# ASCO 2026 | Oricell's GPC3 CAR-T Ori-C101 Hits 66.7% ORR in Late-Line HCC, Signaling Best-in-Class Potential

- Link: https://www.thailand-business-news.com/pr-news/asco-2026-oricells-gpc3-car-t-ori-c101-hits-66-7-orr-in-late-line-hcc-signaling-best-in-class-potential
- Published: 2026-06-01T09:37:00+07:00
- Author: PR Newswire

CHICAGO, June 1, 2026 /PRNewswire/ — Oricell Therapeutics, a clinical-stage biotech
company pioneering cancer immunotherapy, today announced that its lead asset, Ori-
C101, a GPC3-targeted CAR-T therapy, achieved a 66.7% objective response rate (ORR)
in patients with Late-line refractory hepatocellular carcinoma (HCC). The data, 
selected for an oral presentation at the 2026 American Society of Clinical Oncology(
ASCO) Annual Meeting, highlight a potential new benchmark for patients who have 
exhausted standard therapies.

**Landmark Efficacy in a High-Unmet Need Setting**

Hepatocellular carcinoma (HCC) remains a critical global health challenge, particularly
in China, which accounts for more than one-third of the world’s over 800,000 annual
deaths from the disease. While frontline treatments have evolved, options for patients
failing second-line therapy are scarce, with historical ORRs typically below 13%.

Oricell’s registrational Phase Ib BEACON study challenges this status quo. As of
April 3, 2026, among 18 efficacy-evaluable patients with advanced, heavily pretreated
HCC:

 ◦ Overall ORR reached 50%.
 ◦ At the Recommended Phase 2 Dose (RP2D), ORR surged to 66.7%, with a disease control
   rate (DCR) nearing 90%.
 ◦ Durability was profound: One patient achieved a complete response (CR) lasting
   24 months.
 ◦ Safety was manageable: No immune effector cell-associated neurotoxicity syndrome(
   ICANS) or off-tumor toxicity was observed, with cytokine release syndrome (CRS)
   contained within controllable grades.

**Long-Term Validation: From 2021 ASCO Poster to Registrational Data**

Notably, as early as 2021, Oricell’s investigator-initiated trial (IIT) data for
Ori-C101 were selected for a poster presentation at ASCO. At that time, a striking
response was observed in a late-line HCC patient following a single infusion: the
first efficacy assessment showed a partial response (PR), with target lesions shrinking
by 96.1% (from 155.45 mm to 6 mm) and alpha-fetoprotein (AFP) levels plummeting 
by 99.1% (from >80,000 ng/mL to 742 ng/mL). The patient achieved an overall survival(
OS) of nearly three years.

[[

The now-unveiled registrational clinical data further validate the clinical value
of Ori-C101, reinforcing the consistency and reproducibility of Oricell’s approach
from early proof-of-concept to pivotal trials.

**Technology Backbone: A ****"****Three-in-One****" ****Engine Addressing Solid 
Tumor Barriers**

Ori-C101’s exceptional performance stems from Oricell’s proprietary technology platforms,
systematically addressing major challenges in CAR-T therapy for solid tumors: antigen
heterogeneity, immunosuppressive tumor microenvironment (TME), and manufacturing
efficiency.

**1. Ori®Ab (AI-Powered Antibody Discovery Platform****）**
The Ori®Ab platform 
features a massive library comprising up to 10¹¹ fully human scFv and nanobody sequences.
Utilizing a live-cell-based high-throughput screening strategy, the platform specifically
identifies native conformational antigens, including challenging targets such as
GPCRs, thereby avoiding the false-positive risks associated with purified protein-
based screening. Furthermore, AI-assisted algorithms have compressed the antibody
discovery and screening cycle from a traditional 12 months to just 3 months, significantly
enhancing both efficiency and quality. The resulting high-specificity, optimally
affine GPC3 antibody sequence equips Ori-C101 with a robust safety profile, effectively
minimizing the risk of off-tumor toxicity.

**2. Ori®Armoring (Structure-Enhanced Cell Platform)**
The Ori®Armoring platform
incorporates customized "armoring" elements designed to modulate T cell metabolic
pathways and signal transduction based on the specific tumor microenvironment (TME).
This engineering strategy enriches young, stem-like memory T cell subsets (Tscm),
significantly enhancing the in vivo persistence of Ori-C101. By remodeling the local
immune microenvironment, the platform effectively reverses immunosuppression, converting"
cold tumors" into "hot tumors," thereby promoting the infiltration and activation
of effector T cells. This approach overcomes the dual bottlenecks of the immunosuppressive
TME and T cell exhaustion in solid tumors, ensuring durable, long-term responses.
Additionally, the platform integrates logic-gating strategies—including ‘OR’ gating
to prevent antigen escape and ‘AND’ gating to improve targeting precision—which 
collectively optimize the therapeutic index of the product.

**3. Ori®OnGo: Flexible Manufacturing Platform (Classic / Rapid / In Vivo)**
Built
on a "Quality by Design" (QbD) philosophy, this platform includes proprietary manufacturing
technologies. The rapid manufacturing process reduces ex vivo culture time to just
3 days, significantly improving productivity and lowering cost of goods (COGS). 
It ensures final product cell viability consistently above 95%, and compresses the
vein-to-vein time to within 15 days. Moreover, the platform’s in vivo CAR-T product
design and process capabilities open broader future applications for CAR-T therapy.
This integrated manufacturing approach enables scalable, cost-effective production
while maintaining product quality and patient access.

**Executive Outlook**

"Securing a third ASCO oral presentation validates our integrated platform strategy,"
said Dr. Helen Yang, Co-Founder and CEO of Oricell. "We are accelerating the pivotal
Phase II development to bring this therapy to market. We are also actively seeking
global partnerships to expand the reach of our technology and deliver hope to patients
worldwide."

**About Oricell Therapeutics**

Oricell is a clinical-stage global biotechnology company dedicated to becoming a
pioneer in tumor immunotherapy. Focused on solving unmet medical needs in oncology
and immunology, by powering a proprietary technology triad: Ori®Ab (antibody discovery),
Ori®Armoring (T-cell enhancement), and OnGo CMC (rapid manufacturing), Oricell has
successfully established a robust pipeline targeting both solid and hematological
tumors. The company’s clinical translation capabilities have been recognized globally,
with multiple data readouts selected for oral presentations at major international
conferences including ASCO and EHA, and published in top-tier journals such as The
Lancet Haematology. For more information, visit [www.oricell.com](https://www.oricell.com/).

**Forward-Looking Statements**

This press release contains "forward-looking statements" which are not historical
facts, but instead are predictions about future events based on the beliefs as well
as assumptions made by and information currently available to the management of 
Oricell Therapeutics Holdings Limited ("the Company" or "Oricell"). The words "anticipate,""
believe," "continue," "could," "estimate," "expect," "intend," "may," "plan," "potential,""
predict," "project," "should," "target," "will," "would" and similar expressions
are intended to identify forward-looking statements, although not all forward-looking
statements contain these identifying words. Such forward-looking statements involve
known and unknown risks, uncertainties and other important factors that could cause
the actual results, performance or achievements of the Company, or industry results,
to differ materially from any future results, performance or achievement implied
by such forward-looking statements. Any forward-looking statements contained in 
this press release speak only as of the date of this press release. The Company 
assumes no obligation to update any forward-looking statement, whether as a result
of new information, future events or otherwise.

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