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BioWorld - Sunday, April 5, 2026
Breaking News: Best of BioWorld Science: Q1Breaking News: Best of BioWorld Science: Q1Breaking News: Best of BioWorld Science: Q1
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3D representation of tumor
Cancer

ADRX-0706, a next-generation Nectin-4-targeting ADC with improved therapeutic window

April 23, 2024
Researchers from Adcentrx Therapeutics Inc. recently reported preclinical data for the Nectin-4-targeting antibody-drug conjugate (ADC) ADRX-0706, currently in phase I development for the treatment of solid tumors (NCT06036121).
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Liver disease
Gastrointestinal

Ochre Bio partners with Boehringer Ingelheim on regenerative treatments for chronic liver diseases

April 23, 2024
Ochre Bio Ltd. has established a partnership with Boehringer Ingelheim Pharma GmbH & Co. KG focused on the discovery and development of novel first-in-class regenerative treatments for chronic liver diseases, such as late-stage metabolic dysfunction-associated steatohepatitis (MASH) cirrhosis.
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Steadying hand while reaching for glass
Neurology/Psychiatric

AAV-CaV1.3-shRNA ameliorates parkinsonian symptoms in aged macaques

April 23, 2024
Proof-of-concept findings had shown that mRNA silencing of striatal Cav1.3 channels prevented and reversed established levodopa-induced dyskinesia in parkinsonian rats, with these effects being maintained in aged rats.
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Cancer

Haihe’s SOS1 inhibitor HH-100937 slows tumor growth in preclinical models

April 23, 2024
Son of sevenless homolog 1 (SOS1) plays a crucial role in the conversion of KRAS from its GDP- to its GTP-bound form independently of KRAS mutational status, thus being a promising therapeutic target for all tumors driven by KRAS. Haihe Biopharma Co. Ltd. has presented a potent SOS1 inhibitor, HH-100937, that has been found effective as monotherapy or when combined with drugs targeting the KRAS/MAPK pathway.
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Lung cancer driven by the Kras oncogene shown in purple
Cancer

Broader KRAS inhibition methods include chaperoning, gluing, vaccinating

April 23, 2024
By Anette Breindl
The existence of two approved therapies, Lumakras (sotorasib, Amgen Inc.) and Karzati (adagrasib, Mirati Therapeutics Inc.), has been a triumphant success against KRAS, a protein that was once considered undruggable. KRAS is the most frequently mutated oncogene in solid tumors. KRAS driver mutations are found in about 30% of non-small-cell lung cancers (NSCLC), about half of colorectal cancers, and more than 90% of pancreatic cancers. Lumakras and Karzati both target the G12C mutation. Inhibitors that target other mutations, like G12D, are now making their way through preclinical and clinical development, while some companies are developing therapies that would target mutated KRAS more broadly, irrespective of the specific mutation that is activating the protein.
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E3 ubiquitin-protein ligase RNF25
Cancer

Outrun emerges from stealth with $10M for E3 ligase inhibitors

April 22, 2024
By Nuala Moran
Newco Outrun Therapeutics Ltd. has raised $10 million in a seed round to develop small-molecule E3 ubiquitin ligase inhibitors that prevent programmed protein degradation. The lead program targeting an E3 ligase that tags a tumor suppressor protein for destruction will now advance to preclinical development.
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Cancer

New KIF18A inhibitors disclosed in Genescience Pharmaceuticals patent

April 22, 2024
Genescience Pharmaceuticals Co. Ltd. has described fused ring kinesin-like protein KIF18A inhibitors reported to be useful for the treatment of cancer.
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Cancer

Oncopia Therapeutics presents new CRBN ligands and its PROTACs

April 22, 2024
Oncopia Therapeutics Inc. (dba Proteovant Therapeutics Inc.) has divulged protein cereblon (CRBN) ligands and its PROTACs reported to be useful for the treatment of cancer.
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Infection

Aligos Therapeutics describes new prodrugs to treat hepatitis B and D virus infections

April 22, 2024
Aligos Therapeutics Inc. has identified prodrugs reported to be useful for the treatment of hepatitis B and hepatitis D viral infections.
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Cancer

Xuanzhu Pharma divulges new KIF18A inhibitors for cancer

April 22, 2024
Xuanzhu Pharma Co. Ltd. has synthesized kinesin-like protein KIF18A inhibitors reported to be useful for the treatment of cancer.
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