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Biosight Reports Final Primary Endpoint Data from Phase 2b Study of Aspacytarabine (BST-236) for First-Line Acute Myeloid Leukemia Therapy
January 06, 2022 16:05 ET | BioSight Ltd.
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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Biosight Announces Initiation of Phase 2 Clinical Trial of Aspacytarabine for MDS and AML
November 12, 2021 08:00 ET | BioSight Ltd.
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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Biosight Encourages Advaxis Stockholders to Vote “FOR” Proposed Merger
November 11, 2021 08:00 ET | BioSight Ltd.
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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Biosight Announces Upcoming Presentation at the 63rd American Society of Hematology Annual Meeting
November 04, 2021 09:36 ET | BioSight Ltd.
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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Biosight Announces Initiation of Investigator Sponsored Phase 2 Clinical Trial of Aspacytarabine for Relapsed/Refractory AML and MDS with the Groupe Francophone des Myélodysplasies
August 16, 2021 08:00 ET | BioSight Ltd.
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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Biosight Presents Updated Clinical Data from Ongoing Phase 2b Study of Aspacytarabine (BST-236) in an Oral Presentation at the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting
June 04, 2021 08:00 ET | BioSight Ltd.
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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Biosight Appoints Dr. Darrel Cohen as Chief Medical Officer
May 18, 2021 09:05 ET | BioSight Ltd.
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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Biosight Completes Enrollment in Phase 2b Study of Aspacytarabine (BST-236) for First-Line Acute Myeloid Leukemia Therapy
May 11, 2021 08:30 ET | BioSight Ltd.
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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Biosight to Present Updated Clinical Data from Ongoing Phase 2b Study of Aspacytarabine (BST-236) at the 2021 ASCO Annual Meeting
April 28, 2021 16:31 ET | BioSight Ltd.
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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Biosight Receives Orphan Medicinal Product Designation from the European Medicines Agency for Aspacytarabine (BST-236) for the Treatment of Acute Myeloid Leukemia
December 17, 2020 08:00 ET | BioSight Ltd.
AIRPORT CITY, Israel, Dec. 17, 2020 (GLOBE NEWSWIRE) -- Biosight Ltd., a pharmaceutical development company developing innovative therapeutics for hematological malignancies and disorders, today...