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BioWorld - Friday, May 15, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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Replimune’s lead candidate misses two phase II endpoints

Dec. 5, 2023
By Lee Landenberger
Replimune Group Inc.’s lead candidate, RP-1 (vusolimogene oderparepvec), took a solid hit as it missed both primary endpoints in the Cerpass phase II study of skin cancer. Despite some better results from the study and good news from other studies along with a plan to drop some programs, the company’s stock still suffered.
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Samsung-Bioepis lab

Samsung Bioepis, Intocell partner for ADC drug development

Dec. 5, 2023
By Marian (YoonJee) Chu
Samsung Bioepis Co. Ltd. will partner with South Korean biotech Intocell Inc. to develop antibody-drug conjugate (ADC) drugs, continuing the Samsung Group and the wider industry’s hunt for novel ADCs. Under the joint research agreement inked on Dec. 5, the Daejon-based ADC platform technology firm Intocell will supply the Songdo, Incheon-based Samsung Bioepis its linker technology, coined OHPAS, or ortho-hydroxy protected aryl sulfate, upon which Samsung Bioepis will develop ADC drugs for up to five cancer targets.
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Handshake with charts, maps, data

Abbisko out-licenses pimicotinib to Merck KGaA in $605M deal

Dec. 5, 2023
By Tamra Sami
Abbisko Therapeutics Co. Ltd. has out-licensed China rights to its colony-stimulating factor 1 receptor inhibitor, pimicotinib, to Merck KGaA in a deal worth up to $605.5 million. Pimicotinib is in phase III trials in patients with tenosynovial giant cell tumors in China, the U.S., Canada and Europe.
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Lilly’s Jaypirca gets another accelerated nod for lymphoma

Dec. 4, 2023
By Karen Carey
Eli Lilly and Co., through its Loxo@Lilly oncology unit, secured its second accelerated approval for non-covalent Bruton’s tyrosine kinase (BTK) inhibitor Jaypirca (pirtobrutinib), this time to treat adults with chronic lymphocytic leukemia or small lymphocytic lymphoma. The U.S. FDA approval of 100-mg and 50-mg tablets is for patients who have received two prior lines of therapy, including another BTK inhibitor and a BCL-2 inhibitor. It is based on phase I/II data from a subset of 108 patients participating in the open-label, single-arm, multi-cohort Bruin trial.
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Acute myeloid leukemia illustration

Targeting gene coactivation factors with Cellcentric's inobrodib

Dec. 1, 2023
By Shyama Ghosh
Cellcentric's inobrodib, a novel drug with a distinct mechanism of action, shows promise in treating various hematological malignancies, as revealed in a recent publication in Cancer Cell.
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Engeneic dream vector nanocells extend overall survival in end-stage pancreatic cancer

Nov. 30, 2023
By Tamra Sami
Patients with end-stage pancreatic ductal adenocarcinoma achieved unprecedented survival rates after being treated with the Engeneic dream vector nanocells, with 88% of patients doubling the historical survival rates, Engeneic Ltd. co-CEO Jennifer MacDiarmid told BioWorld.
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Acquisition puzzle

To engineer Elahere: Abbvie sees bright future in $10B Immunogen takeover

Nov. 30, 2023
By Randy Osborne
Buying out Immunogen Inc. in a whopper cash deal valued at about $10.1 billion, Abbvie Inc. has major plans for an expanded label on the antibody-drug conjugate Elahere (mirvetuximab soravtansine-gynx), already approved for treating platinum-resistant ovarian cancer.
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Phenomic signs $509M deal with Boehringer for cancer targets

Nov. 29, 2023
By Lee Landenberger
Companies have invested billions for decades to crack the problem of treating the deep complexities involving stromal cancers, Phenomic AI CEO Girish Aakalu told BioWorld. Now he and his company are on the receiving end as they enter a new collaboration with Boehringer Ingelheim GmbH.
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FDA investigating risk with CAR T-cell therapies

Nov. 28, 2023
By Mari Serebrov
Reports of T-cell malignancies, including lymphoma, have the U.S. FDA investigating the risks for patients who received certain autologous CAR T-cell immunotherapies.
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British pound symbol

CRUK warns UK government of shortfall in funding for cancer research

Nov. 28, 2023
By Nuala Moran
Cancer Research UK (CRUK) is worried that rising prices and its total dependence on public donations mean its funding model is becoming unsustainable. The charity is calling on the U.K. government to step in and plug a £1 billion (US$1.23 billion) shortfall it said will open up over the next decade, in order to maintain investment at 2019 levels in real terms.
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