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Design Therapeutics to Host Investor Webcast to Review Data from RESTORE-FA Trial of DT-216P2 for Friedreich’s Ataxia on Monday, May 18, 2026

Key Takeaway: Design Therapeutics will present data from its Phase 1/2 RESTORE-FA trial of DT-216P2 for Friedreich's ataxia on May 18, 2026. The company is focused on developing therapies for serious genetic diseases using its GeneTAC platform. The webcast will be accessible to investors and archived for later viewing.
Price reaction · baseline $14.37 (2026-05-15 close) · clean, no other DSGN news in the window
day 0 close
-25.5%
day 1 · peak
-27%
day 3
-23.4%

Market Sentiment Analysis

POSITIVE FACTORS

  • Design Therapeutics is advancing innovative therapies for genetic diseases.
  • The RESTORE-FA trial is a significant step in treating Friedreich's ataxia.
  • Management is engaging with investors through a webcast to share important data.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+78%
120-day peak, hindsight
Typical move
2%
average across 2 past catalysts
Cash runway
~40 mo
Minimal dilution risk
Lead asset
Alectinib- Usual
Phase 2 · Non-small Cell Lung Cancer

Full Press Release Details

CARLSBAD, Calif., May 17, 2026 (GLOBE NEWSWIRE) -- Design Therapeutics, Inc. (Nasdaq: DSGN), a clinical-stage biotechnology company developing treatments for serious degenerative genetic diseases, will announce data from the ongoing Phase 1/2 RESTORE-FA trial evaluating DT-216P2 in patients with Friedreich’s ataxia (FA) on Monday, May 18, 2026. Management will host a conference call and webcast at 8:00 a.m. ET.
A live webcast of the presentation will be availablehereand in the investors section of the company’s website atwww.designtx.com. The webcast will be archived for at least 30 days following the presentation.
About Design TherapeuticsDesign Therapeutics is a clinical-stage biotechnology company developing a new class of therapies based on its platform of GeneTAC®gene targeted chimera small molecules. The company’s GeneTAC®molecules are designed to either dial up or dial down the expression of a specific disease-causing gene to address the underlying cause of disease. In addition to its clinical-stage GeneTAC®programs, DT-216P2, in development for patients with Friedreich ataxia, DT-168, for Fuchs endothelial corneal dystrophy, and DT-818, for myotonic dystrophy type-1, the company is advancing a program in Huntington’s disease. Discovery efforts are underway for multiple genomic medicines. For more information, please visit designtx.com.

Contact:Renee Leck, THRUSTrenee@thrustsc.com

Frequently Asked Questions

What is the RESTORE-FA trial?

The RESTORE-FA trial is a Phase 1/2 study evaluating DT-216P2 for Friedreich's ataxia.

When will the investor webcast take place?

The investor webcast will be held on May 18, 2026, at 8:00 a.m. ET.

What is DT-216P2?

DT-216P2 is a therapy being developed by Design Therapeutics for Friedreich's ataxia.

Where can I access the webcast?

The webcast will be available on Design Therapeutics' website and archived for 30 days.

Last updated: May 17, 2026