.
A vizsgálat típusa
Beavatkozással járó
A vizsgált kezelések
  • SAR445419
  • fludarabine
  • cytarabine
A regiszteradat frissítve
2026. június 5.
Miért állt le
Sponsor's decision

Ki vehet részt

Életkor
18 év felett
Nem
Nők és férfiak
Egészséges önkéntesek
Nem vehetnek részt

A regiszter feltételei, szó szerint

Mind a 12 feltétel megnézéseKevesebb

Ki vehet részt

  • Participant must be 18 years of age inclusive
  • Participants with confirmed diagnosis of relapsed or primary refractory acute myeloid leukemia (AML), according to World Health Organization (WHO) classification, including:
  • Participants with relapsed AML after allogeneic stem cells transplantation, including those who have received donor lymphocyte infusions,
  • Isolated central nervous system (CNS) or extramedullary disease,
  • At least 1 prior line of therapy which includes chemotherapy, hypomethylating agents, venetoclax or targeted therapy; Participants with a weight ≥42 kg

Ki nem vehet részt

  • Pregnant or breast-feeding women, female participants of childbearing potential, and male participants with female partners of childbearing potential who are not willing to avoid pregnancy by using a highly effective method of contraception (2 barrier method or 1 barrier method with a spermicide, intrauterine device, or hormonal contraception with inhibition of ovulation, for 2 weeks prior to the first dose of SAR445419, during treatment, and 6 months after the last dose of fludarabine). A woman is considered of childbearing potential, i.e., fertile, following menarche and until becoming postmenopausal unless permanently sterile
  • Receiving at the time of first SAR445419 administration corticosteroid as a concomitant medication with corticosteroid dose >10 mg/day of oral prednisone or the equivalent, except steroid inhaler, nasal spray, or ophthalmic solution
  • Concurrent treatment with other investigational drugs; The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial
  • Second primary malignancy that requires active therapy. Adjuvant hormonal therapy is allowed
  • Known acquired immunodeficiency syndrome (AIDS-related illnesses) or human immunodeficiency virus (HIV) disease requiring antiretroviral treatment, or having active hepatitis B or C infection, or symptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection
  • History of solid organ transplant, including corneal transplant
  • Known contraindication to any of the non-investigational medicinal products (NIMPs) (fludarabine, cytarabine, acetaminophen and diphenhydramine)

Helyszínek itt: Egyesült Államok

  • ~MD Anderson Cancer Center Site Number : 8400002Houston, Egyesült Államok
  • University of Nebraska Medical Center Site Number : 8400003Omaha, Egyesült Államok
  • Albert Einstein College of Medicine Site Number : 8400001The Bronx, Egyesült Államok

A vizsgálatról

Mit akar kideríteni a vizsgálat

This is a single group, Phase 1, single-arm, dose escalation study to determine the candidate dose(s), and evaluate safety, tolerability, and preliminary anti-tumor activity of SAR445419 administered after fludarabine and cytarabine conditioning for the treatment of relapsed or refractory acute myeloid leukemia (R/R AML). Adult participants with R/R AML will be eligible for treatment.

A teljes eredeti leírásKevesebb

The study is intended to assess the candidate dose(s) by the occurrence of dose-limiting toxicity (DLT) from start of chemotherapy until 28 days after the first administration of SAR445419.

The duration of the study for a participant will include:

* Screening period up to 21 days prior to initiating chemotherapy, * Treatment period of 5 days chemotherapy followed by SAR445419 administered for 2 weeks and end of treatment visit 56 days after first SAR445419 administration, * Survival follow-up period up to 1 year after the last participant has started treatment with SAR445419.

A vizsgálat csoportja

  • SAR445419A vizsgált kezelés

    Treatment consists of chemotherapy with fludarabine 30mg/m2/day and cytarabine 2g/m2/day administered for 5 days (Day -6 to Day -2), followed by 6 doses of SAR445419 given thrice weekly for 2 weeks beginning Day 1.

    Kezelés: SAR445419, fludarabine és cytarabine

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
A Phase I, Single-arm, Open Label, Dose Escalation, Multicenter Study of Off-the-shelf Natural Killer (NK) Cells (SAR445419) in Participants With Relapsed or Refractory Acute Myeloid Leukemia (R/R AML)
A regiszteradat frissítve
2026. június 5.