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Noticias de ALLO
Eventos de ALLO
Allogene Therapeutics CFO Geoffrey Parker to Retire on November 6
Allogene Therapeutics announced that Geoffrey Parker, executive VP and CFO, will retire effective November 6. Parker will continue to lead the finance organization through his retirement date as the company conducts an external search for his successor.
Allogene Therapeutics Files $500M Mixed Securities Shelf
Allogene Therapeutics files $500M mixed securities shelf
Allogene Reports Q2 Revenue of $4.64M, Exceeding Expectations
Reports Q2 revenue $4.64M, consensus $2,220. "When we reset our strategy in 2024, we started with the patient and focused on where the distinct attributes of allogeneic CAR T could create a clinical advantage," said Zachary Roberts, President and Chief Executive Officer of Allogene. "ALPHA3 is the clearest expression of that strategy: identifying patients at high risk of relapse, treating before disease returns clinically, and enabling CAR T delivery where patients already receive care. We took the same patient-first approach with ALLO-329, recognizing early that chemotherapy-based lymphodepletion and treatment interruptions associated with leukapheresis in autologous therapy could create meaningful burdens for patients with autoimmune disease. Together, these programs demonstrate that the value of allogeneic CAR T extends well beyond off-the-shelf availability, offering the flexibility to address clinical and practical barriers other approaches cannot. We believe the scale of that opportunity will become increasingly apparent as our programs continue to advance."
Allogene Therapeutics Receives FDA RMAT and Fast Track Designations
Allogene Therapeutics announced that the FDA has granted Regenerative Medicine Advanced Therapy, or RMAT, and Fast Track designations to cemacabtagene ansegedleucel for the treatment of adult patients with large B-cell lymphoma who, at the completion of first-line therapy, are in complete or partial response suitable for observation but test positive for minimal residual disease. Together, the designations enable more frequent FDA engagement and support an efficient development and review process.
Allogene Publishes Complete Phase 1 Data for ALLO-316
Allogene Therapeutics announced the publication of complete Phase 1 data from the TRAVERSE study of ALLO-316 in advanced or metastatic renal cell carcinoma in the Journal of Clinical Oncology. "TRAVERSE represents a potential breakthrough for both Allogene and the broader CAR T field," said Zachary Roberts, president and CEO of Allogene. "CAR T has transformed hematologic malignancies while solid tumors have remained one of the field's most difficult challenges. When we designed ALLO-316 with the Dagger technology, our goal was to address two of the most persistent barriers in solid tumors - achieving robust CAR T expansion with standard lymphodepletion and translating that biology into durable responses. These results show that a well-designed allogeneic CAR T product, developed for a defined population, can expand, persist, and produce durable responses in metastatic, treatment refractory solid tumors. Importantly, the robust CAR T expansion and durable persistence in this trial provides clinical validation of our Dagger technology platform and has direct read-through to our broader clinical and preclinical pipeline of next-generation AlloCAR T candidates."
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