Suzetrigine (Journavx) PI Todd Bertoch, MD, identifies the sweet spot where he thinks the new NaV1.8 inhibitor will be most effective in post-surgical and other moderate-to-severe acute pain.
Anesthesiologist Todd Bertoch, MD, led clinical research that supported the FDA's approval last week of the novel nonopioid analgesic suzetrigine, marketed by Vertex Pharmaceuticals as Journavx. Suzetrigine is an oral highly selective voltage-gated sodium channel (NaV1.8) inhibitor and represents the first new approach to acute pain management in more than 2 decades.1
The company describes the approval as an historic milestone for the 80 million Americans who are prescribed a medication for moderate-to-severe acute pain every year.2 Patient Care sat down with Bertoch to learn more about where he feels the new option will find the greatest utility along the continuum of acute pain care. He describes the clinical scenario in the short video above.
Cebranopadol Achieves Positive Phase 3 Results for Treatment of Moderate-to-Severe Acute Pain
January 22nd 2025Cebranopadol, an investigational oral dual-NMR agonist, satisfied the primary endpoint of statistically significant reduction in pain intensity compared to placebo following abdominoplasty surgery.
Cebranopadol Achieves Positive Phase 3 Results for Treatment of Moderate-to-Severe Acute Pain
January 22nd 2025Cebranopadol, an investigational oral dual-NMR agonist, satisfied the primary endpoint of statistically significant reduction in pain intensity compared to placebo following abdominoplasty surgery.
2 Commerce Drive
Cranbury, NJ 08512