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About Laekna

HKEX Stock Code: 2105.HK

Patient needs in major disease areas—such as metabolic diseases, oncology, and liver fibrosis—remain the driving force behind our mission. Laekna, a science-driven biotechnology company, is committed to bringing novel therapeutics to patients around the world.

Leveraging our tremendous experience and extensive know-how in disease biology, we have built a pipeline of over 20 internally discovered innovative drug candidates with proprietary intellectual property rights. We keep expanding our global reach through strategic partnerships, fostering collaborative success across regions.

In oncology, the Phase III clinical trial of LAE002 (afuresertib, an AKT inhibitor) for breast cancer (AFFIRM-205) was completed and successfully met its primary endpoint. We plan to submit NDA to the CDE in 2026, which will mark Laekna’s pivotal transition from clinical development to commercialization. Laekna has entered into an exclusive licensing agreement with Qilu Pharma to further accelerate the delivery of this novel therapeutic to patients across China.

In metabolic diseases, building on our deep expertise and extensive knowhow in the ActRII pathway, we have established a globally competitive, differentiated portfolio comprising LAE102, LAE103, and LAE123. Top-line results from Phase I studies of LAE102 (ActRIIA monoclonal antibody) for obesity, conducted in both China and the United States, consistently demonstrated dose-dependent trends in lean mass increase and fat mass reduction, as well as a well-tolerated safety profile. The Phase I study in the U.S. was completed in collaboration with the global R&D leader Eli Lilly, aiming to jointly accelerate the global development of this high-quality weight management therapy. The Phase I SAD study of LAE103 (ActRIIB monoclonal antibody) has been commenced in Australia.

From our laboratory in Zhangjiang Pharma Valley in Shanghai, to clinical trials conducted across China, the U.S., and Australia, our footprint spans the globe. Looking ahead, Laekna will continue to collaborate with international partners to accelerate delivery of novel therapeutics to patients worldwide.

For more information, please visit: https://www.laekna.com/ or https://www.linkedin.com/company/74110713/

Our Vision
Our Vision

Instead of  chasing the next big trend, commit to the work in front of you and refine every detail; with decade‑long discipline, time will make you a force that leads the way. 

Chris Lu, Ph.D.
Chairman & CEO
Scientific Advisory Board
Jeff Porter
Ph.D.
Chairman/Advisor

Jeff Porter, Ph.D. was appointed as Chairman of Scientific Advisory Board of Laekna in March 2022. He has over 25 years of global R&D leadership and strategic expertise, having most recently served as Vice President, Global Head of Chemical Biology & Therapeutics for the Novartis Institutes for BioMedical Research (NIBR).

 

As a senior member of the Leadership team at the NIBR from its inception, Jeff developed an enabling target and lead discovery approach focused on biological pathways, a fundamental tool for the success of NIBR. The diverse research group he led developed a dynamic multidisciplinary platform that merged pathway biology and disease area expertise with enabling technology. Their efforts led to numerous seminal discoveries, from fundamental insights to novel targets and clinical candidates that showed benefits in early proof of concept human trials and beyond. Examples include the discovery of multiple key targets/drug candidates in the core pathways of Developmental biology as well as the ‘drug-ability’ of RNA splicing.

 

Prior to Novartis, Jeff worked with Ontogeny (now Curis, Inc.) for over 5 years, starting as a staff scientist and advancing to serve as its Vice President of Research. He received a Ph.D. in Biochemistry at the Johns Hopkins University School of Medicine and performed postdoctoral work in the Department of Molecular Biology and Genetics in the Howard Hughes Medical Institute at Johns Hopkins.

Peter ten Dijke
Ph.D.
Advisor

Dr. Peter ten Dijke was appointed as advisor of Scientific Advisory Board of Laekna in 2021. He is the professor of molecular cell biology at Leiden University. His laboratory studies how subverted TGF family signaling is involved in cancer, vascular and bone diseases. They combine chemistry with biology  to develop novel synthetic molecules for therapeutic gain.

 

He received his Ph.D. degree in 1991 from Wageningen University, The Netherlands based on his research on the identification of the third isoform of TGF-β performed at Oncogene Science, Inc., New York, USA. He did his postgraduate studies with Kohei Miyazono and Carl-Henrik Heldin at the Ludwig Institute for Cancer Research (LICR), Uppsala, Sweden. In 1994, he became group leader at LICR and in 1999 he moved to the Netherlands Cancer Institute, Amsterdam, The Netherlands. In 2005 he moved to the Leiden University Medical Center, Leiden, The Netherlands.

Scott L. Friedman
M.D.
Advisor

Dr. Scott L. Friedman was appointed as advisor of Scientific Advisory Board of Laekna in 2022. He is the Dean for Therapeutic Discovery and Chief of the Division of Liver Diseases, at the Icahn School of Medicine at Mount Sinai. He has performed pioneering research into the underlying causes of scarring, or fibrosis associated with chronic liver disease, affecting millions worldwide. Dr. Friedman was among the first to isolate and characterize the hepatic stellate cell, the key cell type responsible for scar production in liver. His work has spawned an entire field that is now realizing its translational and therapeutic potential, with new anti-fibrotic therapies for liver disease reaching clinical trials.

 

He is widely recognized as a dynamic and a respected author, with over 300 peer-reviewed publications. He has mentored over 85 postdoctoral fellows and students. He has been a member of the American Society of Clinical Investigation, the Association of American Physicians, and was elected as a Fellow of the American Gastroenterological Association, the Am. College of Physicians, the American Assn. for the Study of Liver Diseases and the American Association for the Advancement for Science.

 

Dr. Scott L. Friedman was recognized with the Distinguished Achievement Awards from both the American Assn for the Study of Liver Diseases and the American Liver Foundation. In 2013 he was awarded the Shanghai Magnolia Gold Award by the Mayor of Shanghai and the China Friendship Award from the Premier of China in 2014 in recognition of his efforts to improve the health of the residents of Shanghai and China through his research achievements.

Counde Oyang
Ph.D.
Advisor

Dr. Oyang was appointed as advisor of Scientific Advisory Board of Laekna in 2021. He has had over 40 years of experience in drug discovery. From 2013 to 2018, he was with the Novartis Institutes for BioMedical Research (China) where he served as Head of Global Discovery Chemistry (China) and managed chemistry portfolio in drug and target discovery for various disease areas. From 2010 to 2013, he was with BioDuro where he served as Vice President of Chemistry. At BioDuro, he oversaw all programs in synthetic chemistry, medicinal chemistry and provided integrated services to clients. From 1982 to 2010, Dr. Oyang worked at Roche – in Palo Alto and at Syntex (acquired by Roche) where he served in roles of increasing responsibility including Director of Medicinal Chemistry. At Roche, he led multiple small molecule programs that advanced to the clinic. Dr. Oyang is an author of over 60 publications and patents.

 

Dr. Oyang obtained his Ph.D. in Chemistry from Loyola University of Chicago (with Professor James W. Wilt) and pursued postdoctoral research at Massachusetts Institute of Technology (with Professor Frederick D. Greene) and the University of Chicago (with Professor Josef Fried).

Jeff Porter
Ph.D.
Chairman/Advisor

Jeff Porter, Ph.D. was appointed as Chairman of Scientific Advisory Board of Laekna in March 2022. He has over 25 years of global R&D leadership and strategic expertise, having most recently served as Vice President, Global Head of Chemical Biology & Therapeutics for the Novartis Institutes for BioMedical Research (NIBR).

 

As a senior member of the Leadership team at the NIBR from its inception, Jeff developed an enabling target and lead discovery approach focused on biological pathways, a fundamental tool for the success of NIBR. The diverse research group he led developed a dynamic multidisciplinary platform that merged pathway biology and disease area expertise with enabling technology. Their efforts led to numerous seminal discoveries, from fundamental insights to novel targets and clinical candidates that showed benefits in early proof of concept human trials and beyond. Examples include the discovery of multiple key targets/drug candidates in the core pathways of Developmental biology as well as the ‘drug-ability’ of RNA splicing.

 

Prior to Novartis, Jeff worked with Ontogeny (now Curis, Inc.) for over 5 years, starting as a staff scientist and advancing to serve as its Vice President of Research. He received a Ph.D. in Biochemistry at the Johns Hopkins University School of Medicine and performed postdoctoral work in the Department of Molecular Biology and Genetics in the Howard Hughes Medical Institute at Johns Hopkins.

Peter ten Dijke
Ph.D.
Advisor

Dr. Peter ten Dijke was appointed as advisor of Scientific Advisory Board of Laekna in 2021. He is the professor of molecular cell biology at Leiden University. His laboratory studies how subverted TGF family signaling is involved in cancer, vascular and bone diseases. They combine chemistry with biology  to develop novel synthetic molecules for therapeutic gain.

 

He received his Ph.D. degree in 1991 from Wageningen University, The Netherlands based on his research on the identification of the third isoform of TGF-β performed at Oncogene Science, Inc., New York, USA. He did his postgraduate studies with Kohei Miyazono and Carl-Henrik Heldin at the Ludwig Institute for Cancer Research (LICR), Uppsala, Sweden. In 1994, he became group leader at LICR and in 1999 he moved to the Netherlands Cancer Institute, Amsterdam, The Netherlands. In 2005 he moved to the Leiden University Medical Center, Leiden, The Netherlands.

Scott L. Friedman
M.D.
Advisor

Dr. Scott L. Friedman was appointed as advisor of Scientific Advisory Board of Laekna in 2022. He is the Dean for Therapeutic Discovery and Chief of the Division of Liver Diseases, at the Icahn School of Medicine at Mount Sinai. He has performed pioneering research into the underlying causes of scarring, or fibrosis associated with chronic liver disease, affecting millions worldwide. Dr. Friedman was among the first to isolate and characterize the hepatic stellate cell, the key cell type responsible for scar production in liver. His work has spawned an entire field that is now realizing its translational and therapeutic potential, with new anti-fibrotic therapies for liver disease reaching clinical trials.

 

He is widely recognized as a dynamic and a respected author, with over 300 peer-reviewed publications. He has mentored over 85 postdoctoral fellows and students. He has been a member of the American Society of Clinical Investigation, the Association of American Physicians, and was elected as a Fellow of the American Gastroenterological Association, the Am. College of Physicians, the American Assn. for the Study of Liver Diseases and the American Association for the Advancement for Science.

 

Dr. Scott L. Friedman was recognized with the Distinguished Achievement Awards from both the American Assn for the Study of Liver Diseases and the American Liver Foundation. In 2013 he was awarded the Shanghai Magnolia Gold Award by the Mayor of Shanghai and the China Friendship Award from the Premier of China in 2014 in recognition of his efforts to improve the health of the residents of Shanghai and China through his research achievements.

Counde Oyang
Ph.D.
Advisor

Dr. Oyang was appointed as advisor of Scientific Advisory Board of Laekna in 2021. He has had over 40 years of experience in drug discovery. From 2013 to 2018, he was with the Novartis Institutes for BioMedical Research (China) where he served as Head of Global Discovery Chemistry (China) and managed chemistry portfolio in drug and target discovery for various disease areas. From 2010 to 2013, he was with BioDuro where he served as Vice President of Chemistry. At BioDuro, he oversaw all programs in synthetic chemistry, medicinal chemistry and provided integrated services to clients. From 1982 to 2010, Dr. Oyang worked at Roche – in Palo Alto and at Syntex (acquired by Roche) where he served in roles of increasing responsibility including Director of Medicinal Chemistry. At Roche, he led multiple small molecule programs that advanced to the clinic. Dr. Oyang is an author of over 60 publications and patents.

 

Dr. Oyang obtained his Ph.D. in Chemistry from Loyola University of Chicago (with Professor James W. Wilt) and pursued postdoctoral research at Massachusetts Institute of Technology (with Professor Frederick D. Greene) and the University of Chicago (with Professor Josef Fried).

Milestones
2026
  • June, entered into an exclusive license agreement with Vasque Bio for LAE118 in Ex-China Region
  • April, Phase III clinical trial of LAE002 (afuresertib) for HR+/HER2- breast cancer (AFFIRM-205) successfully met its primary endpoint
  • March, positive topline results from U.S. Phase I SAD study of LAE102( in collaboration with Eli Lilly)showed encouraging trends toward lean mass increase and fat mass reduction
  • February, an article titled "Afuresertib plus fulvestrant for pretreated HR-positive, HER2-negative, advanced breast cancer: a phase Ib trial" was published in Nature Communications
2025
  • December, first subject dosed in Phase I SAD study of LAE103 in Australia
  • November, entered into an exclusive licensing agreement of LAE002 (afuresertib) for the treatment of breast cancer in China with Qilu Pharma
  • September, announced positive preliminary results of LAE102 MAD Study
  • July, obtained IND approval of LAE103 from FDA
  • June, presented first-in-human clinical study results of LAE102 and pre-clinical studies results of LAE102, LAE103(ActRllB mAb) and LAE123(ActRllA/llB mAb) at ADA
  • March, initiated LAE102(ActRIIA mAb)  Phase I MAD study for obesity in China
  • February, obtained IND approval of LAE120 (USP1 inhibitor) from FDA
2024
  • December, completed LAE102 Phase I SAD study for obesity in China with positive results
  • November, entered into a clinical collaboration agreement with Eli Lilly of LAE102 for obesity in the U.S.
  • October, initiated subcutaneous dosing cohort of LAE102 phase I SAD study for obesity in China
  • September, announced robust phase 1b data of LAE002 for breast cancer at ESMO
  • June, first subject dosed in phase I clinical trial of LAE102 for the treatment of obesity
  • May, first patient enrolled in AFFIRM-205, a phase III clinical study of LAE002 (afuresertib) plus fulvestrant for the treatment of breast cancer
  • Q2, obtained IND approval of LAE102(ActRIIA mAb) for the treatment of obesity from FDA and CDE
2023
  • September, included as a constituent of the Hang Seng Composite Index, and listed in the Stock Connect
  • June, listed on the Main Board of the HKEX
  • May, received IND approval for Phase I/II study of LAE102 from FDA in the United States
2022
  • April, completed Series D financing
  • March, received IND approval for Phase II LAE002 and LAE001 combination study in patients with mCRPC in South Korea
  • January, received IND approval for Phase I/II combination therapy of LAE002 with sintilimab, targeting patients with solid tumors with prior PD-1/PD-L1 treatments from NMPA in China
2021
  • September, completed Phase I clinical trial of LAE001 for mCRPC in China, and entered Phase II stage
  • August, received IND approval for Phase Ib/III study of LAE002 plus fulvestrant in patients with locally advanced or metastatic HR+/HER2- breast cancer from NMPA in China
  • July, entered into a collaboration agreement with Innovent to develop a combination therapy of LAE002 with sintilimab, targeting patients with solid tumors with prior PD-1/PD-L1 treatments
  • June, received IND approval for Phase Ib/III study of LAE002 plus fulvestrant in patients with locally advanced or metastatic HR+/HER2- breast cancer from FDA in the United States
  • May, declared the first internally discovered pre-clinical candidate, ActRIIA antibody for immunotherapy of cancers and advanced it to IND-enabling studies
  • March, completed Series C financing
  • February, completed Phase I LAE002 and LAE001 combination study in patients with mCRPC in the United States, and entered Phase II stage
2020
  • December, received IND approval for Phase I/II clinical trial of LAE002 combined with LAE005 and nab-paclitaxel for TNBC from NMPA in China
  • August, received IND approval for pivotal Phase II MRCT study of LAE002 plus paclitaxel versus paclitaxel in patients with PROC from NMPA in China
  • February, acquired global license of LAE005 from Novartis
  • February, completed Series B financing
2019
  • November, received IND approval for pivotal Phase II MRCT study of LAE002 plus paclitaxel versus paclitaxel in patients with PROC from FDA in the United States
  • May, received IND approval for Phase I LAE002 and LAE001 combination MRCT study in patients with mCRPC from FDA in the United States
  • January, received IND approval for Phase I/II clinical trial of LAE001 for mCRPC from NMPA in China
2018
  • May, acquired global licenses of LAE002 and LAE003 from Novartis
  • May, completed Series A financing
  • January, completed onshore Series Seed financing
2017
  • June, acquired global licenses of LAE001 from Novartis
2016
  • Laekna establised
Recognition & Awards
  • 2026

    Healthcare Executive · Top100 Chinese Pharmaceutical Innovative Enterprises

    Gelonghui · Outstanding Company in ESG Sustainability / ESG Excellence PR Team

  • 2025

    Zhitong Finance · Most Valuable Pharmaceutical Company / IR Team of the Year

    Gelonghui · Outstanding Company of the Year: Investment Value Award

    Healthcare Executive · China Pharma SMEs ESG Progress Top 10

    CIPRA · China PR Industry Best Case Competition - ESG & Corporate Image, Bronze Award

    Shanghai Public Relations Association · 12th Excellent PR Cases - Model Case

  • 2024

    PCIC · 2024 Person of The Year

    Gelonghui · Most Popular Stock Connect Enterprises / IR Team of the Year

    Zhitong Finance · Most Valuable Pharmaceutical and Healthcare Company

    Shanghai Pudong New Area Health Supervision Institute: Health Model Companyin Zhangjiang

  • 2023

    Shanghai Zhangjiang · Life & Health Startup of the Year

    Influential Tech Innovation Company of the Year

    Healthcare Executive · Top 100 Chinese Pharmaceutical Innovation Seed Enterprises

    Gelonghui · Annual Innovation Award

    Zhitong Finance · Most Valuable Pharmaceutical and Healthcare Company

    bioPR · Best Communication Case in the Pharmaceutical Industry

  • 2022

    Healthcare Executive · Top 100 Chinese Pharmaceutical Innovation Seed Enterprises

    China STAR Market Daliy · Scientist-Entrepreneur Pioneer

    KPMG · China Future 50 - Biotech

  • 2021

    Xinhua NewsNet · China Corporate Social Responsibility Virtual Summit - CSR Good Practice

    Healthcare Executive · Top 100 Chinese Pharmaceutical Innovation Seed Enterprises

    China STAR Market Daliy · China’s Leading Sci-Tech Companies — Biomedicine Pioneer 10

    Frost & Sullivan · Top 100 Tech Powerhouses - Top 50 Innovative Companies

  • 2020

    CSCO · Top 20 Breakthrough Oncology Technologies of the Year

  • 2019

    CHC&CITIC Securities · China Healthcare Investment & Financing Honors — Top 20 Healthcare Rising Stars

  • 2018

    Zhangjiang Venture Capital · Insights Zhangjiang Top 100

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