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Trevi Therapeutics Announces Upcoming Presentations at the European Respiratory Society (ERS) Congress 2026

Trevi Therapeutics (Nasdaq: TRVI) will present two abstracts on oral nalbuphine extended-release (ER) for chronic cough at the European Respiratory Society (ERS) Congress 2026 in Barcelona, Spain, from September 5-9, 2026.

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Trevi Therapeutics (Nasdaq: TRVI) will present two abstracts on oral nalbuphine extended-release (ER) for chronic cough at the European Respiratory Society (ERS) Congress 2026 in Barcelona, Spain, from September 5-9, 2026.

One oral presentation will cover quality-of-life outcomes from the Phase 2b CORAL trial in idiopathic pulmonary fibrosis (IPF)-related chronic cough, and one poster will address quality-of-life outcomes from the Phase 2a RIVER trial in refractory chronic cough (RCC), both using the Leicester Cough Questionnaire (LCQ).

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Argus Aug 26 session 1 alert
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News Market Reaction – TRVI

$2.82B Market Cap

On Aug 26, the day this news came out, TRVI closed 0.17% below the previous close. Relative volume reached 3.0x the daily average during tracking.

Data tracked by StockTitan Argus for the Aug 26 session.

Key Figures

Abstracts Accepted: 2 abstracts CORAL Trial Phase: Phase 2b RIVER Trial Phase: Phase 2a +3 more
Abstracts Accepted
2 abstracts
ERS Congress 2026
CORAL Trial Phase
Phase 2b
Nalbuphine ER in IPF-related chronic cough
RIVER Trial Phase
Phase 2a
Nalbuphine ER in refractory chronic cough
Congress Dates
September 5-9, 2026
Barcelona, Spain
Oral Presentation
September 7, 11:00 a.m. to 12:15 p.m. CEST
ERS Congress 2026
Poster Presentation
September 7, 12:30 p.m. to 2:00 p.m. CEST
ERS Congress 2026

Historical Context

5 past events · Latest: Aug 06
5 events
  1. Aug 06

    Q2 earnings report

    24h Move
    +0.1%

    Q2 results advanced trials and reported cash supporting development programs.

  2. Jul 30

    Earnings date notice

    24h Move
    -0.8%

    Scheduled Q2 results webcast and corporate update for August 6 at 4:30 p.m. ET.

  3. Jul 28

    Conference participation

    24h Move
    +1.7%

    Announced participation in two August 2026 biotech conferences, including a fireside chat.

  4. Jun 17

    Event schedule notice

    24h Move
    +6.3%

    Announced June-July attendance at BIO International and two therapeutic forums.

  5. May 05

    Q1 earnings report

    24h Move
    -2.7%

    Reported Q1 results, equity proceeds, cash runway, and clinical development plans.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

idiopathic pulmonary fibrosis, interstitial lung disease, extended-release
3 terms
idiopathic pulmonary fibrosis medical
"treatment of patients with idiopathic pulmonary fibrosis"
Idiopathic pulmonary fibrosis is a chronic lung disease in which the air‑carrying tissue becomes progressively thickened and scarred for no identifiable reason, making the lungs stiff and less able to move oxygen—similar to a sponge that hardens and loses its pores. It matters to investors because it is life‑limiting with limited effective treatments, so clinical trial outcomes, regulatory approvals, pricing and reimbursement decisions can strongly affect the commercial value of therapies and the financial prospects of companies developing treatments.
interstitial lung disease medical
"patients with IPF, non-IPF interstitial lung disease"
A group of lung conditions that cause inflammation and scarring of the thin tissue between the air sacs, which makes it harder for oxygen to pass into the blood; imagine the lungs’ fine filters becoming stiff and less effective. Investors care because reports of interstitial lung disease can affect a drug’s safety profile, trigger regulatory warnings or label changes, and shift demand for treatments or create liability risks that influence a company’s valuation.
extended-release technical
"Nalbuphine extended-release for chronic cough"
Extended-release is a drug formulation designed to release its active ingredient slowly over an extended period so the medicine stays at steadier levels in the body and usually needs to be taken less often—think of a timed-release coffee versus sipping many short espressos. Investors care because extended-release versions can improve patient adherence, reduce side effects, and create product differentiation that supports higher pricing, longer commercial lifecycles, and clearer revenue visibility, while also attracting specific regulatory and manufacturing considerations.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Professor Marlies Wijsenbeek will give an oral presentation on the quality-of-life outcomes assessed by the LCQ from the Phase 2b CORAL trial of nalbuphine ER for the treatment of patients with IPF-related chronic cough

Dr. Imran Satia will give a poster presentation on the quality-of-life outcomes assessed by the LCQ from the Phase 2a RIVER trial of nalbuphine ER for the treatment of patients with RCC

NEW HAVEN, Conn., Aug. 26, 2026 (GLOBE NEWSWIRE) -- Trevi Therapeutics, Inc. (Nasdaq: TRVI), a clinical-stage biopharmaceutical company developing the investigational therapy 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 the acceptance of two abstracts for presentation at the European Respiratory Society (ERS) Congress 2026, taking place from September 5-9, 2026, in Barcelona, Spain.

Abstract: Nalbuphine extended-release for chronic cough in patients with idiopathic pulmonary fibrosis: assessment of quality of life using the Leicester Cough Questionnaire in the Phase 2b CORAL trial
Oral Presentation Session: 325 – Moving forward in interstitial lung disease: new data on novel therapies
Date & Time: September 7, 11:00 a.m. to 12:15 p.m. CEST
Location: 3K
Oral Presenter: Marlies S. Wijsenbeek, MD, PhD

Abstract: Quality of life outcomes assessed by the Leicester Cough Questionnaire in the Phase 2a RIVER trial of nalbuphine extended-release in refractory chronic cough
Poster Session: 343 – Novel cough therapeutics: the airway microbiome
Date & Time: September 7, 12:30 p.m. to 2:00 p.m. CEST
Location: PS-15
Poster Presenter: Imran Satia, MB, BChir, PhD, MRCP

Registration Details

About the Phase 2b CORAL Trial
The Phase 2b Cough Reduction in IPF with nalbuphine ER (CORAL) trial was a double-blind, randomized, placebo-controlled, parallel-arm trial evaluating three doses of nalbuphine ER (27 mg, 54 mg, and 108 mg twice daily) compared to placebo for the treatment of chronic cough in patients with IPF over a 6-week treatment period. 165 patients with IPF chronic cough were randomized 1:1:1:1 to one of three nalbuphine ER dose groups or placebo with an initial 2-week titration period to the target dose followed by 4 weeks of fixed dosing. The primary efficacy endpoint for the trial was the relative change in 24-hour cough frequency (coughs per hour), as determined by an objective cough monitor, for the modified intent-to-treat (mITT) population at the end of Week 6 versus Baseline for nalbuphine ER compared to placebo. The mITT population consisted of all patients who were randomized and received at least one dose of study drug or placebo.

About the Phase 2a RIVER Trial
The Phase 2a Refractory Chronic Cough Improvement Via Nalbuphine ER (RIVER) trial was a randomized, double-blind, placebo-controlled, two-treatment, two-period, crossover study designed to evaluate the efficacy, safety, and tolerability of nalbuphine ER for the treatment of patients with RCC. Each treatment period lasted 21 days, separated by a 21-day washout period. During the nalbuphine ER treatment period, patients were titrated with assessments at 27 mg twice daily (BID), 54 mg BID, and 108 mg BID for objective cough and other assessments at each dose. The primary endpoint of the trial was the mean change in 24-hour cough frequency, as determined by an objective cough monitor, for the full analysis set (FAS) population at Day 21. The FAS population included all patients who received at least one dose of study drug and have objective cough count data on both Baseline and Day 21 in at least one treatment period.

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). In clinical trials, Haduvio showed a statistically-significant reduction in cough frequency, consistent across baseline cough frequencies, and showed improvements in patient-reported outcomes, in both patients with IPF-related chronic cough and in patients with RCC. Haduvio is believed to act 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 
IR@trevitx.com

Media Contact
Rosalia Scampoli
914-815-1465
rscampoli@marketcompr.com


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What is Trevi Therapeutics (TRVI) presenting at the ERS Congress 2026?

Trevi Therapeutics will present two abstracts on oral nalbuphine ER for chronic cough. According to Trevi, one covers IPF-related chronic cough (CORAL trial) and the other refractory chronic cough (RIVER trial), both focusing on quality-of-life outcomes using the Leicester Cough Questionnaire.

When and where will Trevi Therapeutics present nalbuphine ER data at ERS 2026?

Trevi presentations will take place on September 7, 2026, at the ERS Congress in Barcelona. According to Trevi, the oral session runs 11:00 a.m.–12:15 p.m. CEST and the poster session 12:30 p.m.–2:00 p.m. CEST, both on September 7.

What will the RIVER trial poster from Trevi Therapeutics (TRVI) cover at ERS 2026?

The RIVER trial poster will report Leicester Cough Questionnaire quality-of-life outcomes in refractory chronic cough. According to Trevi, this Phase 2a study evaluates nalbuphine extended-release in RCC and is scheduled in Poster Session 343 on September 7, 2026.

Who will present Trevi Therapeutics’ nalbuphine ER data at ERS Congress 2026?

Professor Marlies S. Wijsenbeek will deliver the CORAL oral presentation and Dr. Imran Satia will present the RIVER poster. According to Trevi, both experts will discuss Leicester Cough Questionnaire quality-of-life outcomes in chronic cough populations.

In which ERS 2026 sessions will Trevi Therapeutics’ nalbuphine ER data be shown?

The CORAL trial will appear in Oral Session 325, focused on interstitial lung disease therapies. According to Trevi, the RIVER trial data will be in Poster Session 343, centered on novel cough therapeutics and the airway microbiome, both on September 7, 2026.

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