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BioWorld - Thursday, January 1, 2026
Home » Keywords » HER2-positive cancers

Items Tagged with 'HER2-positive cancers'

ARTICLES

Illustration of cancer cells and immunotherapy treatment
Immuno-oncology

Abpro and Celltrion announce IND filing for T-cell engager

Dec. 16, 2025
No Comments
Abpro Holdings Inc. and Celltrion Inc. have announced the submission of an IND application to the FDA for ABP-102 (CT-P72), a HER2 x CD3 T-cell engager. Pending clearance, a phase I trial in patients with HER2-positive cancers, including breast and gastric cancers, is anticipated to begin in the first half of next year.
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3D illustration of T cells fighting cancer
Immuno-oncology

Preclinical data on bispecific TCE support further development

Dec. 1, 2025
No Comments
HER2-targeted antibody-drug conjugates (ADCs) have significantly improved cancer therapy in recent decades. However, ADCs can cause toxicity and resistance, while T-cell engagers (TCEs) show promising antitumor activity in solid tumors but are limited by substantial adverse effects.
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Immuno-oncology

Tagworks’ radioimmunoconjugate TGW-211 cleared for clinical trial

Oct. 16, 2025
No Comments
Tagworks Pharmaceuticals BV has announced approval by the Dutch regulatory authorities for a clinical trial application.
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Adenovirus cells
Immuno-oncology

Vironexis exits stealth with 10+ AAV-delivered immuno-oncology candidates

Sep. 13, 2024
By Brian Orelli
Vironexis Biotherapeutics Inc. has come out of stealth mode, disclosing that it has more than 10 product candidates it’s been developing over the last three years. The therapies are built on the company’s AAV-based platform, Transjoin, which is designed to have patients' livers express bispecific antibodies that bind to both CD3 on T-cells and various targets on tumor cells.
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Adenovirus cells
Newco news

Vironexis exits stealth with 10+ AAV-delivered immuno-oncology candidates

Sep. 12, 2024
By Brian Orelli
Vironexis Biotherapeutics Inc. came out of stealth mode today, disclosing that it has more than 10 product candidates it’s been developing over the last three years. The therapies are built on the company’s AAV-based platform, Transjoin, which is designed to have patients' livers express bispecific antibodies that bind to both CD3 on T-cells and various targets on tumor cells.
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Cancer

Chinese researchers present new antibody-drug conjugates for HER2-positive cancers

Aug. 16, 2024
Scientists from Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have disclosed antibody-drug conjugates (ADC) comprising antibodies targeting HER2 bound to an eribulin derivative through a linker reported to be useful for the treatment of cancer.
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Gastric distress: ALX shares upset by phase II evorpacept data

Aug. 1, 2024
By Randy Osborne
Investors wanted more from ALX Oncology Holdings Inc.’s phase II study testing evorpacept (evo) combination therapy in gastric tumors, and the stock (NASDAQ:ALXO) tumbled 36% or $1.77 to close Aug. 1 at $3.04.
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Immuno-oncology

Sorrento Therapeutics presents new antibody-drug conjugates for cancer

Oct. 3, 2023
Sorrento Therapeutics Inc. has divulged antibody-drug conjugates comprising antibodies targeting HER2 covalently linked to exatecan through a linker. They are reported to be useful for the treatment of cancer.
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Transparent tumor tomography image of a mouse model for HER2-positive breast cancer.
Immuno-oncology

Abpro partners with Celltrion to advance ABP-102, a bispecific antibody for HER2+ cancers

Sep. 22, 2022
Abpro Corp. has entered into a strategic partnership with Celltrion Holdings Co. Ltd. for ABP-102, a bispecific antibody therapy for patients with HER2+ cancer, including breast, gastric and pancreatic cancers.
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Precirix closes €80M series B with plans to complete phase II cancer trial

March 16, 2022
By Nuala Moran
Targeted radiopharmaceutical specialist Precirix NV has closed an €80 million (US$87.8 million) series B financing, enabling it to complete phase II development of CAM-H2, a potential treatment for HER2-positive metastatic breast cancer and gastric cancer. The round follows initial data showing there were no dose limiting toxicities in the first cohort of patients in the phase I/II trial, and a positive review from the safety committee.
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