Press Releases April 28, 2026 04:05 PM

Trevi Therapeutics to Report First Quarter 2026 Financial Results and Provide a Corporate Update on May 5, 2026

Trevi Therapeutics announces Q1 2026 financial results release and corporate update with focus on Haduvio development for chronic cough.

By Marcus Reed TRVI
Trevi Therapeutics to Report First Quarter 2026 Financial Results and Provide a Corporate Update on May 5, 2026
TRVI

Trevi Therapeutics, a clinical-stage biopharmaceutical firm, will report its first quarter 2026 financial results and provide a corporate update on May 5, 2026. The company is developing Haduvio (oral nalbuphine ER), targeting chronic cough in patients with idiopathic pulmonary fibrosis, non-IPF interstitial lung disease, and refractory chronic cough. Haduvio is the first investigational therapy showing statistically significant reductions in cough frequency for these conditions, which currently lack FDA-approved treatments. The update will include financials and progress on the development of Haduvio.

Key Points

  • Trevi Therapeutics will report Q1 2026 financial results on May 5, 2026, alongside a corporate update.
  • The company is advancing Haduvio, an investigational treatment for chronic cough associated with IPF, non-IPF ILD, and refractory chronic cough, with positive clinical trial results.
  • Chronic cough related to IPF, non-IPF ILD, and RCC represents a significant unmet medical need with a large patient population in the US, impacting respiratory and biopharmaceutical sectors.

NEW HAVEN, Conn., April 28, 2026 (GLOBE NEWSWIRE) -- Trevi Therapeutics, Inc. (Nasdaq: TRVI), a clinical-stage biopharmaceutical company developing the investigational therapy Haduvio™ (oral nalbuphine ER) 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), today announced that senior management will host a conference call and live audio webcast on Tuesday, May 5, 2026, at 4:30 p.m. ET, to provide a corporate update and review the Company's financial results for the quarter ended March 31, 2026. 

Conference Call and Webcast
To register for the live conference call and webcast, please visit the ‘Investors & News’ section of the Company’s website or access directly at ir.trevitherapeutics.com/news-events/events. Please note for phone participants: Once registered, you will receive an email with unique call-in details. An archived replay of the webcast will also be available for 30 days on the Company's website following the event.

About Trevi Therapeutics, Inc.     
Trevi Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing the investigational therapy 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 chronic cough and in patients with RCC. Haduvio 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. Nalbuphine is not currently scheduled by the U.S. Drug Enforcement Agency. 

Chronic cough in patients with IPF and non-IPF ILD is a condition with high unmet need and no FDA-approved therapies. There are ~140,000 U.S. patients with IPF, and two-thirds of these patients are faced with uncontrolled chronic cough. Additionally, there are ~228,000 U.S. patients with non-IPF ILD, with 50-60% having uncontrolled chronic cough. The impact of chronic cough is significant, with patients coughing up to 1,500 times per day. This consistent cough, and any associated damage, may lead to a higher risk of morbidity and mortality, including worsening disease, a higher risk of progression, increased respiratory hospitalizations, and a decline in patients' quality of life.    

RCC is a condition with high unmet need and no FDA-approved therapies. RCC is defined as a persistent cough lasting >8 weeks despite treatment for an underlying condition (i.e., asthma, gastroesophageal reflux disease, non-asthmatic eosinophilic bronchitis, upper airway cough syndrome, or post-nasal drip) and includes unexplained chronic cough. There are ~2-3 million U.S. patients with RCC, and it is believed to be associated with cough reflex hypersensitivity involving both the central and peripheral nervous systems. RCC is highly debilitating and may impact patients physically, psychologically, and socially.   

Trevi intends to propose Haduvio as the trade name for oral nalbuphine ER. Its safety and efficacy have not been evaluated by any regulatory authority.  
  
For more information, visit www.TreviTherapeutics.com and follow Trevi on X (formerly Twitter) and LinkedIn.  

Investor Contact   
Jonathan Carlson   
Trevi Therapeutics, Inc.   
(203) 654 3286   
[email protected]

Media Contact   
Rosalia Scampoli   
914-815-1465   
[email protected]


Risks

  • Haduvio is still investigational and has not been evaluated or approved by any regulatory authority, reflecting development and regulatory risks.
  • The company operates in a competitive and uncertain biopharmaceutical market with risks related to clinical trial outcomes and commercial adoption.
  • Financial results may reveal challenges in funding ongoing development and commercialization efforts, impacting overall business viability.

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