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BioWorld - Sunday, June 21, 2026
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Gloved hands holding mRNA vaccine vial
Immune

Korean consortium to develop mRNA vaccine for SFTS virus

Dec. 10, 2025
No Comments
A consortium including Korea Disease Control and Prevention Agency (KDCA), International Vaccine Institute (IVI), ST Pharm Co. Ltd. and Seoul National University (SNU) is joining forces with CEPI to advance a new AI-designed mRNA vaccine to protect against tick-borne severe fever with thrombocytopenia syndrome (SFTS) virus, or Dabie bandavirus. CEPI is providing up to US$16 million to the project, led by IVI, to test the vaccine’s safety and ability to generate a suitable immune response in healthy adults in preclinical and phase I/II trials in Korea.
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Cancer

Ideaya seeks IND clearance for KAT6/7 dual inhibitor IDE-574

Dec. 10, 2025
No Comments
Ideaya Biosciences Inc. has submitted an IND application to the FDA for IDE-574, a KAT6/7 dual inhibitor with potential to treat hormone receptor-positive breast cancer and lung adenocarcinoma. A phase I trial of IDE-574 monotherapy is expected to begin in the first quarter of next year.
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Illustration of brain with electrical activity background
Neurology/psychiatric

ABS-1230 controls seizures in KCNT1-driven severe epilepsy

Dec. 10, 2025
No Comments
Mutations in the KCNT1 gene produce gain-of-function effects that lead to overactivation of the potassium channel and consequent disruption of normal neuronal electrical signaling. These alterations give rise to a severe, early-onset developmental and epileptic encephalopathy that is typically associated with a high seizure burden and resistance to standard antiseizure medications.
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3D illustration of pancreatic cancer
Immuno-oncology

Akari’s AKTX-101 shows potential for KRAS-mutant PDAC

Dec. 10, 2025
No Comments
Akari Therapeutics plc has released new preclinical data indicating the therapeutic potential of AKTX-101 in pancreatic cancer driven by KRAS mutations. AKTX-101 is an antibody-drug conjugate (ADC) that delivers a novel RNA spliceosome modulating payload, PH1, into cancer cells that express TROP2.
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Hematologic

GB-3226: a first-in-class dual ENL-YEATS/FLT3 inhibitor for AML

Dec. 10, 2025
No Comments
ENL-YEATS is an epigenetic reader that sustains transcriptional programs essential for AML, whereas FLT3 mutations, present in approximately 30% of patients, drive malignant proliferation. Dual inhibition of ENL-YEATS and FLT3 may therefore more effectively disrupt complementary drivers of leukemogenesis than FLT3 targeting alone.
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GSK goes away, Ideaya synthetic lethality bids in-house again

Dec. 9, 2025
By Randy Osborne
No Comments
GSK plc said in paperwork filed with the U.S. SEC that the potentially whopping deal inked in the summer of 2020 with Ideaya Biosciences Inc. has gone down the tubes. The two firms were collaborating on three of Ideaya’s synthetic lethality programs, MAT2A (methionine adenosyltransferase 2a), Pol Theta (polymerase theta) and Werner Helicase.
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Real fluorescence microscopic view of human neuroblastoma cells
Cancer

Romidepsin offers hope for high-risk neuroblastoma

Dec. 9, 2025
By Tamra Sami
No Comments
Australian researchers have found a drug combination that can bypass the cellular defenses in neuroblastoma that lead to relapse, and the discovery could lead to better treatment strategies for children whose cancers have stopped responding to standard chemotherapy.
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Cancer

Merck Sharp & Dohme discovers new GTPase KRAS degradation inducers

Dec. 9, 2025
Merck Sharp & Dohme LLC has described proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a GTPase KRAS G12D mutant-targeting moiety via a linker reported to be useful for the treatment of cancer.
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Immuno-oncology

New antibody-drug conjugates disclosed in Genome & Co. patent

Dec. 9, 2025
Genome & Co. has divulged antibody-drug conjugates consisting of antibodies targeting basal cell adhesion molecules (BCAM) covalently linked to a cytotoxic drug through a linker reported to be useful for the treatment of cancer.
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Cancer

Uppthera describes new PLK1 degradation inducers

Dec. 9, 2025
Uppthera Inc. has identified proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a serine/threonine-protein kinase PLK1 (STPK13)-targeting moiety reported to be useful for the treatment of cancer.
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