Trevi Therapeutics
TRVINASDAQUSD
- Source valuation snapshot. Not a live recalculation.
- Latest filed annual earnings; price snapshot date unavailable. Not forward P/E.
- Diluted earnings per share from the latest filed annual.
- $14.91 Prior regular-session close from the quote source.
- $14.48–$15.12 Regular-session low and high so far today.
- 1.5M Regular-session shares traded · Nov 11, 4:00 PM ET.
- Feb 8 projected Projected for 2027-02-08 from the company’s own results filings (SEC 8-K Item 2.02). The company has not confirmed the date.
- $9.82–$20.22 52-week trading low and high returned by the quote source.
Understand the Business
Why the Stock Moved
Period-matched expectations history is not yet available. Current metrics are not a substitute for a historical explanation.
The core investment thesis
Own TRVI if TRVI is a focused, single-asset clinical biotech whose value depends on Haduvio proving it can become an approved, differentiated chronic-cough therapy before cash burn and dilution consume the upside.
TRVI price history
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Investment thesis
What must happen next
Haduvio’s differentiated value rests on proving that oral nalbuphine ER can deliver clinically meaningful chronic-cough relief with tolerability good enough for long-term use in IPF, non-IPF ILD, and refractory chronic cough.HoldingMateriality: High
Item 1 Business describes Trevi as focused on developing and commercializing Haduvio for chronic cough in IPF, non-IPF ILD, and RCC. If this holds, Trevi owns a potentially scarce therapy in underserved cough populations; if it breaks, the core asset and most of the equity value are impaired.
Watch: A late-stage Haduvio trial fails to show cough-frequency or patient-reported benefit adequate for FDA approval.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Item 1 Business describes Trevi as focused on developing and commercializing Haduvio for chronic cough in IPF, non-IPF ILD, and.
Open source ↗Trevi’s upside depends on the same Haduvio mechanism being relevant across several chronic-cough populations, not just one narrow indication.StrengtheningMateriality: High
Item 1 Business names three target areas for Haduvio: chronic cough in IPF, non-IPF ILD, and refractory chronic cough. If indication breadth holds, the asset can support a larger commercial or partnering opportunity; if not, the addressable market and negotiating leverage shrink.
Watch: Clinical data show Haduvio works only in one cough population and does not translate to RCC or non-IPF ILD.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Item 1 Business names three target areas for Haduvio: chronic cough in IPF, non-IPF ILD, and refractory chronic cough.
Open source ↗Trevi must keep enough financial runway to reach value-changing Haduvio clinical and regulatory events before needing highly dilutive capital.HoldingMateriality: Medium
FY2025 cash was $18.914 million, while FY2025 total assets were much larger at $193.439 million, implying liquidity assessment requires more detail than cash alone. For owners, successful science only compounds per-share value if the company can finance the path without giving away too much of the upside.
Watch: A required trial expansion, manufacturing requirement, or regulatory delay forces a financing before a data catalyst.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
FY2025 cash was $18.914 million, while FY2025 total assets were much larger at $193.439 million, implying liquidity assessment requires more.
Open source ↗Trevi’s small-company focus must keep burn tied to Haduvio development rather than premature commercial infrastructure or unfocused pipeline expansion.StrengtheningMateriality: Medium
Trevi had 34 employees as of December 31, 2025, including 21 engaged in research, indicating a compact development organization. A lean model preserves optionality and negotiating leverage; an early cost build would raise the amount of clinical success needed just to protect per-share value.
Watch: Management begins building a full commercial sales organization well before approval or partnership clarity.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Trevi had 34 employees as of December 31, 2025, including 21 engaged in research, indicating a compact development organization.
Open source ↗A low-liability balance sheet gives Trevi strategic flexibility, but that advantage must persist as Haduvio advances through more expensive development stages.StrengtheningMateriality: Medium
FY2025 liabilities were $10.195 million against $193.439 million of total assets. Low debt preserves upside for equity holders and improves negotiating leverage; onerous liabilities or secured financing would shift value away from common shareholders.
Watch: Trevi takes on secured debt, restrictive covenants, or royalty-backed financing to fund trials.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
FY2025 liabilities were $10.195 million against $193.439 million of total assets.
Open source ↗
Full investment case & evidence
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Original research
Haduvio’s differentiated value rests on proving that oral nalbuphine ER can deliver clinically meaningful chronic-cough relief with tolerability good enough for long-term use in IPF, non-IPF ILD, and refractory chronic cough. If this holds, Trevi owns a potentially scarce therapy in underserved cough populations; if it breaks, the core asset and most of the equity value are impaired.
Trevi’s upside depends on the same Haduvio mechanism being relevant across several chronic-cough populations, not just one narrow indication. If indication breadth holds, the asset can support a larger commercial or partnering opportunity; if not, the addressable market and negotiating leverage shrink.
Trevi must keep enough financial runway to reach value-changing Haduvio clinical and regulatory events before needing highly dilutive capital. For owners, successful science only compounds per-share value if the company can finance the path without giving away too much of the upside.
Trevi’s small-company focus must keep burn tied to Haduvio development rather than premature commercial infrastructure or unfocused pipeline expansion. A lean model preserves optionality and negotiating leverage; an early cost build would raise the amount of clinical success needed just to protect per-share value.
A low-liability balance sheet gives Trevi strategic flexibility, but that advantage must persist as Haduvio advances through more expensive development stages. Low debt preserves upside for equity holders and improves negotiating leverage; onerous liabilities or secured financing would shift value away from common shareholders.
All standing thesis claims
Original report summary
TRVI is a focused, single-asset clinical biotech whose value depends on Haduvio proving it can become an approved, differentiated chronic-cough therapy before cash burn and dilution consume the upside.
Bull case and bear case
Bull case and bear case for Trevi Therapeutics
Where the evidence on Trevi Therapeutics stands: Holding on the latest evidence (Nov 10, 2026). Of its 5 thesis points, 3 strengthening and 2 holding.
Bull case: what the evidence supports
Haduvio’s differentiated value rests on proving that oral nalbuphine ER can deliver clinically meaningful chronic-cough relief with tolerability good enough for long-term use in IPF, non-IPF ILD, and refractory chronic cough.
Trevi’s upside depends on the same Haduvio mechanism being relevant across several chronic-cough populations, not just one narrow indication.
Trevi must keep enough financial runway to reach value-changing Haduvio clinical and regulatory events before needing highly dilutive capital.
Trevi’s small-company focus must keep burn tied to Haduvio development rather than premature commercial infrastructure or unfocused pipeline expansion.
A low-liability balance sheet gives Trevi strategic flexibility, but that advantage must persist as Haduvio advances through more expensive development stages.
Bear case: what would count against it
A late-stage Haduvio trial fails to show cough-frequency or patient-reported benefit adequate for FDA approval.
Clinical data show Haduvio works only in one cough population and does not translate to RCC or non-IPF ILD.
A required trial expansion, manufacturing requirement, or regulatory delay forces a financing before a data catalyst.
Thesis-Break Engine
What has broken in Trevi Therapeutics’s thesis
Each break OptimistFi flagged on Trevi Therapeutics, dated — with what has historically followed the same kind of break across the market, not a forecast for Trevi Therapeutics.
- Sharp drawdowncondition set before this filing
Across all companies, this kind of break has happened 15,428 times before. Those stocks beat comparable companies by a median of 1% over the next six months, and 33% of them trailed it by 10 points or more.
Early warning
The break condition read on the trailing twelve months through Trevi Therapeutics’s latest quarterly report, ahead of the annual figure it is written on.
- Net loss, trailing 12 months
Across all companies, this kind of early warning has happened 2,059 times before. Those stocks beat comparable companies by a median of 1% over the next six months, and 35% of them trailed it by 10 points or more.
MARKET + FINANCIAL SNAPSHOT
The numbers behind the thesis
What Changed
- MixedReported results of operations (earnings release).
Trevi Therapeutics filed an SEC 8-K on 2026-11-09: Reported results of operations (earnings release). It is a dated development that tests the current thesis.
- MixedReported results of operations (earnings release).
Trevi Therapeutics filed an SEC 8-K on 2026-08-06: Reported results of operations (earnings release). It is a dated development that tests the current thesis.
- MixedReported results of operations (earnings release).
Trevi Therapeutics filed an SEC 8-K on 2026-05-05: Reported results of operations (earnings release). It is a dated development that tests the current thesis.
Risks / falsifiers
What could break the thesis
- A late-stage Haduvio trial fails to show cough-frequency or patient-reported benefit adequate for FDA approval.
- Clinical data show Haduvio works only in one cough population and does not translate to RCC or non-IPF ILD.
- A required trial expansion, manufacturing requirement, or regulatory delay forces a financing before a data catalyst.
- Management begins building a full commercial sales organization well before approval or partnership clarity.
- Trevi takes on secured debt, restrictive covenants, or royalty-backed financing to fund trials.
TRVI news
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Financial statements
TRVI income statement
Annual filed results · USD · Oldest to newest. Margins are calculated from the reported figures.
TRVI: quick answers
- When does Trevi Therapeutics (TRVI) report earnings next?
- Trevi Therapeutics's next results are projected for February 8, 2027, from the dates of its own results filings with the SEC. The company has not confirmed the date. It last reported on November 9, 2026. Earnings calendar
- What is TRVI's short interest?
- As of October 30, 2026, 16.9M TRVI shares were sold short, 11.8% of its shares outstanding, up 5.3% from the count before. At the stock's average daily volume that is 10 days to cover. FINRA publishes the count twice a month. TRVI short interest history
- Which well-known investors own TRVI?
- 1 of the 37 well-known funds tracked here reported TRVI shares in their latest 13F filing. By share of the fund's portfolio: Viking Global Investors (Andreas Halvorsen), 0.1%. Fund portfolios
TRVI in well-known investors’ portfolios
1 of 37 funds reported TRVI shares in their latest 13F filing. A 13F shows quarter-end positions and arrives up to 45 days later.
| Fund | Of its portfolio | Value | Change | Quarter |
|---|---|---|---|---|
| Andreas HalvorsenViking Global Investors | 0.08% | $28.8M | — | Q2 2026 |
