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Compugen to Present at the Oppenheimer 31st Annual Healthcare Conference
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HOLON, Israel, March 8, 2021 /PRNewswire/ Compugen Ltd. (NASDAQ: CGEN), a leader in predictive discovery and development of first-in-class therapeutics for cancer immunotherapy, today announced that management will present at the Oppenheimer 31
st Annual Healthcare Conference (virtual), on Tuesday, March 16, 2021 at 10:40 AM ET.
A live webcast of the presentation will be available on Compugen s website. A replay will be available after the presentation ends.
About Compugen
Compugen is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable, predictive computational discovery platforms to identify novel drug targets and develop therapeutics in the field of cancer immunotherapy. Compugen s lead product candidate, COM701, a first-in-class anti-PVRIG antibody, for the treatment of solid tumors, is undergoing a P
IsraelTel-avivElana-holzmanJosephine-belluardoBob-yedidLifesci-advisorsCompugen-ltdCorporate-communications-compugen-ltdCompugenNasdaqLifesci-communicationsTel-aviv-stock-exchangeCompugen Reports Fourth Quarter and Full Year 2020 Results
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Encouraging signals of anti-tumor activity demonstrated across COM701 Phase 1 combination and monotherapy studies with durable responses, including a complete response, in tumor types typically unresponsive to checkpoint inhibitors
Expansion of DNAM axis clinical programs to include Phase 1b cohort expansion of COM701 with Opdivo® in Q2 2021 and Phase 1 COM701 with COM902 dual combination study in 2H 2021
Initial data from ongoing dose escalation studies of triple combination of COM701 with Bristol Myers Squibb s Opdivo® and TIGIT Inhibitor, and COM902 monotherapy, both on track for Q4 2021
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ChinaUnited-statesIsraelTel-avivElana-holzmanJosephine-belluardoBob-yedidLifesci-advisorsCompugen-ltdCompugenNasdaqExchange-commissionPublished: Feb 03, 2021
- First potentially disease-modifying gene therapy for GM2 gangliosidosis to enter clinical studies
- Expect to continue patient identification, screening, and enrollment in Stage 1 of the study throughout 2021
NEW YORK and RESEARCH TRIANGLE PARK, N.C., Feb. 03, 2021 (GLOBE NEWSWIRE) Sio Gene Therapies Inc. (NASDAQ: SIOX), a clinical-stage company focused on developing gene therapies to radically transform the lives of patients with neurodegenerative diseases, today announced that the first patient with infantile Tay-Sachs disease has been dosed in a Phase 1/2 trial evaluating AXO-AAV-GM2, an investigational gene therapy for the treatment of GM2 gangliosidosis, also known as Tay-Sachs or Sandhoff disease.
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