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
Market Cap
344M
52 Wk Range
$1.10 - $5.48
Previous Close
$3.42
Open
$3.59
Volume
22,132
Day Range
$3.43 - $3.64
Enterprise Value
267.6M
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 & Indication | Stage & Event | Catalyst 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 | |
UCARTCS1 Details Cancer, Multiple myeloma, Menkes Disease | Failed Discontinued | |
ALLO-501 Details Non-Hodgkin lymphoma, Cancer | Failed Discontinued | |
UCART19 (anti-CD19) Details Cancer, Multiple myeloma, Acute lymphoblastic leukemia | Failed Discontinued | |
ALLO-715 Details Cancer, Multiple myeloma | Failed Discontinued |
