REGENXBIO Inc. (RGNX)

NASDAQ: RGNX · Real-Time Price · USD
12.05
+0.21 (1.82%)
Jun 30, 2026, 12:50 PM EDT - Market open
Market Cap622.70M +21.7%
Revenue (ttm)87.82M -44.0%
Net Income-290.01M
EPS-5.60
Shares Out 51.70M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume637,466
Open11.85
Previous Close11.83
Day's Range11.70 - 12.26
52-Week Range5.46 - 16.19
Beta1.03
AnalystsBuy
Price Target24.36 (+102.24%)
Earnings DateAug 6, 2026

About RGNX

REGENXBIO Inc., a clinical-stage biotechnology company, provides gene therapies that deliver functional genes to cells with genetic defects in the United States. Its gene therapy product candidates are based on NAV Technology Platform, a proprietary adeno-associated virus gene delivery platform. The company’s products in pipeline includes ABBV-RGX-314 for the treatment of wet age-related macular degeneration, diabetic retinopathy, and other chronic retinal diseases; and RGX-202 for the treatment of Duchenne muscular dystrophy, as well as RGX-12... [Read more]

Industry Biotechnology
Sector Healthcare
IPO Date Sep 17, 2015
Employees 371
Stock Exchange NASDAQ
Ticker Symbol RGNX
Full Company Profile

Financial Performance

In 2025, REGENXBIO's revenue was $170.44 million, an increase of 104.54% compared to the previous year's $83.33 million. Losses were -$193.88 million, -14.63% less than in 2024.

Financial Statements

Analyst Summary

According to 11 analysts, the average rating for RGNX stock is "Buy." The 12-month stock price target is $24.36, which is an increase of 102.24% from the latest price.

Price Target
$24.36
(102.24% upside)
Analyst Consensus: Buy
Stock Forecasts

News

Regenxbio says first patient dosed in Phase IIb/III NAAVIGATE trial

Regenxbio (RGNX) announced the first patient has been dosed in the Phase IIb/III NAAVIGATE clinical trial of investigational surabgene lomparvovec (sura-vec, ABBV-RGX-314) in diabetic retinopathy usin...

Other symbols: ABBV
1 day ago - TheFly

REGENXBIO Announces First Patient Dosed in Phase IIb/III NAAVIGATE Trial of Surabgene Lomparvovec in Diabetic Retinopathy; Company to Receive $100 Million Milestone

New long-term data from diabetic retinopathy and wet AMD programs to be presented at American Society of Retina Specialists (ASRS) 2026 ROCKVILLE, Md., June 29, 2026 /PRNewswire/ -- REGENXBIO Inc. (Na...

1 day ago - PRNewsWire

Regenxbio completes dosing in confirmatory study of RGX-202

Regenxbio (RGNX) announced the successful completion of dosing in the confirmatory study of RGX-202, a potential best-in-class gene therapy for Duchenne muscular dystrophy. This milestone positions Re...

6 days ago - TheFly

REGENXBIO Completes Dosing in Confirmatory Study of RGX-202, Marking Completion of Registrational Development Program and Supporting Planned BLA Submission in Q3 2026

Confirmatory study completed ahead of schedule due to strong patient demand and robust investigator interest On track to initiate BLA in Q3 2026 under the accelerated approval pathway supporting poten...

6 days ago - PRNewsWire

Regenxbio price target raised to $32 from $27 at Baird

Baird raised the firm’s price target on Regenxbio (RGNX) to $32 from $27 and keeps an Outperform rating on the shares. The firm updated its model the reflect the FDA-aligned…

7 days ago - TheFly

H.C. Wainwright notes Regenxbio doesn’t need more studies for BLA resubmission

After Regenxbio (RGNX) announced that it has aligned with the FDA regarding the resubmission of the Biologics License Application for Navsunli for Mucopolysaccharidosis II or Hunter syndrome, H.C. Wai...

8 days ago - TheFly

Regenxbio aligns with FDA on path forward for Navsunli

Regenxbio (RGNX) announced it has aligned with the U.S. FDA regarding the next steps needed for a potential accelerated approval of Navsunli, the only potential one-time treatment and gene therapy…

8 days ago - TheFly

REGENXBIO Announces Alignment with FDA on Path Forward for NAVSUNLI™ BLA Resubmission for Accelerated Approval; First Potential Gene Therapy for MPS II

FDA confirmed no additional studies required, existing longer-term data from the CAMPSIITE ® study will be reviewed on an expedited basis for approval via the accelerated approval pathway The Company ...

8 days ago - PRNewsWire

FDA to reverse rejection of Regenxbio's rare-disease drug, WSJ reports

The ​U.S. Food ‌and Drug ​Administration ​will reverse ⁠its ​earlier ​rejection of a ​rare-disease ​therapy from Regenxbio , ‌the ⁠Wall Street ​Journal ​reported ⁠on Monday.

8 days ago - Reuters

Regenxbio up 25% after saying FDA will reverse rejection, consider application

Regenxbio (RGNX) shares are up $1.97, or 25% to $9.77 in pre-market trading after after Chief Executive Curran Simpson said the Food and Drug Administration has agreed to reverse its…

8 days ago - TheFly

Regenxbio tells WSJ that FDA will reverse rejection of drug

Regenxbio (RGNX) Chief Executive Curran Simpson said the Food and Drug Administration has agreed to reverse its rejection of an experimental gene therapy for a rare and fatal brain disease…

Other symbols: QUREREPL
8 days ago - TheFly

FDA Will Reverse Rejection of Third Rare-Disease Drug, Regenxbio Says

The company plans to refile its application for its gene therapy for a fatal brain disease after the FDA dropped demands to give a placebo to some study subjects.

8 days ago - WSJ

Regenxbio price target lowered to $26 from $30 at H.C. Wainwright

H.C. Wainwright analyst Yi Chen lowered the firm’s price target on Regenxbio (RGNX) to $26 from $30 and keeps a Buy rating on the shares. The firm says RGX202 deliveded…

25 days ago - TheFly

REGENXBIO Transcript: RBC Capital Markets Global Healthcare Conference 2026

Plans are underway for a rolling BLA filing for Duchenne gene therapy, with strong efficacy and safety data supporting accelerated approval. Wet AMD pivotal trials are well-powered and on track, while the Hunter program is advancing post-clinical hold. Patient advocacy and product differentiation remain central.

5 weeks ago - Transcripts

REGENXBIO to Participate in Upcoming Investor Conferences

ROCKVILLE, Md., May 18, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced it will participate in the following investor conferences: 2026 RBC Capital Markets Global Healthcare Confere...

6 weeks ago - PRNewsWire

Regenxbio price target lowered to $16 from $17 at Morgan Stanley

Morgan Stanley lowered the firm’s price target on Regenxbio (RGNX) to $16 from $17 and keeps an Overweight rating on the shares.

6 weeks ago - TheFly

Regenxbio price target lowered to $14 from $25 at BofA

BofA lowered the firm’s price target on Regenxbio (RGNX) to $14 from $25 and keeps a Buy rating on the shares. The firm views the RGX-202 AFFINITY DUCHENNE topline update…

6 weeks ago - TheFly

Regenxbio price target lowered to $12 from $37 at Barclays

Barclays analyst Eliana Merle lowered the firm’s price target on Regenxbio (RGNX) to $12 from $37 and keeps an Overweight rating on the shares. The firm thinks further updates on…

6 weeks ago - TheFly

REGENXBIO Earnings release: Q1 2026

REGENXBIO released its Q1 2026 earnings on May 14, 2026, summarizing the period's financial results.

6 weeks ago - Filings

REGENXBIO Quarterly report: Q1 2026

REGENXBIO has published its Q1 2026 quarterly earnings report on May 14, 2026.

6 weeks ago - Filings

Regenxbio reports Q1 EPS ($1.72) vs. 12c last year

Reports Q1 revenue $6.4M vs. $89M last year. “REGENXBIO (RGNX) enters a transformative year with positive momentum, reaching significant late-stage milestones to support our potential first- and best-...

6 weeks ago - TheFly

Regenxbio expects cash, equivalents to fund operations into early 2027

Regenxbio (RGNX) expects its balance in cash, cash equivalents and marketable securities of $150.5M as of March 31 to fund its operations into early 2027. This cash runway guidance is…

6 weeks ago - TheFly

Regenxbio’s RGX-202 shows efficacy in Phase 3 Duchenne trial

Regenxbio (RGNX) announced positive topline and interim functional data from the pivotal Phase III portion of the Phase I/II/III AFFINITY DUCHENNE trial of RGX-202, a potential best-in-class gene ther...

6 weeks ago - TheFly

REGENXBIO Transcript: Study result

Pivotal phase III data for RGX-202 in Duchenne Muscular Dystrophy showed high microdystrophin expression, strong correlation with functional improvement, and a favorable safety profile. Investigators and families observed meaningful benefits, supporting plans for accelerated approval in 2027.

6 weeks ago - Transcripts

REGENXBIO Press release: Study result

REGENXBIO issued a press release on May 14, 2026, disclosing material business information to investors.

6 weeks ago - Filings