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BioWorld - Monday, March 2, 2026
Home » Topics » Drugs » Immuno-oncology

Immuno-oncology
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Antibody-drug conjugates floating on light purple background
Immuno-oncology

Next-generation dual-payload ADCs advance in oncology pipelines

March 2, 2026
No Comments
Researchers from Sutro Biopharma Inc. presented data on dual-payload antibody-drug conjugates (ADCs) engineered to overcome drug resistance, demonstrating enhanced cytotoxicity and potential efficacy in resistant cancer models.
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Cancer cell in the cross-hairs
Immuno-oncology

ARV-6723 shows robust efficacy in solid tumors

March 2, 2026
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Mitogen-activated protein kinase kinase kinase kinase 1 (HPK1) is a serine/threonine protein kinase that is expressed in the hematopoietic compartment, exerting regulatory functions in myeloid and innate immune cells. It has been associated with decreased T-cell activation and proliferation.
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B-cell releasing antibodies
Immuno-oncology

Characterization of HXN-1031 for B-cell malignancies

March 2, 2026
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Autoantibodies and B cells are drivers of progressive autoimmune diseases, but targeting B cells or plasma cells alone is not sufficient to address them. Earendil Labs has presented data on HXN-1031, a novel T-cell engager targeting both CD19 and B-cell maturation protein (BCMA).
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CAR T cell attacking cancer cells
Immuno-oncology

HITting solid tumors with a closer look and a stronger CAR T cell

March 2, 2026
By Anette Breindl
No Comments
CAR T cells have been groundbreaking for the treatment of B-cell cancers. But 8 years after Kymriah (tisagenlecleucel, Novartis AG) became the first CAR T-cell therapy to be approved, there are no CAR Ts approved for solid tumors.
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Acute myeloid leukemia
Immuno-oncology

Nanobody-based CLL-1-targeted CAR T cells enhance AML killing with reduced off-target effects

Feb. 26, 2026
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To overcome the challenges of current CAR T-cell strategies and enhance their efficacy and specificity for acute myeloid leukemia, researchers at the Sino-American Cancer Foundation and collaborating institutions have developed a nanobody-based CAR T-cell platform directed against C-type lectin-like molecule-1 (CLL-1).
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Antibody-drug conjugate illustration
Immuno-oncology

Kivu reports KIVU-305 data, gains clearance to enter clinic

Feb. 26, 2026
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Kivu Bioscience Inc. has announced receipt of Human Research Ethics Committee approval and clinical trial notification clearance in Australia to initiate a first-in-human trial of KIVU-305, its CEACAM5-targeted antibody-drug conjugate.
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Photo of magnifying glass inspecting moles on person's back
Immuno-oncology

Almirall nominates LAD-116 for non-melanoma skin cancer

Feb. 24, 2026
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Almirall SA has nominated LAD-116 as a novel therapy targeting non-melanoma skin cancer for further development in IND-enabling studies. LAD-116 is based on collaborator Etherna Immunotherapies NV’s intratumoral mRNA/lipid nanoparticle (LNP) platform.
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Immuno-oncology

ANK-203: first CD137-anchored therapy with strong antitumor activity

Feb. 24, 2026
No Comments
CD137 is a potent immune costimulatory receptor that promotes T-cell activation and enhances antitumor immune responses. However, systemic activation of CD137 can result in excessive immune stimulation and associated safety risks, such as hepatotoxicity, limiting its clinical use.
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Colorectal cancer 3D illustration
Immuno-oncology

L. monocytogenes vaccine enhances immunotherapy efficacy in CRC

Feb. 23, 2026
No Comments
In a recent study, researchers from Stony Brook University Renaissance School of Medicine and Cold Spring Harbor Laboratory investigated whether in vivo targeting of gastrointestinal tissues via foodborne delivery of Lm-based cancer vaccines could control tumor growth in murine models of colorectal cancer.
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Bispecific antibodies with heavy chain in green and pink, light chain in blue and yellow
Immuno-oncology

First-in-class LTβR x EDB bispecific antibody overcomes checkpoint resistance

Feb. 23, 2026
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Researchers from Agni Bio Inc. reported the preclinical profile of AGB-201, a bispecific antibody designed to simultaneously target EDB and LTβR, while minimizing unwanted immune activation.
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