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CureGene Achieves First-Dose Milestone for Antiplatelet Drug CG-0255 IV Formulation in US Clinical Trial

2024-05-08 10:00:00

CureGene proudly announced the successful administration of the first dose of its groundbreaking new generation antiplatelet drug CG-0255 injection to a subject in a US clinical trial. This milestone marks its potential for CG-0255 in the field of cardiovascular and cerebrovascular disease treatment.

CG-0255 has garnered considerable industry attention due to its remarkable efficacy and distinctive benefits. Notably, it boasts a rapid onset, with peak effects occurring within 15 minutes of intravenous injection, aligning perfectly with the exigencies of clinical practice. The rapid action of CG-0255 post-administration enables prompt intervention in arterial thrombosis formation, markedly enhancing therapeutic outcomes. It circumvents the variabilities associated with oral medications, such as gastrointestinal absorption and drug interactions, offering patients a swift and targeted therapeutic intervention.

CG-0255 is safety profile is also commendable. It has demonstrated outstanding safety in clinical trials with minimal variability among individuals. The sophisticated metabolic pathway of CG-0255 renders it largely unaffected by drug interactions, offering clinicians flexibility and convenience in its application. This translates to a significant reduction in patient discomfort and side effect risks, optimizing treatment efficacy and prognostic expectations. 

Given that cardiovascular and cerebrovascular diseases are leading causes of mortality globally, the enhancement of treatment protocols is imperative. CG-0255, characterized by its rapid onset, efficacy, and safety, is poised to have substantial clinical utility. It is expected to broaden the spectrum of treatment options available to patients and offer renewed hope to those afflicted with cardiovascular and cerebrovascular conditions. 


About CG-0255
CG-0255 is a revolutionary antiplatelet drug with truly unique and innovative design, it has been developed in two formulations: intravenous injection and oral tablets. It is currently undergoing clinical development for indications such as acute coronary syndrome, recent myocardial infarction, recent stroke, and peripheral arterial disease to address the shortcomings of existing treatment options, unmet clinical needs, and to provide better antiplatelet solutions for all patients. CG-0255 has rapid onset of action, good safety profile, and shows minimal individual variations, overcoming widely present resistant issue with current treatment. CG-0255 also has little drug-drug interactions. It has the potential to become the best-in-class P2Y12 antagonist antiplatelet drug and fully meet the clinical needs in various medication scenarios.












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