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BioWorld - Monday, February 16, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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It’s the climb: Matterhorn debuts to develop T-cell receptor therapies

Aug. 5, 2020
By Lee Landenberger
Matterhorn Bioscience AG has launched to develop T-cell receptor therapies based on the power of MR1T cells that have been found to find and kill a range of tumors in various tissue organs.
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Acute myeloid leukemia illustration
Newco news

Australia’s Race Oncology resurrects bisantrene following promising phase II AML results

Aug. 5, 2020
By Tamra Sami
PERTH, Australia – Patients with relapsed or refractory acute myeloid leukemia (r/r AML) who have received three or more lines of therapy are often too sick to get much-needed bone marrow transplants and often run out of options. Melbourne-based Race Oncology Ltd. hopes to change those outcomes with a new take on an old drug that slipped through the cracks in the 1980s.
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Not sleepy or hollow, hopes for Legend high despite loss of head

Aug. 4, 2020
By Randy Osborne
With Glaxosmithkline plc (GSK) having sailed through an FDA advisory panel meeting July 14 centered on its belantamab mafodotin (belantamab), an antibody-drug conjugate (ADC) for multiple myeloma (MM), others in the B-cell maturation antigen (BCMA) space such as Legend Biotech Corp. are further piquing Wall Street’s interest.
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Simcere licenses CDK4/6 inhibitor from G1 Therapeutics in $170M deal

Aug. 4, 2020
By Elise Mak
Nanjing, China-based Simcere Pharmaceutical Co. Ltd. became the second Chinese player to seek assets from G1 Therapeutics Inc., of Research Park Triangle, N.C., this year. On Tuesday, it licensed trilaciclib, an intravenous CDK4/6 inhibitor, from G1 Therapeutics in a $170 million deal for Greater China rights.
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FDA Approved stamp

Morphosys, Incyte win FDA nod for Monjuvi in DLBCL

Aug. 3, 2020
By Nuala Moran
LONDON – Morphosys AG finally has some heft to put behind its U.S. commercialization ambitions following FDA approval for its long-nurtured anti-CD19 antibody, Monjuvi (tafasitamab-cxix) in relapsed or refractory diffuse large B-cell lymphoma (r/rDLBCL).
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Henlius’ Herceptin biosimilar wins EU approval, marks Chinese players entry to Europe

July 31, 2020
By Elise Mak
Chinese biosimilar maker Shanghai Henlius Biotech Inc. won EMA approval for its Zercepac, a biosimilar to Roche Holding AG’s Herceptin (trastuzumab) on July 28. Henlius CEO Scott Liu told BioWorld that Zercepac will be the first Chinese monoclonal antibody biosimilar to enter the EU market, setting a precedent for Chinese drugmakers seeking to join the global race in biosimilars.
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Target with off-center arrow

Red pill, blue pill? Neoantigen matrix proving tricky as Wall Street hacks Genocea results

July 30, 2020
By Randy Osborne
Unraveling the eagerly awaited data from Genocea Biosciences Inc.’s phase I/IIa study with neoantigen cancer vaccine GEN-009 turned out less than simple, and the rollout of results – characterized by the company as positive, albeit early – were followed by a haircut for shares (NASDAQ:GNCA), which closed at $3.45, down $1.52, or 31%.
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Terns out-licenses BCR-ABL inhibitor for CML to Hansoh to accelerate entry to clinic

July 30, 2020
By Elise Mak
Terns Pharmaceuticals Inc., a NASH specialist based in San Francisco and Shanghai, has out-licensed the Greater China rights of its BCR-ABL inhibitor, TRN-000632, for treating chronic myeloid leukemia (CML) to Chinese pharma giant Hansoh Pharmaceutical Group Co. Ltd. to move the preclinical oncology asset to the clinic faster.
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Gold dollar sign

Bright Peak Therapeutics emerges from stealth with $35M series A for synthetic biologics

July 28, 2020
By Cormac Sheridan
DUBLIN – Versant Ventures is committing $35 million in series A funding to Bright Peak Therapeutics Inc., which is developing a pipeline of engineered cytokines that are produced using a novel chemical synthesis technique rather than the recombinant methods that have underpinned more than four decades of biotechnology development.
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Two ways about it? Spectrum sorts for cohorts’ purport after NSCLC win

July 28, 2020
By Randy Osborne
The bad cohort 1 news from Spectrum Pharmaceuticals Inc. in late April with poziotinib in the phase II Zenith20 study turned itself around in a stock-boosting way as the Henderson, Nev.-based firm unveiled data from cohort 2.
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