Vertex Unveils Full Phase III Data for Non-Opioid Pain Candidate, Touts Safety Profile

Entrance to Vertex's office in Boston, Massachusetts

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BMO Capital Markets analyst Evan Seigerman in a note to investors said the late-stage data for Vertex’s experimental non-opioid pain medication “reaffirms our confidence in the strength of suzetrigine’s profile.” However, William Blair analysts view these data as “an incremental positive” as the company faces challenges in targeting the acute pain market.

Vertex Pharmaceuticals’ investigational non-opioid pain therapy suzetrigine has a cleaner safety profile than standard pain relief medicines and even placebo, according to full Phase III data presented over the weekend at the 2024 annual meeting of the American Society of Anesthesiologists in Philadelphia.

In study participants who were undergoing abdominoplasty—more commonly known as a tummy tuck—adverse events of any severity arose in 50% of patients given suzetrigine. By comparison, toxicities were detected in 60.7% of patients managed with hydrocodone bitartrate/acetaminophen (HB/APAP) and in 56.3% of placebo comparators.

Suzetrigine continued to have a better safety profile than HB/APAP and placebo even after disaggregating according to severity. Severe toxicities developed in 1.8% of abdominoplasty patients in the suzetrigine arm, versus 2% and 2.7% in HB/APAP and placebo counterparts, respectively. One patient in the placebo arm died.

Similar safety findings were observed in patients who underwent bunionectomy, which is a surgical procedure to correct a bone deformity in the toes.

Aside from the positive safety data, Vertex also reported an efficacy update for suzetrigine at ASA 2024. In abdominoplasty patients, suzetrigine monotherapy led to a 48.4-point improvement in pain scores, as measured by SPID48, a tool that measures time-weighted pain intensity from 0 to 48 hours after surgery. This effect was statistically significant, with a p-value less than 0.0001, according to Vertex’s presentation.

While suzetrigine’s effect seems to be weaker in bunionectomy patients, it still remained significantly better than placebo. Mean SPID48 scores were 29.3 points higher after suzetrigine treatment versus placebo.

Compared with the HB/APAP combo, however, suzetrigine monotherapy did not lead to significantly better pain relief. Mean SPID48 scores improved by only 6.6 points in abdominoplasty patients versus HB/APAP, an effect that fell short of significance. Meanwhile, in bunionectomy patients, mean SPID48 scores appear to have worsened by 20.2 points in the suzetrigine arm, which was statistically significant.

Suzetrigine is an orally available pain signal inhibitor that works by targeting and binding to the NaV1.8 voltage-gated sodium channel. Typically found on pain-sensing neurons, these channels help transmit pain signals from the peripheral nervous system back to the spine and brain. NaV1.8 channels are validated pain targets.

In July 2024, the FDA accepted Vertex’s New Drug Application for suzetrigine for moderate to severe acute pain, with a target action date on Jan. 30, 2025. If approved, suzetrigine could provide patients with an effective non-opioid option for pain relief.

BMO Capital Markets analyst Evan Seigerman in a note to investors said the detailed late-stage data for Vertex’s non-opioid pain medication “reaffirms our confidence in the strength of suzetrigine’s profile in acute pain.”

However, William Blair analysts in a note to investors said they view Vertex’s presentation at ASA 2024 as “an incremental positive” for suzetrigine with some challenges as the company targets the acute pain market.

“In the post-surgical outpatient setting, we continue to believe suzetrigine has a strong argument for inclusion in the market but note that pricing remains a point of investor contention along with how this impacts reimbursement, formulary placement, and prior authorization requirements, the latter of which Vertex is keen to avoid,” the analysts wrote.

Truist Securities analyst Joon Lee in a note said his firm is “not entirely sold yet on the commercial case for suzetrigine in acute pain,” adding that “if there is indeed will to use non-opioid analgesic, we think there are numerous options that are readily available that will be significantly cheaper than suzetrigine.”

Tristan is an independent science writer based in Metro Manila, with more than eight years of experience writing about medicine, biotech and science. He can be reached at tristan.manalac@biospace.com, tristan@tristanmanalac.com or on LinkedIn.
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