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BioWorld - Friday, February 13, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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T cells

Yeeha at EHA: Sierra’s two-in-one approach with momelotinib welcomed in MF

July 7, 2021
By Randy Osborne
The whopper June buyout of by Morphosys AG of Constellation Pharmaceuticals Inc. brought renewed attention to myelofibrosis (MF) and other players in the space, such as Sierra Oncology Inc.
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Gadeta and Apeiron head to clinic with cell therapies aimed at solid tumors

July 7, 2021
By Richard Staines
Getting cell therapies to work against solid tumors is proving difficult – but two biopharma firms have begun early-stage studies with technologies that aim to crack this tough nut. Gadeta B.V. and Apeiron Biologics AG are using two different approaches to cell therapy that they hope will be effective against tough-to-treat solid tumors.
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Lilly takes equity stake in Mina Therapeutics

July 6, 2021
By Nuala Moran
LONDON – Following on from the $25 million up-front payment received on sealing their recent research collaboration, Mina Therapeutics Ltd. is now in line for a $15 million equity investment from Eli Lilly and Co. Inc.
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Stock merger illustration

Biosight just right for Advaxis praxis; merger deal sealed

July 6, 2021
By Randy Osborne
Advaxis Inc.’s long journey is ending happily by way of a merger with Biosight Ltd. that leaves the new firm with $50 million to help advance aspacytarabine (BST-236), a prodrug of cytarabine for acute myeloid leukemia and myelodysplastic syndromes.
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Kintara’s phase II GBM data incrementally improves

July 1, 2021
By Lee Landenberger
New top-line data from Kintara Therapeutics Inc.’s phase II study of its lead candidate, VAL-083, in recurrent glioblastoma multiforme were incrementally better than data released in April, and that’s just fine with CEO Saiid Zarrabian. “Normally, in my experience, top-line data usually regresses a little,” Zarrabian told BioWorld. “The fact that it improved could be a reflection of the small size of the study, but it adds a little more interest to top-line data.”
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Rylaze box and via

Jazz wins FDA approval for Erwinaze alternative, Rylaze

July 1, 2021
By Michael Fitzhugh
Just months after Jazz Pharmaceuticals plc's inventory of a therapy key to treating certain acute lymphoblastic leukemia and lymphoblastic lymphoma patients appears to have run out, FDA approval has arrived for an alternative: a recombinant version of the medicine the company developed, Rylaze (asparaginase Erwinia chrysanthemi (recombinant)).
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Lung cancer illustration

Arrivent raises a $150M series A to in-license oncology assets

June 30, 2021
By Lee Landenberger
Arrivent Biopharma Inc. has raised a series A financing worth up to $150 million to in-license compounds from China and bring them to the rest of the world. Arrivent’s focus is in oncology and its first in-licensed asset is furmonertinib, a third-generation EFGR tyrosine kinase inhibitor from Shanghai-based Allist Pharmaceuticals Co. Ltd.
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Knowledge center latest tool in EU cancer fight

June 30, 2021
By Mari Serebrov
As the first flagship action of Europe’s plan to beat cancer, the European Commission launched its Cancer Knowledge Center June 30. The new online platform will map the latest evidence on cancer, provide health care guidelines and quality assurance schemes, and monitor and project trends in cancer incidence and mortality across the EU, where cancer is the No. 1 killer for people younger than 65.
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Currus-Biologics-team-6-29
Newco news

Currus Biologics launches with AU$10M series A to tackle CAR T combo in solid tumors

June 29, 2021
By Tamra Sami
PERTH, Australia – Startup Currus Biologics Pty Ltd. has launched with a AU$10 million (US$7.5 million) series A round with the mission of improving the success of CAR T-cell therapies against solid tumors such as breast, ovarian and pancreatic cancers.
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Back to the dojo

Underwhelmed by lead cancer vaccine, Sensei moves to reprioritize, refocus

June 29, 2021
By Michael Fitzhugh
Shares of Sensei Biotherapeutics Inc. (NASADQ:SNSE) fell 16% to $9.10 on June 29 after an announcement by President and CEO John Celebi that the antigen display technology used in its prior lead candidate, SNS-301, "is suboptimal for use in an active cancer vaccine." A phase I/II trial evaluating it will be discontinued, he said. Now, work on a next-generation vaccine, SNS-401-NG, and the monoclonal antibody SNS-VISTA will take precedence in a portfolio reprioritization at the company, with IND-enabling studies for the anti-VISTA program planned to start by the end of 2021 and for the next-gen vaccine in second half of 2022.
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