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Legend’s experimental cell therapy shows promise in blood cancer patients

By Thomson Reuters Jun 2, 2026 | 8:31 AM

June 2 (Reuters) – Legend Biotech’s experimental therapy showed early signs that its approach of generating disease-fighting cells within patients may work for a type of blood cancer, ​sending shares of the company up nearly 30%.

Unlike traditional ‌CAR‑T therapies that require extracting, modifying and reinfusing a patient’s immune cells, Legend aims to generate them inside the body using its in vivo dual-targeting therapy, LB2501.

In the highly anticipated early-stage trial data reported on Tuesday, ‌12 ​patients with relapsed/refractory B-cell non-Hodgkin lymphoma were ⁠treated across two dose ⁠levels as of April 1.

In the higher-dose cohort, the preliminary data showed all six patients responded, while five had a complete response.

The data points “to a potentially best-in-class profile in the ​in vivo CAR-T space and best-in-disease profile in NHL,” Oppenheimer analyst Kostas Biliouris said, adding that it strengthened chances of ⁠Legend’s acquisition.

Several pharmaceutical companies including AstraZeneca ⁠and Eli Lilly have recently struck deals in ​the in vivo CAR-T field.

LB2501 is designed to generate CAR-T cells ​directly within the patient through a single, direct infusion, ‌eliminating the need for ex vivo cell engineering and manufacturing.

“By generating CAR-T cells directly within the patient, this approach has the potential to simplify treatment delivery and expand access for patients ⁠who may not be able to receive traditional CAR-T cell therapies,” said CEO Ying Huang.

While a longer follow-up was warranted, the data highlights ⁠the potential of ‌LB2501 as a scalable, readily accessible “off-the-shelf” immunotherapy ⁠for B-cell malignancies, Legend said.

It did not provide ​additional ‌dose-level details and said further data would be ​shared at ⁠a medical meeting later this month.

The company said no dose-limiting toxicities, serious adverse events or fatal cases were reported. Infusion-related reactions occurred in nine patients, but were resolved within a two-day median, it said.

(Reporting by Sriparna Roy and Mariam Sunny in Bengaluru; Editing ​by Pooja Desai)