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Vertex Pharmaceuticals Discontinues VX-993 Development After Phase 2 Failure in Acute Pain

7 days ago2 min read

Key Insights

  • Vertex Pharmaceuticals announced that its experimental non-opioid pain reliever VX-993 failed to significantly outperform placebo in a Phase 2 trial for acute pain treatment.

  • The company will discontinue development of VX-993 as a single-agent medicine for acute pain, with CEO Reshma Kewalramani stating they do not expect it to be superior to existing NaV1.8 inhibitors.

  • VX-993 was designed as a next-generation version of Vertex's recently approved pill Journavx, with potential for higher dosing and IV infusion formulation.

Vertex Pharmaceuticals announced Monday that its experimental non-opioid pain medication VX-993 failed to demonstrate statistically significant improvement over placebo in a Phase 2 clinical trial, prompting the company to halt development of the drug as a monotherapy for acute pain.
The investigational compound, designed as a next-generation version of Vertex's recently approved pain medication Journavx, was engineered to potentially allow higher dosing and formulation as an intravenous infusion. The company had hoped this enhanced profile could provide superior pain relief or serve as an alternative to IV opioids in clinical settings.

Trial Results and Company Response

The Phase 2 trial evaluated VX-993's efficacy and safety as a treatment for acute pain without opioid use. Results showed no meaningful difference between patients receiving VX-993 and those given placebo in pain reduction measures.
"We do not plan to advance VX-993 as monotherapy in acute pain, because we do not expect that it will be superior to our [existing] NaV1.8 inhibitors," CEO Reshma Kewalramani stated during Monday's earnings call with investors. The comment referenced the drug class that includes both VX-993 and Journavx, which target the NaV1.8 sodium channel.

Continued Development in Diabetic Neuropathy

Despite discontinuing acute pain development, Vertex will maintain its clinical program testing VX-993 in patients with diabetes who experience chronic nerve pain. This ongoing trial represents a different therapeutic application that may yield more favorable results given the distinct pathophysiology of chronic versus acute pain conditions.

Strategic Implications

The failure represents a setback for Vertex's pain portfolio expansion, particularly as the pharmaceutical industry continues seeking effective non-opioid alternatives amid ongoing concerns about opioid dependence and abuse. The company's decision to halt monotherapy development while continuing the diabetic neuropathy program suggests a more targeted approach to the drug's therapeutic potential.
VX-993's failure to outperform placebo in acute pain settings highlights the ongoing challenges in developing effective non-opioid pain medications, despite significant investment and research efforts across the pharmaceutical industry.
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NCT06619847CompletedPhase 2
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Sources

VX-993 - Page 1 - BioWorld

bioworld.comAug 6, 2025

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