Silexion Therapeutics Announces Selection of CRO to Support Upcoming Ph 2/3 Clinical Trials for SIL204

“Selecting AMS as our CRO partner represents a critical milestone as we advance SIL204 toward clinical development,” said Ilan Hadar, Chairman and CEO of Silexion Therapeutics. “This partnership brings the deep oncology expertise and regulatory knowledge essential for executing our dual-route administration strategy effectively. AMS’s strong experience with Phase 3 oncology trials brings a unique level of proven expertise which we believe will bolster our clinical program. With SIL204 having recently demonstrated up to 97% inhibition rates in preclinical studies and our manufacturing partnership with Catalent already in place, we are building the comprehensive foundation needed to bring this potentially transformative RNAi therapy to patients with KRAS-driven cancers.”

Share:

More News

“The positive outcome of our pre-IND interactions with the FDA reinforces the development pathway for MaaT034 and supports its continued advancement toward the clinic. It also represents an important step in MaaT Pharma’s expansion into immuno-oncology, highlighting the broader potential of our first in class co-cultivated microbiome donor-independent platform across

“Patients with metastatic RAS G12D non-squamous NSCLC, occurring in approximately 4% of cases, represent an underserved population, with no approved targeted treatment options. Initial clinical data evaluating zoldonrasib in combination with standard of care pembrolizumab and platinum doublet chemotherapy in patients with previously untreated metastatic RAS G12D non-squamous NSCLC showed

“At Georgiamune, we are focused on uncovering novel mechanisms that control immune-cell function and translating that biology into first-in-class medicines across autoimmune disease and oncology,” said Samir N. Khleif, M.D., Founder and Chief Executive Officer of Georgiamune. “GIM-621 is one of multiple programs to emerge from that work, alongside three

“Our team’s outstanding execution has enabled us to rapidly advance three programs into the clinic in 2026 and make significant progress in developing next-generation IO, ADC and combination therapies. Together with our partner, Kelun-Biotech, we have achieved seven IND clearances to date, and by mid-2027, we expect more than 2,000