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portfolios on TandT
Bookmarked by
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Avg position size
—
of holders' portfolios
13F filers
0
institutions
Market cap
$284.7M
101M shares
52-week range
$1.42 – $5.48
37% from low
Exchange
NASDAQ
ADRC
Borrow rate
0.31%
Easy to borrow
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| 2018 | 2019 | 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | |
|---|---|---|---|---|---|---|---|---|
| Revenue | $12.7M | $15.2M | $51.1M | $30.3M | $19.2M | $755.0K | $41.5M | $72.9M |
| Cost of revenue | $2.7M | $11.4M | $2.0M | $1.8M | $8.5M | $7.4M | $9.2M | $9.8M |
| Gross profit | $10.0M | $3.8M | $49.1M | $28.5M | $10.7M | −$6.7M | $32.3M | $63.2M |
| Gross margin | 78.5% | 25.0% | 96.2% | 93.9% | 55.7% | -882.6% | 77.9% | 86.6% |
| R&D | $76.6M | $92.0M | $77.0M | $117.8M | $97.5M | $87.6M | $90.5M | $93.5M |
| Operating income | −$105.1M | −$123.6M | −$42.3M | −$103.5M | −$89.7M | −$97.3M | −$59.6M | −$33.1M |
| EBITDA | −$93.8M | −$105.7M | −$43.3M | −$78.4M | −$76.4M | −$92.6M | −$9.5M | −$39.8M |
| Net income | −$78.7M | −$102.1M | −$81.1M | −$114.2M | −$106.1M | −$101.1M | −$36.8M | −$67.6M |
| Net margin | -618.1% | -672.1% | -158.8% | -376.3% | -553.6% | -13385.3% | -88.6% | -92.7% |
| EPS (diluted) | -1.93 | -2.14 | -1.71 | -1.93 | -2.33 | -1.77 | -0.41 | -0.68 |
Annual figures · source: Financial Modeling Prep
| Year | Est. revenue | Est. EPS | EPS range | # Analysts |
|---|---|---|---|---|
| 2026 | $61M | $-0.92 | $-1.26–$-0.74 | 6 |
| 2027 | $118M | $-0.74 | $-1.10–$-0.50 | 5 |
| 2028 | $73M | $-1.30 | $-2.51–$-0.36 | 2 |
| 2029 | $80M | $-1.46 | $-2.80–$-0.40 | 1 |
Forward consensus · source: Financial Modeling Prep
Cellectis SA is a clinical stage biotechnological company, employing the core proprietary technologies to develop products based on gene-editing, with a portfolio of allogeneic Chimeric Antigen Receptor T-cells, or UCART, product candidates in the field of immuno-oncology and gene-edited hematopoietic stem and progenitor cells, or HSPC product candidates in other therapeutic indications.
www.cellectis.comNo one on the platform currently holds CLLS.
No tracked institution reports a position in CLLS as of their last filing.
No one on the platform has traded CLLS yet.
| $985M |
| — |
| DBVTDBV Technologies S.A. | $16.00 | -0.06% | $383M | — |
| DRTSAlpha Tau Medical Ltd | $11.22 | +3.13% | $1.0B | — |
Source: Financial Modeling Prep · peers by sector/industry
Click to see transaction details on SEC.gov. Form 4s cover trades by officers, directors, and 10%+ owners, due within 2 business days of the trade.
$CLLS shared final Phase 1 data showing 100% response rate for lasme‑cel and promising early results for eti‑cel at the EHA 2026 Congress.
View on StockTwits ↗$CLLS (+5.4% pre) Cellectis receives FDA RMAT designation for blood cancer therapy https://ooc.bz/l/104705
View on StockTwits ↗CLLS Stock Rallies Over 24% After Hours — Here's Why $CLLS https://stocktwits.com/news/equity/markets/clls-stock-rallies-after-hours-heres-why/cZ0UqzWR7Rq
View on StockTwits ↗After Hours Top Gainers PT2 $CLLS $HKPD $HKIT $YYGH $CGTL
View on StockTwits ↗$CLLS got FDA RMAT for lasme-cel, an off-the-shelf CAR-T therapy for hard-to-treat leukemia that may speed up patient access. https://notreload.xyz/xy/fda-grants-rmat-to-cellectis-lasme-cel-car-t-therapy/
View on StockTwits ↗$CLLS up 13.31% Cellectis Secures FDA Regenerative Medicine Advanced Therapy Designation For lasme-cel, CD22-Targeting Allogeneic CAR-T Cell Therapy Product Candidate, For Treatment Of r/r B-ALL $CLLS $XBI
View on StockTwits ↗$CLLS Share Price: $3.67 Contract Selected: Nov 20, 2026 $2.5 Calls Buy Zone: $1.99 – $2.46 Target Zone: $3.33 – $4.07 Potential Upside: 58% ROI Time to Expiration: 177 Days | Updates via https://fxcapta.com/stockinfo/
View on StockTwits ↗$CLLS LTC deal is just another frivolous suit. It’s an another he said she said bullshit claim to get at that cash. Argh… Just another money grab eh RK. At the same time there could be some credibility. Licensing can be a fickle thing. It can also be simply adjusted to rectify. This shit happens all the time. I see this as posturing. Someone woke up, saw the glitch with some good hard legal beagle work and here we stand. Cellectis runs a tight ship. I see this as nothing. But Cellectis is my Baby. And no one puts Baby in the corner.
View on StockTwits ↗$CLLS On April 20, 2026, Life Technologies Corporation ("LTC"), a subsidiary of Thermo Fisher, claimed to terminate licensing agreements between LTC and Cellectis in 2014, which grant Cellectis non-exclusive rights under certain patents, namely Halle Patent Therapeutic License, Halle Patent Research License and GeneArt and Seamless Cloning Patent Therapeutic License (the "LTC Agreements"). This alleged termination follows TFS's allegations that we did not comply with our obligations under the LTC Agreements, as previously indicated. Simultaneously, LTC brought arbitration proceedings before the American Arbitration Association, designating Cellectis S.A. and Cellectis Bioresearch, Inc. as defendants. LTC's arbitration request alleges that Cellectis violated the LTC Agreements, by underpaying sub-licensing fees and more generally by not complying with our obligations under the LTC Agreements.
View on StockTwits ↗$CLLS Cellectis announced two presentations at the European Hematology Association (EHA) 2026 congress: 🔵 Lasme-cel - Oral presentation | June 13 The full Phase 1 BALLI-01 dataset highlight the promising safety profile and response rates in patients with r/r B-ALL, who have relapsed following multiple prior targeted therapies including autologous CD19 CAR-T. These data form the basis for our pivotal Phase 2 program, currently recruiting in Europe and North America. ➡️ First interim pivotal Phase 2 analysis expected in Q4 2026. 🔵 Eti-cel - Poster presentation | June 13 Early mechanistic insights from the NATHALI-01 study in r/r B-NHL, exploring how lymphodepletion optimization drives cellular expansion and clinical response for our dual-targeting CD20×CD22 allogeneic CAR-T. ➡️ Full Phase 1 data expected in Q4 2026.
View on StockTwits ↗$CLLS ASGCT abstract 3414 In vivo targeted gene insertion using AAV and LNP formulated TALEN mRNA drives phenylalanine lowering and metabolic rescue in a PKU model 1Alexion Pharmaceuticals, Cambridge, MA, United States, 2Cellectis, New York, NY, United States, 3Astrazeneca 4Cellectis, Paris, France, 5Alexion Pharmaceuticals, Boston, MA, Phenylketonuria (PKU) is caused by inherited deficiency of phenylalanine hydroxylase (PAH), most often due to missense PAH mutations, impairing conversion of phenylalanine to tyrosine. Elevated phenylalanine in blood and brain causes neurotoxicity and developmental impairment. Current standard of care including life-long dietary protein restriction and approved therapies such as sapropterin and pegvaliase are either ineffective or carry black box warnings, underscoring the need for new therapies.
View on StockTwits ↗Recent $TICKER stream from stocktwits.com — refreshed every 5 minutes. Sentiment tags are self-reported by posters. Not investment advice.
Trading at 5.5× sales vs its 8.5× historical median P/S.
Fair value ≈ $4.50 · price $2.94 today
Fair-value line = the stock's median historical P/S × sales per share. Price below the orange line = cheap vs its own history; above = expensive. Not investment advice.