Estrella Immunopharma
Estrella Immunopharma is a clinical-stage biopharmaceutical company developing CD19 and CD22-targeted ARTEMIS T-cell therapies for B-cell non-Hodgkin's lymphoma, autoimmune diseases, and solid tumors. Lead candidate EB103 showed 100% complete response in Phase I high-dose cohort.
- Company typePublic
- Founded2022
- HeadquartersEmeryville, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Estrella Immunopharma does
Estrella Immunopharma is a clinical-stage biopharmaceutical company developing CD19 and CD22-targeted T-cell therapies for the treatment of B-cell malignancies, autoimmune diseases, and solid tumors. Founded in 2022 as a Delaware corporation headquartered in Emeryville, California, the company went public on NASDAQ (tickers ESLA and ESLAW) in October 2023 following a SPAC business combination with TradeUP Acquisition Corp. that provided approximately $23.11 million in cash. Its product candidates are built on the ARTEMIS (Antibody Redirected T Cells with Endogenous Modular Immune Signaling) platform, licensed from parent company Eureka Therapeutics, which uses a modular antibody-T-cell-receptor (AbTCR) architecture designed to mimic natural T-cell receptor signaling.
The lead product candidate, EB103, is a CD19-redirected ARTEMIS T-cell therapy in Phase I/II STARLIGHT-1 clinical trials for relapsed/refractory B-cell Non-Hodgkin's Lymphoma. The company reported a 100% complete response rate in the high-dose cohort of the Phase I trial (n=9 patients) with no treatment-related serious adverse events and no Grade 3 or higher cytokine release syndrome. Additional pipeline assets include EB104 (a dual CD19/CD22-targeted ARTEMIS T-cell therapy for B-cell malignancies), EB201 (an ARTEMIS T-cell candidate for Systemic Lupus Erythematosus), and a Mark-and-Kill combination approach developed in partnership with Imugene Limited using the CF33-CD19t oncolytic virus to address solid tumors.
As a pre-revenue clinical-stage company, Estrella does not currently generate product revenue. The business model relies on periodic equity capital raises — including a $3.35 million private placement in May 2025 and an $8.0 million registered direct offering in January 2026 — to fund clinical development, with future revenue dependent on regulatory approval and commercialization. Investigational therapies are currently distributed exclusively through clinical trial sites: UC Davis Comprehensive Cancer Center (primary site) and Baylor Scott & White Research Institute. Parent company Eureka Therapeutics, founded and led by CEO Dr. Cheng Liu, is also Estrella's primary technology licensor and equity holder, creating a concentrated ownership and technology structure.
Estrella Immunopharma firmographics
Firmographics- Name
- Estrella Immunopharma
- Legal name
- Estrella Immunopharma, Inc.
- Website
- https://estrellabio.com
- Company type
- Public
- Founded year
- 2022
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Estrella Immunopharma is a clinical-stage biopharmaceutical company developing CD19 and CD22-targeted ARTEMIS T-cell therapies for B-cell non-Hodgkin's lymphoma, autoimmune diseases, and solid tumors. Lead candidate EB103 showed 100% complete response in Phase I high-dose cohort.
- Ownership category
- akta.pro rank
Estrella Immunopharma industry classification
Industry- Product category
- Cell Therapy Biopharmaceuticals
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414)
- SIC
- Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
- akta.pro primary industry
- CAR-T & TCR-T Therapies (HLAAABAC)
Keywords
Where Estrella Immunopharma is headquartered
LocationHeadquarters
- HQ city
- Emeryville
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Estrella Immunopharma business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales, Others
Revenue model
- T-cell Therapy Development and Commercialization: As a clinical-stage biopharmaceutical company, Estrella does not currently generate revenue. The company is developing CD19 and CD22-targeted ARTEMIS T-cell therapies for treatment of cancers and autoimmune diseases. Lead product EB103 is in Phase I/II clinical trials for relapsed/refractory B-cell Non-Hodgkin's Lymphoma. Revenue will be generated through commercialization of therapeutic products upon regulatory approval.
Go-to-market motion1 record
Distribution channels2 records
Marketing channels5 records
Estrella Immunopharma product offering
Product offeringCore offering
Estrella Immunopharma is a clinical-stage biopharmaceutical company developing next-generation T-cell immunotherapies built on the ARTEMIS platform licensed from Eureka Therapeutics. Its lead candidate EB103 is a CD19-redirected ARTEMIS T-cell therapy in a Phase I/II trial (STARLIGHT-1) for relapsed/refractory B-cell Non-Hodgkin's Lymphoma, with additional candidates EB104 (dual CD19/CD22) and EB201 (autoimmune disease) in preclinical/early development.
Product overview
Estrella Immunopharma is a clinical-stage biopharmaceutical company developing a portfolio of ARTEMIS T-cell therapies. The company's core products include EB103 (CD19-targeted) as the lead candidate for B-cell Non-Hodgkin's Lymphoma, EB104 (CD19/CD22 dual-targeted) for DLBCL and ALL, and EB201 for autoimmune diseases like Systemic Lupus Erythematosus. The company also employs a proprietary "mark-and-kill" approach combining EB103 with oncolytic viruses for solid tumor applications. All therapies utilize the ARTEMIS (Antibody Redirected T Cells with Endogenous Modular Immune Signaling) technology platform licensed from parent company Eureka Therapeutics.
Differentiator
Problem solved
Functional benefit
Products and services
- EB103 (CD19-Redirected ARTEMIS T-Cell Therapy) Lead product candidate, a CD19-targeted ARTEMIS T-cell therapy in Phase I/II clinical development for adult patients with relapsed/refractory B-cell Non-Hodgkin's Lymphoma (NHL), including aggressive subtypes such as DLBCL. EB103 utilizes ARTEMIS technology licensed from Eureka Therapeutics to target the CD19 protein expressed on B-cell leukemia and lymphoma surfaces, and is designed to reduce Cytokine Release Syndrome and neurotoxicity versus conventional CAR-T therapies.
- EB104 (Dual CD19/CD22-Targeted ARTEMIS T-Cell Therapy) ARTEMIS T-cell therapy candidate designed to simultaneously target both CD19 and CD22 proteins expressed on most B-cell malignancies, including diffuse large B-cell lymphoma (DLBCL) and Acute Lymphocytic Leukemia (ALL).
- EB201 (ARTEMIS T-Cell Therapy for Autoimmune Disease) ARTEMIS T-cell therapy candidate being developed for autoimmune diseases, specifically Systemic Lupus Erythematosus (SLE), applying the company's modular T-cell platform beyond oncology.
- EB103 + Oncolytic Virus Combination (Mark-and-Kill Approach) Investigational combination strategy pairing CD19-Redirected ARTEMIS T-cells (EB103) with an oncolytic virus (CF33-CD19t) that forces solid tumor cells to express CD19 on their surface, enabling ARTEMIS T-cells to target and kill CD19-labeled solid tumors.
Quantifiable outcome
- 100% Complete Response rate in high-dose cohort at Month 1 in Phase I STARLIGHT-1 trial
- +4 more outcomes
Companies that use Estrella Immunopharma
Customer profileSegments4 records
Ideal customer profiles2 records
Estrella Immunopharma technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Estrella Immunopharma partnerships and signals
Strategic signalPartnerships
Three partnerships are on record, tiered core and minor.
- Eureka Therapeutics, Inc.coreEureka Therapeutics is Estrella's parent company that developed and owns the ARTEMIS technology. Estrella has a license agreement with Eureka to utilize ARTEMIS technology for CD19 and CD22-targeted T-cell therapies. Dr. Cheng Liu, Estrella's CEO and President, is also the Founder, President, and CEO of Eureka Therapeutics.
- Imugene LimitedcoreCollaboration with Imugene Limited and its product candidate CF33-CD19t, an oncolytic virus, to research the use of EB103 in conjunction with CF33-CD19t to treat solid tumors using a 'mark and kill' strategy. This partnership expands Estrella's pipeline to address solid tumors beyond blood cancers.
- Winston & Strawn LLPminorLegal counsel to the company for the January 2026 financing transactions.
Scale indicators7 records
Recent moves7 records
Expansion highlights5 records
Estrella Immunopharma competitors and assessment
Company assessmentDirect peers
- Gilead Sciences (Kite Pharma): Markets Yescarta and Tecartus, the leading approved CD19 CAR-T therapies for R/R B-cell NHL. Direct competitor to Estrella's lead candidate EB103 in the same indication, with established commercial infrastructure, real-world evidence base, and manufacturing scale.
- Novartis: Markets Kymriah, the first FDA-approved CD19 CAR-T therapy for R/R B-cell NHL and ALL. Competes head-to-head with EB103 in the same patient population with an entrenched franchise and global commercial reach.
- Bristol-Myers Squibb: Markets Breyanzi, a CD19 CAR-T approved for R/R B-cell NHL. Direct competitor to EB103 with established physician relationships and a growing real-world dataset in aggressive B-cell lymphomas.
- Allogene Therapeutics: Clinical-stage company developing allogeneic (off-the-shelf) CAR-T therapies for hematologic cancers including CD19-targeted candidates. Comparable in clinical-stage status and competing in the same R/R B-cell NHL space.
- Caribou Biosciences: Clinical-stage allogeneic CAR-T developer with CD19 programs for B-cell malignancies. Direct peer in the autologous/allogeneic CD19 CAR-T space with similar clinical-stage profile.
- CRISPR Therapeutics: Developing gene-edited allogeneic CAR-T therapies including CD19-targeted candidates for B-cell malignancies. Comparable in modality and clinical-stage development, with significant capital backing.
- Autolus Therapeutics: Clinical-stage CAR-T developer with CD19 and other hematologic targets. Comparable in clinical-stage positioning and competing in the R/R B-cell NHL space with next-generation CAR-T constructs.
- Adicet Bio: Developing gamma-delta T cell therapies for cancer and autoimmune diseases, including CD19-directed candidates. Closely comparable to Estrella's ARTEMIS platform, which also leverages gamma/delta TCR architecture.
- Nkarta: Clinical-stage developer of allogeneic NK cell therapies for cancer and autoimmune disease, including CD19-directed candidates. Comparable in targeting autoimmune (SLE) indications via cell therapy, similar to Estrella's EB201 program.
Others
- Eureka Therapeutics: Estrella's parent company and licensor of the ARTEMIS technology platform. While not a direct commercial competitor, Eureka is the originating developer of Estrella's core technology and shares leadership with Estrella, making it a strategically relevant ecosystem participant.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat3 records
Key risks6 records
Key highlights6 records
Customer concentration
Estrella Immunopharma financial estimates
Financial estimateRevenue estimate
Valuation estimate
Estrella Immunopharma leadership team
Management profileNumber of profiles
Profiles8 records
Estrella Immunopharma funding detail
Funding detailFunding overview
Funding rounds3 records
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Estrella Immunopharma M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Estrella Immunopharma
What does Estrella Immunopharma do?
Estrella Immunopharma is a clinical-stage biopharmaceutical company developing next-generation T-cell immunotherapies built on the ARTEMIS platform licensed from Eureka Therapeutics. Its lead candidate EB103 is a CD19-redirected ARTEMIS T-cell therapy in a Phase I/II trial (STARLIGHT-1) for relapsed/refractory B-cell Non-Hodgkin's Lymphoma, with additional candidates EB104 (dual CD19/CD22) and EB201 (autoimmune disease) in preclinical/early development.
Is Estrella Immunopharma a public or private company?
Estrella Immunopharma is a public company. It is classified as public and is currently operating.
When was Estrella Immunopharma founded?
Estrella Immunopharma was founded in 2022. It employs 11 to 50 people.
Where is Estrella Immunopharma based?
Estrella Immunopharma is headquartered in Emeryville, United States, in the North America region.
How does Estrella Immunopharma make money?
One revenue line is on record: T-cell Therapy Development and Commercialization.
Who are Estrella Immunopharma's main competitors?
Direct peers on record are Gilead Sciences (Kite Pharma), Novartis, Bristol-Myers Squibb, Allogene Therapeutics, Caribou Biosciences, CRISPR Therapeutics, Autolus Therapeutics, Adicet Bio and Nkarta. Eureka Therapeutics is listed as an others.
Does Estrella Immunopharma have an API?
No public API is recorded for Estrella Immunopharma.
What industry is Estrella Immunopharma in?
Estrella Immunopharma's product category is Cell Therapy Biopharmaceuticals. Its primary akta.pro industry code is HLAAABAC, CAR-T & TCR-T Therapies. Its NAICS code is 325414 and its SIC code is 2836.