HAYA Therapeutics

HAYA Therapeutics website preview
biotech Lausanne, CH 4 sources
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HAYA Therapeutics develops RNA-guided therapies and programmable therapeutics to reprogram disease-driving cell states and restore health through causal biology.

Classification

Lausanne CH biotech licensing b2b bioinformatics BiotechRna-Guided MedicinesRegulatory GenomePrecision MedicineHealth Restoration

Profile

Tech stack
RNA-guided therapies

Funding

Funding details not yet available.

Business model
💡 Value Proposition

RNA-guided therapies that reprogram disease-driving cell states to reverse disease at its roots, restoring health through causal biology.

👥 Customer Segments

Pharmaceutical companies, biotech firms, and research institutions in the DACH region.

💰 Revenue Model

Up-front licensing fees and milestone payments from pharma partners · Royalties on future product sales (once candidates are commercialized) · Grant funding / non-dilutive awards for early-stage research (e.g., Struengmann Award)

📡 Channels

Direct sales and partnerships with biotech/pharma firms for therapeutic development.

🤝 Key Partnerships

biopharma partnerships

⚖️ Cost Structure

R&D for developing RNA-guided therapeutics and causal biology platforms.

🏗️ Key Resources

Proprietary RNA-guided therapeutic platform and causal biology methodology for programming lasting health.

⚙️ Key Activities

Developing programmable therapeutics to reprogram cell states and reverse disease-driving conditions.

💬 Customer Relationships

Sales-led relationships with enterprise biotech and pharmaceutical clients.

Strategic analysis
🏁 Competitive landscape

Competes in the RNA therapeutics space by differentiating through causal biology and cell state reprogramming rather than traditional symptom management.

🎯 Market pains

Disease-driving cell states that require reversal to restore health rather than just managing symptoms.

💎 Improvement suggestions
  • Diversify revenue early - pursue additional non-exclusive licensing deals with mid-size pharma to generate milestone cash before IND fili
♟️ Strategic implications

First-mover advantage in lncRNA therapeutics can translate into high-value licensing deals if the platform proves reproducible across diseas · Capital efficiency hinges on converting scientific milestones into partnership revenue; delaying this may strain cash-runway given high R&D · Regulatory clarity will be a make-or-break factor; early engagem

🛡️ Credibility notes
  • Scientific leadership - CEO Samir Ounzain discovered the cardiac lncRNA Wisper, a validated target that underpins the lead program, dem
Team
Unknown Founder
CEO and Co-Founder
Investors

No investors recorded yet.

Sources & references

Web verified · 4 sources
Enriched 18 Jun 2026