REGENXBIO Inc. (RGNX)
| Market Cap | 413.59M +3.4% |
| Revenue (ttm) | 161.32M +91.3% |
| Net Income | -177.92M |
| EPS | -3.46 |
| Shares Out | 50.62M |
| PE Ratio | n/a |
| Forward PE | n/a |
| Dividend | n/a |
| Ex-Dividend Date | n/a |
| Volume | 182,350 |
| Open | 8.00 |
| Previous Close | 8.04 |
| Day's Range | 7.98 - 8.22 |
| 52-Week Range | 5.04 - 16.19 |
| Beta | 1.05 |
| Analysts | Strong Buy |
| Price Target | 29.13 (+256.55%) |
| Earnings Date | Mar 12, 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, which is in Phase III clinical trial for the treatment of Duchenne... [Read more]
Financial Performance
In 2024, REGENXBIO's revenue was $83.33 million, a decrease of -7.66% compared to the previous year's $90.24 million. Losses were -$227.10 million, -13.81% less than in 2023.
Financial StatementsAnalyst Summary
According to 8 analysts, the average rating for RGNX stock is "Strong Buy." The 12-month stock price target is $29.13, which is an increase of 256.55% from the latest price.
News
Regenxbio: Cautiously Bullish After FDA Setbacks
REGENXBIO's NAV AAV platform has given them a diversified pipeline. They have RGX-314 and RGX-202 as primary value drivers with promising 2026 catalysts. RGX-314 is being developed in partnership with...
FDA Rejection Clouds Path For REGENXBIO's Rare Disease Treatment
In May 2025, the FDA accepted the RGX-121 BLA under the accelerated approval pathway; however, the Prescription Drug User Fee Act (PDUFA) goal date was extended from November 9, 2025, to February 8, 2...
US FDA declines to approve Regenxbio's rare disease drug
Regenxbio said on Monday the U.S. Food and Drug Administration has declined to approve its drug for a rare disease.
REGENXBIO Announces Regulatory Update on RGX-121 BLA for MPS II
FDA issues Complete Response Letter for RGX-121 (clemidsogene lanparvovec) for treatment of Mucopolysaccharidosis II (MPS II) REGENXBIO plans to work with FDA on a path forward with the goal of resubm...
RGNX Investors Have Opportunity to Join REGENXBIO Inc. Fraud Investigation with the Schall Law Firm
LOS ANGELES--(BUSINESS WIRE)---- $RGNX--RGNX Investors Have Opportunity to Join REGENXBIO Inc. Fraud Investigation with the Schall Law Firm.
Investigation into Regenxbio: Questions Arise Over Disclosure Completeness Prior to FDA Action
(NASDAQ: RGNX) NEW YORK, Jan. 29, 2026 /PRNewswire/ -- Levi & Korsinsky, LLP is investigating Regenxbio Inc. (NASDAQ: RGNX) regarding potential gaps between information provided to investors and under...
FDA Clinical Hold Knocks REGENXBIO Stock
REGENXBIO Inc. (NASDAQ: RGNX) shares are tumbling on Wednesday with a session volume of 3.83 million versus an average volume of 684.271 thousand.
US FDA places clinical hold on Regenxbio's gene therapy trials
Regenxbio said on Wednesday the U.S. Food and Drug Administration has placed a clinical hold on two of its experimental gene therapy programs for rare childhood diseases after a brain tumor was found ...
REGENXBIO Announces Regulatory Update on Ultra Rare MPS Programs
ROCKVILLE, Md., Jan. 28, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced that the U.S. Food and Drug Administration (FDA) placed a clinical hold on its investigational gene therapy,...
REGENXBIO: Key FDA Decision On Hunter Syndrome Just Weeks Away
Regenxbio Inc. faces pivotal catalysts in 2026, notably RGX-121's FDA decision and RGX-202 Duchenne data, potentially transforming it into a commercial-stage gene therapy company. RGX-121 offers a uni...
REGENXBIO Inc. (RGNX) Presents at 44th Annual J.P. Morgan Healthcare Conference Transcript
REGENXBIO Inc. (RGNX) Presents at 44th Annual J.P. Morgan Healthcare Conference Transcript
REGENXBIO Highlights Key 2026 Catalysts and Announces Positive Long-Term Functional Outcomes in Lead Duchenne Gene Therapy Program
New Phase I/II RGX-202 functional data demonstrates long-term, durable treatment effect at pivotal dose at 18 months Robust patient enrollment in confirmatory trial continues, expect majority of pati...
REGENXBIO to Present at the 44th Annual J.P. Morgan Healthcare Conference
ROCKVILLE, Md. , Dec. 18, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced it will present at the 44th Annual J.P.
REGENXBIO to Participate in Upcoming Investor Conference
ROCKVILLE, Md. , Nov. 25, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced it will participate in the following investor conference: Piper Sandler 37th Annual Healthcare Conference F...
REGENXBIO Inc. (RGNX) Q3 2025 Earnings Call Transcript
REGENXBIO Inc. ( RGNX) Q3 2025 Earnings Call November 6, 2025 8:00 AM EST Company Participants Patrick Christmas - Executive VP & Chief Strategy and Legal Officer Curran Simpson - President, CEO & Di...
REGENXBIO Reports Third Quarter 2025 Financial Results and Operational Highlights
RGX-202 program for Duchenne muscular dystrophy advancing rapidly, topline results expected early Q2 2026 and BLA submission mid-2026 Pivotal trial enrollment completed in October; confirmatory trial ...
REGENXBIO Announces Completion of Pivotal Enrollment and Initiates Commercial Production in Duchenne Gene Therapy Program
Patients treated with RGX-202 demonstrate consistent, robust microdystrophin expression and functional improvement compared to natural history in Phase I/II portion of AFFINITY DUCHENNE® trial support...
REGENXBIO to Host Conference Call on November 6 to Discuss Third Quarter 2025 Financial Results and Operational Highlights
ROCKVILLE, Md. , Oct. 29, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced that it will host a conference call on Thursday, November 6, at 8:00 a.m.
REGENXBIO to Participate in Upcoming Investor Conferences
ROCKVILLE, Md. , Oct. 15, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced it will participate in the following investor conferences: Chardan's 9th Annual Genetic Medicines Conferenc...
REGENXBIO Announces Presentation at the American Academy of Ophthalmology 2025 Annual Meeting
ROCKVILLE, Md. , Oct. 9, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced that it will present interim data from the Phase II ALTITUDE® trial evaluating suprachoroidal delivery of su...
REGENXBIO Announces Completion of Enrollment in Pivotal Trials of Subretinal Surabgene Lomparvovec for Wet AMD
Over 1,200 participants enrolled in ATMOSPHERE® and ASCENT® pivotal trials, representing largest global gene therapy program ever conducted Subretinal surabgene lomparvovec on track to be first gene t...
REGENXBIO Announces Presentation at the World Muscle Society
ROCKVILLE, Md. , Sept. 29, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced Chief Medical Officer, Steve Pakola, M.D.
Regenxbio: Poised For Breakthrough With RGX-121 Gene Therapy In Hunter Syndrome
Regenxbio's RGX-121 gene therapy for Hunter syndrome is the main catalyst, with FDA approval targeted for February 2026. Recent clinical data shows RGX-121 can address neurological decline, a major un...
REGENXBIO Inc. (RGNX) Presents At Morgan Stanley 23rd Annual Global Healthcare Conference Transcript
REGENXBIO Inc. (NASDAQ:RGNX) Morgan Stanley 23rd Annual Global Healthcare Conference September 8, 2025 11:30 AM EDT Company Participants Curran Simpson - President, CEO & Director Steve Pakola - Exec...
Regenxbio: Remains A "Buy Rating" Despite BLA Review Delay Of RGX-121 For Hunter Syndrome
Regenxbio's RGX-121 for Hunter syndrome saw its FDA review delayed to February 8, 2026, but strong 12-month surrogate endpoint data supports its potential as a gene therapy. Late-stage Sura-vec trials...