Trevi Therapeutics to Report Third Quarter 2025 Financial Results and Provide a Corporate Update on November 13, 2025
MWN-AI** Summary
Trevi Therapeutics, Inc. (Nasdaq: TRVI), a clinical-stage biopharmaceutical company, is set to report its financial results for the third quarter of 2025 and provide a corporate update on November 13, 2025, at 4:30 p.m. ET. Investors and stakeholders can participate in the conference call via phone or through a live audio webcast, accessible from the company’s website.
Trevi focuses on developing Haduvio™ (oral nalbuphine ER), an investigational therapy targeting chronic cough linked to idiopathic pulmonary fibrosis (IPF), non-IPF interstitial lung disease (non-IPF ILD), and refractory chronic cough (RCC). Haduvio represents a significant advancement in this area, being the first investigational treatment to demonstrate a statistically significant reduction in cough frequency among patients suffering from these conditions during clinical trials.
Chronic cough associated with IPF and non-IPF ILD poses a substantial unmet need, affecting a large patient population without effective FDA-approved therapies. It is estimated that approximately 150,000 patients in the U.S. suffer from IPF, with two-thirds experiencing uncontrolled chronic cough. Likewise, around 228,000 individuals are affected by non-IPF ILD, with 50-60% confronting similar challenges. The debilitating nature of chronic cough can lead to severe health consequences, diminished quality of life, and increased healthcare utilization.
Further, RCC impacts an estimated 2-3 million Americans, characterized by a persistent cough lasting more than eight weeks despite existing treatment for underlying conditions. Trevi’s Haduvio aims to address these critical health concerns by acting on the cough reflex arc through its unique mechanism as a kappa agonist and mu antagonist.
For more updates, stakeholders can visit Trevi’s official website and follow the company on social media platforms.
MWN-AI** Analysis
As Trevi Therapeutics (Nasdaq: TRVI) prepares to report its third quarter 2025 financial results on November 13, 2025, investors should closely monitor several key factors that could impact the company's valuation and future performance. Trevi is in the clinical-stage biopharmaceutical sector, primarily focused on bringing Haduvio™ (oral nalbuphine ER) to market, targeting chronic cough treatments for patients suffering from idiopathic pulmonary fibrosis (IPF) and non-IPF interstitial lung disease.
Recent clinical trials have shown Haduvio to provide significant reductions in cough frequency, marking it as a potentially groundbreaking therapy for an ailment that currently has no FDA-approved treatments. This presents a unique opportunity for Trevi, given that there are approximately 150,000 U.S. patients with IPF, and up to 60% of the estimated 228,000 patients with non-IPF ILD experience chronic cough. The unmet medical need in this domain may be a strong catalyst for Trevi, particularly if they continue demonstrating positive clinical outcomes.
During the upcoming conference call, investors should pay attention to updates on Haduvio's development timeline, any new partnerships or collaborations that may enhance its market position, and insights into the company's financial health, including revenue projections and cash runway. Key indicators to consider include the current liquidity position and anticipated expenditures, given the often high burn rate seen in clinical-stage companies.
Market sentiment surrounding Trevi will hinge heavily on the clarity provided regarding Haduvio's trajectory and regulatory progress. Positive developments could drive shares upward, whereas any setbacks might have the opposite effect. With a robust pipeline and a pressing need for effective treatments, Trevi Therapeutics remains an intriguing prospect within the biopharma landscape, but investors should remain vigilant and ready to react to the findings announced on November 13.
**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.
PR Newswire
Conference call and webcast to be held at 4:30 p.m. ET
NEW HAVEN, Conn., Nov. 6, 2025 /PRNewswire/ -- 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 Thursday, November 13, 2025, at 4:30 p.m. ET, to provide a corporate update and review the Company's financial results for the quarter ended September 30, 2025.
To participate in the live conference call by phone, please dial (877) 870 4263 (domestic) or (412) 317 0790 (international) and ask to join the Trevi Therapeutics call. No code is necessary for access. A live audio webcast will be accessible from the 'Investors & News' section on the Company's website at www.TreviTherapeutics.com. 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 of 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 ~150,000 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.
Refractory chronic cough 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
carlsonj@trevitherapeutics.com
Media Contact
Rosalia Scampoli
914-815-1465
rscampoli@marketcompr.com
SOURCE Trevi Therapeutics, Inc.
FAQ**
What key milestones has Trevi Therapeutics Inc. TRVI achieved regarding the development of Haduvio™ since the last financial report, and how do these milestones impact the timeline for potential regulatory submission?
Can Trevi Therapeutics Inc. TRVI provide insights into the financial performance for Q3 2025, including any changes in operational expenses related to the ongoing clinical trials for Haduvio™?
Given the significant unmet need in treating chronic cough in IPF and non-IPF ILD patients, what strategies is Trevi Therapeutics Inc. TRVI considering to enhance market penetration once Haduvio™ receives regulatory approval?
How has patient feedback and data from recent clinical trials influenced Trevi Therapeutics Inc. TRVI's approach to finalizing the trade name and branding of Haduvio™ in preparation for its potential market launch?
**MWN-AI FAQ is based on asking OpenAI questions about Trevi Therapeutics Inc. (NASDAQ: TRVI).
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