REGENXBIO Inc. (RGNX) Research

REGENXBIO Inc. is a biotechnology company operating in the clinical stage, dedicated to developing gene therapy candidates. These therapies are designed to introduce genes into cells, aiming either to rectify genetic deficiencies or to stimulate the body's own cells to produce therapeutic proteins or antibodies to combat diseases. Central to its therapeutic development is the proprietary NAV Technology Platform, an adeno-associated virus-based gene delivery system. The company's primary investigational asset, RGX-314, is currently in Phase III clinical trials for treating wet age-related macular degeneration. Its pipeline also includes RGX-121 and RGX-111, both in Phase I/II trials for mucopolysaccharidosis type II and type I, respectively; RGX-181, which is in preclinical development for late-infantile neuronal ceroid lipofuscinosis type II disease; RGX-202, undergoing Phase I/II evaluation for Duchenne muscular dystrophy; and RGX-381, at the preclinical stage for addressing the ocular manifestations of CLN2 disease. In addition to its internal programs, REGENXBIO Inc. licenses its NAV Technology Platform to other biotech and pharmaceutical enterprises. It also maintains a collaborative and licensing agreement with Neurimmune AG for the advancement of innovative gene therapies. Founded in 2008, REGENXBIO Inc. maintains its headquarters in Rockville, Maryland.

Market snapshot

Symbol
RGNX
Price
$7.80
Day change
-1.27%
Market cap
$403.2M
P/E ratio
-1.41x
52-week range
5.455-16.19
Sector
Healthcare
Industry
Biotechnology
Next earnings
in 2 months
Analyst price target
$22.86

Recent news

  • REGENXBIO Advances Duchenne Gene Therapy Toward Accelerated Approval

    REGENXBIO Inc. (NASDAQ:RGNX) on Thursday released topline and interim functional data from the pivotal Phase 1/2/3 AFFINITY DUCHENNE trial evaluating RGX-202, its investigational gene therapy for Duchenne muscular dystrophy.

  • Regenxbio's muscle disorder therapy meets main goal in late-stage study

    Regenxbio said on Thursday that ​its experimental therapy to ‌treat a muscle-wasting disorder met the main goal in ​a late-stage study.

Peer companies

  • Absci Corporation (ABSI)
  • Corvus Pharmaceuticals, Inc. (CRVS)
  • 4D Molecular Therapeutics, Inc. (FDMT)
  • Gossamer Bio, Inc. (GOSS)
  • KalVista Pharmaceuticals, Inc. (KALV)
  • MoonLake Immunotherapeutics (MLTX)
  • Olema Pharmaceuticals, Inc. (OLMA)
  • Prothena Corporation plc (PRTA)

Recent insider activity

  • Tasse Daniel — A-Award (46600 shares) on 2026-05-29
  • Tasse Daniel — A-Award (9807 shares) on 2026-05-29
  • STUMP DAVID C — A-Award (46600 shares) on 2026-05-29
  • STUMP DAVID C — A-Award (9807 shares) on 2026-05-29
  • Zachary Jennifer — A-Award (46600 shares) on 2026-05-29

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