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
- NCT05712278
- U1111-1279-2948
- 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.