Financials
Cash Data
- Monthly Burn
- Burn Trend
- Dilution Risk
- SEC Filing
Key Stats
Upcoming Catalysts
FDA decisions, readouts and PDUFA dates · scored by probability of approval
| Catalyst | Drug / Treatment | Stage | Prob. of Approval | Description | Drug Type | Therapeutic Area | Source |
|---|---|---|---|---|---|---|---|
PDUFA 2026 | Example Drug Treatment for example condition requiring FDA review | Phase 3 | Small Molecule | Oncology | - |
ABEO Catalyst Timeline
Dated clinical, regulatory and corporate events for Abeona Therapeutics Inc.
Catalyst Timeline
Dated clinical, regulatory & corporate events for Abeona Therapeutics Inc.
Upcoming catalysts 2
Event history 50
Past FDA Catalysts and PDUFA Decisions
How ABEO actually traded into and out of each decision
| Date | Drug | Catalyst | Stage | Reaction | Event Move % | Best Trade % |
|---|---|---|---|---|---|---|
| 2025-04-29 | Prademagene zamikeracel (pz-cel) | PDUFA Date Approved | PDUFA |
Drug Pipeline Intelligence
| Product | Revenue | Prior period | Change |
|---|---|---|---|
| ZEVASKYN | $23M | - | - |
| Drug | Indication | Phase | PTRS | rNPV | Status | Enroll | Velocity | Design | Est. Completion | ML Signal | Last Change |
|---|---|---|---|---|---|---|---|---|---|---|---|
| LZRSE-Col7A1 Engineered Autologous Epidermal Sheets Monoclonal antibodyCompletedNCT01263379 | Epidermolysis Bullosa Dystrophica | Phase 1 | COMPLETED | 12 | Mar 9, 2022 |
Clinical Trial Results
Readouts, endpoints and source filings for every ABEO program
| Drug Name | Indication | Phase | Date | Trial Results Summary | Title | Source |
|---|---|---|---|---|---|---|
| ZEVASKYN PriorityOrphanRare Pediatric | recessive dystrophic epidermolysis bullosa | Phase 3 | 2025-06-24 | significant improvements in wound healing and pain reduction following a single treatmentRead More | Abeona Therapeutics Announces Publication in The Lancet of Phase 3 VIITAL™ Study Data in Recessive Dystrophic Epidermolysis BullosaRead More |
Inside Trades
| Insider | Side | Shares | Price | Value | Date |
|---|---|---|---|---|---|
| Vasanthavada MadhavOfficer (Chief Commercial Officer) | Sell | -4,902 285,721 held | $5.16 | 09/29/2026 |
Hedge Fund 13F Activity
Hedge Funds invested in ABEO
| Fund | % of Portfolio | Current MV | Shares Owned | Activity |
|---|---|---|---|---|
| SILVERARC CAPITAL MANAGEMENT, LLC | 0.4 % (33.3 %) | 3.77 M | 610.41 K | -5.94% ( -38.53 K) |
ABEO Institutional Ownership Trends
Options Data
Option Volume
Option Chain Statistics
| Expiry | Call Vol | Put Vol | Vol P/C | Call OI | Put OI | OI P/C | IV Call | IV Call OI-Wtd | IV Call Vol-Wtd | IV Put | IV Put OI-Wtd | IV Put Vol-Wtd |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2026-10-16 | ||||||||||||
Real-Time Option Chain
| Calls | Strike | Puts | ||||
|---|---|---|---|---|---|---|
| Last | Vol | OI | Last | Vol | OI | |
| No data available | ||||||
Calls vs Puts by Expiry
Competitive positioning
How ABEO ranks across every disease it competes in
ABEO News
Abeona Therapeutics® Announces New Employee Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Abeona Therapeutics announced the granting of equity awards to new non-executive employees as an inducement to employment, in compliance with Nasdaq Listing Rule 5635(c)(4). The awards, totaling up to 7,200 restricted shares, will vest over three years. This move reflects the company's commitment to attract and retain talent while advancing its gene therapy initiatives.
Read more →Abeona Therapeutics® Congratulates Ultragenyx on U.S. FDA Approval of FAYUVI™ Gene Therapy for Sanfilippo Syndrome Type A (MPS IIIA)
Abeona Therapeutics congratulated Ultragenyx on the FDA approval of FAYUVI, a gene therapy for Sanfilippo syndrome type A. This approval marks a significant achievement for patients suffering from this rare disease, which has limited treatment options. The therapy was developed from research at The Ohio State University and was advanced by Abeona before being licensed to Ultragenyx. Abeona is set to receive milestone payments and royalties from future sales.
Read more →Abeona Therapeutics® Announces Activation of University of Florida Health as Newest Qualified Treatment Center for ZEVASKYN®
Abeona Therapeutics has activated the University of Florida Health as the eighth Qualified Treatment Center for ZEVASKYN, a gene-modified therapy for recessive dystrophic epidermolysis bullosa (RDEB). This partnership aims to enhance access to innovative treatment for patients in Florida and the Southeastern U.S. ZEVASKYN is designed to improve wound healing in RDEB patients by incorporating the COL7A1 gene into their skin cells.
Read more →Abeona Therapeutics® Announces Participation in Upcoming Investor Conferences
Abeona Therapeutics Inc. announced its participation in several investor conferences in September 2026. The events include the Cantor Global Healthcare Conference, H.C. Wainwright 28th Annual Global Investment Conference, and Morgan Stanley 24th Annual Global Healthcare Conference. Management will engage in fireside chats and investor meetings, enhancing the company's visibility in the investment community.
Read more →Abeona Therapeutics® Reports Second Quarter 2026 Results and Provides Business Update
Abeona Therapeutics reported a 31% increase in ZEVASKYN revenue for Q2 2026, totaling $11.4 million. The company treated five patients with ZEVASKYN in Q2 and expanded its qualified treatment center network to seven sites. Notably, ZEVASKYN received CMS New Technology Add-On Payment status, expected to improve access for Medicare patients. However, the company reported a net loss of $(20.2) million for the quarter.
Read more →Abeona Therapeutics® to Host Second Quarter 2026 Financial Results Conference Call on August 13, 2026
Abeona Therapeutics Inc. will hold a conference call on August 13, 2026, to discuss its second quarter financial results and provide a corporate update. The call will be accessible via phone and a live webcast. The company is known for its development of cell and gene therapies, including ZEVASKYN for treating RDEB.
Read more →CMS Grants New Technology Add-On Payment (NTAP) Status for ZEVASKYN®
Abeona Therapeutics announced that CMS has granted New Technology Add-On Payment (NTAP) status for ZEVASKYN, enhancing reimbursement for this innovative therapy. This designation aims to support patient access and treatment center economics. ZEVASKYN is the first autologous cell sheet-based gene therapy for treating wounds in patients with recessive dystrophic epidermolysis bullosa (RDEB).
Read more →Cincinnati Children's Activated as the Seventh Qualified Treatment Center for ZEVASKYN®
Abeona Therapeutics has announced the activation of Cincinnati Children's as the seventh Qualified Treatment Center for ZEVASKYN, a novel gene-modified therapy for recessive dystrophic epidermolysis bullosa (RDEB). This collaboration aims to improve access to ZEVASKYN for patients suffering from this severe skin condition. The therapy has shown promising results in wound healing and pain reduction.
Read more →Abeona Therapeutics Announces New Employee Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Abeona Therapeutics announced the granting of equity awards to new non-executive employees under Nasdaq Listing Rule 5635(c)(4). On May 31, 2026, the company's Compensation Committee approved 13,800 restricted shares as an inducement for the seven newly hired individuals. The vesting period for these awards spans three years, contingent upon continued employment. This move underscores Abeona's strategy to attract and retain talented personnel as it continues to develop its pipeline of cell and gene therapies.
Read more →Abeona Therapeutics Announces Participation in Upcoming Investor Conferences
Abeona Therapeutics Inc. will participate in significant investor conferences in June 2026, including the Jefferies Global Healthcare Conference and the Goldman Sachs Annual Global Healthcare Conference. The management team will engage with investors, highlighting their focus on advancing cell and gene therapies for serious diseases. The events will also feature a live webcast of a fireside chat, accessible on their website. This engagement reflects Abeona's commitment to their innovative therapies and maintaining investor relations.
Read more →Abeona Therapeutics® Reports First Quarter 2026 Results and Provides Pipeline Update
Abeona Therapeutics reported strong first quarter results for 2026, highlighting increased adoption of ZEVASKYN with three patients treated. The company expanded its qualified treatment center network to six sites, enhancing patient access. Financially, Abeona saw a significant rise in net product revenue, although it also reported a net loss of $(17.1) million for the quarter.
Read more →Abeona Therapeutics® Announces Activation of Children's Hospital of Philadelphia as a New Qualified Treatment Center for ZEVASKYN®
Abeona Therapeutics has announced the activation of the Children's Hospital of Philadelphia as a Qualified Treatment Center for ZEVASKYN, a gene-modified therapy for recessive dystrophic epidermolysis bullosa (RDEB). This collaboration aims to improve access to treatment for patients in the east coast. ZEVASKYN has demonstrated significant wound healing and pain reduction, although there are potential risks associated with its use.
Read more →Abeona Therapeutics® Announces Date of First Quarter Financial Results
Abeona Therapeutics Inc. announced a conference call scheduled for May 13, 2026, to discuss its first quarter financial results and corporate progress. The call will be accessible via phone and webcast. The company is known for its ZEVASKYN gene therapy, which targets recessive dystrophic epidermolysis bullosa, and is actively developing additional therapies.
Read more →Abeona Therapeutics® Announces Appointment of Keith A. Goldan to its Board of Directors
Abeona Therapeutics has appointed Keith A. Goldan to its Board of Directors as of April 1, 2026. Goldan, who has over two decades of financial leadership experience, will also chair the Audit Committee. His expertise is anticipated to support Abeona's growth as a commercial-stage biotech company, particularly in advancing its strategic priorities.
Read more →Abeona Therapeutics® Announces New Qualified Treatment Center for ZEVASKYN® in New York
Abeona Therapeutics has activated NewYork-Presbyterian/Columbia University Irving Medical Center as a Qualified Treatment Center for ZEVASKYN, enhancing patient access in the Northeast. This partnership aims to provide world-class care for patients with recessive dystrophic epidermolysis bullosa (RDEB). ZEVASKYN is the first gene-modified cellular therapy for this condition, demonstrating significant healing potential.
Read more →