Press Releases April 23, 2026 08:30 AM

Vericel to Report First-Quarter 2026 Financial Results on May 7, 2026

Vericel Corporation Schedules Q1 2026 Financial Results Release and Conference Call for May 7, 2026

By Ajmal Hussain
Share
Twitter Reddit Facebook LinkedIn
VCEL

Vericel Corporation announced that it will report its first-quarter 2026 financial results on May 7, 2026. The company will hold a conference call and webcast to discuss the financial results and business highlights. Vericel specializes in advanced therapies for sports medicine and severe burn care, marketing three main products in the United States.

Vericel to Report First-Quarter 2026 Financial Results on May 7, 2026
VCEL
Summarize with
ChatGPT Perplexity Claude Grok Gemini

Key Points

  • Vericel focuses on advanced cell therapies for sports medicine and severe burn care, with products including MACI, Epicel, and NexoBrid.
  • The company is set to release its Q1 2026 financial results and host an investor conference call on May 7, 2026.
  • Vericel holds exclusive North American rights to NexoBrid, an orphan product for eschar removal in burn patients.

CAMBRIDGE, Mass., April 23, 2026 (GLOBE NEWSWIRE) -- Vericel Corporation (NASDAQ:VCEL), a leader in advanced therapies for the sports medicine and severe burn care markets, today announced that the Company will report its first-quarter 2026 financial results on Thursday, May 7, 2026. Vericel’s management will host a conference call and webcast at 8:30 a.m. ET to discuss its financial results and business highlights.

The live webcast can be accessed on the Investor Relations section of the Vericel website at http://investors.vcel.com/events-presentations. Presentation slides for the conference call will be available on the webcast and on the website. A replay of the webcast will be available until May 7, 2027.

To participate by telephone, dial 800-330-6730 or +1-312-471-1351 if connecting from outside the U.S. When connected, please use passcode: 244506.

About Vericel Corporation
Vericel is a leading provider of advanced therapies for the sports medicine and severe burn care markets. The Company combines innovations in biology with medical technologies, resulting in a highly differentiated portfolio of innovative cell therapies and specialty biologics that repair injuries and restore lives. Vericel markets three products in the United States. MACI® (autologous cultured chondrocytes on porcine collagen membrane) is an autologous cellularized scaffold product indicated for the repair of symptomatic, single or multiple full-thickness cartilage defects of the knee with or without bone involvement in adults. Epicel® (cultured epidermal autografts) is a permanent skin replacement for the treatment of patients with deep dermal or full thickness burns greater than or equal to 30% of total body surface area. Vericel also holds an exclusive license for North American rights to NexoBrid® (anacaulase-bcdb), a biological orphan product containing proteolytic enzymes, which is indicated for eschar removal in adults and pediatric patients with deep partial-thickness and/or full-thickness burns. For more information, please visit www.vcel.com. Epicel and MACI are registered trademarks of Vericel Corporation. NexoBrid is a registered trademark of MediWound Ltd. and is used under license to Vericel Corporation. © 2026 Vericel Corporation. All rights reserved.

Investor Contact:
Eric Burns
ir@vcel.com
+1 (734) 418-4411


Risks

  • Financial results could underperform market expectations, potentially impacting stock performance in biotech and healthcare sectors.
  • Dependencies on regulatory approvals and market adoption of advanced therapies in regenerative medicine and burn care.
  • Competition in biotechnology and specialty biologics markets; potential challenges in product sales or reimbursement.

More from Press Releases

Agios Showcases RISE UP Phase 3 Results at EHA 2026 Plenary Session Reinforcing Strong Anti-Hemolytic Profile of Mitapivat in Sickle Cell Disease Jun 13, 2026 Rhythm Pharmaceuticals Presents Positive Interim Six-month Data from Phase 2 Trial of Setmelanotide in Patients with Prader-Willi Syndrome (PWS) at ENDO 2026 Jun 13, 2026 Intellia Therapeutics Reports Additional Positive Phase 3 Results for Lonvoguran Ziclumeran (lonvo-z) in Patients with Hereditary Angioedema Jun 13, 2026 Arcadia Biosciences (RKDA) Announces Closing of $4 Million Private Placement Priced At-The-Market Under Nasdaq Rules Jun 12, 2026 Belite Bio Completes Rolling Submission of New Drug Application to U.S. Food and Drug Administration for Tinlarebant for the Treatment of Stargardt Disease Type 1 Jun 12, 2026