Regeneron Tessera Partner on TSRA-196 Gene-Writing Therapy for AATD with $275M Deal

Regeneron Tessera Partner on TSRA-196 Gene-Writing Therapy for AATD with $275M Deal

Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Tessera Therapeutics announced a global collaboration to develop and commercialize TSRA-196, Tessera’s lead investigational in vivo Gene Writing program for alpha‑1 antitrypsin deficiency (AATD).

Deal Structure & Financial Terms

ComponentAmount/Term
Upfront & EquityUSD 150 million (cash + Regeneron investment)
Near/Mid‑Term MilestonesUp to USD 125 million
Total Potential ValueUSD 275 million (plus profit sharing)
Cost/Profit Sharing50/50 worldwide for TSRA-196
LeadershipTessera leads first‑in‑human trial; Regeneron leads subsequent development/commercialization

Program Overview & Mechanism

  • TSRA-196: In vivo Gene Writing therapy designed to precisely correct the genetic mutation causing AATD.
  • Goal: Restore functional alpha‑1 antitrypsin (AAT) protein production via a one‑time, durable treatment.
  • Regulatory Timeline: Tessera expects to file IND and multiple CTAs with the U.S. FDA by end‑2025.

Strategic Rationale & Platform Synergy

PartnerCore Contribution
RegeneronIndustry‑leading genetics capabilities; proven track record in advancing novel genetic medicines
TesseraProprietary Gene Writing platform; non‑viral delivery technologies
Combined ValueAccelerates TSRA-196 from preclinical to global markets

Market Context & Competitive Landscape

  • AATD Market: ~100,000 patients in US/EU; current standard of care (protein augmentation) requires lifelong weekly infusions.
  • Gene Writing Differentiation: First platform to enable precise correction of disease‑causing mutations in vivo, potentially offering a curative approach.
  • Commercial Opportunity: Analysts project >US$2 billion peak sales potential for a functional cure in AATD.

Forward‑Looking Statements
This brief contains forward‑looking statements regarding TSRA-196 development, regulatory filings, and collaboration milestones. Actual results may differ due to clinical, regulatory, and competitive risks.-Fineline Info & Tech