Home Jiangsu Kangyuan Pharma and Shengpu Zetai Achieve Milestone: AI-Powered KYS2301 Gel Successfully Submits IND Application

Jiangsu Kangyuan Pharma and Shengpu Zetai Achieve Milestone: AI-Powered KYS2301 Gel Successfully Submits IND Application

Jul 04, 2025 18:41 CST Updated 18:41
Kanion Pharmaceutical

A large traditional Chinese medicine enterprise integrating R&D, production, and trade

Space Peptides

One-Stop Platform Service Provider for Peptide Drugs


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On June 30, 2025, Jiangsu Kanion Pharmaceutical Co., Ltd. and Space Peptides jointly announced that their innovative drug project KYS2301 Gel (C-C Chemokine Receptor Type 8 (CCR8) Peptide Inhibitor), developed based on AI technology, has successfully completed the submission of a new drug clinical trial application (IND). This isTo date, the world's first peptide inhibitor targeting CCR8, as well as the world's first peptide drug designed using AI technology to reach the IND stage., ushering in a new era of AI-driven peptide drug research and development.



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Schematic Diagram of AI-Assisted New Drug Molecular Discovery

A Model of Intelligent Transformation for Traditional Pharmaceutical Enterprises


As a traditional pharmaceutical company with the modernization of Chinese medicine at its core, Kanion Pharmaceutical's collaboration with AI pharmaceutical enterprise Space Peptides has successfully achieved an important transformation towards intelligent innovation for traditional pharmaceutical companies. As the world's first CCR8 peptide inhibitor,KYS2301 Gel Rapidly and Precisely Discovers New Drug Molecules Through AI Technology, Taking Only 4 Months from Target Discovery to PCC (Preclinical Candidate Compound) Acceptance, taking only 18 months to reach the IND application stage, which is more than 60% shorter than the traditional R&D cycle, marking a significant breakthrough in the company's First-in-Class innovative drug pipeline. Notably, this project successfully overcame the technical challenge of transdermal absorption for peptides with a molecular weight exceeding 2000, providing an important reference for the subsequent development of peptide-based drugs.

KYS2301 Gel Provides a New Treatment Option for Patients with Moderate to Severe Atopic Dermatitis



Atopic Dermatitis (Atopic Dermatitis (AD) is a chronic inflammatory skin disease, often characterized by recurrent eczematous lesions (i.e., poorly demarcated, erythematous (red) plaques, with early exudation, blistering and crusting, and later scaling, fissuring, and lichenification (thickening)), intense pruritus, and discomfort. AD is associated with varying degrees of lesion severity and imposes a broad symptom burden, including pruritus, skin pain, sleep disturbances, and mental health disorders, negatively impacting quality of life. Current treatment options include topical medications (e.g., corticosteroids, calcineurin inhibitors), oral immunosuppressants (e.g., JAK inhibitors), and biologics (e.g., dupilumab), but existing therapies still present issues such as insufficient efficacy, safety risks, or inconvenient administration.

Breakthrough Therapy Addresses Clinical Pain Points



KYS2301 Gel, as the world's first CCR8 peptide inhibitor, demonstrates significant advantages through the precise optimization of molecular structure using AI technology:

Excellent Safety:Peptide drugs have low immunogenicity, high stability, can replace hormones, and local topical administration can avoid systemic adverse reactions;

Patient-Friendly Design:Gel formulations are convenient for patients to apply autonomously, especially suitable for children, the elderly, and those with difficulties in oral administration, significantly improving treatment compliance.

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Schematic Diagram of AI-Simulated Receptor and Peptide Drug Molecule Fitting

AI Empowers R&D, Breaking Through Industry Bottlenecks


The rapid development of KYS2301 gel is attributed to Space Peptides' AI drug discovery platform. By utilizing deep learning algorithms to analyze vast amounts of compound data, the platform completed the screening and optimization of active molecules in just one-third of the time required by traditional research and development methods, significantly shortening the preclinical research cycle. The Investigational New Drug (IND) application for KYS2301 gel (a CCR8 peptide inhibitor), an innovative drug project developed based on AI technology, has officially been approved by the Center for Drug Evaluation (CDE) under China's National Medical Products Administration (NMPA). This approval validates the core value of AI technology in drug design, toxicity prediction, and formulation optimization, offering a replicable innovation model for the industry.

Three Core Advantages, Reshaping the AD Treatment Landscape



Technological Leadership:The world's first targetedTopical Peptide Inhibitor of CCR8: AI-Driven Molecular Design Achieves Dual Breakthrough in "High Activity + Low Toxicity"

Clinical Needs Orientation:Covering Moderate to SevereAD patient population, especially addressing the unmet treatment needs of children and special populations;

Industrialization Potential:The production process of gel dosage forms is mature, with controllable costs, and it is expected to become a promising option in the future.First-line therapy for AD.


Looking Ahead

According to the plan, KYS2301 gel will conduct multi-center clinical trials in China, focusing on evaluating its efficacy and safety in patients with moderate to severe AD. As the atopic dermatitis market size is expected to exceed 4 billion US dollars by 2030, this product is expected to become an important participant in the global AD treatment field. This cooperation not only brings newHope to further push China's innovative drug research and development into the "AI Intelligent Manufacturing" era.

Both parties will continue to deepen the "AI + pharmaceuticals" strategic cooperation, accelerate the development and commercialization of breakthrough therapies, and benefit patients worldwide.






About the Partner


Jiangsu Kanion Pharmaceutical Co.,Ltd.

(Stock Code: 600557) is a leading innovative pharmaceutical company in China, focusing on the modernization of traditional Chinese medicine while also expanding into biologics, chemical drugs, and novel therapies. The company owns a national-level enterprise technology center and a postdoctoral research workstation, with a primary focus on developing innovative drugs in the fields of oncology, immunology, and metabolic diseases. Its representative products include modern Chinese medicine formulations such as Reduning Injection and Ginkgo Diterpene Lactone Meglumine Injection, along with several biologics currently in clinical stages. The KYS2301 gel, co-developed with Space Peptides, marks the company’s first innovative drug project optimized rapidly through AI technology, signifying an important breakthrough in intelligent drug manufacturing.


Space Peptides

Space Peptides, a pioneer in the AI pharmaceutical field, focuses on the application of artificial intelligence and computational biology in drug development. The company's self-developed generative AI molecular design platform (SP-PDGA) and molecular dynamics simulation system (SP-PMDA) can significantly improve the efficiency of candidate molecule screening and reduce R&D costs. Currently, Space Peptides has established innovative drug R&D collaborations with more than 10 pharmaceutical companies in China and abroad. The successful submission of KYS2301 gel validates the core value of its AI technology in drug optimization and preclinical research.


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