Zai Lab Announces Strategic Partnership with MediLink Therapeutics to Develop a Novel LRRC15 Antibody-Drug Conjugate
Zai Lab (NASDAQ: ZLAB; HKEX: 9688) has announced a strategic collaboration and worldwide license agreement with MediLink Therapeutics to develop ZL-6201, a novel LRRC15 antibody-drug conjugate (ADC). The partnership will utilize MediLink's TMALIN® ADC platform combined with an antibody discovered by Zai Lab.
The collaboration expands Zai Lab's global oncology pipeline with a potential first-in-class ADC targeting multiple solid tumors. ZL-6201 has shown promising preclinical data, with an Investigational New Drug (IND) filing expected in 2025. This partnership builds upon ongoing clinical trials for ZL-1310 and reinforces Zai Lab's commitment to developing ADC-based cancer therapies.
Zai Lab (NASDAQ: ZLAB; HKEX: 9688) ha annunciato una collaborazione strategica e un accordo di licenza mondiale con MediLink Therapeutics per sviluppare ZL-6201, un nuovo coniugato di anticorpo-farmaco (ADC) contro LRRC15. Questa partnership utilizzerà la piattaforma ADC TMALIN® di MediLink combinata con un anticorpo scoperto da Zai Lab.
La collaborazione amplia il portafoglio globale di oncologia di Zai Lab con un potenziale ADC di prima classe mirato a diversi tumori solidi. ZL-6201 ha mostrato dati preclinici promettenti, con un deposito di Nuovo Farmaco in Sperimentazione (IND) previsto per il 2025. Questa partnership si basa su trial clinici in corso per ZL-1310 e rafforza l'impegno di Zai Lab nello sviluppo di terapie oncologiche basate su ADC.
Zai Lab (NASDAQ: ZLAB; HKEX: 9688) ha anunciado una colaboración estratégica y un acuerdo de licencia mundial con MediLink Therapeutics para desarrollar ZL-6201, un nuevo conjugado de anticuerpo-fármaco (ADC) dirigido a LRRC15. La asociación utilizará la plataforma de ADC TMALIN® de MediLink combinada con un anticuerpo descubierto por Zai Lab.
La colaboración amplía la cartera global de oncología de Zai Lab con un posible ADC de primera clase que apunta a múltiples tumores sólidos. ZL-6201 ha mostrado datos preclínicos prometedores, con una solicitud de Nuevo Fármaco en Investigación (IND) prevista para 2025. Esta alianza se basa en ensayos clínicos en curso para ZL-1310 y refuerza el compromiso de Zai Lab en el desarrollo de terapias contra el cáncer basadas en ADC.
자이랩 (NASDAQ: ZLAB; HKEX: 9688)읶 메디링크 테라퓨틱스와 LRRC15를 겨냥한 새로운 항체-약물 접합체(ADC)인 ZL-6201을 개발하기 위한 전략적 협력 및 전 세계 라이센스 계약을 발표했습니다. 이 파트너십읶 메디링크의 TMALIN® ADC 플랫폼과 자이랩이 발견한 항체를 결합하여 사용할 것입니다.
이번 협력읶 자이랩의 글로벌 종양학 포트폴리오를 확대하며, 여러 고형 종양을 타겟으로 하는 최초의 ADC가 될 잠재력을 지니고 있습니다. ZL-6201읶 유망한 전임상 데이터를 보여주었으며, 2025년에는 임상 시험 신약(IND) 신청이 예상됩니다. 이 파트너십읶 ZL-1310에 대한 진행 중인 임상 시험을 기반으로 하며, ADC 기반 암 치료 개발에 대한 자이랩의 헌신을 강화합니다.
Zai Lab (NASDAQ: ZLAB; HKEX: 9688) a annoncé une collaboration stratégique et un accord de licence mondial avec MediLink Therapeutics pour développer ZL-6201, un nouvel anticorps-conjugué médicament (ADC) ciblant LRRC15. Ce partenariat utilisera la plateforme d'ADC TMALIN® de MediLink combinée à un anticorps découvert par Zai Lab.
Cette collaboration élargit le portefeuille mondial d'oncologie de Zai Lab avec un ADC potentiel de classe première ciblant plusieurs tumeurs solides. ZL-6201 a montré des données précliniques prometteuses, avec un dépôt d'Investigational New Drug (IND) prévu pour 2025. Ce partenariat s'appuie sur des essais cliniques en cours pour ZL-1310 et renforce l'engagement de Zai Lab à développer des thérapies contre le cancer basées sur les ADC.
Zai Lab (NASDAQ: ZLAB; HKEX: 9688) hat eine strategische Zusammenarbeit und eine weltweite Lizenzvereinbarung mit MediLink Therapeutics bekannt gegeben, um ZL-6201, ein neuartiges LRRC15-Antikörper-Wirkstoff-Konjugat (ADC), zu entwickeln. Die Partnerschaft wird die ADC-Plattform TMALIN® von MediLink in Kombination mit einem von Zai Lab entdeckten Antikörper nutzen.
Die Zusammenarbeit erweitert die globale Onkologie-Pipeline von Zai Lab mit einem potenziellen ADC der Klasse „first-in-class“, der auf mehrere solide Tumoren abzielt. ZL-6201 hat vielversprechende präklinische Daten gezeigt, und die Einreichung eines Antrags auf einen Neuen Wirkstoff (IND) wird für 2025 erwartet. Diese Partnerschaft baut auf laufenden klinischen Studien für ZL-1310 auf und stärkt das Engagement von Zai Lab für die Entwicklung von ADC-basierten Krebstherapien.
- Expansion of global oncology pipeline with potential first-in-class ADC
- Worldwide license agreement secured for novel LRRC15 ADC technology
- Promising preclinical data for ZL-6201
- IND filing timeline established for 2025
- None.
Insights
This strategic partnership marks a significant expansion in Zai Lab's ADC development capabilities. The collaboration leverages MediLink's TMALIN® platform technology with Zai Lab's antibody discovery expertise to develop ZL-6201, targeting LRRC15 - a promising target in solid tumors. LRRC15 (Leucine Rich Repeat Containing 15) is particularly interesting as it's expressed in cancer-associated fibroblasts and certain tumor cells, making it a compelling dual-targeting approach.
The deal structure appears to be a worldwide license agreement, giving Zai Lab global commercialization rights - a substantial value driver compared to regional deals. The IND filing timeline in 2025 suggests the program is in late preclinical development, with encouraging data supporting its progression. For context, the ADC market is experiencing rapid growth, with successful launches like Enhertu and Padcev demonstrating the commercial potential of next-generation ADCs.
This builds on Zai Lab's existing ADC program ZL-1310, creating a complementary pipeline in this high-value therapeutic class. The partnership demonstrates Zai Lab's strategic focus on building a globally competitive oncology portfolio through both internal development and strategic licensing.
From a financial perspective, this deal strengthens Zai Lab's position in the lucrative ADC market, which is projected to reach
For a company with a market cap of
Having multiple ADC programs reduces development risk through pipeline diversification while potentially creating platform value. Early-stage biotech investors typically assign higher valuations to companies with platform technologies and global rights, particularly in hot areas like ADCs.
Through this collaboration, Zai Lab further expands its global oncology pipeline with another potential first-in-class ADC targeting multiple solid tumors and addressing significant unmet medical needs. ZL-6201 has demonstrated encouraging preclinical data with an IND expected to be filed in 2025.
“MediLink has built a differentiated proprietary ADC technology platform, and we are excited to broaden our global partnership,” said Rafael G. Amado, M.D., President, Head of Global Research and Development at Zai Lab. “Building on the promising findings from our ongoing clinical trials for ZL-1310, this new collaboration demonstrates our continued focus on developing cancer therapies with ADC drugs and enriches our global oncology pipeline to address unmet medical needs. We look forward to working with MediLink to advance this compound into the clinic soon.”
“Zai Lab’s strong commitment to innovation and proven track record of global development impressed us through our existing collaboration,” said Tony Xue, PhD, CEO at MediLink. “This new partnership further validates our technology and enhances our strategic partnership. We believe our collaboration with Zai Lab will bring this innovative therapy to patients worldwide.”
About LRRC15
Leucine-rich repeat-containing protein 15 (LRRC15) is a type I transmembrane protein involved in cell-cell and cell-extracellular matrix (ECM) interactions. It is overexpressed in various mesenchymal tumors such as sarcoma, glioblastoma and melanoma, where it promotes tumor metastasis. Additionally, LRRC15 is upregulated in cancer-associated fibroblasts (CAFs) across various cancer types, contributing to immune-excluded and immune-suppressive tumor microenvironment (TME). This makes LRRC15 an appealing target for cancer therapy.
About Zai Lab in ADC
Zai Lab is building a portfolio of potential first- and/or best-in-class ADCs around the world. In addition to this next-generation ADC, the company has one near to commercial stage asset TIVDAK (tisotumab vedotin) and two next-generation ADC programs, ZL-1310 and ZL-6301, with exclusive worldwide rights. ZL-1310, a potential first-in-class ADC, is an investigational DLL3-targeted ADC being developed in a Phase 1 trial. Zai Lab presented encouraging efficacy and safety results for ZL-1310 from the ongoing Phase 1 study in patients with recurrent extensive-stage small cell lung cancer (SCLC) at the 2024 EORTC-NCI-AACR (ENA) Annual Symposium.
About Zai Lab
Zai Lab Limited (NASDAQ: ZLAB; HKEX: 9688) is an innovative, research-based, commercial-stage biopharmaceutical company based in
For additional information about Zai Lab, including our products, business activities and partnerships, research, and other events or developments, please visit or follow us at .
Zai Lab Forward-Looking Statements
This press release contains forward-looking statements relating to our future expectations, plans, and prospects, for Zai Lab, including, without limitation, statements relating to our prospects and plans for developing and commercializing next generation ADCs, the potential benefit of ADCs, and the potential treatment of solid tumors. All statements, other than statements of historical fact, included in this press release are forward-looking statements, and can be identified by words such as “aim,” “anticipate,” “believe,” “could,” “estimate,” “expect,” “forecast,” “goal,” “intend,” “may,” “plan,” “possible,” “potential,” “will,” “would,” and other similar expressions. Such statements constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are not guarantees or assurances of future performance. Forward-looking statements are based on our expectations and assumptions as of the date of this press release and are subject to inherent uncertainties, risks and changes in circumstances that may differ materially from those contemplated by the forward-looking statements. We may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in our forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results may differ materially from those indicated by forward-looking statements as a result of various important factors, including but not limited to (1) our ability to successfully commercialize and generate revenue from our approved products, (2) our ability to obtain funding for our operations and business initiatives, (3) the results of our clinical and pre-clinical development of our product candidates, (4) the content and timing of decisions made by the relevant regulatory authorities regarding regulatory approvals of our product candidates, (5) risks related to doing business in
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FAQ
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