Inventiva
IVAPhase 3Inventiva 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.
IVA · Stock Price
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
77 drugs in pipeline, 1 in Phase 3
| Drug | Indication | Stage |
|---|---|---|
| IVA337 + Placebo | NASH - Nonalcoholic Steatohepatitis | Phase 3 |
| IVA337 + Placebo | Scleroderma, Diffuse | Phase 2 |
| Odiparcil | Mucopolysaccharidosis VI | Phase 2 |
| IVA337 + IVA337 + Placebo | Non-Alcoholic Steatohepatitis (NASH) | Phase 2 |
| IVA337 + Placebo + Empagliflozin | NASH - Nonalcoholic Steatohepatitis | Phase 2 |
Funding History
2Total raised: $50M
Opportunities
Risk Factors
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.
Company Info
Trading
Contact
Therapeutic Areas
Sectors
Partners
Claim your profile to update information, add pipeline data, and connect with investors.
Claim profile