Trevi Therapeutics Execs to Present at Key August Conferences

  • Trevi Therapeutics execs to present at Oppenheimer's Biotech in the Berkshires (Aug 4) and Stifel's Biotech Summer Summit (Aug 10-12).
  • CEO Jennifer Good and CFO David Hastings scheduled for fireside chat at Stifel event.
  • Haduvio™ (oral nalbuphine ER) remains investigational with no FDA approval yet.
  • Company targets chronic cough in IPF, non-IPF ILD, and refractory chronic cough markets.

Trevi Therapeutics is positioning itself as a key player in the chronic cough treatment space, targeting both IPF-related and refractory chronic cough indications. The upcoming conference presentations come at a critical time as the company seeks to build investor confidence ahead of potential regulatory milestones for Haduvio. With no FDA-approved therapies currently available for these conditions, Trevi has an opportunity to capture significant market share if it can successfully navigate the regulatory pathway.

Regulatory Pathway
Whether Trevi can secure FDA approval for Haduvio given the high unmet need in chronic cough indications.
Market Positioning
How Trevi differentiates itself in a competitive landscape with no current FDA-approved therapies for these conditions.
Clinical Data
The pace at which additional clinical data will be released to support Haduvio's efficacy and safety profile.