Initiation Meeting of FDA-FE Clinical Study of Vicagrel Capsules
Published Time:
2021-08-18 08:19
Source:
On August 18, the kick-off meeting of the FDA-FE clinical study of Vicagrel Capsules, a Class I new drug of Jiangsu Vcare Pharmatech Co., Ltd. (Jaingsu Vcare), was held at the Phase I Clinical Research Center of the First Hospital of Jilin University. This marks the official launch of the FDA clinical study of Vicagrel in the United States and the supporting Phase III clinical study in China.
Vicagrel plans to apply for marketing authorization in the United States following the 505(b)(2) pathway and improve the development efficiency through two key clinical pharmacological studies. As a Class I anti-thrombotic new drug, through the ingenious design of the drug structure, the in-vivo active metabolite of Vicagrel is the same as that of Clopidogrel. It breaks through and avoids the metabolic pathway of Clopidogrel, completes the key metabolic activation steps with the help of esterase, retains the safe and effective advantages of Clopidogrel, is expected to overcome the major defect of "Clopidogrel resistance", avoid the adverse reactions such as the high bleeding risk of Ticagrelor (especially for the elderly population taking the drug), and solve the problems of common combined medication with drugs like Repaglinide and Proton Pump Inhibitors. More notably, the equivalent dose of Vicagrel is only one-fifteenth of that of Clopidogrel, which means that the dose-related side effects are greatly reduced, and it is a potential new anti-platelet drug that meets the urgent clinical needs.
Liu Yongqiang, Chairman of Jaingsu Vcare, Gong Yanchun, General Manager, Lai Xiaojuan, Director of the Clinical Center, etc. participated in the meeting via remote video together with Ding Yanhua, Director of the Phase I Clinical Research Center of the First Hospital of Jilin University, and other researchers.
Director Ding Yanhua said, "We are very glad to cooperate with Jaingsu Vcare again in the clinical development of Vicagrel. The previous research results suggest that Vicagrel is a very promising new anti-thrombotic drug. We have great confidence in the clinical study of Vicagrel and look forward to the exciting trial results."
Chairman Liu Yongqiang delivered a speech: "Jaingsu Vcare focuses on the research, development and production of better pharmaceutical products for patients. Vicagrel is a differentiated innovative drug developed to meet the unmet clinical needs, and there is an urgent clinical demand for it. The Phase I Clinical Research Center of the First Hospital of Jilin University is a well-known domestic Phase I clinical research base, with a high-level research team and rich project experience. We would like to thank the center for its strong support in project scheduling. We hope that under the leadership of Director Ding, we can complete the relevant research with high quality as planned, help Vicagrel obtain approval for marketing as soon as possible, and enable more patients with cardiovascular and cerebrovascular diseases to use good and reliable drugs as soon as possible."
About the Phase I Clinical Research Center of the First Hospital of Jilin University
The Phase I Clinical Research Center of the First Hospital of Jilin University is a professional early-stage clinical trial platform for new drugs. It was established in 2011. The ward currently has 55 employees and 114 beds. Over the past 10 years, the center has undertaken 326 Phase I clinical trials of drugs, including 170 Phase I clinical trials of new drugs and 156 bioequivalence and biosimilar drug comparison trials. It is the Phase I center that has undertaken and completed the most clinical trials of innovative drugs in China.
The center attaches great importance to the protocol design and result analysis of early-stage clinical trials of innovative drugs, and uses model simulation technology combined with pre-clinical and human trial PK/PD data to predict the effective dose of drugs. It especially attaches importance to the Ia/IIb clinical trials with patients as subjects, and has a fast enrollment speed. It can achieve seamless connection from trials on healthy people to trials on patients, and enter Phase II and Phase III clinical trials as soon as possible. It is proficient in bioequivalence trials with high difficulty such as dual filings in China and the United States and high variability, and can complete the design of Chinese and English protocols and the writing of summary reports.
The center passed the FDA project inspection in 2015 without any deficiencies and has passed 48 inspections by the National Medical Products Administration. It has cooperated with more than a hundred domestic and foreign pharmaceutical companies and has become a professional Phase I clinical trial research center of international level.
About Vicagrel
Vicagrel is an industry-university-research cooperation project between Jaingsu Vcare and China Pharmaceutical University, and the company owns all the rights and interests of the project. Some of the preliminary work of the project was fully published in the Journal of Medicinal Chemistry under the American Chemical Society, and was highlighted and recommended by the journal SciBX under Nature.

Related News
30
2024
/
12
On December 30, 2024, the first administration of VC005 tablets was completed in the Phase III clinical trial of oral treatment of moderate-to-severe atopic dermatitis (AD). VC005 is a new-generation highly selective JAK1 inhibitor independently developed by Jiangsu Vcare Pharmatech Co., Ltd. (Jiangsu Vcare). Positive top-line data were obtained from the unblinded Phase II clinical study of VC005 for AD, with primary endpoints showing superiority over the best drugs in the same class. Meanwhile, the overall safety and tolerability of the drug are good. In particular, the decreases in neutrophil and platelet counts caused by high dosage VC005 were smaller, compared with the positive control group of tofacitinib, and no significant reduction in lymphocyte count was observed.
18
2024
/
11
Jiangsu Vcare Selected Among "2024 China’s Top 500 Hidden Unicorn Enterprises"
At the 2024 China Hidden Unicorn 500 Summit, theDevelopment Report on China’s Top 500 Hidden Unicorn Enterprises 2024was released.Jiangsu Vcare Pharmatech Co., Ltd.(Jiangsu Vcare) debuted on this list, showcasing its strong technical accumulation and continuous innovation in independent R&D of innovative drugs and full-chain CRO/CDMO services for pharmaceuticals.
01
2024
/
11
Recently, the Nanjing Municipal Science and Technology Bureau announced the acceptance results of 2024 provincial-level engineering research centers and academician workstations. The"Jiangsu (Vcare) Chemical Innovative Drug Engineering Research Center", established byJiangsu Vcare Pharmatech Co., Ltd.(Jiangsu Vcare), successfully passed project acceptance.
28
2024
/
10
Jiangsu Vcare Included in "2024 Jiangsu Provincial Sci-Tech Enterprise Listing Cultivation Program"
Recently, the Jiangsu Provincial Department of Science and Technology announced the "2024 Proposed Enterprises for Provincial Sci-Tech Enterprise Listing Cultivation Program," withJiangsu Vcare Pharmatech Co., Ltd.(Jiangsu Vcare) successfully included.
23
2024
/
10
Jiangsu Vcare Selected Among "Top 100 China Pharma Innovation Seed Enterprises 2024"
Recently, the "Top 100 China Pharma Innovation Seed Enterprises 2024" list was released, withJiangsu Vcare Pharmatech Co., Ltd.(Jiangsu Vcare) ranked in the second tier. This list, compiled by a non-governmental organization, evaluates enterprises based on innovation foundation, process, and outcomes—using patent data, clinical trial data, etc.—selected from over 5,000 Chinese pharmaceutical companies.
22
2024
/
10
Jiangsu Vcare's Oral Treatment VC005 for Atopic Dermatitis enters Phase III Clinical Study
VC005 tablets, developed by Jiangsu Vcare Pharmatech Co., Ltd. (Jiangsu Vcare), is a new-generation highly selective JAK1 inhibitor. The oral treatment of moderate-to-severe atopic dermatitis has initiated a Phase III clinical trial. It is a multicenter, randomized, double-blind, placebo parallel-controlled Phase III clinical study, aiming to evaluate the efficacy and safety of VC005 tablets for adult patients with moderate-to-severe atopic dermatitis. The trial is led by the Institute of Dermatology, Chinese Academy of Medical Sciences.