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Inventiva (IVA) Stock Price & Analysis
IVA Stock Chart & Stats
- Day’s Range
- EUR 3.17 - EUR 3.34
- 52-Week Range
- EUR 2.57 - EUR 6.20
- Previous Close
- EUR 3.35
- Volume
- 253.81K
- Average Volume (3M)
- 656.15K
- Market Cap
- EUR 760.35M
- Enterprise Value
- EUR 781.47M
- Total Cash (Recent Filing)
- EUR 166.13M
- Total Debt (Recent Filing)
- EUR 66.66M
- Price to Earnings (P/E)
- ―
- Beta
- 0.15
- Next Earnings
- Mar 31, 2027 (Est.)
- EPS Estimate
- -0.29
- Next Dividend Ex-Date
- N/A
- Dividend Yield
- N/A
Bulls Say, Bears Say
Bulls Say
Phase III Execution
Completing recruitment and final patient visits keeps Inventiva on a defined clinical timetable and reduces enrollment execution risk. The large, biopsy-confirmed cohort provides a meaningful validation event that could support regulatory progress and commercial planning over the next several quarters.
Clinical Efficacy Evidence
The phase II-B results provide a substantive efficacy foundation for lanifibranor before the pivotal readout. Consistent improvements across fibrosis, MASH resolution, and the composite endpoint strengthen the clinical rationale and support potential differentiation if Phase III confirms the effect.
Near-Term Funding Runway
Funding that extends through the expected Phase III readout and potential NDA filing gives Inventiva time to reach important value-creating milestones without an immediate financing requirement. This improves execution continuity, although later extension depends on additional conditions and financing outcomes.
Bears Say
Negative Equity And Leverage
Negative equity indicates that accumulated losses have overwhelmed the capital base, limiting financial flexibility and weakening the balance sheet ahead of major development decisions. Increased debt further raises leverage pressure and can constrain the company's ability to absorb setbacks or fund future programs.
Persistent Cash Burn And Losses
Persistent negative operating and free cash flow shows that development activity is consuming substantial cash rather than funding itself. Worsening 2025 outflows increase dependence on external capital and make the company's ability to sustain the pipeline sensitive to financing access and clinical progress.
Unapproved Lead Candidate
The core investment case remains dependent on an unapproved drug and a pending Phase III outcome, leaving regulatory and clinical risk unresolved. Until NATiV3 delivers supportive data, the projected filing and commercial launch are plans rather than established revenue drivers.
Inventiva News
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Company Description
Inventiva
Inventiva S.A. is a biopharmaceutical firm currently in the clinical development phase, specializing in creating orally administered small molecule treatments for conditions such as non-alcoholic steatohepatitis (NASH), mucopolysaccharidoses (MPS), and various other ailments. Their primary drug candidate, Lanifibranor, has successfully concluded Phase IIb clinical trials for the management of NASH. Furthermore, the company is advancing Odiparcil, a compound that has finished Phase IIa clinical testing specifically for treating the MPS VI subtype. Beyond these, Inventiva maintains a development pipeline featuring several early-stage projects targeting oncology and other medical conditions. Strategic partnerships are in place with AbbVie to address autoimmune diseases, and with Boehringer Ingelheim International GmbH for innovating therapies for idiopathic pulmonary fibrosis. Established in 2011, Inventiva S.A. operates from its headquarters in Daix, France.
- Sector
- General
- Industry
- Biotechnology
- CEO
- Andrew Obenshain
- Employees
- 87
- Website
- www.inventivapharma.com
- Address
- 50 rue de Dijon, Daix, BF, 21121, FR
Inventiva (IVA) Earnings & Revenues
IVA Earnings Call
Earnings Call SentimentPositive
The call was strongly focused on positive clinical, regulatory, commercial, and financing progress: NATiV3 is fully recruited with the final 72-week visit completed, phase II-B results were described as robust, the balance sheet was strengthened, and cash runway covers the expected Q4 2026 readout and potential 2027 filing. The principal negatives were the pending phase III outcome, known weight gain and edema effects, lower-end liver stiffness results, increased marketing and G&A expenses, and financing runway beyond Q2 2027 remaining conditional. Highlights significantly outweighed the stated challenges.
View all FR:IVA earnings summariesTechnical Analysis
Overall Consensus
| Indicator | Bullish | Neutral | Bearish |
|---|---|---|---|
| Overall Consensus | 7 | 5 | 10 |
| Technical Analysis | 3 | 5 | 2 |
| Moving Averages | 4 | 0 | 8 |





