🎯HIT identification in muscle drug discovery: how many of your « hits » actually hold up?

Most screening teams already know the answer — and it's not good. Standard 2D assays generate volume, but oversimplified biology means false positives flood your pipeline. Compounds that look active in a flat monolayer fail the moment they meet a more relevant system. And when programs stall downstream, fingers point back at screening.

MyoScreen™ changes that equation.

Multiplexed, phenotypic-quality readouts — morphology, function, spatial organisation — from a single well, at genuine screening scale. You get richer hit profiles at the primary stage, so you triage smarter and advance chemical matter that actually holds up.

Built for HTS workflows, not against them: 

✓ 384-well format — runs on your existing protocols

âś“ Standardised micropatterned muscle models with tight assay windows

✓ Disease-relevant myoblasts (primary or immortalised) — assay-ready, not months of development

✓ AI-powered automated analysis — processes thousands of wells, no expert bottleneck

✓ Toxicity and cytostatic assessment built in — orthogonal data without extra experiments

đź’ˇ One well. Multiple answers. Better hit rates.

You no longer have to sacrifice biological relevance for throughput. Let’s talk about what that means for your next campaign !

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