Cellectis S.A., a clinical stage biotechnological company, develops products based on gene-editing with a portfolio of allogeneic chimeric antigen receptor T-cells product candidates in the field of immuno-oncology and gene therapy product candidates in other therapeutic indications. The company is developing ALLO-501 to treat large B-cell lymphoma; ALLO-316, a gene-edited allogeneic CAR T-cell product targeting CD70; ALLO-819 to treat acute myeloid leukemia; ALLO-213 for the treatment of small cell lung cancer; and ALLO-182 to treat gastric and pancreatic cancer. It also develops UCART22 for the treatment of relapsed or refractory B-cell acute lymphoblastic leukemia; UCART123 to treat acute myeloid leukemia; UCART 20x22 for relapsed or refractory B-Cell non-hodgkin's lymphoma; and cema-cel to treat relapsed/refractory chronic lymphocytic leukemia/small lymphocytic lymphoma. The company was founded in 1999 and is headquartered in Paris, France. Show more

8, rue de la Croix Jarry, Paris, 75013, France

Biotechnology
Healthcare
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Market Cap

398.3M

52 Wk Range

$1.10 - $5.48

Previous Close

$3.90

Open

$3.96

Volume

39,876

Day Range

$3.92 - $4.04

Enterprise Value

237M

Cash

190.2M

Avg Qtr Burn

-1.571M

Insider Ownership

0.00%

Institutional Own.

17.04%

Qtr Updated

09/30/25


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Drug & IndicationStage & EventCatalyst Date
UCART22 Details
Relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL)

Phase 1/2

Update

UCART123 Details
Cancer, Relapsed/refractory acute myeloid leukemia

Phase 1

Data readout

UCART20x22 Details
Cancer, Non-Hodgkin lymphoma

Phase 1

Data readout

ALLO-715 Details
Cancer, Multiple myeloma

Failed

Discontinued

UCARTCS1 Details
Cancer, Multiple myeloma, Menkes Disease

Failed

Discontinued

UCART19 (anti-CD19) Details
Cancer, Multiple myeloma, Acute lymphoblastic leukemia

Failed

Discontinued

ALLO-501 Details
Non-Hodgkin lymphoma, Cancer

Failed

Discontinued