HomeTrialNCT05826535
NCT05826535Phase 1Phase 2RECRUITING

Study of Rondecabtagene Autoleucel in Aggressive Large B-Cell Lymphoma

Study Summary

This is a Phase 1/2, multi-center, open-label study evaluating the safety and efficacy of rondecabtagene autoleucel (ronde-cel) also known as LYL314, a dual-targeting chimeric antigen receptor (CAR) targeting cluster of differentiation (CD)19 and CD20 in participants with aggressive large B-cell lymphoma.

View on ClinicalTrials.gov ↗
Study Details
Enrollment270 participants
Primary Completion
Lead SponsorLyell Immunopharma, Inc.
Data Retrieved2026-04-11 04:20:24.455729+00:00
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 1 trials primarily test safety and dosing in a small number of participants (typically 20–100). Results do not yet speak to efficacy. FDA approval is typically many years away from this stage.

Phase 2 trials begin testing efficacy in a larger patient group (100–300). This is often where biotech binary events occur — positive Phase 2 data can significantly advance a company's pipeline narrative, while failures can be terminal for a program.

Status & Expected Data

Currently recruiting: the trial is enrolling patients. A data readout is not expected until after enrollment closes and the follow-up period is complete.

Enrolled: 270 participants
Sponsor Catalyst Profile

Lyell Immunopharma (LYEL) is the sponsoring company for this trial. BiotechSign currently grades this company D (44/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

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