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   <title>Estrella Immunopharma adds Baylor site to lymphoma trial</title>
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   <description>&lt;p&gt;Estrella Immunopharma, Inc. (NASDAQ: ESLA) has activated Baylor Scott &amp; White Research Institute in Dallas, Texas, as a second clinical site for its STARLIGHT-1 Phase I/II trial evaluating EB103, a CD19-directed T-cell therapy, in patients with relapsed or refractory B-cell non-Hodgkin's lymphoma (NHL).&lt;/p&gt;&lt;p&gt;According to a press release, the Dallas site has begun screening and enrolling patients. The trial's first site, UC Davis Comprehensive Cancer Center, remains active. The study is registered at clinicaltrials.gov under NCT06343311.&lt;/p&gt;&lt;p&gt;The expansion phase of the trial is a multi-center, open-label study evaluating the safety and efficacy of EB103 at the recommended Phase II dose in patients</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
   <link>http://www.streetinsider.com/Press+Releases/Estrella+Immunopharma+Activates+Baylor+Scott+%26amp%3B+White+Research+Institute+as+Second+Clinical+Site+for+Phase+III+STARLIGHT-1+Trial+in+B-cell+Non-Hodgkin%E2%80%99s+Lymphoma/26830864.html</link>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
   <link>http://www.streetinsider.com/Press+Releases/Estrella+Immunopharma+Activates+Baylor+Scott+%26amp%3B+White+Research+Institute+as+Second+Clinical+Site+for+Phase+III+STARLIGHT-1+Trial+in+B-cell+Non-Hodgkin%E2%80%99s+Lymphoma/26830864.html</link>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
   <link>http://www.streetinsider.com/Business+Wire/Estrella+Immunopharma+Activates+Baylor+Scott+%26amp%3B+White+Research+Institute+as+Second+Clinical+Site+for+Phase+III+STARLIGHT-1+Trial+in+B-cell+Non-Hodgkin%E2%80%99s+Lymphoma/26830864.html</link>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
   <link>http://www.streetinsider.com/Business+Wire/Estrella+Immunopharma+Activates+Baylor+Scott+%26amp%3B+White+Research+Institute+as+Second+Clinical+Site+for+Phase+III+STARLIGHT-1+Trial+in+B-cell+Non-Hodgkin%E2%80%99s+Lymphoma/26830864.html</link>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <pubDate>Wed, 29 Jul 2026 08:00:00 -0400</pubDate>
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   <title>Estrella Immunopharma Activates Baylor Scott &amp;amp; White Research Institute as Second Clinical Site for Phase I/II STARLIGHT-1 Trial in B-cell Non-Hodgkin’s Lymphoma</title>
   <link>http://www.streetinsider.com/Business+Wire/Estrella+Immunopharma+Activates+Baylor+Scott+%26amp%3B+White+Research+Institute+as+Second+Clinical+Site+for+Phase+III+STARLIGHT-1+Trial+in+B-cell+Non-Hodgkin%E2%80%99s+Lymphoma/26830864.html</link>
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&lt;p&gt;    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 the activation of a second clinical site for its ongoing STARLIGHT-1 Phase I/II clinical trial evaluating EB103, a CD19-Redirected ARTEMIS® T-cell therapy, in patients with relapsed or refractory (“R/R”) B-cell non-Hodgkin’s lymphoma (“NHL”). The new site, Baylor Research Institute d/b/a Baylor Scott &amp;amp; White Research Institute in Dallas, Texas, has begun screening and enrolling patients.&lt;/p&gt;&lt;p&gt;“Partnering with Baylor Scott &amp;amp; White Research Institute, a nationally recognized</description>
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   <title>Estrella Immunopharma doses first patient in EB103 expansion trial</title>
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   <description>&lt;p&gt;Estrella Immunopharma, Inc. (NASDAQ: ESLA) announced that the first patient has been dosed in the dose-expansion phase of its STARLIGHT-1 Phase I/II clinical trial, which is evaluating EB103, a CD19-redirected T-cell therapy, in patients with relapsed or refractory B-cell non-Hodgkin's lymphoma (NHL).&lt;/p&gt;&lt;p&gt;The expansion phase follows data from the dose-escalation cohort showing that, at a six-month assessment of evaluable Phase I patients without central nervous system involvement, all patients who achieved a complete response remained in complete response.&lt;/p&gt;&lt;p&gt;&quot;This marks an important milestone for Estrella and STARLIGHT-1,&quot; said Cheng Liu, PhD, Chief Executive Officer of Estrella. &quot;The sustained complete responses observed to</description>
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   <pubDate>Fri, 24 Jul 2026 08:00:35 -0400</pubDate>
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   <title>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</title>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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&lt;p&gt;    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/refractory (R/R) B-cell non-Hodgkin’s lymphoma (NHL).

&lt;/p&gt;&lt;p&gt;
Estrella’s dosing of the first patient in the dose-expansion cohort follows encouraging efficacy data from the dose-escalation cohort. At the 6-month assessment of evaluable Phase I patients with no CNS involvement,</description>
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