TMCnet News
Biosight Raises $19M in Series C Funding to Support Clinical Stage Oncology ProgramsAIRPORT CITY, Israel, March 11, 2020 (GLOBE NEWSWIRE) -- Biosight Ltd., a pharmaceutical development company developing innovative therapeutics for hematological malignancies and disorders, today announced the raising of a $19M Series C financing. The investment is led by Israel Biotech Fund (IBF) with participation by SBI JI Innovation Fund, Arkin Bio Ventures, and additional new and existing investors. The new capital will advance the clinical development of Biosight’s lead asset BST-236 (aspacytarabine), currently being investigated in a Phase 2b study as a single-agent, first-line treatment of acute myeloid leukemia (AML). “We are thrilled with this financing,” said Dr. Ruth Ben Yakar, Chief Executive Officer of Biosight. “The increase of our investor base as well as the continued support from our existing shareholders are testaments to the potential of BST-236 as an important new therapy to cancer patients with limited therapeutic options. With this funding we are well positioned to complete enrollment of our ongoing Phase 2b trial in patients with AML, and to advance BST-236 to additional indications to address the unmet needs in the treatment of patients who are currently medically unfit to receive intensive chemotherapy.” Dr. David Sidransky of IBF said, “The encouraging interim data presented at the 2019 ASH Annual Meeting bolster our confidence in the ability of BST-236 to serve as a safer and more tolerable chemotherapy agent. We believe BST-236 has the potential to dramatically change standard of care for patients with hematologic malignancies and are thrilled to partner with the Biosight team to help the company succeed in its clinical development.” About BST-236 (Aspacytarabine) BST-236 was granted Orphan Drug Designation from the FDA, which entitles Biosight to seven years of market exclusivity upon BST-236 marketing approval for the treatment of AML. Integrated results from an ongoing Phase 2b study and a completed Phase 1/2a study of BST-236 as a single-agent first-line AML therapy for patients unfit for standard chemotherapy were presented at the ASH 2019 Annual Meeting. The data include a 57% complete remission (CR) rate in de novo AML patients, a 45% CR rate in patients with adverse cytogenetics, and a potential increase in overall survival. For more information regarding the Phase 2b clinical study of BST-236, please visit www.clinicaltrials.gov. About Biosight Ltd. About Israel Biotech Fund About Arkin Bio Ventures Contact: |
