Pharmaceutical composition comprising GLP-1 and GIP dual-receptor agonist and use thereof
By adding stabilizers, buffer salts and antibacterial agents to the GLP-1 and GIP dual receptor agonists to prepare a liquid injection, the stability and safety issues of multi-dose injections are solved, and the effectiveness and safety of the drug in multi-dose use are achieved, making it suitable for the treatment of metabolic disorders.
Patent Information
- Application Number
- PCT/CN2025/082004
- Authority / Receiving Office
- WO · WO
- Patent Type
- Applications
- Current Assignee / Owner
- Priority Date
- 2024-03-14
- Filing Date
- 2025-03-12
- Publication Date
- 2025-09-18
AI Technical Summary
There are currently no reports on multi-dose injection prescriptions of GLP-1 and GIP dual receptor agonists, which leads to stability and safety issues in clinical applications.
Provided is a pharmaceutical composition comprising a GLP-1 and GIP dual receptor agonist, which is prepared into a liquid injection by adding excipients such as stabilizers, buffer salts and antibacterial agents to ensure the stability and safety of the drug during multi-dose use.
The good stability of the GLP-1 and GIP dual receptor agonists in liquid preparations is achieved, aggregation and degradation are avoided, the effectiveness and safety of the drugs are ensured, and they are suitable for the prevention and treatment of metabolic disorder-related diseases such as diabetes and obesity.
Smart Images

Figure PCTCN2025082004-FTAPPB-I100001 
Figure PCTCN2025082004-FTAPPB-I100002 
Figure PCTCN2025082004-FTAPPB-I100003
Abstract
Claims
1. A pharmaceutical composition comprising a GLP-1 and GIP dual receptor agonist, comprising a GLP-1 and GIP dual receptor agonist, a stabilizer, a buffer salt, and an antibacterial agent; The GLP-1 and GIP dual receptor agonist is a compound as shown in Formula I or a pharmaceutically acceptable salt, ester, solvate, optical isomer, tautomer, isotope-labeled substance or prodrug thereof:
2. The pharmaceutical composition according to claim 1, characterized in that The pharmaceutical composition is a liquid preparation; Preferably, the pharmaceutical composition is an injection.
3. The pharmaceutical composition according to claim 1, characterized in that The concentration of the GLP-1 and GIP dual receptor agonist is 2 to 36 mg / mL; Preferably, the concentration of the GLP-1 and GIP dual receptor agonist is 5 to 30 mg / mL.
4. The pharmaceutical composition according to claim 1, characterized in that The antibacterial agent is phenol or m-cresol; Preferably, when the antibacterial agent is phenol, the concentration of the antibacterial agent is 5.3-5.5 mg / mL; When the antibacterial agent is m-cresol, the concentration of the antibacterial agent is 2.4-3.0 mg / mL.
5. The pharmaceutical composition according to claim 1, characterized in that The concentration of the stabilizer in the pharmaceutical composition is 10 to 20 mg / mL; the stabilizer is a polyol; Preferably, the stabilizer is propylene glycol, mannitol or glycerol; More preferably, the stabilizer is propylene glycol.
6. The pharmaceutical composition according to claim 1, characterized in that The buffer salt is selected from hydrogen phosphate, hydrogen phosphate hydrate, citrate, citrate hydrate, acetate or acetate hydrate; Preferably, the buffer salt is hydrogen phosphate hydrate, citrate hydrate or acetate hydrate.
7. The pharmaceutical composition according to claims 1-6, characterized in that The concentration of the buffer salt in the pharmaceutical composition is 7 to 23 mM; Preferably, the concentration of the buffer salt is 10 mM.
8. The pharmaceutical composition according to any one of claims 1 to 7, characterized in that The pH value of the pharmaceutical composition is 6.5 to 8.5; Preferably, the pH value of the pharmaceutical composition is 7.0 to 8.4; More preferably, the pH value of the pharmaceutical composition is 7.2 to 8.2; More preferably, the pH value of the pharmaceutical composition is 7.2-7.
6.
9. A method for preparing the pharmaceutical composition according to any one of claims 1 to 8, comprising the steps of: dissolving a stabilizer, a buffer salt, and an antibacterial agent in a solvent, adding a GLP-1 and GIP dual receptor agonist to prepare a solution, and adjusting the pH of the solution to a target value.
10. Use of the pharmaceutical composition according to any one of claims 1 to 8 in the preparation of a medicament for preventing and / or treating diseases related to metabolic disorders; Preferably, the metabolic disorder-related disease is diabetes, diabetic complications, obesity or obesity complications.
Citation Information
Patent Citations
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