Compare

REGENXBIO/$RGNX

1D1W1M3M6MYTD1Y5YMAX

About REGENXBIO

Regenxbio Inc is a clinical-stage biotechnology company focused on the development of gene therapy treatments. Its product candidates are designed to deliver genes to cells to address genetic defects or enable the production of therapeutic proteins. The company is developing a pipeline of investigational gene therapy treatments using its NAV Technology Platform based on adeno-associated virus (AAV) vectors. Its internal research and development programs are focused on therapies for retinal, neuromuscular, and neurodegenerative diseases.
Ticker
$RGNX
Sector
Health
Primary listing
NASDAQ
Employees
371

REGENXBIO Metrics

BasicAdvanced
$472M
-
-$3.77
0.93
-

What the Analysts think about REGENXBIO

Analyst ratings (Buy, Hold, Sell) for REGENXBIO stock.
Analyst projections of the future price of REGENXBIO stock.

Bulls say / Bears say

RGX-202 met its Phase 3 primary endpoint, with 93% of evaluable participants reaching the prespecified microdystrophin threshold; early one-year functional results also favoured treatment over external controls. That gives REGENXBIO a credible potential Duchenne approval catalyst. (NeurologyLive)
The AbbVie-partnered retinal programme offers another late-stage growth opportunity: REGENXBIO reported durable vision and treatment-burden results in longer-term wet AMD follow-up, with pivotal wet AMD data expected in the fourth quarter of 2026. (REGENXBIO)
The company’s post-July cash position of about $313 million is expected to fund operations into the fourth quarter of 2027, covering key planned Duchenne and retinal milestones and easing near-term financing pressure. (REGENXBIO)
The FDA placed RGX-121 on clinical hold after spine MRI findings in five participants, and the company no longer expects to resubmit its application in the near term. This removes a potential approval catalyst and leaves the programme’s timing and prospects uncertain. (BioPharma Dive)
RGX-202’s pivotal cohort included two treatment-related serious events: myocarditis and liver injury, although both resolved. These events add safety and regulatory risk to the company’s lead Duchenne opportunity. (NeurologyLive)
The cash runway depends partly on a one-off AbbVie milestone and proceeds from a share offering, while US ZOLGENSMA royalties fell after patent expiry and the company continues to incur losses. That leaves future funding and dilution risks if development or launches take longer than planned. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 17 Oct 2026.

REGENXBIO Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

REGENXBIO Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Real-time US market data is sourced from the IEX order book provided by Polygon. After-hours US market data is 15 minutes delayed and may differ significantly from the actual tradable price at market open.