Actuate Therapeutics' elraglusib, a GSK-3β inhibitor, received EMA Orphan Medicinal Product Designation for pancreatic ductal adenocarcinoma (PDAC) treatment. Positive Phase 2 trial interim results showed significant clinical benefits, aiming to expedite elraglusib's development as a novel mPDAC treatment.
Actuate Therapeutics' drug elraglusib received EMA's Orphan Medicinal Product Designation for treating pancreatic ductal adenocarcinoma, showing promise in Phase 2 trials with improved survival rates. The company plans to report topline data in 2025 and has also gained FDA's rare pediatric disease designation for Ewing sarcoma treatment.
Actuate Therapeutics' elraglusib, a GSK-3β inhibitor, received EMA Orphan Medicinal Product Designation for treating pancreatic cancer. Positive Phase 2 trial results show significant clinical benefits, aiming to expedite elraglusib's development as a novel treatment for metastatic pancreatic cancer.
Actuate Therapeutics' elraglusib, a GSK-3β inhibitor, received EMA Orphan Medicinal Product Designation for treating pancreatic ductal adenocarcinoma (PDAC). Positive Phase 2 trial results showed significant clinical benefits, aiming to expedite elraglusib's development as a novel treatment for metastatic PDAC.
Actuate Therapeutics' elraglusib reduced death risk by 37% in a Phase I/II metastatic pancreatic cancer trial, doubling one-year survival rate to 43.6% in the treatment arm vs 22.5% in the control arm. The company plans a Phase III study based on these encouraging results.