Pluripotent stem cell (PSC) therapies provide hope to patients with incurable diseases. But current approaches to bringing them to market are challenging.
Development is risky and often poorly planned, manufacturing processes are unpredictable and costly, and income models are unreliable.
That’s where Alder Therapeutics comes in.
Officially founded in 2022, the vision of Alder Therapeutics took root a decade earlier. Our co-founder, Kristian Tryggvason, motivated by a discussion with his father, Professor Karl Tryggvason, and a belief in the untapped potential of laminin technology, set the stage for what would become a transformative force in pluripotent cell therapy.
Fast forward to 2022, when the data from animal studies clearly showed the benefit of the photoreceptor cell differentiation and cardiac cell differentiation methods, which had been further developed by Professor Tryggvason with the support of Duke-NUS and other external parties.
It was then that Alder Therapeutics materialized. Kristian, together with Stijn Heessen and Ricardo Baptista attracted the attention of Linc and Flerie. Early in 2023, our team licensed the technology from Duke-NUS, successfully transferred the manufacturing process to a CDMO, and generated innovative analytical methods that further bolstered our operations.
Come September 2023, we ambitiously aim to secure funding to take our groundbreaking ALD01 eye project to Phase I. Looking beyond, 2024 will usher in a new phase of rigorous verification studies and the initiation of GLP Tox studies, paving the way for a landmark clinical trial in 2026.
But Alder Therapeutics’ journey is more than a recount of milestones. It's a testament to our dedication to medical innovation, patient outcome, and our enduring commitment to cure the incurable.
Drawing on extensive academic and commercial cell therapy experience, we work in accordance with the AlderEdge philosophy, which focuses on de-risking cell therapy development by keeping the commercial product in mind from the start.
Any cell therapy program progressed according to the AlderEdge principles will consider critical determinants of success from the get-go:
In this way, we streamline development and manufacturing, and maximize the chances of program success which benefits patients and our investors.

Using the AlderEdge™ methodology, we’re progressing two game-changing allogeneic stem cell therapies through development — the first for the treatment of Retinitis Pigmentosa and a second for the treatment of heart failure.
Both candidates are backed by promising, high-quality preclinical data. We are on track to bring our lead therapy to first-in-human trials in 2026.
Want to support us on our journey to shape the future of regenerative medicine?