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MediLink Therapeutics Announces Latest Business Progress with Nona Biosciences

SUZHOU, CHINA, December 15th , 2023 -- MediLink Therapeutics (“MediLink”), today announced that it has entered into a supplemental agreement to the license agreement with Nona Biosciences (“Nona”, a wholly-owned subsidiary of HBM Holdings) in which Nona is entitled to license the ADC product HBM9033 (YL215) jointly developed by the two parties to a licensed independent third party., Pfizer Inc.. (“Pfizer”). MediLink has the right to receive a certain percentage of sub-licensing payment based on the collaboration between Nona and Pfizer.

2023-12-15Learn more

MediLink Therapeutics Welcomes Steve Chin, M.D., As Chief Medical Officer (CMO)

On Oct. 23rd, 2023, MediLink Therapeutics is pleased to announce the appointment of Dr. Steve Chin as Chief Medical Officer (CMO). Dr. Chin will be responsible for MediLink’s clinical trial execution, product registration and optimization of clinical capability in both China and the US.

2023-10-23Learn more

MediLink Therapeutics Announces Strategic Collaboration and Worldwide License Agreement with BioNTech

MediLink Therapeutics (“MediLink”), announced today that it has entered into a strategic research collaboration and worldwide license agreement with BioNTech SE (Nasdaq: BNTX, "BioNTech"), a next generation immunotherapy company pioneering novel therapies for cancer and other serious diseases, on the development of a next-generation antibody-drug conjugate candidate (“ADC”), against Human Epidermal Growth Factor Receptor 3 (HER3).

2023-10-12Learn more

MediLink Therapeutics: Focuses on ADC research and development to promote new prospects for cancer treatment

GUANGZHOU, China, Sept. 23, 2023 /PRNewswire/ -- On September 23, 2023, oncologists and experts from more than 60 clinical research centers across the country gathered in Guangzhou to participate in the YL201 Phase I/II Investigators Meeting hosted by Suzhou MediLink Therapeutics Co., Ltd. The chair of this meeting was Professor Li Zhang, from the Cancer Center of Sun Yat-sen University, who gathered the wisdom and experience of experts, to discuss the development strategy of the clinical trial protocol in depth, and lay a solid foundation for the efficient drug development of YL201.

2023-09-23Learn more

MediLink Therapeutics is studying YL202 in advanced lung and breast cancer patients.

Working as a Clinical Research Coordinator I frequently find myself in the situation of balancing trial demands, patients’ comfort and executing protocol instructions correctly. I make the best of my resources and ask for assistance when needed. Hence, it should go without saying, having a reliable team is of paramount importance! Here is where, in my most recent experience, MediLink Therapeutics excels.

2023-08-25Learn more

PHARMCUBE interview - Dr. Xue, founder of Medilink Therapeutics

2023-03-02Learn more

MediLink Dosed 1st Patient in Phase I Study with ADC YL202

MediLink Therapeutics today announced that the first patient has been successfully dosed with its Antibody Drug Conjugate (ADC) product YL202 in the United States and the first dose was well tolerated without any adverse events (AEs) observed. This is a multi-center nonrandomized, open-label, first-in-human phase I study to evaluate the safety, tolerability, pharmacokinetics, and efficacy of YL202 in patients with locally advanced or metastatic epidermal growth factor receptor (EGFR)-mutated Non-small cell lung cancer (NSCLC) or hormone receptor (HR)-positive and HER2-negative breast cancer (BC). “The initiation of this study represents a significant milestone for MediLink Therapeutics, as it marks the second program of our ADC platform to enter the clinic in less than one year”, stated Tony Xue, PhD, Chairman, Founder & CEO.

2023-02-14Learn more

ADC treatment for cancer, how to take the future path

Antibody-drug conjugates (ADCs) combine the specificity of monoclonal antibodies with the potency of highly cytotoxic drugs, effectively delivering the drug payload to tumor sites and potentially reducing the severity of side effects. They are often referred to as the "magic bullets" of cancer therapy.

2023-06-17Learn more

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