Inventiva

Inventiva

IVAPhase 3

Inventiva is a public biopharma company (Euronext: IVA) focused on discovering and developing oral small molecule therapies for significant unmet needs in fibrosis, lysosomal diseases, and oncology. Its core asset is lanifibranor, a unique pan-PPAR agonist in a pivotal global Phase 3 trial (NATiV3) for NASH/MASH, with topline results expected in H2 2026. The company's strategy is built on a robust discovery platform, a deep chemistry library, and key partnerships, positioning it as a potential leader in the evolving NASH treatment landscape.

Market Cap
$1.2B
Employees
80-100
Focus
Small Molecules

IVA · Stock Price

USD 5.785.32 (-47.93%)

Historical price data

AI Company Overview

Inventiva is a public biopharma company (Euronext: IVA) focused on discovering and developing oral small molecule therapies for significant unmet needs in fibrosis, lysosomal diseases, and oncology. Its core asset is lanifibranor, a unique pan-PPAR agonist in a pivotal global Phase 3 trial (NATiV3) for NASH/MASH, with topline results expected in H2 2026. The company's strategy is built on a robust discovery platform, a deep chemistry library, and key partnerships, positioning it as a potential leader in the evolving NASH treatment landscape.

Technology Platform

A proprietary drug discovery platform specializing in nuclear receptors, transcription factors, and epigenetic modulation, supported by an in-house chemical library of 240,000 molecules and a team of ~80 scientists.

Pipeline Snapshot

7

7 drugs in pipeline, 1 in Phase 3

DrugIndicationStage
IVA337 + PlaceboNASH - Nonalcoholic SteatohepatitisPhase 3
IVA337 + PlaceboScleroderma, DiffusePhase 2
OdiparcilMucopolysaccharidosis VIPhase 2
IVA337 + IVA337 + PlaceboNon-Alcoholic Steatohepatitis (NASH)Phase 2
IVA337 + Placebo + EmpagliflozinNASH - Nonalcoholic SteatohepatitisPhase 2

Funding History

2

Total raised: $50M

PIPE$50MSofinnova PartnersJun 15, 2021
IPOUndisclosedUndisclosedJul 15, 2017

Opportunities

The primary opportunity is launching the first-in-class pan-PPAR agonist for the vast, treatment-naive NASH/MASH market, projected to be multi-billion dollar.
Success could also validate the company's platform, enabling expansion into other fibrotic, metabolic, and lysosomal diseases.
Existing partnerships provide a foundation for ex-European market access.

Risk Factors

High clinical risk from the ongoing Phase 3 trial (NATiV3), with binary outcomes expected in H2 2026.
Intense competition in NASH from other late-stage candidates.
Financial risk as a pre-revenue company funding an expensive global trial.
Pipeline concentration risk on a single lead asset.

Competitive Landscape

Competes in the crowded NASH space against companies like Madrigal, 89bio, and Akero. Lanifibranor's key differentiation is its unique pan-PPAR mechanism, designed to comprehensively address steatosis, inflammation, and fibrosis. Its oral administration and FDA Breakthrough Therapy designation are competitive advantages, but it must demonstrate superior or differentiated efficacy/safety to capture market share.

Publications
20
Pipeline
7

Company Info

TypeTherapeutics
Employees80-100
LocationFrance
StagePhase 3
RevenuePre-revenue

Trading

TickerIVA
ExchangeEuronext

Therapeutic Areas

FibrosisLysosomal Storage DiseasesOncologyMetabolic Disease

Partners

Sino BiopharmHepalys Pharma, Inc.
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