REGENXBIO Shareholder Notice Issued
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 24 2026
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Should l Buy RGNX?
Source: PRnewswire
- Shareholder Notice Issued: The Gross Law Firm has issued a notice encouraging shareholders who purchased REGENXBIO (NASDAQ:RGNX) shares between February 9, 2022, and January 27, 2026, to contact them regarding potential lead plaintiff appointment, although this status is not required for recovery participation.
- Allegations Overview: The complaint alleges that REGENXBIO misled investors about the development of its RGX-111 gene therapy by providing false and misleading information while concealing significant adverse facts related to the clinical trial, resulting in investor losses.
- FDA Clinical Hold: On January 28, 2026, REGENXBIO announced that the FDA placed a clinical hold on RGX-111 after a participant in the trial developed an intraventricular CNS tumor, causing the stock price to plummet by 17.8% in a single day.
- Next Steps for Shareholders: Shareholders must register for the class action by April 14, 2026, and upon registration, they will receive updates on the case's progress through a monitoring system, with no costs or obligations to participate.
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Analyst Views on RGNX
Wall Street analysts forecast RGNX stock price to rise
7 Analyst Rating
7 Buy
0 Hold
0 Sell
Strong Buy
Current: 8.690
Low
19.00
Averages
29.71
High
45.00
Current: 8.690
Low
19.00
Averages
29.71
High
45.00
About RGNX
REGENXBIO Inc. is a clinical-stage biotechnology company seeking to improve lives through the curative potential of gene therapy. The Company has developed a pipeline of gene therapy programs using its proprietary adeno-associated virus (AAV) gene therapy delivery platform (NAV Technology Platform) to address genetic diseases. It is focused on its internal development pipeline in three areas: retinal, neuromuscular, and neurodegenerative diseases. Its investigational AAV therapeutics include ABBV-RGX-314, RGX-202, RGX-121, and RGX-111. It is developing ABBV-RGX-314 in collaboration with AbbVie to treat large patient populations impacted by wet age-related macular degeneration, diabetic retinopathy (DR) and other chronic retinal diseases characterized by loss of vision. It is developing RGX-202 to treat Duchenne muscular dystrophy (Duchenne). The Company is developing RGX-121 to treat Mucopolysaccharidosis type II (MPS II), a progressive, neurodegenerative lysosomal storage disorder.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
REGENXBIO Presents RGX-202 Gene Therapy Updates at MDA Conference
- Clinical Data Presentation: REGENXBIO will showcase clinical data on RGX-202 at the 2026 Muscular Dystrophy Association Conference, including preclinical and Phase I/II safety, biomarker, and functional data, which is expected to bolster investor confidence in the company's R&D capabilities.
- Key Presentation Schedule: Clinical Professor Carolina Tesi Rocha will present oral data on RGX-202 on March 11, 2026, at 11:45 AM, highlighting its potential in treating Duchenne muscular dystrophy, which may attract more attention and collaboration opportunities.
- Poster Presentation Insights: Dr. Steven Foltz from REGENXBIO will present research on microdystrophin's protective effects against pharmacologically induced cardiac damage in mice, further validating RGX-202's therapeutic mechanism and potentially advancing subsequent clinical studies.
- Symposium Details: The company will host a symposium titled “Advancing Duchenne Gene Therapy Trials in a New Era” on March 9, 2026, featuring industry experts discussing optimized trial design and interpretation, aimed at enhancing the understanding and application of gene therapies in the field.
See More
REGENXBIO Investors Urged to Discuss Legal Rights Amid Significant Losses
- Legal Investigation: Faruqi & Faruqi LLP is investigating potential claims against REGENXBIO due to possible false statements made during securities transactions from February 9, 2022, to January 27, 2026, which may have harmed investors' interests.
- Clinical Trial Hold: On January 28, 2026, REGENXBIO announced that the FDA placed a clinical hold on its gene therapies RGX-111 and RGX-121 after a participant developed a tumor, causing the stock price to drop by 17.9% to $11.01 per share, significantly impacting market confidence.
- Class Action Deadline: Investors must apply by April 14, 2026, to serve as lead plaintiffs in the class action lawsuit to represent other affected investors, ensuring their rights are protected in the legal process.
- Information Solicitation: Faruqi & Faruqi LLP is urging anyone with knowledge of REGENXBIO's conduct, including former employees and shareholders, to provide information to support the ongoing legal investigation, enhancing the case's effectiveness.
See More
Notice of Class Action Lawsuit Against REGENXBIO Securities
- Class Action Deadline: Rosen Law Firm reminds investors who purchased REGENXBIO (NASDAQ:RGNX) securities between February 9, 2022, and January 27, 2026, that they must apply to be lead plaintiff by April 14, 2026, to participate in the class action and seek compensation.
- No Upfront Fees: Investors joining the class action will incur no out-of-pocket fees or costs, as the law firm operates on a contingency fee basis, thereby reducing the financial burden on investors.
- Case Background: The lawsuit alleges that defendants provided false and misleading information regarding REGENXBIO's RGX-111 gene therapy development, leading to investor losses when the true facts emerged, negatively impacting the company's reputation and stock price.
- Law Firm Credentials: Rosen Law Firm specializes in securities class actions and has recovered over $438 million for investors in 2019 alone, demonstrating its extensive experience and success in handling such cases, prompting investors to carefully select qualified legal counsel.
See More
REGENXBIO Faces Class Action Lawsuit
- Class Action Initiated: Robbins LLP reminds investors of a class action filed on behalf of shareholders who purchased REGENXBIO (NASDAQ:RGNX) securities between February 9, 2022, and January 27, 2026, highlighting serious concerns regarding the company's transparency and investor communication.
- Drug Candidate Issues: The lawsuit alleges that REGENXBIO misled investors about the safety of its clinical-stage drug RGX-111, which was touted as receiving FDA Fast Track designation and reporting positive clinical results, while serious safety concerns were concealed from the public.
- FDA Clinical Hold: On January 28, 2026, the FDA placed a clinical hold on RGX-111 and RGX-121 due to a reported case of CNS tumor in a trial participant, causing REGENXBIO's stock to plummet 17.8% in one day, from $13.41 to $11.01 per share, reflecting a significant loss of investor confidence.
- Shareholder Action Guidance: Shareholders can submit their papers to become lead plaintiffs in the class action by April 14, 2026, indicating a need for improved corporate governance to protect investor rights, as participation in the lawsuit is not required for potential recovery.
See More
REGENXBIO to Participate in Multiple Investor Conferences
- Investor Conference Schedule: REGENXBIO will participate in the Leerink Partners and Barclays Global Healthcare Conferences on March 9 and 10 in Miami, showcasing its latest advancements in gene therapy, which is expected to attract investor interest and enhance the company's visibility.
- Virtual Conference Participation: The company will also attend the RBC Inaugural Virtual Ophthalmology Conference on March 24, further expanding its influence in the ophthalmology field by presenting its treatment options for wet AMD and diabetic retinopathy.
- Pioneering Gene Therapy: Since its founding in 2009, REGENXBIO has made significant strides in AAV gene therapy, advancing a late-stage pipeline for rare and retinal diseases, demonstrating its leadership position in the biotechnology sector.
- Patient Treatment Potential: The gene therapies developed by the company have provided treatment opportunities for thousands of patients, particularly with ZOLGENSMA® in collaboration with Novartis, indicating the potential of its treatment options to transform healthcare delivery for millions.
See More
Notice of REGENXBIO Securities Class Action
- Class Action Deadline: Purchasers of REGENXBIO, Inc. (NASDAQ: RGNX) securities between February 9, 2022, and January 27, 2026, should note that the deadline to apply as lead plaintiff is April 14, 2026, and failure to act may result in losing the opportunity to represent other investors.
- Lawsuit Context: The lawsuit alleges that defendants misled investors by providing overly positive information about RGX-111 gene therapy while concealing critical adverse facts regarding the trial's safety and efficacy, leading to investor losses when the truth emerged.
- Law Firm Credentials: The Rosen Law Firm specializes in securities class actions and has recovered over $438 million for investors in 2019 alone, being ranked first in 2017 for the number of securities class action settlements, showcasing its expertise and success in this field.
- Participation Instructions: Investors can join the class action by visiting the Rosen Law Firm's website or calling toll-free at 866-767-3653 for more information, with no upfront fees required, ensuring that investor rights are protected.
See More
REGENXBIO Presents RGX-202 Gene Therapy Updates at MDA Conference
- Clinical Data Presentation: REGENXBIO will showcase clinical data on RGX-202 at the 2026 Muscular Dystrophy Association Conference, including preclinical and Phase I/II safety, biomarker, and functional data, which is expected to bolster investor confidence in the company's R&D capabilities.
- Key Presentation Schedule: Clinical Professor Carolina Tesi Rocha will present oral data on RGX-202 on March 11, 2026, at 11:45 AM, highlighting its potential in treating Duchenne muscular dystrophy, which may attract more attention and collaboration opportunities.
- Poster Presentation Insights: Dr. Steven Foltz from REGENXBIO will present research on microdystrophin's protective effects against pharmacologically induced cardiac damage in mice, further validating RGX-202's therapeutic mechanism and potentially advancing subsequent clinical studies.
- Symposium Details: The company will host a symposium titled “Advancing Duchenne Gene Therapy Trials in a New Era” on March 9, 2026, featuring industry experts discussing optimized trial design and interpretation, aimed at enhancing the understanding and application of gene therapies in the field.
See More
REGENXBIO Investors Urged to Discuss Legal Rights Amid Significant Losses
- Legal Investigation: Faruqi & Faruqi LLP is investigating potential claims against REGENXBIO due to possible false statements made during securities transactions from February 9, 2022, to January 27, 2026, which may have harmed investors' interests.
- Clinical Trial Hold: On January 28, 2026, REGENXBIO announced that the FDA placed a clinical hold on its gene therapies RGX-111 and RGX-121 after a participant developed a tumor, causing the stock price to drop by 17.9% to $11.01 per share, significantly impacting market confidence.
- Class Action Deadline: Investors must apply by April 14, 2026, to serve as lead plaintiffs in the class action lawsuit to represent other affected investors, ensuring their rights are protected in the legal process.
- Information Solicitation: Faruqi & Faruqi LLP is urging anyone with knowledge of REGENXBIO's conduct, including former employees and shareholders, to provide information to support the ongoing legal investigation, enhancing the case's effectiveness.
See More
Notice of Class Action Lawsuit Against REGENXBIO Securities
- Class Action Deadline: Rosen Law Firm reminds investors who purchased REGENXBIO (NASDAQ:RGNX) securities between February 9, 2022, and January 27, 2026, that they must apply to be lead plaintiff by April 14, 2026, to participate in the class action and seek compensation.
- No Upfront Fees: Investors joining the class action will incur no out-of-pocket fees or costs, as the law firm operates on a contingency fee basis, thereby reducing the financial burden on investors.
- Case Background: The lawsuit alleges that defendants provided false and misleading information regarding REGENXBIO's RGX-111 gene therapy development, leading to investor losses when the true facts emerged, negatively impacting the company's reputation and stock price.
- Law Firm Credentials: Rosen Law Firm specializes in securities class actions and has recovered over $438 million for investors in 2019 alone, demonstrating its extensive experience and success in handling such cases, prompting investors to carefully select qualified legal counsel.
See More
REGENXBIO Faces Class Action Lawsuit
- Class Action Initiated: Robbins LLP reminds investors of a class action filed on behalf of shareholders who purchased REGENXBIO (NASDAQ:RGNX) securities between February 9, 2022, and January 27, 2026, highlighting serious concerns regarding the company's transparency and investor communication.
- Drug Candidate Issues: The lawsuit alleges that REGENXBIO misled investors about the safety of its clinical-stage drug RGX-111, which was touted as receiving FDA Fast Track designation and reporting positive clinical results, while serious safety concerns were concealed from the public.
- FDA Clinical Hold: On January 28, 2026, the FDA placed a clinical hold on RGX-111 and RGX-121 due to a reported case of CNS tumor in a trial participant, causing REGENXBIO's stock to plummet 17.8% in one day, from $13.41 to $11.01 per share, reflecting a significant loss of investor confidence.
- Shareholder Action Guidance: Shareholders can submit their papers to become lead plaintiffs in the class action by April 14, 2026, indicating a need for improved corporate governance to protect investor rights, as participation in the lawsuit is not required for potential recovery.
See More
REGENXBIO to Participate in Multiple Investor Conferences
- Investor Conference Schedule: REGENXBIO will participate in the Leerink Partners and Barclays Global Healthcare Conferences on March 9 and 10 in Miami, showcasing its latest advancements in gene therapy, which is expected to attract investor interest and enhance the company's visibility.
- Virtual Conference Participation: The company will also attend the RBC Inaugural Virtual Ophthalmology Conference on March 24, further expanding its influence in the ophthalmology field by presenting its treatment options for wet AMD and diabetic retinopathy.
- Pioneering Gene Therapy: Since its founding in 2009, REGENXBIO has made significant strides in AAV gene therapy, advancing a late-stage pipeline for rare and retinal diseases, demonstrating its leadership position in the biotechnology sector.
- Patient Treatment Potential: The gene therapies developed by the company have provided treatment opportunities for thousands of patients, particularly with ZOLGENSMA® in collaboration with Novartis, indicating the potential of its treatment options to transform healthcare delivery for millions.
See More
Notice of REGENXBIO Securities Class Action
- Class Action Deadline: Purchasers of REGENXBIO, Inc. (NASDAQ: RGNX) securities between February 9, 2022, and January 27, 2026, should note that the deadline to apply as lead plaintiff is April 14, 2026, and failure to act may result in losing the opportunity to represent other investors.
- Lawsuit Context: The lawsuit alleges that defendants misled investors by providing overly positive information about RGX-111 gene therapy while concealing critical adverse facts regarding the trial's safety and efficacy, leading to investor losses when the truth emerged.
- Law Firm Credentials: The Rosen Law Firm specializes in securities class actions and has recovered over $438 million for investors in 2019 alone, being ranked first in 2017 for the number of securities class action settlements, showcasing its expertise and success in this field.
- Participation Instructions: Investors can join the class action by visiting the Rosen Law Firm's website or calling toll-free at 866-767-3653 for more information, with no upfront fees required, ensuring that investor rights are protected.
See More
