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PharmaCircleSupervisorMeasurement DisplayIndication: Previously inSeptember 29, 2025From ZhangjiangEccogene Cayman Ltd. Eccogene Inc.(abbreviation "Eccogene”)Filed a prospectus with the Hong Kong Stock Exchange in China. Leave a business card at the back to obtain the prospectus.
1. Overall Layout of the Company
1. Core Technology Platform
Eccogene relies on its independently developedTRANDD Platform(Translational Research and Drug Development Platform) guides decision-making and prioritization for key stages in clinical and preclinical development projects within the cardiovascular metabolic disease and inflammatory disease fields. This platform integrates multiple aspects such as target validation, drug design, and clinical translation, assisting the company in efficiently screening and developing innovative drugs with potential.
2. R&D Pipeline Layout

| | | Research and Development Stage | |
|---|
| ECC5004 | Oral Small Molecule GLP-1 Receptor Agonist | Weight Management, Type 2 Diabetes, MASH | Global Phase 2b (Expected to complete in 2025Q4) | Once-daily low-dose oral administration has the potential to become the best-in-class and the second orally available small molecule GLP-1RA to be launched in the global market. |
| ECC4703 | Oral Liver-Targeted Thyroid Hormone Receptor β Full Agonist | | Preclinical (IND Preparation) | Promising to become the best-in-class and second-to-market MASH treatment, or the first-in-class for weight management: a liver-targeted, selective, full THR-β agonist. |
| ECC0509 | Oral SSAO/VAP-1 Inhibitor | Inflammatory diseases, metabolic diseases | | Targeting Vascular Adhesion Protein-1, with Dual Anti-inflammatory and Metabolic Modulatory Effects |
| GIP Receptor Modulator | | | | Combined use with GLP-1 receptor agonists is expected to enhance weight loss and blood sugar reduction effects. |
| Amylin Receptor Agonist | | | Preclinical (planned to enter clinical stage soon) | Expected to synergize with GLP-1 receptor agonists, improving blood glucose control and weight management. |
3. Business Model
Eccogene adopts a dual-driven model of **"independent R&D + external licensing"**. Its core product, ECC5004, achieves global value maximization through licensing to AstraZeneca (AZ), while retaining the rights to the Chinese market for co-development with AZ; other products are planned for independent development or to find suitable partners.
2. Details of the Transaction with AstraZeneca (AZ)
1. Basic Transaction Information
- Agreement Signing Time
- Transaction Subject: Global development and commercialization rights for the oral small molecule GLP-1 receptor agonist ECC5004 (excluding Greater China)
- Total Transaction Value: Up to$2.01 billion(Including a $185 million upfront payment + $1.825 billion in milestone payments + tiered royalties)
- AZ Shareholding Status: AstraZeneca's wholly-owned subsidiary, AstraZeneca UK Limited, holds 5.02% of the shares, and Hangzhou AstraZeneca Zhongjin Venture Capital holds 2.47% of the shares, with a total shareholding of 7.49%.
2. Payment Structure Details
| | |
|---|
| Down Payment | $185 million (approximately 1.35 billion RMB) | Payment made immediately after the agreement was signed (already paid) |
| Milestone Payment | | Divided into three stages: clinical, registration, and commercialization - Clinical milestones: including completion of key clinical studies, clinical data reaching preset endpoints, etc. - Registration milestones: including approval for marketing in major global markets (such as the United States, European Union, Japan, etc.) - Commercialization milestones: including sales reaching specific thresholds (e.g., $1 billion, $2 billion, etc.)Received: $60 million milestone payment (as of mid-2025) |
| Royalty | Tiered Ratio (High Single Digits to Mid-Double Digits) | Based on the annual net sales of ECC5004 in the AZ authorized region (outside Greater China), the higher the sales, the higher the percentage. |
3. Scope of Authorization and Rights and Obligations
- AstraZeneca ObtainsECC5004 inAll indications in all countries and regions outside of ChinaExclusive rights to development, production, and commercialization
- Eccogene Inc.: Development and commercialization rights in Greater China (Mainland China, Hong Kong, Macao, and Taiwan), in collaboration with AZ
- Eccogene Obligations: Provide technical support, participate in global clinical development plans, and be responsible for the clinical development work in the China region.
- AZ Obligations: Bearing most of the global clinical development costs, responsible for global production and supply chain management, and in charge of commercial promotion in authorized regions.
3. Detailed Terms of Equity Distribution in China
1. Cooperative Development Model
InGreater ChinaECC5004 adopts the cooperation model of **"Co-development + Commercialization Revenue Sharing"**:
- Both parties established a Joint Development Committee (JDC) to jointly formulate clinical development plans, regulatory strategies, and commercialization solutions.
- Clinical development costs are shared by both parties.Share according to the agreed ratio(Specific ratio not disclosed, typically 50:50 or adjusted based on contribution)
- Eccogene is responsible for the execution of clinical research and registration applications in China, while AZ provides global clinical data support and technical guidance.
2. Commercial Rights Distribution
- Net Sales Revenue Split in the Chinese MarketBoth parties share the net sales revenue of ECC5004 in the Chinese market according to the agreed ratio (the specific ratio has not been disclosed, but is typically 50:50).
- Commercial Division of Labor
- Eccogene is responsible for the sales team building, academic promotion, and channel management in the Chinese market.
- AstraZeneca provides global brand support, market access expertise, and international sales network resources.
- Both parties jointly develop pricing strategies and marketing plans.
3. Intellectual Property and Technology Ownership
- The core intellectual property of ECC5004 belongs toEccogene Inc.
- AstraZeneca obtains exclusive rights outside of China and non-exclusive rights within China (shared with Eccogene).
- Both parties jointly own new intellectual property generated during the clinical development process in China.
References:
PharmaCircle Data;
Moxie Pharma pharma.bcpmdata.com (formerly known as Pharma Data Cloud);
https://www1.hkexnews.hk/app/sehk/2025/107767/documents/sehk25100800261_c.pdf
; etc.