The World Peptide Therapeutics Congress 2027 is the flagship gathering for the scientists, executives, regulators, and investors building peptide medicine’s second decade.The first wave is complete: incretins reshaped obesity care, oral peptides reached patients, radioligands became oncology’s fastest-growing category, and AI-designed molecules entered the clinic. The question is no longer “can peptides be drugs?” — it’s “who will build, deliver, scale, and fund the next generation?”
Across 3 days, 5 tracks, and 90+ sessions, the Congress delivers what no other peptide event does:
🔬 First, not repeated. Unpublished Phase 1/2 data, live platform disclosures, and regulatory updates — presented here before journals and before any other 2027 conference.
⚖️ The whole value chain in one room. Discovery science, delivery & formulation, CMC at ton-scale, regulatory implementation, clinical translation, and deal-making — integrated, because that’s how drugs actually succeed.
🤝 A deal venue, not a lecture hall. An AI-matched 1:1 partnering system, investor reverse pitches, and a curated audience where 70% hold Director-level titles or above and service providers are capped — so every conversation has pipeline potential.
🚫 A No-Pitch Charter. Vendor content is limited, flagged, and never occupies main-stage science. Your time is treated as the asset it is.
Whether you’re hunting the post-GLP-1 blockbuster, scaling green manufacturing to tons, navigating finalized ICH guidance, or deploying capital in the peptide supercycle — this is the room where 2027’s roadmap gets written.
AI-Designed Peptides With Clinical Data — The Applied Reality of Generative Drug Design
Second-Generation Oral Peptide Science: Design Rules Written by Approved Products
Radioligands & Peptide-Drug Conjugates: The Post-PSMA Expansion
In Vivo Cell Reprogramming & Extrahepatic RNA Delivery — Peptides as Genetic Medicine Vehicles
Drugging the Undruggable: Molecular Glue Peptides, De Novo Miniproteins & Peptide Degraders
Manufacturing at Blockbuster Scale: Green CMC, Tons-Throughput & Sustainable Supply
The Regulatory Implementation Era: ICH Q2(R2), Q14, M10 & New Peptide-Specific Guidances
Clinical First-Disclosures: Oncology, Immunology & Pandemic Preparedness
Capital, M&A & IP in the Peptide Supercycle
Dedicated first-disclosure slots with managed embargoes: Phase 2 readouts, platform data, and regulatory interpretations debuting on our stage up to 12 months before they appear at competing conferences or in journals.
Advisory committee sessions, compendial-body workshops, and former regulators answering your CMC, immunogenicity, and filing questions directly — in rooms of 30, not auditoriums of 600.
Practicing oncologists and endocrinologists grade the peptide pipeline live — telling you, before you spend $50M, what treating physicians will actually prescribe.
In vivo T-cell reprogramming, molecular glue macrocycles, ton-scale green manufacturing, AI-inventorship IP — the modalities and constraints that will define the next deal cycle, programmed before any other event touches them.
Average delegate reports: 27 new qualified contacts, 9 follow-up meetings booked on-site, and 3 pipeline decisions accelerated per event. If your meeting count isn’t met, we credit your registration. That’s how confident we are.








Sponsor and exhibitor slots are capped and service-provider attendance limited to 30%. Your competitors at other events are shouting into rooms full of other vendors. Here, you’re one of a deliberately limited set and every booth conversation happens with a buyer, not a seller.
Our delegates hold budget: 70% Director+, 40% from large pharma, 25% from funded biotech actively outsourcing. The people evaluating CDMO transfers, hiring discovery platforms, and releasing 2028 R&D budgets are in this room with meeting slots reserved for you.
Contact us if you have any questions about the agenda, team discounts or anything else…