Duchenne News Tags: REGENXBIO

October 31, 2025
On October 30, 2025, REGENXBIO Inc. announced the completion of enrollment in the AFFINITY DUCHENNE® pivotal trial of RGX-202, an investigational gene therapy for the treatment of Duchenne muscular dystrophy,...
June 5, 2025
Updates include positive functional, safety and biomarker data for RGX-202, REGENXBIO's potential best-in-class, investigational gene therapy for Duchenne muscular dystrophy.
April 2, 2025
On March 24, REGENXBIO Inc. shared a Letter to the Duchenne Community announcing updates to their RGX-202 AFFINITY DUCHENNE gene therapy for the treatment of Duchenne muscular dystrophy. To view...
March 14, 2025
On March 13, 2025, REGENXBIO Inc. reported financial results and recent operational highlights for the fourth quarter and year ended December 31, 2024. Please continue reading to view full updates....
November 19, 2024
Updates on dosing and more for REGENXBIO's open-label trial of RGX-202 for Duchenne muscular dystrophy.
November 7, 2024
On November 6, 2024, reported financial results and recent operational highlights for the third quarter ended September 30, 2024. Please continue reading to view their full press release. ROCKVILLE, Md., Nov....
August 6, 2024
Data updates for Phase I/II AFFINITY DUCHENNE® trial of RGX-202.
June 24, 2024
REGENXBIO shares a press release detailing updates on its Phase I/II AFFINITY DUCHENNE® trial.
May 10, 2024
REGENXBIO shares financial results for the first quarter ending March 31, 2024.
March 5, 2024
REGENXBIO reports additional interim safety and efficacy data in the Phase I/II AFFINITY DUCHENNE® trial of RGX-202 in patients with Duchenne.
February 8, 2024
REGENXBIO announces completion of enrollment in the Phase I/II AFFINITY DUCHENNE® trial of RGX-202.
November 30, 2023
REGENXBIO announces that the first patient received RGX-202 at dose level 2 in the Phase I/II AFFINITY DUCHENNE® trial.
November 9, 2023
On November 9, 2023, REGENXBIO announced financial results for the third quarter ended September 30, 2023, and recent operational highlights, including a strategic pipeline prioritization and corporate restructuring intended to...

Experience the magic this summer!

How is the rare disease community accomplishing goals?

Tune in on February 29 to hear from our panel and moderators on how they are accomplishing goals and living life to the fullest!

Your gift helps Jett Foundation provide programming and opportunities, such as Camp Promise, to many families impacted by Duchenne muscular dystrophy each year.

Accessible Vehicle Fund Applications Open