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FDA greenlights Vertex's pain drug suzetrigine NDA process

EditorEmilio Ghigini
Published 04/18/2024, 08:32 PM
VRTX
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BOSTON - Vertex Pharmaceuticals (NASDAQ:VRTX) Incorporated (NASDAQ:VRTX) announced significant progress in its suzetrigine pain treatment program, which could introduce a novel class of medication for acute and neuropathic pain management.

The Food and Drug Administration (FDA) has accepted a rolling New Drug Application (NDA) submission for suzetrigine, an oral selective NaV1.8 pain signal inhibitor, for the treatment of moderate-to-severe acute pain. The company has commenced the submission process and aims to complete it by the second quarter of 2024.

Suzetrigine has previously received Fast Track and Breakthrough Therapy designations from the FDA for its potential use in acute pain scenarios. Following these designations and positive Phase 3 results earlier this year, the rolling NDA submission marks a critical step towards bringing the drug to market.

Additionally, Vertex is preparing to initiate a Phase 3 program for suzetrigine in the second half of 2024, targeting pain associated with diabetic peripheral neuropathy (DPN). The company recently concluded a successful end-of-phase 2 meeting with the FDA and has been granted a Breakthrough Therapy designation for suzetrigine in the treatment of DPN-associated pain.

The upcoming Phase 3 program will consist of two 12-week randomized, double-blind, placebo-controlled studies to assess suzetrigine's efficacy and safety in DPN patients. The primary goal is to evaluate changes in pain intensity, with approximately 1,100 patients expected to enroll in each study. Following these studies, participants will have the opportunity to continue in an open-label study to determine the long-term safety and effectiveness of the drug.

Vertex is also progressing with its Phase 2 study of suzetrigine in patients with lumbosacral radiculopathy (LSR), with enrollment completion anticipated by the year's end.

Carmen Bozic, M.D., Executive Vice President of Vertex, emphasized the potential of suzetrigine to offer a non-opioid alternative for managing acute and peripheral neuropathic pain for millions of patients.

As part of its broader pain portfolio strategy, Vertex is advancing the development of additional NaV1.8 and NaV1.7 pain signal inhibitors. The company plans to move its next-generation NaV1.8 inhibitor, VX-993, into Phase 2 studies for acute pain and peripheral neuropathic pain later this year, and to initiate a Phase 1 study of an intravenous formulation of VX-993.

This news is based on a press release statement from Vertex Pharmaceuticals Incorporated.

InvestingPro Insights

As Vertex Pharmaceuticals (NASDAQ:VRTX) forges ahead with its suzetrigine pain treatment program, the company's financial health and stock performance metrics provide insights into its market position. With a robust Market Cap of $101.6 billion and a Price / Book ratio of 5.78 as of the last twelve months ending Q4 2023, Vertex stands as a substantial entity in the biotech industry.

InvestingPro Tips reveal that Vertex holds more cash than debt on its balance sheet, which could be a sign of financial stability as it invests in the development of suzetrigine and other pain treatments. Moreover, the company's stock is currently trading at a high P/E ratio, 28, relative to near-term earnings growth, which may suggest investor confidence in its future prospects. Additionally, with analysts predicting the company will be profitable this year, and given its profitable performance over the last twelve months, Vertex seems to be on a solid trajectory.

Investors looking to delve deeper into Vertex's financials and stock performance can explore more tips on InvestingPro, where they can find a total of 13 additional InvestingPro Tips for Vertex. For those interested in gaining comprehensive insights, use the coupon code PRONEWS24 to get an extra 10% off a yearly or biyearly Pro and Pro+ subscription at InvestingPro.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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