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About MediLink

Company Profile

    Founded on July 08, 2020, MediLink Therapeutics is an innovative drug development company focusing on antibody-drug conjugates (ADC) and related technologies.

    ADC drugs have both the powerful killing effects of the small molecule and tumor targeting properties of antibody. The recent technology breakthrough has led to nine new ADC approvals in the past three years for cancer treatment.

    As one of the most sophisticated class of drug modalities, ADC has several components including antibody, payload and linkers with a concerted mechanism of functions. New structures are emerging regularly to hit the new clinical applications, and the indications are also moving rapidly from oncology to non-oncology fields.

    MediLink Therapeutics was formed by experienced scientists from both small and large molecule drug development fields. The management team has collectively put over 20 new compounds into clinical developments, 3 of them are antibody drug conjugates. The team also has strong background in corporate governance and capital operations.

Our History

2024.12

YL201 Granted Orphan-Drug Designation by the US FDA

2024.12

YL201 Phase 3 trial initiation for NPC in China

2024.11

YL201 Phase 3 trial initiation for SCLC in China

2024.05

multi-target TMALIN® ADC technology platform license agreement with BioNTech

2024.05

YL205 was approved by CDE for clinical trials

2024.01

YL211 collaborates with Roche

2024.01

CFO onboarding

2023.12

YL215 was relicensed to Pfizer by Harbour

2023.11

YL201 received orphan drug designation from the FDA

2023.10

CMO onboarding

2023.10

YL202 collaborates with BioNTech

2023.10

YL201 launched phase I/II Study

2023.04

YL212 collaborates with Zai Lab

2022.11

YL202 was approved by CDE for clinical trials

2022.09

YL202 project IND has received approval from the FDA

2022.07

YL201 was approved by CDE for clinical trials

2022.06

Establishment of Singapore subsidiary and YL project enrolled first subject in clinical trial

2022.04

YL201 project IND has received approval from the FDA

2022.03

Completed $70 million Series B financing

2021.12

YL202 project into pharmacology and toxicology

Subsidiaries in Boston and Hong Kong were established

2021.08

YL201 project entered the formal stage of pharmacology and toxicology

Suzhou production subsidiary Eigong Source, Shanghai subsidiary was established

2021.05

Suzhou Biobay research and development site put into use

2021.02

Completed A round of 350 million RMB financing

2020.12

Product IP Layout

Initiate research and development site design

Two collaborations were reached

2020.11

Key personnel in place

Two projects were approved

Develop toxin Linker design