Estrella Immunopharma announces additional site for STARLIGHT-1 trial
Clinical Trial Update: Estrella Immunopharma has activated a second clinical site for its STARLIGHT-1 Phase I/II trial, which is testing the EB103 therapy for patients with relapsed or refractory B-cell non-Hodgkin's lymphoma.
New Enrollment Site: The Baylor Research Institute in Dallas, Texas, is now open for patient enrollment in the ongoing clinical trial.
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- Successful Financing: Estrella Immunopharma has closed a registered direct offering with a single healthcare-focused institutional investor, issuing 4,063,290 shares of common stock and 1,000,000 pre-funded warrants, raising approximately $8 million, which enhances the company's financial resources for clinical development.
- Advancing Product Development: The proceeds will support the Phase II clinical trial of Estrella's lead product candidate, EB103, aimed at providing new treatment options for patients with cancers and autoimmune diseases who are not eligible for existing therapies, highlighting its significant clinical value.
- Investor Confidence: The CEO stated that this financing underscores continued investor support for the company's clinical vision, indicating strong market confidence in Estrella's future growth, which may facilitate further advancements in the biopharmaceutical sector.
- Compliance and Transparency: The financing adheres to SEC registration requirements, ensuring compliance in all securities transactions, while the company commits to filing registration statements with the SEC, thereby enhancing investor trust in the company's transparency.
- Successful Financing: Estrella Immunopharma closed a registered direct offering with a single healthcare-focused institutional investor, raising approximately $8 million by issuing 4,063,290 shares of common stock and 1,000,000 pre-funded warrants, thereby strengthening its financial position to support clinical objectives.
- Advancing Clinical Programs: The financing will provide Estrella with the necessary resources to advance its lead product EB103 into Phase II clinical trials, aimed at offering treatment options for cancer patients who are ineligible for currently marketed therapies, which holds significant market potential.
- Investor Confidence: The CEO stated that this financing underscores continued investor support for the company's clinical vision, indicating market recognition of its ARTEMIS T-cell therapies, which may enhance future fundraising capabilities.
- Compliance Assurance: The offering was conducted under SEC registration statements, ensuring compliance, and through a registration rights agreement with the investor, Estrella will file registration statements to cover the resale of common stock, thereby boosting investor confidence.

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Clinical Trial Expansion: Estrella Immunopharma has activated a second clinical site at Baylor Research Institute for its STARLIGHT-1 Phase I/II trial of EB103, a CD19-Redirected ARTEMIS® T-cell therapy aimed at treating relapsed or refractory B-cell non-Hodgkin's lymphoma.
Therapeutic Approach: EB103 utilizes innovative ARTEMIS® technology to target and destroy CD19-positive cancer cells, representing a potential advancement in safer and more effective treatments for patients with advanced NHL.

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