FDA approves and designates Roche Tina-qant Lp Assay as a Breakthrough Device
Roche's FDA-approved Tina-quant® identifies patients for innovative Lp(a) lowering therapy, addressing cardiovascular risk.
According to the reports, Roche revealed that the U.S. FDA approved its Tina-quant ® lipoprotein Lp(a) RxDx as a Breakthrough Device. The device will help to identify patients who can benefit from the innovative Lp(a) lowering therapy, which is currently being developed.
Lp (a) proves to be a critical marker for people at risk of cardiovascular disease. However, the healthcare sector needs more solutions to address this problem effectively. By collaborating with Amgen, Roche has paved a new path to make the elevated Lp(a) an actionable marker, said Matt Sause, the CEO of Roche Diagnostics.
Tina-quant ® lipoprotein Lp(a) RxDx is the result of combining Amgen's year-long legacy and expertise in cardiovascular disease with Roche’s diagnostic expertise.
After its approval, the new Tina-quant® test shall be available to identify the patients who benefit from the Lp(a)- lowering therapy.
My international experience as a researcher in Taiwan for three years has equipped me with a global perspective, enabling me to create content that resonates with an international audience.
More from Pharma News
All stories →
Tonix Plans Adaptive Phase 2 Trial for Seasonal Lyme Disease Prevention Therapy, Advances Program Following FDA Type C Meeting
Medicus Pharma Appoints Dr. Faisal Mehmud as CEO of UK Subsidiary Antev, Strengthens Leadership to Advance Global Development of Teverelix®
Discussion