Trevi Therapeutics announces June and July event schedule
Trevi Therapeutics announced its senior management will attend the BIO International Convention, Leerink Partners Therapeutics Forum, and ERS Cough Conference in June and July. The company is developing Haduvio for chronic cough in IPF, non-IPF ILD, and RCC patients. Haduvio has shown statistically-significant reduction in cough frequency in clinical trials.

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Trevi Therapeutics, Inc. has announced that its senior management will participate in several upcoming conferences in June and July. The clinical-stage biopharmaceutical company, which is developing the investigational therapy Haduvio for chronic cough, will engage with investors and industry professionals at three key events. The schedule underscores the company's commitment to advancing its pipeline and communicating its progress to stakeholders.
Conference Schedule
Trevi Therapeutics will attend the following events, with specific executives representing the company:
| Event | Date | Location | Trevi Representatives |
|---|---|---|---|
| BIO International Convention | June 22-25, 2026 | San Diego, California | Jennifer Good, President and CEO; Farrell Simon, Pharm.D., CCO |
| Leerink Partners Therapeutics Forum 2026 | July 14-15, 2026 | Boston, Massachusetts | David Hastings, CFO; Farrell Simon, Pharm.D., CCO |
| ERS Cough Conference 2026 | July 15-17, 2026 | London, United Kingdom | Jennifer Good, President and CEO; James Cassella, Ph.D., CDO |
About Trevi Therapeutics
Trevi Therapeutics, Inc. is focused on developing Haduvio (oral nalbuphine extended-release) for the treatment of chronic cough in patients with idiopathic pulmonary fibrosis (IPF), non-IPF interstitial lung disease (non-IPF ILD), and refractory chronic cough (RCC). Haduvio is the first and only investigational therapy to show a statistically-significant reduction in cough frequency in clinical trials across both patients with IPF-related chronic cough and in patients with RCC. The therapy acts on the cough reflex arc both centrally and peripherally as a kappa agonist and a mu antagonist (KAMA), targeting opioid receptors that play a key role in controlling chronic cough.
Chronic cough in patients with IPF and non-IPF ILD represents a high unmet need with no FDA-approved therapies. There are approximately 140,000 U.S. patients with IPF, two-thirds of whom experience uncontrolled chronic cough. Additionally, there are approximately 228,000 U.S. patients with non-IPF ILD, with 50-60% having uncontrolled chronic cough. RCC affects approximately 2-3 million U.S. patients and is defined as a persistent cough lasting more than 8 weeks despite treatment for an underlying condition. Trevi intends to propose Haduvio as the trade name for oral nalbuphine ER, though its safety and efficacy have not been evaluated by any regulatory authority.
What key data or milestones does Trevi Therapeutics plan to highlight during these conferences to advance Haduvio's development?
How might investor engagement at these events influence Trevi's funding strategies or partnerships for Haduvio's commercialization?
What regulatory hurdles or timelines should investors anticipate for Haduvio's approval in the U.S. and other markets?
























