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Ocugen CEO to Present at Oppenheimer Movers in Rare Disease Summit

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Ocugen (NASDAQ: OCGN) announced that Dr. Shankar Musunuri, chairman, CEO, and co-founder, will present at the Oppenheimer Movers in Rare Disease Summit at the Sofitel New York on Thursday, December 11, 2025. The presentation is a fireside chat titled "Fireside Chat with Aldeyra and Ocugen: Setting Sights on Inherited Retinal Dystrophies" scheduled for 9:45–10:05 a.m. ET in the Second Floor Ballroom, Track 1.

Ocugen said its executive team will also hold one-on-one investor meetings to review the company’s gene-modifier therapy platform, clinical development strategy, and expected catalysts in 2026.

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Key Figures

Summit date Thursday, December 11, 2025 Oppenheimer Movers in Rare Disease Summit presentation
Presentation time 9:45–10:05 a.m. ET Fireside chat with Aldeyra and Ocugen
Event location Second Floor Ballroom, Track 1 Summit presentation venue
Catalyst timing 2026 Upcoming catalysts highlighted in investor meetings

Market Reality Check

$1.21 Last Close
Volume Volume 2,578,895 is below the 20-day average of 2,998,464 (relative volume 0.86x). normal
Technical Price $1.21 is trading above the 200-day MA at $1.04, after a 0.83% 24h gain.

Peers on Argus

Peers show mixed moves: FDMT -4.45%, MBX -7.96%, DSGN -5.5% versus BNTC +0.91% and LRMR +8.04%, suggesting stock-specific rather than broad sector action around this CEO summit appearance.

Historical Context

Date Event Sentiment Move Catalyst
Nov 20 Conference presentation Neutral -2.6% CEO presentation at NobleCon21 and investor meetings on strategy.
Nov 05 Earnings update Positive -1.4% Q3 2025 results, financing and clinical progress for OCU400/OCU410ST.
Oct 23 Earnings call setup Neutral +1.3% Scheduled webcast to discuss Q3 2025 results and business update.
Oct 02 Conference schedule Positive +5.4% Participation in three major October conferences and BLA timeline goals.
Sep 15 Licensing deal Positive +12.2% Exclusive Korean OCU400 license with milestones and 25% royalties.
Pattern Detected

Recent conference and business updates often saw positive or modest price gains, while one earnings/business update and one presentation event drew mild negative reactions, showing mixed but generally constructive responses to visibility and partnership news.

Recent Company History

Over the past six months, Ocugen highlighted strategic progress across conferences, financing, and partnerships. In September 2025, a Korean OCU400 license with potential milestones drove a 12.15% gain. October conference participation and BLA goals coincided with a 5.36% rise. Earnings and business updates in November 2025 produced modest declines despite financing and clinical milestones. The latest November conference presentation saw a small pullback. Today’s Oppenheimer rare disease summit appearance continues this pattern of investor-focused visibility and discussion of the modifier gene therapy platform and upcoming catalysts.

Market Pulse Summary

This announcement highlights Ocugen’s continued visibility push, with its CEO presenting at the Oppenheimer Movers in Rare Disease Summit and holding investor meetings. It reinforces focus on a novel modifier gene therapy platform and a gene-agnostic approach for rare and age-related blindness diseases. In recent months, the company combined licensing deals, conference exposure, and financing activity with ambitions for multiple BLAs. Investors may watch upcoming 2026 catalysts, funding developments, and progress in inherited retinal dystrophies.

Key Terms

gene therapies medical
"a pioneering biotechnology leader in gene therapies for blindness diseases"
Gene therapies are medical treatments that change or replace a person’s genetic instructions to fix or counteract a disease, using biological delivery methods to get the new material into cells — like repairing or swapping pages in a faulty instruction manual. They matter to investors because they can offer one-time or long-lasting cures with large market potential, but carry high development costs, regulatory scrutiny and manufacturing challenges that make outcomes binary and investment risky.
modifier gene therapy medical
"sharing more about Ocugen’s novel modifier gene therapy platform"
Modifier gene therapy is a treatment that changes the activity of genes that influence how severe or how a disease progresses, rather than directly fixing the original faulty gene. Think of it as turning a volume knob on disease symptoms: it can make conditions milder or slow progression, which matters to investors because it can expand the number of patients who benefit, affect how quickly and cheaply a product can reach the market, and change commercial and regulatory risk and reward.

AI-generated analysis. Not financial advice.

MALVERN, Pa., Dec. 10, 2025 (GLOBE NEWSWIRE) -- Ocugen, Inc. (Ocugen or the Company) (NASDAQ: OCGN), a pioneering biotechnology leader in gene therapies for blindness diseases, today announced that Dr. Shankar Musunuri, Chairman, CEO, and Co-founder, will present at the Oppenheimer Movers in Rare Disease Summit taking place at the Sofitel New York on Thursday, December 11, 2025.

“For the second year in a row, we will join leaders advancing groundbreaking discoveries for rare disease at this significant meeting,” said Dr. Musunuri. “I look forward to sharing more about Ocugen’s novel modifier gene therapy platform with a gene-agnostic approach that has the potential to treat the entire disease and in turn large patient populations—in both rare and age-related blindness diseases.”

Details regarding the fireside chat are as follows:
Title: Fireside Chat with Aldeyra and Ocugen: Setting Sights on Inherited Retinal Dystrophies
Date: Thursday, December 11, 2025
Location: Second Floor Ballroom, Track 1
Time: 9:45-10:05 a.m. ET  

In addition to Dr. Musunuri’s session, members of Ocugen’s executive team will conduct one-on-one meetings with investors to highlight the Company’s business and clinical development strategy and upcoming catalysts in 2026.

About Ocugen, Inc.
Ocugen, Inc. is a pioneering biotechnology leader in gene therapies for blindness diseases. Our breakthrough modifier gene therapy platform has the potential to address significant unmet medical need for large patient populations through our gene-agnostic approach. Unlike traditional gene therapies and gene editing, Ocugen’s modifier gene therapies address the entire disease—complex diseases that are potentially caused by imbalances in multiple gene networks. Currently we have programs in development for inherited retinal diseases and blindness diseases affecting millions across the globe, including retinitis pigmentosa, Stargardt disease, and geographic atrophy—late stage dry age-related macular degeneration. Discover more at www.ocugen.com and follow us on X and LinkedIn.

Cautionary Note on Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995, which are subject to risks and uncertainties. We may, in some cases, use terms such as “predicts,” “believes,” “potential,” “proposed,” “continue,” “estimates,” “anticipates,” “expects,” “plans,” “intends,” “may,” “could,” “might,” “will,” “should,” or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Such statements are subject to numerous important factors, risks, and uncertainties that may cause actual events or results to differ materially from our current expectations. These and other risks and uncertainties are more fully described in our periodic filings with the Securities and Exchange Commission (SEC), including the risk factors described in the section entitled “Risk Factors” in the quarterly and annual reports that we file with the SEC. Any forward-looking statements that we make in this press release speak only as of the date of this press release. Except as required by law, we assume no obligation to update forward-looking statements contained in this press release whether as a result of new information, future events, or otherwise, after the date of this press release.

Contact:
Tiffany Hamilton
AVP, Head of Communications
Tiffany.Hamilton@ocugen.com 


FAQ

When will Ocugen (OCGN) present at the Oppenheimer Movers in Rare Disease Summit?

Ocugen will present on December 11, 2025, with the fireside chat at 9:45–10:05 a.m. ET.

What is the title of Ocugen's (OCGN) presentation at the December 11, 2025 summit?

The session is titled "Fireside Chat with Aldeyra and Ocugen: Setting Sights on Inherited Retinal Dystrophies".

Who from Ocugen (OCGN) will speak at the Oppenheimer Rare Disease Summit?

Dr. Shankar Musunuri, chairman, CEO, and co-founder, will deliver the fireside chat and represent the company.

Where is Ocugen's (OCGN) fireside chat being held on December 11, 2025?

The fireside chat will be held at the Sofitel New York, Second Floor Ballroom, Track 1.

Will Ocugen (OCGN) meet with investors at the summit and what will they discuss?

Yes; Ocugen's executive team will hold one-on-one investor meetings to discuss the gene-modifier therapy platform, clinical development strategy, and 2026 catalysts.

What therapeutic focus will Ocugen (OCGN) highlight at the Oppenheimer summit?

Ocugen will highlight its novel modifier gene therapy platform and its gene-agnostic approach for inherited and age-related blindness diseases.
Ocugen Inc

NASDAQ:OCGN

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374.78M
307.65M
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17.46%
Biotechnology
Biological Products, (no Disgnostic Substances)
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United States
MALVERN