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DRUG:

FATE-NK100

i
Other names: adaptive NK cell cancer immunotherapy, FATE-NK100, FATE NK100
Associations
Company:
Fate Therap, University of Minnesota
Drug class:
NK cell stimulant, Cell therapy
Related drugs:
Associations
almost3years
FATE-NK100 as Monotherapy and in Combination With Monoclonal Antibody in Subjects With Advanced Solid Tumors (clinicaltrials.gov)
P1, N=44, Completed, Fate Therapeutics | Active, not recruiting --> Completed | N=100 --> 44 | Trial completion date: Oct 2022 --> Dec 2020
Clinical • Trial completion • Enrollment change • Trial completion date • Combination therapy
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2)
|
Herceptin (trastuzumab) • Erbitux (cetuximab) • FATE-NK100
over4years
[VIRTUAL] APOLLO: A phase I study of adaptive memory natural killer (NK) cells in recurrent ovarian cancer. (ASCO 2020)
FATE-NK100 via IP port was tested using 3 dose cohorts ([DC]; 1 × 107 cells/kg; >1 × 107 cells/kg to ≤3 × 107 cells/kg; or >3 × 107 to ≤10 × 107 cells/kg) after lympho-conditioning with fludarabine 25 mg/m2 IV and cyclophosphamide 300 mg/m2 IV on days −6 and −5. IP delivery of FATE-NK100 is safe, with clinical benefit in 3/9 patients treated. The allogeneic product cells persist and have enhanced function compared to patient NK cells for up to 21 days, even after retreatment. This phase I study in recurrent/refractory ovarian cancer shows promise for IP NK cell delivery.
P1 data
|
IFNG (Interferon, gamma)
|
fludarabine IV • FATE-NK100 • cyclophosphamide intravenous
almost5years
FATE-NK100 as Monotherapy and in Combination With Monoclonal Antibody in Subjects With Advanced Solid Tumors (clinicaltrials.gov)
P1, N=100, Active, not recruiting, Fate Therapeutics | Recruiting --> Active, not recruiting
Clinical • Enrollment closed • Combination therapy
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2)
|
Herceptin (trastuzumab) • Erbitux (cetuximab) • FATE-NK100