First-in-human study of in vivo CAR-T therapy GT801 in adults with relapsed or refractory CD19-positive B-cell hematologic malignancies.
7079 Background: Despite high initial cure rates, patients with B-cell hematologic malignancies, including B-ALL and B-NHL, experience substantial relapse, with markedly reduced disease-free and overall survival after second-line therapy. GT801 is a first-in-human, in vivo CAR-T therapy that uses antibody-displayed lipid nanoparticle (LNP) to deliver CD19 CAR mRNA directly to T cells, enabling in vivo reprogramming without ex vivo cell manufacturing or lymphodepletion. We report initial safety and efficacy data from an open-label, single-arm phase I study (NCT07205315). Methods: GT801 was evaluated using a modified 3+3 dose-escalation design across three dose levels (0.5, 1.5, and 3.0 mg). Patients received up to 4 treatment cycles, each consisting of a single intravenous administration of GT801 on Day 1 of a 7-day cycle. The primary endpoint was safety, including treatment-emergent adverse events (TEAEs), graded per CTCAE v5.0. Secondary endpoints included 3-month overall response rate (ORR), best overall response (BOR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS), assessed per Lugano 2014 criteria. Results: As of January 13, 2026, 3 patients were enrolled (median age 60 years; median three prior therapies). One patient received 3 doses at 0.5 mg, and two patients received 4 doses at 1.5 mg. All patients had B-NHL. Premedication included dexamethasone, NSAIDs, antihistamines. Most AEs were Grade 1-2. Common TEAEs included cytokine release syndrome (CRS), cytopenia, and transient liver enzyme elevations. Grade ≥3 events were hematologic toxicities and CRS. No neurotoxicity or organ failure was observed. At Week 4, all patients demonstrated a treatment response. Peripheral blood flow cytometry showed rapid CAR-T generation, with CD8 + CAR-T cells detectable within 4 hours post-infusion and peak levels on Day 1. Reprogramming efficiency reached up to 93% and was maintained with repeat dosing. Minimal off-target CAR expression was detected in monocytes. Complete peripheral B-cell depletion occurred within 4 hours after the first dose and was sustained for at least 7 days; after the third dose, B-cell depletion and CAR-T detection were observed in both peripheral blood and bone marrow. Conclusions: GT801 demonstrated a manageable safety profile and early signs of antitumor activity in heavily pretreated B-NHL patients. The ability to generate functional CAR-T cells in vivo without lymphodepletion supports further clinical evaluation of GT801 as a promising therapeutic approach. Clinical trial information: NCT07205315 . Research sponsor: Vivacta Biotechnology (Shanghai) Co., Ltd.
Authors
- P Wang
- Wei Xu
- Lihua Yan (ORCID: https://orcid.org/0000-0003-0915-6864)
- Hang Chen
- Xianchao Ding
- Liqing Ma
- Jingwei Sun
- Li Wang
- Derun Shen
- Yarong Liu
- Zhiyang Xu
- Jing Yu
- Zhenzhen Wang
Institutions
- University of Southern California (US)
- Shanghai CASB Biotechnology (China) (CN)
- Zhengzhou City Hospital (CN)
- Viva Biotech (China) (CN)
Publication Details
- Journal
- Journal of Clinical Oncology
- Published
- 2026-05-27
- DOI
- https://doi.org/10.1200/jco.2026.44.16_suppl.7079
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00