

Galapagos NV abandoned an oral immunology drug during its corporate meltdown. Now a startup founded by the drug's former Galapagos scientist just raised $125 million from Novo Holdings, Regeneron Ventures, and others to prove the big company was wrong.
When a big pharma company abandons a drug, the story usually ends there. The asset gets shelved, the scientists move on, and nobody writes about it again.
But sometimes, someone picks up the discarded thing and bets enormous money that the original owner was wrong. That's exactly what just happened with COL-5671, an oral immunology drug that Galapagos NV let go during a messy corporate restructuring. On April 28, a startup called Coultreon Biopharma closed a $125 million Series A to take this orphaned molecule into bigger clinical trials.
The round was oversubscribed. The investor list reads like a who's who of serious biotech money: Sofinnova Investments led, with Forbion and Novo Holdings co-leading. Regeneron's venture arm, Galapagos itself, Samsara BioCapital, Longwood Fund, Balyasny Asset Management, and others piled in.
For a Phase 1 drug at a company that didn't exist two years ago, that's a remarkable vote of confidence.
To understand Coultreon, you have to understand the chaos it emerged from.
Galapagos NV spent the last two years in a corporate identity crisis. In January 2025, the Belgian company announced plans to split itself in two. By May, they'd paused that plan. By October, they were winding down their entire cell therapy business, cutting approximately 365 employees.
Think of it like a restaurant that kept changing its concept every few months: French, then Italian, then "actually, we're closing the kitchen entirely." Amid all that turmoil, promising research programs got orphaned.
Pierre Raboisson, who previously ran discovery and preclinical development at Galapagos, saw an opportunity. He left in June 2025 and founded what was then called Onco3R Therapeutics. Galapagos transferred full ownership of COL-5671 in April 2025, along with a €20 million convertible loan facility to get things started. The company later rebranded as Coultreon Biopharma to reflect its focus on immunology.

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COL-5671 targets something called SIK3 (salt-inducible kinase 3). If that means nothing to you, think of SIK3 as a light switch inside immune cells that controls two things simultaneously.
When you flip this switch off with the drug, two things happen. First, the immune system dials down its production of inflammatory molecules like TNFα, IL-12, and IL-23 (the chemicals that drive autoimmune flares). Second, it ramps up production of IL-10, a molecule that calms the immune system down.
It's like having a thermostat that both turns off the heater and turns on the AC at the same time. Most existing drugs only do one or the other. They block a single inflammatory signal but don't actively promote resolution. COL-5671 theoretically does both, in one pill, taken once a day.
That dual mechanism is what investors are paying $125 million to test in humans.
Coultreon's drug enters a crowded immunology market, but it has one major structural advantage: it's a pill.
The biggest drugs in autoimmune disease (think Humira, Stelara, Skyrizi) are all injectable biologics. Patients have to give themselves shots every few weeks, often with drugs that cost tens of thousands of dollars per year. Oral drugs are cheaper to manufacture, easier to take, and don't require cold-chain shipping.
The oral immunology space already has some players. JAK inhibitors like Rinvoq (upadacitinib) and the newer TYK2 inhibitor Sotyktu (deucravacitinib) have proven that pills can compete with biologics. But JAK inhibitors carry safety baggage: black box warnings about blood clots, infections, and cancer risk that make doctors hesitant.
COL-5671 takes a completely different approach from JAK inhibitors. By working through the SIK3 pathway, it could potentially sidestep those safety concerns entirely. That "potentially" is doing a lot of heavy lifting, though; the drug is still in Phase 1, so safety data in larger groups remains years away.
Coultreon plans to advance COL-5671 into Phase 2 trials for psoriasis and ulcerative colitis, with proof-of-concept data expected in 2027. The target list also includes Crohn's disease, psoriatic arthritis, and rheumatoid arthritis, though those are further out.
If the science works, Coultreon would essentially be offering a single oral drug that mimics what currently takes multiple expensive biologics to achieve. That's a big "if," but it explains why Novo Holdings' partner Max Klement joined the board, and why Regeneron's venture arm wrote a check.
Coultreon's raise fits a growing pattern. Big pharma companies are shedding assets during restructurings, and nimble startups are scooping them up with venture backing. Bristol Myers Squibb's cast-off autoimmune assets launched Beeline Medicines with $300 million. Now Galapagos' discarded SIK3 program has found a $125 million home.
The lesson? In biotech, "abandoned" doesn't always mean "failed." Sometimes it just means the original owner had other problems. Coultreon is betting that Galapagos' loss is their gain, and some very smart money agrees.
Now they just have to prove the drug actually works.
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