https://chimerictherapeutics.com/wp-content/uploads/2021/12/Chimeric-Therapeutics-Newsletter-December-2021.pdf
Following up on @stockrock's comment:
the NK cells used in this phase 1 trial are not even going to be used the same way or at all in the future trials I believe. They are enhancing it, using them in a combination study and also developing CaR-NK cells…
As mentioned in the newsletter above, CORE-NK is merely the platform to build CAR-NK products:
(same link as above)
@turbo already mentioned a few highlights of this platform:
1. Established an efficacy signal.
2. Shown absence of GvHD = universal therapy.
3. Demonstrated cell persistence up to 28 days.
4. Successful cell expansion = efficient manufacturing.
5. Provided the basis for further developments.
Unlike FDA-approved CAR-T cells that come with heavy side-effects such as Cytokine Release Syndrome and also some patients developed GvHD, such side effects have not been reported when using CAR-NK cells. This has been mentioned in the thePhase 1 Clinical Data Presentation (07/03/2022):
CORE-NK however seems to address specifically known CAR-NK challenges:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140022/
See @turbo's points 3 & 4:
limited proliferative potential of NK cells (4.):
https://chimerictherapeutics.com/wp-content/uploads/2022/03/CORE-NK-Platform-Phase-1-Clinical-Data-Presentation-7-March-2022.pdf
limited persistence upon infusion (3.):
(same link as above)
I found a few very promising statements in the nature article published by Dr Wald et al who designed and developed the CORE-NK platform:
https://www.nature.com/articles/s41598-019-51287-6
Whilst this is based on a preclinical study, the data is very promising and I'm looking forward to clinical results of CHM 1301,
CHM 2301, CHM 3301.
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