May 8, 2027Research
— / —No executable quote
Research candidateOpen
Z-rostudirsen
Dyne Therapeutics · Duchenne muscular dystrophy amenable to exon 51 skippingJan 21, 2027 target
Will the FDA approve Z-rostudirsen for Duchenne muscular dystrophy amenable to exon 51 skipping?
DYN-YES/ USDC
Outcome claim / Research candidate
Executable price
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Change across observed prices in this windowImplied YES probability—Price-based, not a clinical forecast
Market not listed
No market price yet.
This program has no funded pool or observed trading history. Start with the evidence, or explore a clearly labeled scenario.
0 trading observationsNo live price feed
YES —NO —
This chart stays empty until observations exist. Research status is not an approval probability. A sandbox session creates a separate virtual price history.
Rx-DYN-2701 / Evidence
UnlistedPool price—No deployed pool
Dated model P(YES)—No dated model artifact
Days to sponsor target80Date-only guidance
Source publishedJul 20, 2026
Research snapshotOct 28, 2026
FDA targetJan 21, 2027
ASO / siRNANCT05524883
A pool price describes trading inventory; a model estimates an outcome. Neither a live price nor a dated forecast is available for this unlisted catalyst.
Program overview
Sponsor describes a PMO conjugated to an antibody fragment and a January 21, 2027 FDA target.
THERAPEUTIC AREARare disease
DRUG / PROGRAMZ-rostudirsen
INDICATIONDuchenne muscular dystrophy amenable to exon 51 skipping
REGULATORY TARGETJanuary 21, 2027
Agent model / unavailable
No reviewed probability or reasoning artifact is available. A neutral pool opening is not a clinical base rate.
What matters
- Accelerated approval based on surrogate endpoint needs explicit treatment.
- Approval, the stock price and commercial success are different outcomes. A claim only pays on its specified event.
- Future program funding and tokenized financing require separate rights and contracts. An event claim gives no equity, royalty or drug IP.