Quanta Therapeutics develops oral multi-KRAS inhibitors biased to G12D (QTX3034) and G12V (QTX3544), with responses in pancreatic, colorectal, and endometrial cancer.
Quanta Therapeutics, based in South San Francisco, develops oral multi-KRAS inhibitors biased towards G12D, QTX3034, and G12V, QTX3544, with responses reported in pancreatic, colorectal and endometrial cancer. Phase 1 data in October 2025 showed confirmed responses for QTX3034 alone and with cetuximab in colorectal, pancreatic and endometrial cancer, and preclinical data in March 2026 showed both compounds retain activity against resistance mechanisms acquired on the pan-RAS inhibitor daraxonrasib. OnCo links it to pancreatic, colorectal and endometrial cancer, to KRAS and RAS inhibitors, to KRAS as a target and the MAPK pathway, to daraxonrasib and to the bottleneck of undruggable drivers. Whether mutation-biased inhibitors or pan-RAS drugs win on the balance of efficacy and tolerability is the open question. Daraxonrasib has its own page.
The first drug that blocks all active RAS variants, approved by the FDA in August 2026 for metastatic pancreatic cancer, where KRAS drives 90% of tumours.
Shares Covalent chemistry for the RAS mutations that still have no drug, KRAS & RAS inhibitors, The undruggable drivers, RAS / RAF / MEK / ERK (MAPK).
Shares Daraxonrasib, KRAS & RAS inhibitors, KRAS, Pancreatic ductal adenocarcinoma.
Shares Daraxonrasib, KRAS & RAS inhibitors, The undruggable drivers, RAS / RAF / MEK / ERK (MAPK).
Shares KRAS & RAS inhibitors, The undruggable drivers, RAS / RAF / MEK / ERK (MAPK), KRAS.
Shares KRAS & RAS inhibitors, KRAS, Pancreatic ductal adenocarcinoma, Colorectal cancer.
Shares Daraxonrasib, RAS / RAF / MEK / ERK (MAPK), KRAS, Pancreatic ductal adenocarcinoma.
Shares KRAS & RAS inhibitors, The undruggable drivers, RAS / RAF / MEK / ERK (MAPK), KRAS.
Shares Daraxonrasib, KRAS & RAS inhibitors, Pancreatic ductal adenocarcinoma, Colorectal cancer.