a novel class of nk cell engagers overcomes ... - compass · compass bispecific antibody discovery...

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Compass Therapeutics, Cambridge, MA, USA Background Multiple myeloma (MM) is a malignant hematological disease characterized by a dysregulated growth of plasma cells. Different therapeutic options are available for MM patients; however, the disease remains mostly incurable. B‐cell maturation antigen (BCMA) is a promising target in MM because of its restricted expression in normal and malignant plasma cells. NK cells have been implicated in the clinical efficacy of several therapies against MM and may contribute to the success of stem cell transplantation (SCT) by clearing residual cancer cells. In patients with advanced MM, NK cell function is affected by downregulation of CD16A (FcRIIIA) that significantly impairs the efficacy of conventional mAbs currently undergoing clinical testing. In contrast, expression of NKp30 remains stable, providing a compelling rationale for the design of BCMA‐targeted multispecific molecules that redirect NK cell killing by engaging NKp30 to overcome deficiencies in other activating NK receptors. Results Compass bispecific antibody discovery platform CTX‐4419 potently induces tumor cell killing and IFN‐γ production by NK cells in CD16A‐independent manner Primary NK cells were tested against NCI-H929 tumor cells Activity of CTX‐4419 on NKp30 pos,CD16A neg NK cells Glycosylated Fc, CD16A binding Aglycosylated Fc, no CD16A binding Superior tumor cell killing activity preserved in the absence of CD16A engagement CTX‐4419 activates NK cells only in the presence of tumor cells CTX‐4419 induced NK cells cytotoxicity against tumor cells expressing low levels of antigen 0.0001 0.001 0.01 0.1 1 10 100 0 200 400 600 800 1000 1200 Antibody concentration (nM) No Ab 0.0001 0.001 0.01 0.1 1 10 100 0 200 400 600 800 1000 1200 Antibody concentration (nM) No Ab 0.0001 0.001 0.01 0.1 1 10 100 0 200 400 600 800 1000 1200 Antibody concentration (nM) No Ab >100,000 ~100,000 < 30,000 Opportunity for rescuing patients with tumor target downregulation Primary NK cells (NKp30pos,CD16A pos) were tested against high, intermediate and low BCMA-expressing tumor cells More potent induction of target cell lysis than elotuzumab and daratumumab Primary NK cells were tested against MM.1S Superior activity by dual targeting of NKp30 and CD16A Conclusions Compass NK cell engagers lower the threshold for NK cell activation and potently redirect NK cell killing of tumor cells expressing high, medium and low levels of antigen In contrast to other NK targeting antibodies, CTX‐4419, a first‐in‐class NKp30xBCMA bispecific antibody, overcomes CD16A deficiency Compass highly modular bispecific platform can identify best combinations of TAAs and NK cells receptors tailored to target multiple indications Several other TAA combinations are currently under investigation A novel class of NK cell engagers overcomes CD16A deficiency Jennifer Watkins‐Yoon 1 , Jamie Schafer 1 , Allison Nelson 1 , Sara Haserlat 1 , Sri Vadde 1 , Xin Kai 1 , Lucy Liu 1 , Nora Zizlsperger 1 , Amanda Oliphant 1 , Michael Schmidt 1 , Robert Tighe 1 , Monia Draghi 1 1 Compass Therapeutics, Cambridge, MA, USA IFN Killing of tumor Better safety profile than T‐cell based therapies Better efficacy than conventional antibodies currently undergoing clinical testing Primary NK cells were tested against NCI-H929 tumor cells Effectors: Primary NK cells CTX CD137 panel CTX NKp30 panel CTX CD226 panel CTX NKG2D panel CTX BCMA panel Epitope mapping of common light chain antibody leads BCMA NK‐receptor Common light chain bispecific format NKp30xBCMA BiAb Lead CTX‐4419 Surface expression of tumor antigen on MM.1S tumor cells Isotype BCMA CD38 CS1 IgG1 Fc (CD16A binding) Aglyco‐IgG1 Fc (no CD16a binding) Targets: NCI‐H929 Targets: MM.1S Targets: NCI‐H929 Combinatorial screening Targets: RPMI‐8226 Targets: NCI‐H929 Targets: NCI‐H929 0.0001 0.001 0.01 0.1 1 10 0 20 40 60 80 100 Concentration (nM) NK + H929 NK alone 0 150 300 450 600 750 900 CTX-4419 BCMA-IgG1 (mAb) 0.0001 0.001 0.01 0.1 1 10 100 0 10 20 30 40 Antibody concentration (nM) No Ab MM.1S 0.0001 0.001 0.01 0.1 1 10 100 0 20 40 60 Antibody concentration (nM) No Ab NCI‐H929 RPMI‐8226 0.0001 0.001 0.01 0.1 1 10 100 0 10 20 30 40 Antibody concentration (nM) No Ab 0.0001 0.001 0.01 0.1 1 10 0 10 20 30 40 50 60 Concentration of CTX-4419 (nM) % positive NK cells CD137 CD69 NK+ H929 NK in the absence of tumor Assays performed with immortalized NK cell lines 0.0001 0.001 0.01 0.1 1 10 0 10 20 30 40 50 Concentration (nM) No A

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Page 1: A novel class of NK cell engagers overcomes ... - Compass · Compass bispecific antibody discovery platform CTX‐4419 potently induces tumor cell killing and IFN‐γproduction by

Compass Therapeutics, Cambridge, MA, USA

BackgroundMultiple myeloma (MM) is a malignant hematological disease characterized by a dysregulated growthof plasma cells. Different therapeutic options are available for MM patients; however, the diseaseremains mostly incurable. B‐cell maturation antigen (BCMA) is a promising target in MM because ofits restricted expression in normal and malignant plasma cells. NK cells have been implicated in theclinical efficacy of several therapies against MM and may contribute to the success of stem celltransplantation (SCT) by clearing residual cancer cells. In patients with advanced MM, NK cell functionis affected by downregulation of CD16A (FcRIIIA) that significantly impairs the efficacy ofconventional mAbs currently undergoing clinical testing. In contrast, expression of NKp30 remainsstable, providing a compelling rationale for the design of BCMA‐targeted multispecific molecules thatredirect NK cell killing by engaging NKp30 to overcome deficiencies in other activating NK receptors.

ResultsCompass bispecific antibody discovery platform

CTX‐4419 potently induces tumor cell killing and IFN‐γ production by NK cells in CD16A‐independent manner

Primary NK cells were tested against NCI-H929 tumor cells

Activity of CTX‐4419 on NKp30 pos,CD16A neg NK cells

Glycosylated Fc, CD16A binding Aglycosylated Fc, no CD16A binding

Superior tumor cell killing activity preserved in the absence of CD16A engagement 

CTX‐4419  activates NK cells only in the presence of tumor cells

CTX‐4419 induced NK cells cytotoxicity against tumor cells expressing low levels of antigen

0.0001 0.001 0.01 0.1 1 10 1000

200

400

600

800

1000

1200

Antibody concentration (nM)

No Ab

0.0001 0.001 0.01 0.1 1 10 1000

200

400

600

800

1000

1200

Antibody concentration (nM)

No Ab

0.0001 0.001 0.01 0.1 1 10 1000

200

400

600

800

1000

1200

Antibody concentration (nM)

No Ab

>100,000 ~100,000 < 30,000

Opportunity for rescuing patients with tumor target downregulation 

Primary NK cells (NKp30pos,CD16A pos) were tested against high, intermediate and low BCMA-expressing tumor cells

More potent  induction of target cell lysis than elotuzumab and daratumumab

Primary NK cells were tested against MM.1S

Superior activity by dual targeting of NKp30 and CD16A

Conclusions Compass NK cell engagers lower the threshold for NK cell activation and potently

redirect NK cell killing of tumor cells expressing high, medium and low levels of antigen

In contrast to other NK targeting antibodies, CTX‐4419, a first‐in‐class NKp30xBCMAbispecific antibody, overcomes CD16A deficiency

Compass highly modular bispecific platform can identify best combinations of TAAsand NK cells receptors tailored to target multiple indications

Several other TAA combinations are currently under investigation

A novel class of NK cell engagers overcomes CD16A deficiencyJennifer Watkins‐Yoon1, Jamie Schafer1, Allison Nelson1, Sara Haserlat1, Sri Vadde1, Xin Kai1, Lucy Liu1, Nora Zizlsperger1, Amanda Oliphant1, Michael Schmidt1, Robert Tighe1, Monia Draghi1

1Compass Therapeutics, Cambridge, MA, USA

IFN Killing of tumor

Better safety profile than T‐cell based therapies

Better efficacy than conventional antibodies currently undergoing clinical testing

Primary NK cells were tested against NCI-H929 tumor cells

Effectors: Primary NK cells

CTX CD137 panel

CTX NKp30 panel

CTX CD226 panel

CTX NKG2D panel

CTX BCMA panel

Epitope mapping of common light chain antibody leads

BCMA

NK‐receptor

Common light chain bispecific format

NKp30xBCMABiAb Lead

CTX‐4419

Surface expression of tumor antigen on MM.1S tumor cells

Isotype

BCMA

CD38

CS1

IgG1 Fc (CD16A binding) Aglyco‐IgG1 Fc (no CD16a binding)

Targets: NCI‐H929

Targets: MM.1STargets: NCI‐H929

Combinatorial screening

Targets: RPMI‐8226

Targets: NCI‐H929 Targets: NCI‐H929

0.0001 0.001 0.01 0.1 1 100

20

40

60

80

100

Concentration (nM)

NK + H92

9

NK alon

e

0

150

300

450

600

750

900CTX-4419BCMA-IgG1 (mAb)

0.0001 0.001 0.01 0.1 1 10 1000

10

20

30

40

Antibody concentration (nM)

No Ab

MM.1S

0.0001 0.001 0.01 0.1 1 10 1000

20

40

60

Antibody concentration (nM)

No Ab

NCI‐H929 RPMI‐8226

0.0001 0.001 0.01 0.1 1 10 1000

10

20

30

40

Antibody concentration (nM)

No Ab

0.000

10.0

01 0.01 0.1 1 10

0

10

20

30

40

50

60

Concentration of CTX-4419 (nM)

% p

ositi

ve N

K c

ells

CD137

CD69

NK+ H929

NK in the absenceof tumor

Assays performed with immortalized NK cell lines

0.0001 0.001 0.01 0.1 1 100

10

20

30

40

50

Concentration (nM)

No A