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BioWorld - Wednesday, April 8, 2026
Home » solid tumors

Articles Tagged with ''solid tumors''

Immuno-oncology

Nextpoint Therapeutics’ antibodies enhance antitumor immune responses

May 17, 2024
HERV-H LTR-associating protein 2 (HHLA2) is known to play immunosuppressive roles by interacting with killer cell immunoglobulin-like receptor 3DL3 (KIR3DL3). The expression of HHLA2 in cancer is associated with poor patient outcomes, making it a promising therapeutic target for immunotherapy. Nextpoint Therapeutics Inc. has presented data on their monoclonal antibodies NPX-267 and NPX-887, which target KIR3DL3 and HHLA2, respectively.
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3D illustration of tumor
Immuno-oncology

Grant supports Lift Biosciences’ evaluation of IMAN cell therapies in humanized in vivo model systems

May 16, 2024
Lift Biosciences Ltd. has been awarded a grant of over £1 million (US$1.3 million) from Innovate UK that will fund a collaboration between Lift and researchers at the University of Cambridge.
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Radiopharmaceutical illustration
Cancer

Fogpharma and Artbio collaborate to create new class of α-radioligand therapeutics for solid tumors

May 14, 2024
Fogpharma Inc. and Artbio Inc. have established a collaboration to co-develop a new class of α-radioligand therapeutics to maximize efficacy for patients with multiple types of cancer.
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Art concept for monoclonal antibodies
Immuno-oncology

Pheast presents first preclinical data for anti-CD24 antibody-drug candidate

May 14, 2024
Pheast Therapeutics Inc. has announced the presentation of preclinical data for PHST-001, a therapeutic monoclonal antibody targeting CD24, a macrophage checkpoint.
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Poseida, Astellas hit the road in $550M convertibleCAR deal

May 7, 2024
By Jennifer Boggs
As Poseida Therapeutics Inc. anticipates reporting further data this year from allogeneic CAR T-cell therapy P-MUC1C-ALLO1, for which Astellas Pharma Inc. has nabbed first negotiation rights, the two companies inked a second deal aimed at combining their respective cell therapy platforms in an early stage collaboration targeting solid tumors.
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AI-generated image for cancer cells observed under a microscope
Immuno-oncology

Bioatla’s anti-Nectin-4 ADC gains IND clearance

May 7, 2024
Bioatla Inc. has received FDA clearance of its IND application for BA-3361, a conditionally active biologic (CAB)-Nectin-4 antibody-drug conjugate (ADC) for the treatment of multiple tumor types.
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Cancer cell and DNA
Cancer

IND clearance for Eisbach’s allosteric ALC1 inhibitor EIS-12656

May 7, 2024
Eisbach Bio GmbH has announced FDA clearance of its IND application for EIS-12656, a first-in-class orally bioavailable and blood-brain barrier-penetrant allosteric inhibitor of ALC1 (CHD1L), a key molecular machine in DNA repair. Enrollment will open in the second quarter in a phase I/II trial in patients with genetically defined advanced solid tumors, including patients progressing under PARP inhibitor treatment.
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Poseida, Astellas hit the road in $550M convertibleCAR deal

May 1, 2024
By Jennifer Boggs
As Poseida Therapeutics Inc. anticipates reporting further data this year from allogeneic CAR T-cell therapy P-MUC1C-ALLO1, for which Astellas Pharma Inc. has nabbed first negotiation rights, the two companies inked a second deal aimed at combining their respective cell therapy platforms in an early stage collaboration targeting solid tumors.
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Cancer

Potent and highly selective CDK7 inhibitor, KRLS-017, shows antitumor efficacy in multiple xenograft models

April 24, 2024
Researchers from Kirilys Therapeutics Inc. presented findings from the preclinical evaluation of KRLS-017, a novel reversible cyclin-dependent kinase 7 (CDK7) inhibitor being developed for the treatment of advanced solid tumors.
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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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