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CGeneTech Partners with Yunxuan Pharmaceuticals for CXCR4 Antagonist Broad Distribution

  • Categories:Company News
  • Author: BioBAY
  • Origin:
  • Time of issue:2020-04-16
  • Views:0

(Summary description)CGeneTech, a company focused on both internal R&D and outbound alliances, recently announced that it has signed an exclusive collaboration and license agreement with Yunxuan Pharmaceuticals to acquire exclusive global development and commercialization rights for one of its preclinical chemokine receptor type 4 (CXCR4) antagonists.

CGeneTech Partners with Yunxuan Pharmaceuticals for CXCR4 Antagonist Broad Distribution

(Summary description)CGeneTech, a company focused on both internal R&D and outbound alliances, recently announced that it has signed an exclusive collaboration and license agreement with Yunxuan Pharmaceuticals to acquire exclusive global development and commercialization rights for one of its preclinical chemokine receptor type 4 (CXCR4) antagonists.

  • Categories:Company News
  • Author: BioBAY
  • Origin:
  • Time of issue:2020-04-16
  • Views:0

CGeneTech, a company focused on both internal R&D and outbound alliances, recently announced that it has signed an exclusive collaboration and license agreement with Yunxuan Pharmaceuticals to acquire exclusive global development and commercialization rights for one of its preclinical chemokine receptor type 4 (CXCR4) antagonists.

CXCR4 belongs to a family of cytokine receptors that form the?CXCR4/SDF-1 signaling axis with its natural ligand, stromal cell-derived factor-1 (SDF-1), and plays an important role in the infiltration and metastasis of malignant tumors, migration and homing of stem cells, the immune and inflammatory response of the body, and HIV virus infection. According to the cutting-edge international research, this selective antagonist can be applied in the following therapeutic areas: (i) overcoming malignant tumor brain metastasis, overcoming primary and secondary tumor drug resistance in combination with immunotherapy, reducing tumor stem cell escape in combination with targeted angiogenic drugs, etc., and reducing tumor recurrence in combination with radiotherapy and chemotherapy. ②As a small molecule stem cell mobilizer, it is used in first-line consolidation and second-line salvage autologous hematopoietic stem cell transplantation for patients with multiple myeloma and non-Hodgkin's lymphoma. ③For the treatment of WHIM syndrome, an inherited primary autoimmune rare disease, for which there is still no effective therapeutic drug approved.

Professor Xiaohu Zhang, founder of Yunxuan Pharmaceuticals, said, "As an old classmate of the same year in the chemistry department of Peking University, I am very familiar with the entrepreneurial team of CGeneTech, and I most appreciate the execution and control of the project by Torping Ding and Qiang Yu. I believe they can take this compound I designed and synthesized, continue to nurture it like a child, and eventually turn it into a good drug."

Dr. Qiang Yu, CEO of CGeneTech, thanked his old classmate for his trust and said, "Through preclinical head-to-head experimental comparisons, we believe that Professor Zhang's compound has best-in-class or first-in-class potential in multiple therapeutic areas, which is in line with CGeneTech's R&D philosophy We are in the process of completing our diabetes pipeline. After improving our pipeline in diabetes, we have recently started to develop our portfolio in antineoplastic and rare diseases. With the introduction of this variety, it is just as well that the whole package is vivid with the fall of Tianyuan."

It is reported that according to the terms of the agreement, CGeneTech will pay back to Yunxuan Pharmaceuticals in stages in the form of advance payment, R&D milestone payment and sales commission.

The

The world's first SGLT-2/DPP-4 dual target inhibitor with complementary advantages has been approved for clinical use

Recently, Shengshi Taike's Class 1 innovative drug SGLT-2/DPP-4 dual target inhibitor CGT-2201 has been granted implicit permission for clinical trials by the National Drug Administration. CGT-2201, which targets SGLT-2 and DPP-4, two important targets related to glucose metabolism, can be better used for the treatment of diabetes and its derivatives, including diabetes nephropathy and non-alcoholic fatty liver disease. In 2021, the number of diabetes patients in China will reach 141 million, ranking first in the world. Among the numerous patients with diabetes in China, 20-40% may suffer from complications of diabetes nephropathy. Among the existing hypoglycemic drugs, only sodium glucose cotransporter 2 (SGLT-2) inhibitor has significant renal protection effect in clinical verification, but its inherent reproductive and urinary system infection risks limit its use. Based on SGLT-2 inhibitors and combined with the characteristics of dipeptidyl peptidase 4 (DPP-4) inhibitors, we design and develop a drug that can improve blood sugar, reduce side effects of urinary and reproductive system infections, is not limited by renal function, and has kidney benefits. It is expected to fill the market gap and meet the needs of patients. Based on this market background and target characteristics, Shengshi Taike utilizes its own small molecule chimera drug technology platform to develop multi head multifunctional new drug products with synergistic mechanisms, with CGT-2201 being one of its representative works. It fuses the respective mechanism characteristics of SGLT-2 and DPP-4. On the basis of inhibiting the activity of SGLT-2 to reduce the reabsorption of glucose in the kidney, it also slows down the inactivation of DPP-4 on GLP-1, playing a dual role mechanism to play a superposition effect; While achieving considerable hypoglycemic effect, it can reduce the side effects of existing SGLT-2 drug urinary system infection; At the same time, without kidney excretion, it can reduce the burden of the kidney and reduce the contraindication of diabetes patients with renal insufficiency. Therefore, this drug will have the advantage of better controlling blood sugar and protecting patient kidney function. Shengshi Tyco was founded in Suzhou Industrial Park in 2010. Its core team has decades of experience in the whole life cycle of international drugs, and is committed to the R&D and industrialization of high-quality and differentiated small molecule innovative drugs. The company has built a product pipeline covering multiple disease fields such as hypoglycemic, anticancer, and autoimmune diseases with an integrated drug research and development technology platform and a diversified business perspective. In the field of hypoglycemic drugs, Shenggliptin, the core product independently developed by the company, has submitted an NDA (product launch application) to the National Drug Administration and has been accepted. The results of the Phase 3 clinical trial showed that low doses can reach the predetermined trial endpoint, while the high-dose group can also demonstrate the safety of the drug well. The therapeutic effect of "half the dose" is twice as effective, making it expected to become the best hypoglycemic drug in the class. At the same time, the company has also carried out a comprehensive layout around oral drugs and derivative diseases of various targets related to diabetes. CGT-2201, which was approved for clinical use this time, is one of its pipeline matrix members.
2023-04-20

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