REGENXBIO to Host Webcast on May 14 to Discuss Topline Results from Pivotal Trial of RGX-202 for Duchenne Muscular Dystrophy
REGENXBIO (Nasdaq: RGNX) will host a live webcast on May 14, 2026 at 8:00 a.m. ET to discuss topline results from the pivotal trial of RGX-202, its next-generation investigational gene therapy for Duchenne muscular dystrophy.
Rhea-AI Summary
REGENXBIO (Nasdaq: RGNX) will host a live webcast on May 14, 2026 at 8:00 a.m. ET to discuss topline results from the pivotal trial of RGX-202, its next-generation investigational gene therapy for Duchenne muscular dystrophy.
The company will also report first quarter 2026 financial results and operational highlights pre-market on May 14. The live webcast and an archived replay (available for ~30 days) are accessible via the investor section at regenxbio.com.
Positive
- Topline pivotal trial results for RGX-202 scheduled May 14, 2026
- First quarter 2026 financial results to be released pre-market May 14, 2026
- Webcast will feature three leading Duchenne physicians as presenters
Negative
- None.
Details
News Market Reaction – RGNX
On May 6, the day this news came out, RGNX closed 10.85% above the previous close.
Data tracked by StockTitan Argus for the May 6 session.
Key Figures
- Webcast date
- May 14, 2026
- RGX-202 pivotal topline results discussion
- Webcast time
- 8:00 a.m. ET
- Scheduled RGX-202 topline webcast start time
- Quarter reported
- Q1 2026
- Financial results to be reported with webcast
- Quarter end date
- March 31, 2026
- Period covered by upcoming Q1 2026 results
- Replay availability
- ≈30 days
- Archived webcast replay duration
Previous Clinical trial Reports
-
Positive AFFINITY DUCHENNE Phase I/II interim data for RGX-202 pivotal dose cohort.
-
Positive 12‑month pivotal CAMPSIITE data for RGX-121 in MPS II patients.
-
Preclinical results showing functional benefits of RGX-202 microdystrophin construct.
-
AFFINITY DUCHENNE functional gains and high microdystrophin expression at dose level 2.
-
Positive Phase II fellow-eye data for ABBV-RGX-314 in bilateral wet AMD.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
pivotal trial medical
gene therapy medical
Duchenne muscular dystrophy medical
webcast technical
AI-generated analysis. How Rhea-AI works. Not financial advice.
-- Company will also report first quarter 2026 financial results and operational highlights --
The webcast will feature leading Duchenne physicians including Aravindhan Veerapandiyan, M.D., Director of the Comprehensive Neuromuscular Program and Co-Director of the Muscular Dystrophy Association Care Center at Arkansas Children's Hospital, Carolina Tesi-Rocha, M.D., Clinical Professor, Neurology, Stanford School of Medicine, Stanford Children's Health, and Diana Castro, M.D., Board Certified Neurologist and Neuromuscular Physician, Founder and Director Neurology and Neuromuscular Care Center and Founder and Director Neurology Rare Disease Center.
The company will also report financial results and operational highlights for the first quarter ended March 31, 2026 pre-market Thursday, May 14.
The live webcast can be accessed here and in the Investor section of REGENXBIO's website at www.regenxbio.com. An archived replay of the webcast will be available for approximately 30 days following the presentation.
ABOUT REGENXBIO Inc.
REGENXBIO is a biotechnology company on a mission to improve lives through the curative potential of gene therapy. Since its founding in 2009, REGENXBIO has pioneered the field of AAV gene therapy. REGENXBIO is advancing a late-stage pipeline of one-time treatments for rare and retinal diseases, including RGX-202 for the treatment of Duchenne; clemidsogene lanparvovec (RGX-121) for the treatment of MPS II and RGX-111 for the treatment of MPS I, both in partnership with Nippon Shinyaku; and surabgene lomparvovec (ABBV-RGX-314) for the treatment of wet AMD and diabetic retinopathy, in collaboration with AbbVie. Thousands of patients have been treated with REGENXBIO's AAV platform, including those receiving Novartis' ZOLGENSMA®. REGENXBIO's investigational gene therapies have the potential to change the way healthcare is delivered for millions of people. For more information, please visit WWW.REGENXBIO.COM.
Contacts:
Dana Cormack
Corporate Communications
dcormack@regenxbio.com
Investors:
George E. MacDougall
Investor Relations
IR@regenxbio.com
View original content to download multimedia:https://www.prnewswire.com/news-releases/regenxbio-to-host-webcast-on-may-14-to-discuss-topline-results-from-pivotal-trial-of-rgx-202-for-duchenne-muscular-dystrophy-302763647.html
SOURCE REGENXBIO Inc.
FAQ
AI-generated questions and answers. How Rhea-AI works. Not financial advice.
