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Table 1 The anti-tumor cGAS-STING agonists

From: cGAS-STING, an important pathway in cancer immunotherapy

Molecule

Type

Administration method

Development stage

Ref/note

c(di-GMP)

Prokaryotic CDNs

IT

Pre-clinical

[38]

3′,3′-cGAMP

Prokaryotic CDNs

IP

Pre-clinical

[39]

2′,3′-cGAMP

Eukaryotic CDNs

IT

Pre-clinical

[40]

ML-RR-S2-cGAMP

Synthetic CDN agonists

IT

Pre-clinical

[41]

ADU-S100

Synthetic CDN agonists

IT

Phase 1, Phase 2

[41]

ML-RR-S2-CDG

Synthetic CDN agonists

IT

Pre-clinical

[41]

DMXAA

Non-CDN agonists

IT

Phase1, Phase 2, Phase3

[42]

Amidobenzimidazoles

Non-CDN agonists

IV

Pre-clinical

[43]

ExoSTING

Novel STING agonists

IT

Pre-clinical

SITC 2018 P618

MV-626

ENPP1 inhibitor

IP

Pre-clinical

SITC 2018 P410

SB11285

Novel STING agonists

IP, IT, IV

Phase 1

AACR 2017 P-A25

STACT-TREX1

Novel STING agonists

IT, IV

Pre-clinical

SITC 2018 P235

SYN-STING

Novel STING agonists

IT

Pre-clinical

SITC 2018 P624

  1. Abbreviations: IT intratumoral, IV intravenous, IP intraperitoneal, SITC 2018 Society for the Immunotherapy of Cancer 2018 Annual Meeting, AACR 2017 American Association for Cancer Research 2017 Conference on Tumor Immunology and Immunotherapy