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NantKwest Signs Worldwide License Agreement With ProMab Biotechnologies To Exclusively Develop Select Next Generation Targeted Natural Killer Cell Therapeutics

Published: Mar 4, 2019 8:00 am

Initially Launching a Novel, High-Affinity BCMA CAR Targeting NK Cell De­vel­op­ment Candidate for Multiple Myeloma, with an Option for up to Five Additional CAR Targeting Sequences

NantKwest Signs Worldwide License Agreement With ProMab Biotechnologies To Exclusively Develop Select Next Generation Targeted Natural Killer Cell Therapeutics San Diego, CA (Press Release) – NantKwest, Inc. (Nasdaq:NK), a leading clin­i­cal-stage Natural Killer (NK) cell based thera­peutics com­pany, and ProMab Biotech­nol­ogies to­day an­nounced the estab­lish­ment of a world­wide license to a B-Cell Maturation Antigen (BCMA) targeted anti­body sequence for mul­ti­ple myeloma along with an op­tion for up to five undisclosed targeting sequences for ex­clu­sive use in the devel­op­ment of chi­meric an­ti­gen re­cep­tor (CAR) based NK cell ther­a­pies.

“We are pleased to an­nounce this col­lab­o­ration with ProMab Biotech­nol­ogies, marking another mile­stone for NantKwest in the devel­op­ment of targeted, next gen­er­a­tion, NK cell thera­peutics against mul­ti­ple myeloma and other cancers,” said Dr. Patrick Soon-Shiong, CEO of NantKwest. “With an esti­mated five-year sur­vival rate of around 49% and accounting for 10% of all hema­to­logical malig­nan­cies, patients with mul­ti­ple myeloma are in critical need for more ef­fec­tive treat­ment op­tions. We be­lieve, NantKwest’s CAR-based NK cell ther­apy may rep­re­sent a much needed new treat­ment op­tion for these patients. We eagerly antic­i­pate growing our rela­tion­ship with ProMab and ac­cel­er­ate the devel­op­ment of these new and inno­va­tive, next-gener­a­tion off-the shelf, CAR-based NK cell ther­a­pies.”

“ProMab’s stra­te­gic focus is on the devel­op­ment of mono­clonal anti­bodies and their appli­ca­tion in cell ther­apy through the integration of next gen­er­a­tion sequencing, bio­in­for­matics, high-through­put screen­ing tech­nolo­gies, and novel in vitro in vivo val­i­da­tion tools. This new part­ner­ship allows NantKwest to leverage the breadth of our mono­clonal anti­body gen­er­a­tion and val­i­da­tion plat­form, our human anti­body library screen­ing capabilities, to­geth­er with NantKwest’s strong NK cell engi­neer­ing, manu­fac­tur­ing, and clin­i­cal ex­per­tise,” said John Wu, Pres­i­dent and CEO of ProMab Biotech­nol­ogies. “We look for­ward to work­ing to­geth­er with the NantKwest team to more rapidly bring new NK cell thera­peutics into the clinic.”

Multiple Myeloma

Multiple myeloma is a debilitating blood cancer that while treatable is usually con­sidered incurable, re­sult­ing in over 100,000 deaths annually on a world­wide basis. Representing a sig­nif­i­cant unmet med­i­cal need, without treat­ment, sur­vival is typ­i­cally less than one year. Even with treat­ment, which typ­i­cally in­volves the use of chemo­ther­apy, steroids, targeted ther­apy, and in some cases, stem cell trans­plant, sur­vival often can only be extended to 4 to 5 years. The BCMA pro­tein is im­por­tant in B cell devel­op­ment and preferentially ex­pressed in mature B lym­pho­cytes. BCMA pro­tein is also be­lieved to be in­volved in the devel­op­ment of mul­ti­ple myeloma and other blood cancers and is an im­por­tant target for drug devel­op­ment.

About NantKwest Inc.

NantKwest, a member of the NantWorks ecosystem of com­pa­nies, is an inno­va­tive clin­i­cal-stage immuno­therapy com­pany focused on har­nessing the power of the innate immune sys­tem by using the natural killer cell to treat cancer and virally induced infectious dis­eases.

NantKwest is uniquely positioned to implement pre­ci­sion cancer med­i­cine, with the poten­tial to change the current paradigm of cancer care. Natural Killer (NK) cells are a safeguard in the human body de­signed to recog­nize and detect cells under stress due to cancer or viral in­fec­tion. NantKwest’s “off-the-shelf” activated NK cell plat­form is de­signed to destroy cancer and virally infected cells from the body. The safety of our NK cells as well as their ac­­tiv­ity against a broad range of cancers has been tested in phase I clin­i­cal trials in Canada and Europe as well as in mul­ti­ple phase I and II clin­i­cal trials in the United States. In addi­tion to being a universal cell-based ther­apy that does not re­quire in­di­vid­ualized patient sourcing or matching, our NK cell prod­ucts have been largely admin­istered in the outpatient setting as an “off-the-shelf” living drug.

With the capacity to grow active killer cells as a living cancer ther­apy, our NK cells have been de­signed to induce cell death against cancers and virally infected cells by several mech­a­nisms, in­­clud­ing: innate kill­ing, whereby all of our NK plat­forms recog­nize the stress pro­teins typ­i­cally found on cancer cells, which, upon binding, release toxic granules to im­medi­ately kill their targets; anti­body-mediated kill­ing with our haNK® plat­form, which are NK cells engi­neered to express anti­body re­cep­tors that can bind to thera­peutic anti­body prod­ucts, thereby enhancing the cancer cell kill­ing effect of that anti­body. All three modes of kill­ing (innate, anti­body-mediated, and CAR directed kill­ing) are employed by our t-haNK™ plat­form, which is an inno­va­tive com­bi­na­tion of our aNK, haNK® and taNK® plat­forms in a single prod­uct.

Our haNK®, and t-haNK™ plat­forms have been de­signed to address cer­tain lim­i­ta­tions of CAR T-cell ther­apy in­­clud­ing the ca­pa­bil­i­ty to in­fuse cell ther­apy in an outpatient setting which allows for poten­tial re­duc­tion of risk for serious cytokine storms and protracted serious adverse events. In Phase I and II clin­i­cal trials in patients with late stage cancer, our NK cells have been admin­istered as an inves­ti­ga­tional outpatient in­fusion safely with greater than 300 in­fusions to date at a dose of 2 billion cells per in­fusion.

By leveraging an integrated and extensive genomics and transcriptomics discovery and devel­op­ment engine, to­geth­er with a pipe­line of mul­ti­ple, clin­i­cal-stage, immuno-oncology pro­grams, we be­lieve NantKwest is uniquely positioned to be the premier immuno­therapy com­pany and trans­form med­i­cine by de­livering living drugs in a bag and bringing novel NK cell-based ther­a­pies to routine clin­i­cal care.

NK-92, aNK, haNK, taNK, and t-haNK are trademarks of NantKwest, Inc.

For addi­tional in­for­ma­tion, please visit www.nantkwest.com.

About ProMab Biotech­nol­ogies

ProMab Biotech­nol­ogies is a bio­technology com­pany located in Richmond California, that focuses to de­vel­op and com­mer­cial­ize mouse, rabbit, human mono­clonal anti­bodies as well as chi­meric an­ti­gen re­cep­tor-T Cell (CAR-T) prod­ucts. ProMab’s CAR-T plat­form covers both hema­to­logical and solid cancers with intensive in vitro and in vivo pre-clinical val­i­da­tion de­signed for safer and better treat­ment. As a CRO in the immunology field for 18 years, ProMab offers standard laboratory pro­ce­dures and animal studies for the anti­body discovery through the integration of the newest techniques in anti­body library con­struc­tion, next gen­er­a­tion sequencing, unique humanization modeling, high-through­put screen­ing, and artificial intelligence analysis sys­tems. ProMab aims to out-license anti­bodies val­i­dated in CAR-T ther­apy or bring the CAR-T tech­nolo­gies to the early stage mar­ket of clin­i­cal study. ProMab has part­nered with top bio­technology startups, med­i­cal in­sti­tu­tions, and pharma­ceu­ticals to ad­vance the devel­op­ment of cell ther­a­pies as well as bispecific anti­bodies across mul­ti­ple cancers. For more in­for­ma­tion, visit www.promab.com.

Forward-Looking State­ments

This press release con­tains for­ward-looking state­ments within the meaning of the Private Se­cu­ri­ties Lit­i­ga­tion Reform Act of 1995. Forward-looking state­ments in­clude state­ments con­cern­ing or im­plying the Com­pany will be suc­cess­ful in im­prov­ing the treat­ment of cancer. Risks and un­cer­tain­ties related to this endeavor in­clude, but are not limited to, obtaining FDA ap­prov­al of our NK cells as well as other thera­peutics as part of the NANT Cancer Vaccine plat­form as a cancer treat­ment.

Forward-looking state­ments are based on man­agement's current ex­pec­ta­tions and are subject to var­i­ous risks and un­cer­tain­ties that could cause actual results to differ ma­teri­ally and adversely from those ex­pressed or im­plied by such for­ward-looking state­ments. Accordingly, these for­ward-looking state­ments do not con­sti­tute guar­an­tees of future per­for­mance, and you are cautioned not to place undue reliance on these for­ward-looking state­ments.

These and other risks re­gard­ing our business are described in detail in our Se­cu­ri­ties and Ex­change Com­mis­sion filings, in­­clud­ing in our Quar­ter­ly Report on Form 10-Q for the quarter ended Sep­tem­ber 30, 2018. These for­ward-looking state­ments speak only as of the date hereof, and we disclaim any obli­ga­tion to up­date these state­ments except as may be re­quired by law.

Source: NantKwest.

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