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NCT04555811

FT596 With Rituximab as Relapse Prevention After Autologous HSCT for NHL

Completed Phase 1 Results posted Last updated 9 July 2024
What this trial tests

Phase 1 trial testing FT596 in NHL in 7 participants. Completed in 30 November 2023.

Timeline
22 September 2020
Primary endpoint
8 February 2023
30 November 2023

Quick facts

Lead sponsorMasonic Cancer Center, University of Minnesota
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment7
Start date22 September 2020
Primary completion8 February 2023
Estimated completion30 November 2023
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Masonic Cancer Center, University of Minnesota

Who can join

18 and older, any sex, with NHL or Non Hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Number of Participants Experiencing Dose Limiting Toxicity Events Primary · 28 Days Post FT596 infusion

The component I design (FT596 on day 30) will continue until the MTD is declared or until the first dose is declared to be above MTD. The component I dose limiting toxicity (DLT) is defined as any of the following events within 28 days after the FT596 dosing based on CTCAE v5:Grade 4 hematologic toxicity lasting \> 7 days ,Grade 4 non-hematologic toxicity ,Grade ≥3 Infusion Related Reaction, Grade 2 acute GVHD that requires steroid therapy \>7 days or progression after 3 days of steroids or has partial response after 14 days of treatment, Grade ≥3 acute GVHD, Grade 4 cytokine release syndrome

GroupValue95% CI
FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose0
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose0
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose0
Number of Participants Experiencing Adverse Events Secondary · 1 year post FT596 infusion

Number of participants experiencing adverse events related to FT596 post auto-HSCT in combination with rituximab

GroupValue95% CI
FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose3
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose0
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose1
Percentage of Participants With Relapse/Progression Secondary · 1 year post auto HSCT

Percentage of participants experiencing progression or relapse at 12 months post auto HSCT

GroupValue95% CI
FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose6722 – 100
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose330 – 77
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose00 – 100
Number of Participants Experiencing Non-relapse Mortality Incidents at 100 Days Post HSCT Secondary · 100 days post HSCT

Number of participants experiencing non-relapse mortality at 100 days post auto-HSCT.

GroupValue95% CI
FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose0
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose0
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose0
Percentage of Non-relapse Mortality Incidents at One Year Post HSCT Secondary · one year post auto-HSCT

Percentage of participants experiencing non-relapse mortality at one year post auto-HSCT.

GroupValue95% CI
FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose675 – 95
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose1000 – 100
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose1000 – 100
Progression-Free Survival 12 Months Post Auto-HCT Secondary · 12 Months Post Auto-HCT

Progression-Free Survival 12 Months Post Auto-HCT

GroupValue95% CI
FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose331 – 77
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose675 – 95
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose1000 – 100

Adverse events — posted to ClinicalTrials.gov

Time frame: 1 year. Reporting threshold: 0%. Adverse-event reports describe events observed during the trial — not all are caused by the drug.

FT596 + Rituximab Dose Level 1: 9x10^7 Cells/Dose
Serious: 0/3 (0%)
Deaths: 2/3
FT596 + Rituximab Dose Level 2: 3x10^8 Cells/Dose
Serious: 0/3 (0%)
Deaths: 3/3
FT596 + Rituximab Dose Level 3: 9x10^8 Cells/Dose
Serious: 0/1 (0%)
Deaths: 1/1
Other adverse events (20 terms — click to expand)

ReactionSystemFT596 + Rituximab Dose Lev…FT596 + Rituximab Dose Lev…FT596 + Rituximab Dose Lev…
AnemiaBlood and lymphatic system disorders
FatigueGeneral disorders
DiarrheaGastrointestinal disorders
Lymphocyte count decreasedInvestigations
SinusitisInfections and infestations
HeadacheNervous system disorders
NauseaGastrointestinal disorders
CoughRespiratory, thoracic and mediastinal disorders
HypoxiaRespiratory, thoracic and mediastinal disorders
Non-cardiac chest painGeneral disorders
Infusion related reactionInjury, poisoning and procedural complications
BronchospasmRespiratory, thoracic and mediastinal disorders
HypokalemiaMetabolism and nutrition disorders
ChillsGeneral disorders
Creatinine increasedInvestigations
HypomagnesemiaMetabolism and nutrition disorders
HyponatremiaMetabolism and nutrition disorders
HypocalcemiaMetabolism and nutrition disorders
HypotensionVascular disorders
Lung InfectionInfections and infestations

Data from ClinicalTrials.gov NCT04555811 adverse events section.

Sponsor's own description

This is a Phase I multi-center study to evaluate the safety of FT596 when given with rituximab as relapse prevention in patients who have undergone an autologous hematopoietic stem cell transplant (auto-HSCT) for diffuse large or high-grade B cell lymphoma.

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. CAR race to cancer immunotherapy: from CAR T, CAR NK to CAR macrophage therapy.
    Pan K, Farrukh H, Chittepu VCSR, Xu H, et al · · 2022 · cited 478× · PMID 35361234 · DOI 10.1186/s13046-022-02327-z
  2. Natural killer cell homing and trafficking in tissues and tumors: from biology to application.
    Ran GH, Lin YQ, Tian L, Zhang T, et al · · 2022 · cited 207× · PMID 35768424 · DOI 10.1038/s41392-022-01058-z
  3. Natural killer cells in clinical development as non-engineered, engineered, and combination therapies.
    Lamers-Kok N, Panella D, Georgoudaki AM, Liu H, et al · · 2022 · cited 125× · PMID 36348457 · DOI 10.1186/s13045-022-01382-5
  4. From CAR-T Cells to CAR-NK Cells: A Developing Immunotherapy Method for Hematological Malignancies.
    Lu H, Zhao X, Li Z, Hu Y, et al · · 2021 · cited 81× · PMID 34422667 · DOI 10.3389/fonc.2021.720501
  5. Overcoming tumor resistance mechanisms in CAR-NK cell therapy.
    Valeri A, García-Ortiz A, Castellano E, Córdoba L, et al · · 2022 · cited 73× · PMID 35990652 · DOI 10.3389/fimmu.2022.953849
  6. Engineered and banked iPSCs for advanced NK- and T-cell immunotherapies.
    Cichocki F, van der Stegen SJC, Miller JS. · · 2023 · cited 68× · PMID 36327161 · DOI 10.1182/blood.2022016205
  7. Engineering Induced Pluripotent Stem Cells for Cancer Immunotherapy.
    Zhou Y, Li M, Zhou K, Brown J, et al · · 2022 · cited 44× · PMID 35565395 · DOI 10.3390/cancers14092266
  8. The Next Generation of Cellular Immunotherapy: Chimeric Antigen Receptor-Natural Killer Cells.
    Moscarelli J, Zahavi D, Maynard R, Weiner LM. · · 2022 · cited 40× · PMID 35788086 · DOI 10.1016/j.jtct.2022.06.025

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Other trials of FT596

Trials testing the same drug.

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Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04555811.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing