Home GSK Inks $360M Deal for Syndivia's Preclinical ADC Targeting mCRPC

GSK Inks $360M Deal for Syndivia's Preclinical ADC Targeting mCRPC

Oct 28, 2025 10:04 CST Updated 10:04
Syndivia

Biological Engineering Company

GSK

Pharmaceutical R&D Manufacturer

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On October 27, GSK announced an agreement with Syndivia to obtain global exclusive development and commercialization rights for a preclinical ADC targeting metastatic castration-resistant prostate cancer (mCRPC).


According to the agreement, Syndivia will receive an upfront payment, as well asTotaling up to £268 million (approximately $360 million)The development and sales milestone payments, and will receive tiered royalties on global sales. GSK will assume responsibility for the development, manufacturing, and commercialization of this ADC project worldwide.

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This novel ADC, utilizing Syndivia's next-generation GeminiMab conjugation technology, demonstrates enhanced anti-tumor activity and encouraging safety, showing potential to become a best-in-class drug. Preclinical studies indicate that even at higher doses, the ADC effectively shrinks tumors without a corresponding significant increase in side effects. The ADC can directly target tumors for precise treatment, filling the gap left by current therapies, while offering a more convenient treatment option for mCRPC patients in community healthcare settings.


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GSK has been expanding its ADC drug portfolio in recent years through external acquisition:


On October 23, 2025, GSK announced that the FDA had approved Blenrep in combination with bortezomib and dexamethasone (BVd) for the treatment of adult patients with relapsed or refractory multiple myeloma who have received at least two prior therapies, including a proteasome inhibitor and an immunomodulatory agent. Blenrep is a BCMA ADC developed by Seagen (which has been acquired by Pfizer). In December 2009, GSK reached an agreement with Seagen to obtain the rights for the research, development, manufacturing, and commercialization of the drug.




2In October 2023, GSK introduced the B7-H4 ADC drug HS-20089 from Hansoh Pharma in a deal worth $1.57 billion; in December 2023, GSK again introduced the B7-H3 ADC drug HS-20093 (GSK'227) from Hansoh Pharma in a deal worth $1.71 billion; in December 2024, GSK introduced a preclinical ADC drug DB-1324 from DualityBio in a deal worth $1.005 billion.


GSK is developing a series of innovative product lines, covering ADCs with different antigens and payloads, next-generation small molecules, and T-cell engagers.These diversified solutions (e.g., GSK'227 and this novel ADC)Enable GSK to advance potential treatment options for different stages and types of prostate cancer.


Hesham Abdullah, Senior Vice President and Head of Global Oncology R&D at GSK, stated"Prostate cancer represents a significant health burden for GSK and an emerging growth area for the company. There is an urgent need for targeted therapies among patients with metastatic castration-resistant prostate cancer. The addition of this ADC further strengthens GSK's growing portfolio and its leadership in targeted oncology technologies, which includes the B7-H3-targeted ADC, GSK'227."

Sasha Koniev, CEO of Syndivia, said: "We are honored that GSK is advancing this project globally. This agreement highlights the value of our GeminiMab ADC platform and the opportunity to bring promising new therapies to patients with unmet medical needs."





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