LaStaFium is developing a technology platform of late stage fluorination reactions for the rapid synthesis of ¹⁸F-labeled small-molecule analogues, enabling more accessible and practical Phase 0 and PET studies.
Promising drug candidates still fail late because traditional preclinical models cannot reliably predict distribution, exposure, pharmacokinetics, or tissue penetration in humans. Phase 0 studies — using ¹⁸F-labeled compounds and PET imaging — can deliver real human data before large clinical trials begin.
But there is a fundamental bottleneck: making the right ¹⁸F-labeled molecule. ¹⁸F has a short half-life, and radiolabeling demands a fundamentally different approach from conventional synthetic chemistry. For many candidates, finding a viable labeling route is slow, difficult, and highly specialised.
What is the drug distibution?
Does it reach the intended tissue (brain, tumor)?
Is human PK consistent with the development hypothesis?
Can we decide earlier — before costly Phase I programs?
Rather than relying on a single synthetic route, LaStaFium's platform enables parallel testing of hundreds of reaction conditions — transforming ¹⁸F radiolabeling from a bespoke chemistry problem into a systematic, platform-based discovery process.
Robotic and miniaturised workflows designed for rapid, reproducible experimentation at scale. Procedures are applicable for 18F hot-sytheses.
Parallel evaluation of a broad range of reaction conditions to identify viable labeling routes efficiently. We increse the probablity of finding the reaction that works.
Novel chemical sythesis methods such as electrochemistry, photochemistry. We use human curated, lab-tested database of reactions, updated with novel literature reports.
Generating ¹⁸F-labeled analogues for preclinical studies and Phase 0 in GMP standard.
Every molecule presents a different chemistry problem. Our flexible experimental platform is built around this reality — exploring many chemical possibilities efficiently, with capacity designed to scale with demand.




The future of drug discovery requires faster, more precise decision-making before entering large clinical programmes. LaStaFium is removing one of the key technological barriers limiting broader use of ¹⁸F-based Phase 0 research: the synthesis of the radiolabeled compound itself.
A scalable, automated platform built to handle the diversity of modern drug candidates and radiolabeling challenges.
Human pharmacokinetic and biodistribution data at an earlier stage — before expensive Phase I commitments.
Earlier, higher-confidence go/no-go decisions that reduce late-stage attrition and accelerate development timelines.
Are you developing a drug candidate that could benefit from ¹⁸F labeling or PET research? Are you interested in partnering with LaStaFium?
LaStaFium — Late-Stage Functionalization for ¹⁸F-labeled drug research.
LaStaFium — Late-Stage Functionalization for ¹⁸F-labeled drug research.