Cellectis Announces Arbitral Decision in Dispute with Servier
Rhea-AI Summary
Cellectis (NASDAQ: CLLS) announced an Arbitral Tribunal decision dated December 15, 2025 in its arbitration with Les Laboratoires Servier and IRIS SARL relating to the March 6, 2019 License Agreement.
The Tribunal ordered a partial termination of the License Agreement with respect to product UCART19 V1 (also called ALLO-501) and provided that Cellectis shall, at Allogene’s request, engage in good-faith discussions about granting a direct license to UCART19 V1. All other claims between the parties were dismissed.
Positive
- Arbitral Tribunal decision issued on December 15, 2025
- All other claims between the parties were dismissed
- Tribunal ordered good‑faith discussions for a direct license to UCART19 V1
Negative
- License Agreement partially terminated for UCART19 V1
- Decision changes licensing status of UCART19 V1 (ALLO‑501)
News Market Reaction
On the day this news was published, CLLS gained 2.35%, reflecting a moderate positive market reaction. Argus tracked a trough of -20.0% from its starting point during tracking. Our momentum scanner triggered 16 alerts that day, indicating notable trading interest and price volatility. This price movement added approximately $8M to the company's valuation, bringing the market cap to $354M at that time.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Market Reality Check
Peers on Argus
CLLS fell 10.34% while peers showed mixed moves: ENGN -0.59%, KRRO -4.9%, ABEO -5.75%, GLUE +0.67%, FDMT 0%, pointing to a stock-specific reaction to the arbitration news.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Dec 08 | Clinical data update | Positive | -2.5% | ASH Phase 1 eti-cel data with high ORR and CR rates. |
| Dec 03 | Capital structure update | Neutral | +3.6% | Monthly disclosure of total shares and voting rights. |
| Nov 19 | Scientific publication | Positive | +7.1% | Nature Communications article on non-viral CssDNA gene insertion. |
| Nov 07 | Earnings and pipeline | Positive | +11.3% | Q3 2025 results plus lasme-cel and eti-cel clinical updates. |
| Nov 07 | Capital structure update | Neutral | +1.9% | Monthly report on share count and voting rights. |
Most recent positive scientific/financial updates saw aligned gains, but one strong clinical update drew a modest negative reaction, indicating occasionally contrarian trading around good news.
Over the last months, Cellectis reported multiple developments. On Nov 7, 2025, Q3 results highlighted cash of $225M, nine‑month revenue of $67.4M, and a net loss of $41.3M, with shares rising 11.29%. A Nature Communications paper on Nov 19, 2025 describing efficient non‑viral gene insertion aligned with a 7.06% gain. ASH 2025 eti‑cel data on Dec 8, 2025 showed high response rates but the stock slipped 2.53%. Routine share‑capital updates triggered smaller, generally positive moves.
Regulatory & Risk Context
The company has an active Form F-3 shelf registration filed on 2025-07-02, effective until 2028-07-02, with 0 recorded usages in the provided context, indicating potential but unused capacity for future registered offerings.
Market Pulse Summary
This announcement details an arbitral decision partially terminating the Servier License Agreement for UCART19 V1 and directing good-faith discussions on a potential direct license with Allogene. It follows recent positive clinical and scientific updates, including Q3 2025 data and a Nature Communications paper. Investors may watch for follow-up disclosures on licensing terms, any business update via future Form 6-K filings, and how this interacts with the existing Form F-3 shelf capacity.
Key Terms
arbitral tribunal regulatory
arbitration regulatory
license agreement regulatory
gene-editing medical
cell and gene therapies medical
AI-generated analysis. Not financial advice.
NEW YORK, Dec. 15, 2025 (GLOBE NEWSWIRE) -- Cellectis (the “Company”) (Euronext Growth: ALCLS – NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies, announces that the Arbitral Tribunal has issued its decision in the arbitration proceedings against Les Laboratoires Servier and Institut de Recherches Internationales Servier IRIS SARL (“Servier”), relating to the License, Development and Commercialization Agreement entered into between Servier and Cellectis on March 6, 2019, as amended (the “License Agreement”).
The Tribunal ruled on a partial termination of the License Agreement with respect to product UCART19 V1 (also referred to as “ALLO-501” by Allogene) and provided that Cellectis shall, at Allogene’s request, engage in good-faith discussions regarding the granting of a direct license to product UCART19 V1. All other claims brought by the parties were dismissed.
About Cellectis
Cellectis is a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies. The company utilizes an allogeneic approach for CAR T immunotherapies in oncology, pioneering the concept of off-the-shelf and ready-to-use gene-edited CAR T-cells to treat cancer patients, and a platform to develop gene therapies in other therapeutic indications. With its in-house manufacturing capabilities, Cellectis is one of the few end-to-end gene editing companies that controls the cell and gene therapy value chain from start to finish.
Cellectis’ headquarters are in Paris, France, with locations in New York and Raleigh, NC. Cellectis is listed on the Nasdaq Global Market (ticker: CLLS) and on Euronext Growth (ticker: ALCLS).
To find out more, visit www.cellectis.com and follow Cellectis on LinkedIn and X.
For further information on Cellectis, please contact:
Media contacts:
Pascalyne Wilson, Director, Communications,
+ 33 (0)7 76 99 14 33, media@cellectis.com
Patricia Sosa Navarro, Chief of Staff to the CEO, +33 (0)7 76 77 46 93
Investor Relations contact:
Arthur Stril, Chief Financial Officer & Chief Business Officer, investors@cellectis.com
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