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Estrella Immunopharma Announces First Patient Dosed in Dose-Expansion Phase of STARLIGHT-1 Trial and Reports Durable Response Rate in Advanced B-Cell Non-Hodgkin’s Lymphoma

Key Takeaway: Estrella Immunopharma has announced the successful dosing of the first patient in the dose-expansion phase of its STARLIGHT-1 Phase I/II clinical trial. The trial evaluates EB103, a CD19-redirected ARTEMIS T-cell therapy, specifically for patients with relapsed or refractory advanced B-cell non-Hodgkin's lymphoma. The company also reported a durable response rate in this patient population.

Market Sentiment Analysis

POSITIVE FACTORS

  • First patient dosed in the STARLIGHT-1 trial's expansion phase.
  • Promising durable response rate reported in advanced B-cell lymphoma.
  • Advancement in CD19-targeted ARTEMIS T-cell therapies.

Full Press Release Details

EMERYVILLE, Calif.--(BUSINESS WIRE)--Estrella Immunopharma, Inc. (NASDAQ: ESLA) (“Estrella” or the “Company”), a clinical-stage biopharmaceutical company developing CD19 and CD22-targeted ARTEMIS® T-cell therapies to treat cancer and autoimmune diseases, today announced that the first patient has been successfully dosed in the dose-expansion phase of its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-redirected ARTEMIS® T-cell therapy, in patients with relapsed/refractor

Frequently Asked Questions

What is the STARLIGHT-1 trial?

The STARLIGHT-1 trial is a Phase I/II clinical trial evaluating EB103, a CD19-redirected ARTEMIS T-cell therapy.

What type of patients are involved in the STARLIGHT-1 trial?

The trial involves patients with relapsed or refractory advanced B-cell non-Hodgkin's lymphoma.

What milestone did Estrella Immunopharma achieve recently?

Estrella Immunopharma announced the successful dosing of the first patient in the trial's dose-expansion phase.

What is EB103?

EB103 is a CD19-targeted ARTEMIS T-cell therapy being evaluated in the STARLIGHT-1 trial.

Last updated: Jul 24, 2026