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BioWorld - Sunday, March 15, 2026
Home » Topics » New compound, BioWorld Science

New compound, BioWorld Science
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Skin irritation on hands
Immune

HX-16108 holds promise for treating inflammatory skin diseases

March 11, 2026
No Comments
Atopic dermatitis (AD) is an inflammatory skin disease accompanied by pruritus, for which IL-13 and IL-31 are clinically validated targets. Earendil Labs Inc. has developed a bispecific antibody targeting both IL-13 and IL-31, HX-16108, with an extended half-life.
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Microscopic image of acute myeloid leukemia (AML) cells.
Cancer

Dual degrader shows activity in acute myeloid leukemia models

March 4, 2026
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Researchers in China reported the discovery and preclinical characterization of ZX-079, a novel BRD4/CBP PROTAC degrader.
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Leukemia illustration
Cancer

Newly described selective CDK6 degrader exhibits potential in leukemia models

March 3, 2026
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Researchers from Specally (Wuhan) Life Technology Co. Ltd. have disclosed the discovery and preclinical profile of WWZ-11-098, a non-palbociclib-based, selective cyclin-dependent kinase 6 (CDK6) degrader in models of leukemia.
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Cancer

New compound against tumors with aberrant FGFR2 signaling

Feb. 18, 2026
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Fibroblast growth factor receptor 2 (FGFR2) is a transmembrane tyrosine kinase that regulates signaling pathways controlling cell survival and proliferation. Dysregulation of FGFR2, through amplification or activating mutations, contributes to tumor development, making it an attractive target for therapeutic intervention in oncology.
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Vials, syringes, and pills
Cancer

CZL-077 shows robust preclinical antitumor activity

Feb. 16, 2026
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Researchers from Fudan University reported the development of CZL-077, a p300/CBP bromodomain inhibitor. p300 and CREB-binding protein (CBP) are closely related histone acetyltransferases that play central roles in regulating gene expression. Dysregulation of these proteins has been implicated in tumorigenesis and the development of therapy resistance.
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Illustration of tumor in breast
Cancer

New CDK12/13 dual degrader for TNBC

Feb. 12, 2026
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Triple-negative breast cancer (TNBC) cells depend on the transcriptional kinases CDK12 and CDK13 to maintain DNA damage response gene expression and manage replication stress. Due to their functional overlap, inhibition of a single kinase may permit compensatory activity.
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Cancer

SY-589 suppresses HR-deficient tumors via POLθ inhibition

Feb. 5, 2026
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DNA polymerase θ (POLθ) is a specialized, error-prone DNA polymerase that promotes the repair of DNA double-strand breaks through theta-mediated end joining (TMEJ), an alternative pathway that operates independently of homologous recombination.
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Illustration of rhinovirus particles
Infection

Thiazole derivatives show drug-like properties as broad-spectrum antirhinovirus agents

Feb. 2, 2026
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Challenges in developing antiviral agents against rhinoviruses (RVs) include their genetic heterogeneity (over 160 serotypes), rapid evolution of the viral capsid and serotype-specific immunity. To overcome these limitations, alternative approaches targeting host cellular pathways essential for viral replication have been proposed.
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Neurology/psychiatric

Centessa’s CNT-9982 shows promise for MDD

Jan. 21, 2026
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Orexin OX2 receptor agonists have demonstrated the ability to enhance wakefulness in rodent models, as well as in nonhuman primates and patients with narcolepsy and idiopathic hypersomnia. Based on recent findings, it has been hypothesized that they may also regulate cognition, mood and other neuropsychiatric functions. Furthermore, dysregulated orexin signaling has been reported in patients with major depressive disorder (MDD) with suicide attempts.
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Immuno-oncology

Orum’s ORM-1153 outperforms venetoclax in AML

Dec. 24, 2025
No Comments
Acute myeloid leukemia (AML) is a hematological cancer with limited treatment options and characterized by frequent relapse and poor prognosis. The only approved antibody-drug conjugate for AML is gemtuzumab ozogamicin, which targets CD33.
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