DSGN
Design Therapeutics, Inc.9.62
+0.50+5.48%
Dec 16, 4:00:02 PM EST
Earnings Call Transcripts
This Quarter (Q4 '25)
No earnings call transcript available yet
Last Quarter (Q3 '25)
No earnings call transcript available
Key Stats
Market Cap
547.99MP/E (TTM)
-Basic EPS (TTM)
-1.19Dividend Yield
0%Recent Filings
10-Q
8-K
8-K
Board director transition announced
Design Therapeutics' board saw a seamless shift on September 9, 2025, with Arsani William, M.D., resigning without disagreements, paving the way for Justin Gover's appointment as a Class III director through the 2027 annual meeting and Compensation Committee chair. Gover receives a $40,000 board retainer plus $12,000 for his committee role, alongside an initial option for 30,000 shares vesting over three years and a prorated grant for 15,833 shares over one year. This bolsters governance continuity.
10-Q
Q2 FY2025 results
Design Therapeutics posted a Q2 net loss of $19.1M, up 62% y/y from $11.8M, driven by R&D expenses climbing to $15.7M from $10.5M amid ramped-up clinical work on DT-216P2 for Friedreich ataxia and DT-168 for Fuchs endothelial corneal dystrophy. Operating losses widened to $21.6M from $15.0M, with no revenue yet and interest income dipping to $2.5M from $3.3M. Cash burn quickened, with operating cash use at $31.2M for the half-year versus $23.7M last year, leaving $216.3M in cash and investments at quarter-end—enough for over a year. No debt weighs on the balance sheet. Yet clinical holds from the FDA on DT-216P2's U.S. start pose delays. Cash runway holds firm. Competition in rare diseases sharpens risks.
8-K
Pipeline advances amid FDA hold
Design Therapeutics unveiled early human PK data for DT-216P2, showing favorable translation from non-human primates and an improved profile over prior formulations for its Friedreich Ataxia program, while advancing the RESTORE-FA Phase 1/2 trial outside the U.S. amid an FDA clinical hold. The company kicked off a Phase 2 biomarker study for DT-168 in Fuchs Endothelial Corneal Dystrophy patients. Cash reserves stand at $216.3 million, funding pipeline progress despite a Q2 net loss of $19.1 million. FDA hold resolution remains uncertain.
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