Earendil Labs

HXN-1002 and HXN-1003 (Sanofi)

In Development

Two bispecific antibodies licensed exclusively to Sanofi for autoimmune and inflammatory bowel disease. HXN-1002 targets α4β7 and TL1A for moderate-to-severe ulcerative colitis and Crohn's disease. HXN-1003 targets TL1A and IL-23 and has shown synergistic activity in preclinical colitis and skin-inflammation models.

Latest update Sep 18, 2026

HXN-1002 and HXN-1003 (Sanofi)

01

Current status

Out-licensed to Sanofi in April 2025. Sanofi holds exclusive worldwide rights and is responsible for development. No Sanofi-run clinical start has been announced as of September 18, 2026. Still listed on Earendil's IBD pipeline table.

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Specifications2

Upfront
$125M, plus $50M near-term milestone eligibility
Milestones
Up to $1.72B development and commercial

03

Upcoming milestones1

Announced next steps from Earendil Labs that mention HXN-1002 and HXN-1003 (Sanofi).

  1. Not disclosed

    Sanofi to start human studies of HXN-1002 and HXN-1003

    The April 2025 license put two bispecifics in Sanofi's hands. As of September 18, 2026 Sanofi has not announced a first-in-human study for either asset. A posted trial, an IND, or a Sanofi pipeline listing is the next hard signal that the first deal is more than an upfront payment.

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