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CLLS Overview

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$
0.000
0.000(0.000%)
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0.000(0.000%)Aft-market
ET
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0.000
0.000(0.000%)
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ET
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Intellectia

Loading chart...

High
3.100
Open
3.100
VWAP
3.09
Vol
13.48K
Mkt Cap
309.88M
Low
3.070
Amount
41.66K
EV/EBITDA(TTM)
--
Total Shares
100.61M
EV
172.89M
EV/OCF(TTM)
--
P/S(TTM)
3.98
Cellectis SA is a France-based company active in the field of genome engineering and genomic surgery. The Company specializes in the research, development, and commercialization of rational genome engineering technologies. The Company develops immunotherapies that aim to force the immune system to target and eradicate cancer cells. It has developed an expertise in combining meganucleases with engineered targeting Deoxyribonucleic Acid (DNA) matrices into Meganuclease Recombination Systems (MRS), used for gene excision, correction or replacement. Cellectis SA markets its technologies mainly for use in the research field, in pharmaceutical drug discovery programs, in the agronomics, bioproduction, and biotherapeutics fields. Cellectis SA operates several subsidiaries. The Company operates in France and the United States, among others.
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Events Timeline

(ET)
2026-05-11
16:40:00
Cellectis Reports $188 Million in Cash, Sufficient to Fund Operations into Q4 2027
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2026-05-11
16:40:00
Cellectis Q1 Revenue at $7.5M, Below Consensus
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2026-04-13 (ET)
2026-04-13
16:50:00
Cellectis and Allogene's cema-cel Shows Positive Clinical Data
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2025-12-15 (ET)
2025-12-15
17:50:00
Allogene Therapeutics Wins Arbitration Against Cellectis
select
2025-12-15
17:00:00
Cellectis Announces Arbitration Decision Against Servier
select
2025-11-07 (ET)
2025-11-07
16:32:54
Cellectis announces Q3 adjusted EPS of 2 cents compared to a loss of 22 cents in the previous year.
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News

Newsfilter
2.0
06-11Newsfilter
Cellectis Presents Final Phase 1 Data from BALLI-01 Trial
  • BALLI-01 Trial Results: Cellectis presented final Phase 1 data from the BALLI-01 trial at EHA 2026, showing a 100% overall response rate for lasme-cel in relapsed/refractory B-cell acute lymphoblastic leukemia, with 57% achieving complete remission, highlighting the therapy's significant efficacy.
  • Patient Background Analysis: In the BALLI-01 study, 45 patients were treated, with a median of 5 prior lines of therapy in the target population, indicating the potential of this therapy to provide new treatment options for heavily pretreated patients.
  • Safety Assessment: Lasme-cel demonstrated a manageable safety profile, with ≥ grade 3 cytokine release syndrome and neurotoxicity occurring in 4% of patients, and all adverse events resolved, indicating its acceptability in clinical use.
  • NATHALI-01 Preliminary Data: Cellectis also showcased preliminary data from the NATHALI-01 study, targeting relapsed/refractory B-cell non-Hodgkin lymphoma with eti-cel, revealing an 88% overall response rate and 63% complete response rate, emphasizing the importance of optimizing treatment regimens.
seekingalpha
9.0
06-10seekingalpha
Cellectis CAR-T Therapy Receives FDA RMAT Designation
  • FDA Designation Progress: Cellectis' CD22-targeting CAR-T therapy, lasme-cel, has received FDA Regenerative Medicine Advanced Therapy (RMAT) designation, indicating recognition of its potential to address the urgent medical needs of patients with r/r B-ALL, a severe form of leukemia.
  • Clinical Data Support: The RMAT designation is backed by Phase 1 BALLI-01 trial data, which demonstrates promising efficacy and a manageable safety profile, thereby enhancing investor confidence in the therapy's prospects.
  • Future Presentation Plans: Cellectis is set to present final Phase 1 data for lasme-cel at the 2026 Congress of the European Hematology Association on June 13, which is expected to attract further attention and potentially drive subsequent clinical development.
  • Stock Price Reaction: Following the announcement, Cellectis shares rose over 10% in after-hours trading to $3.30, reflecting the market's positive response to the therapy's designation and its potential commercial value.
stocktwits
8.5
06-09stocktwits
Cellectis Receives FDA RMAT Designation, Stock Soars
  • FDA Designation Impact: Cellectis' cell therapy lasmecabtagene timgedleucel has received FDA's Regenerative Medicine Advanced Therapy (RMAT) designation based on early-stage trial data, which, while not guaranteeing approval, provides early and frequent interaction with the FDA and potential acceleration of the approval process.
  • Stock Reaction: Following the RMAT designation, Cellectis' stock surged over 24% in after-hours trading on Tuesday, indicating strong market recognition of the therapy's potential and reflecting investor optimism about the company's future developments.
  • Analyst Rating: Barclays initiated coverage of Cellectis last month with an 'Overweight' rating and a $9 price target, representing a potential upside of approximately 201% from Tuesday's close, further bolstering market confidence in the company's prospects.
  • Therapeutic Advantages: Cellectis views lasmecabtagene timgedleucel as a ready-to-use option for heavily pretreated patients, and unlike personalized autologous therapies, its use of healthy donor cells allows for quicker treatment response times, opening up previously inaccessible treatment settings.
Newsfilter
9.0
06-09Newsfilter
Cellectis Receives FDA RMAT Designation for CAR-T Therapy
  • FDA Designation Progress: Cellectis' CD22-targeting CAR-T cell therapy, lasmecabtagene timgedleucel (lasme-cel), has received Regenerative Medicine Advanced Therapy (RMAT) designation from the FDA, indicating its potential to address the urgent medical needs of patients with relapsed or refractory B-cell acute lymphoblastic leukemia (r/r B-ALL).
  • Clinical Trial Data Support: The RMAT designation is backed by promising Phase 1 data from the BALLI-01 trial, which will present final results at the European Hematology Association Congress on June 13, further bolstering market confidence in the therapy's efficacy and safety profile.
  • Strategic Implications: Cellectis CEO André Choulika noted that the RMAT designation not only recognizes lasme-cel's potential but also strengthens dialogue with the FDA, facilitating the advancement of the therapy through pivotal clinical trials and enhancing the company's competitive position in the CAR-T market.
  • Trial Enrollment Open: The pivotal Phase 2 of the BALLI-01 trial is now open for enrollment, with participant eligibility and clinical center information available on clinicaltrials.gov, marking a significant step forward for Cellectis in the field of cell and gene therapies.
Newsfilter
1.0
05-20Newsfilter
Cellectis to Hold Annual General Meeting on June 25, 2026
  • Annual Meeting Announcement: Cellectis has announced that it will hold its annual general meeting on June 25, 2026, at 2:30 p.m. CET at the Biopark auditorium in Paris, aiming to update shareholders on company developments and future strategies.
  • Gene Editing Platform Advantage: As a clinical-stage biotechnology company, Cellectis leverages its pioneering gene-editing platform to develop life-saving cell and gene therapies, particularly showcasing unique competitive advantages in CAR T immunotherapies for oncology.
  • End-to-End Control Capability: With in-house manufacturing capabilities, Cellectis is one of the few companies that can control the entire value chain of cell and gene therapies, providing it with a significant strategic position in the market.
  • Global Business Presence: Cellectis is headquartered in Paris, France, with additional locations in New York and Raleigh, NC, demonstrating its global business expansion and market penetration capabilities.
Newsfilter
9.5
05-11Newsfilter
Cellectis Reports Q1 2026 Financial Results and Business Update
  • Clinical Trial Progress: Cellectis' BALLI-01 trial for relapsed or refractory B-cell acute lymphoblastic leukemia shows a 100% objective response rate (ORR) in the target population, with the first interim analysis expected in Q4 2026, potentially paving the way for a future Biologics License Application (BLA).
  • Favorable Safety Data: In the ALPHA3 trial for cema-cel, 58.3% of patients achieved minimal residual disease (MRD) negativity compared to 16.7% in the control group, with no serious adverse events reported, indicating strong safety and efficacy that could support future commercialization efforts.
  • Strong Financial Position: As of March 31, 2026, Cellectis reported $188 million in cash and cash equivalents, providing a runway into Q4 2027; despite a $23 million decrease from 2025, the company demonstrates effective financial management.
  • Increased R&D Spending: R&D expenses for Q1 2026 reached $27.2 million, up $5.3 million from the previous year, primarily due to increased personnel and external costs, reflecting the company's commitment to advancing its innovative therapies and enhancing future market competitiveness.
Wall Street analysts forecast CLLS stock price to rise
4 Analyst Rating
Wall Street analysts forecast CLLS stock price to rise
2 Buy
2 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
4.00
Averages
7.00
High
9.00
Current: 0.000
sliders
Low
4.00
Averages
7.00
High
9.00
Barclays
Overweight
initiated
$9
AI Analysis
2026-05-28
Reason
Barclays
Price Target
$9
AI Analysis
2026-05-28
initiated
Overweight
Reason
Barclays initiated coverage of Cellectis with an Overweight rating and $9 price target. The company is focused on the development of allogenic CAR-T therapeutics for various cancers, the analyst tells investors in a research note. The firm says Cellectis' allogenic platform allows for potentially quicker reaction time from diagnosis to treatment than autologous CAR-T therapies, opening up treatment settings that were previously inaccessible.
Clear Street
Bill Maughan
initiated
$9
2025-12-22
Reason
Clear Street
Bill Maughan
Price Target
$9
2025-12-22
initiated
Reason
Clear Street analyst Bill Maughan initiated coverage of Cellectis with a Buy rating and $9 price target. Cellectis has produced "strong" efficacy data from its initial program, lasme-cel in acute lymphoblastic leukemia, and "an encouraging initial efficacy signal" from eti-cel in non-hodgkin's lymphoma, which the firm believes positions Cellectis well to be among the first companies to bring an allogenic CAR-T product for the treatment of hematological cancers to market.
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Valuation Metrics

The current forward P/E ratio for Cellectis SA (CLLS.O) is 0.00, compared to its 5-year average forward P/E of -1.45. For a more detailed relative valuation and DCF analysis to assess Cellectis SA's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-1.45
Current PE
0.00
Overvalued PE
0.20
Undervalued PE
-3.11

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-2.72
Current EV/EBITDA
-2.20
Overvalued EV/EBITDA
-0.36
Undervalued EV/EBITDA
-5.08

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
4.59
Current PS
5.27
Overvalued PS
6.63
Undervalued PS
2.54

Financials

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Whales Holding CLLS

L
Long Focus Capital Management LLC
Holding
CLLS
+13.99%
3M Return
B
Bpifrance Participations SA
Holding
CLLS
+6.02%
3M Return

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Frequently Asked Questions

What is Cellectis SA (CLLS) stock price today?

The current price of CLLS is 3.1 USD — it has increased 0.65

What is Cellectis SA (CLLS)'s business?

Cellectis SA is a France-based company active in the field of genome engineering and genomic surgery. The Company specializes in the research, development, and commercialization of rational genome engineering technologies. The Company develops immunotherapies that aim to force the immune system to target and eradicate cancer cells. It has developed an expertise in combining meganucleases with engineered targeting Deoxyribonucleic Acid (DNA) matrices into Meganuclease Recombination Systems (MRS), used for gene excision, correction or replacement. Cellectis SA markets its technologies mainly for use in the research field, in pharmaceutical drug discovery programs, in the agronomics, bioproduction, and biotherapeutics fields. Cellectis SA operates several subsidiaries. The Company operates in France and the United States, among others.

What is the price predicton of CLLS Stock?

Wall Street analysts forecast CLLS stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for CLLS is7.00 USD with a low forecast of 4.00 USD and a high forecast of 9.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Cellectis SA (CLLS)'s revenue for the last quarter?

Cellectis SA revenue for the last quarter amounts to NaN USD, decreased

What is Cellectis SA (CLLS)'s earnings per share (EPS) for the last quarter?

Cellectis SA. EPS for the last quarter amounts to USD, decreased

How many employees does Cellectis SA (CLLS). have?

Cellectis SA (CLLS) has 229 emplpoyees as of June 20 2026.

What is Cellectis SA (CLLS) market cap?

Today CLLS has the market capitalization of 309.88M USD.