Cellectis (ALCLS) EHA 2026 Congress presentation summary
Event summary combining transcript, slides, and related documents.
EHA 2026 Congress presentation summary
26 Jun, 2026Background and unmet need
Third-line and beyond B-ALL is highly aggressive, with limited treatment options and frequent resistance mutations.
CD22 remains a viable target in relapsed/refractory B-ALL, especially after CD19-directed therapies.
UCART22 product and mechanism
UCART22 is an allogeneic CAR T-cell therapy targeting CD22, engineered to avoid GvHD and resist alemtuzumab-based lymphodepletion.
TALEN® technology disrupts TCR and CD52, enhancing safety and persistence.
Study design and patient characteristics
BALLI-01 Phase 1 trial enrolled 45 heavily pretreated patients (median 4 prior therapies), many with prior blinatumomab, inotuzumab, and CD19 CAR T exposure.
Two manufacturing processes and multiple dose levels were tested, with lymphodepletion regimens including fludarabine, cyclophosphamide, and alemtuzumab.
Latest events from Cellectis
- Pivot to in vivo gene editing with two lead programs and first clinical data expected in 2027–2028.ALCLS
Investor update - FDA RMAT designation, robust clinical progress, and $169M cash offset lower revenues and net loss.ALCLS
H1 2026 - Lead allogeneic CAR-T therapies show strong efficacy and commercial potential.ALCLS
Corporate presentation - Narrowed net loss, robust cash, and pivotal trial progress set up key milestones for late 2026.ALCLS
Q1 2026 - Lead CAR-Ts delivered high response rates; $211M cash runway supports pivotal milestones into H2 2027.ALCLS
Q4 2025 - UCART22 advances to pivotal Phase II; revenue up, net loss widens, $230M cash funds to H2 2027.ALCLS
Q2 2025 - Net loss narrowed, cash runway extended to 2026, and $140M AstraZeneca investment completed.ALCLS
Q2 2024 - Cash runway extended to 2027 as net loss narrows and CAR-T clinical programs advance.ALCLS
Q3 2024 - Q1 2025 revenues up to $12M, net loss $18.1M; cash runway into H2 2027, key data readouts ahead.ALCLS
Q1 2025