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Complete remission rate of 37%, of which 50% were minimal residual disease negative Single-agent activity and favorable safety demonstrated in most challenging AML patient populations Study results...
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U.S. Based Phase 2 Trial will Evaluate Aspacytarabine in Second Line Relapsed/Refractory MDS and AML across 18 Sites Builds Upon Ongoing Phase 2 Investigator Sponsored Study with the Groupe...
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Combined company, to be named Biosight Therapeutics, expected to be well-positioned to leverage its compelling oncology therapeutics pipeline, strong cash position, and accomplished management and...
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AIRPORT CITY, Israel, Nov. 04, 2021 (GLOBE NEWSWIRE) -- Biosight Ltd., a pharmaceutical development company developing innovative therapeutics for hematological malignancies and disorders, today...
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First Patient Enrolled to the Phase 2 Trial, which will Evaluate Single-Agent Aspacytarabine in Second Line Relapsed/Refractory AML and MDS Study sponsored by Groupe Francophone des Myélodysplasies,...
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Complete remission rate of 39%, of which 63% were minimal residual disease negative, achieved in expanded data set in frontline acute myeloid leukemia Durable responses with median overall survival...
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Industry veteran brings successful track record of clinical development and marketing authorizations of several cancer and leukemia drug products Appointment establishes US presence of senior...
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Encouraging data support single-agent efficacy across key measures including complete remission (CR) with negative minimal residual disease (MRD) rates, duration of response and overall survival in...
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AIRPORT CITY, Israel, April 28, 2021 (GLOBE NEWSWIRE) -- Biosight Ltd., a pharmaceutical development company developing innovative therapeutics for hematological malignancies and disorders,...
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AIRPORT CITY, Israel, Dec. 17, 2020 (GLOBE NEWSWIRE) -- Biosight Ltd., a pharmaceutical development company developing innovative therapeutics for hematological malignancies and disorders, today...