# Antengene Announces Receipt of USD 60 Million Upfront Payment from UCB

- Link: https://www.thailand-business-news.com/pr-news/antengene-announces-receipt-of-usd-60-million-upfront-payment-from-ucb
- Published: 2026-07-13T11:00:00+07:00
- Author: PR Newswire

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SHANGHAI and HONG KONG, July 13, 2026 /PRNewswire/ — Antengene Corporation Limited("**
Antengene**", SEHK: 6996.HK), a leading innovative, commercial-stage global biotech
company dedicated to discovering, developing and commercializing first-in-class 
and/or best-in-class medicines for autoimmune diseases, solid tumors and hematological
malignancies, today announced that **the company has received a USD 60 million upfront
payment from UCB. This payment is made pursuant to the worldwide exclusive license
agreement for ATG-201, a CD19/CD3 bispecific T-cell engager (TCE) antibody, entered
into between the parties in March 2026.**

**ATG-201 is a CD19 targeting bispecific TCE incorporating steric hindrance masking
technology, designed to eliminate CD19-expressing B cells. **This bispecific interaction
with T and B cells through CD3 and CD19 has demonstrated potential in treating B
cell-driven diseases by leveraging the body’s own immune system for precise and 
potent action.

Under the agreement, Antengene grants UCB a worldwide exclusive license to further
develop, manufacture, and commercialize ATG-201, along with access to its associated
manufacturing technology.

China’s National Medical Products Administration (NMPA) approved in June this year
the Investigational New Drug (IND) application for the Phase I ATTRACT study of 
ATG-201 for the treatment of B cell related autoimmune diseases. **Antengene is 
progressing the Phase I study of ATG-201 in China and concurrently preparing for
its clinical development in Australia.**

The receipt of the upfront payment from this license agreement with UCB has further
strengthened Antengene’s cash position, providing robust financial support for the
advancement of our innovative drug pipeline and accelerating benefits to more patients.

Under the terms of the global exclusive license agreement Antengene is eligible 
for additional near-term milestone payments of USD 20 million subject to certain
conditions. The agreement also includes the potential for future success-based development
and commercial milestone payments, as well as tiered royalties on future net sales.

**About Antengene **

Antengene Corporation Limited (**"Antengene"**, SEHK: 6996.HK) is a global, R&D-
driven, commercial-stage biotech company focused on developing first-in-class/best-
in-class therapeutics for diseases with significant unmet medical needs. Its pipeline
spans from preclinical to commercial stages, with key investigational candidates
including ATG-022 (CLDN18.2 ADC), ATG-037 (oral CD73 inhibitor), ATG-101 (PD-L1 
x 4-1BB bispecific antibody), ATG-125 (B7-H3 × PD-L1 bispecific ADC), ATG-207 (αCD3-
TGF-β bifunctional fusion protein), as well as T cell engager (TCE) programs developed
using Antengene’s proprietary AnTenGager^(®) platform.

AnTenGager^(®), is Antengene’s proprietary TCE 2.0 platform, featuring "2+1" bivalent
binding for low expressing targets, steric hindrance masking, and proprietary CD3
sequences with fast on/off kinetics to minimize cytokine release syndrome (CRS) 
and enhance efficacy. These characteristics support the platform’s broad applicability
across autoimmune disease, solid tumors and hematological malignancies, with programs
targeting CD19 x CD3 (ATG-201 for B cell-related autoimmune diseases; partnered 
with UCB), CDH6 x CD3 (ATG-106 for ovarian cancer and kidney cancer), ALPPL2 x CD3(
ATG-112 for gynecological tumors, digestive system malignancies, bladder cancer 
and NSCLC), LY6G6D x CD3 (ATG-110 for microsatellite-stable colorectal cancer), 
GPRC5D x CD3 (ATG-021 for multiple myeloma), LILRB4 x CD3 (ATG-102 for acute myeloid
leukemia and chronic myelomonocytic leukemia) and FLT3 x CD3 (ATG-107 for acute 
myeloid leukemia).

To date, Antengene has obtained 33 investigational new drug (IND) approvals in the
U.S. and Asia, and obtained new drug application (NDA) approvals in 10 Asia Pacific
markets. Its lead commercial asset, XPOVIO^(®) (selinexor), is approved in the Mainland
of China, Taiwan China, Hong Kong China, Macau China, South Korea, Singapore, Malaysia,
Thailand, Indonesia and Australia, and has been included in the national insurance
schemes in five of these markets (Mainland of China, Taiwan China, Australia, South
Korea and Singapore).

**Forward-looking statements**

The forward-looking statements made in this article relate only to the events or
information as of the date on which the statements are made in this article. Except
as required by law, we undertake no obligation to update or revise publicly any 
forward-looking statements, whether as a result of new information, future events
or otherwise, after the date on which the statements are made or to reflect the 
occurrence of unanticipated events. You should read this article completely and 
with the understanding that our actual future results or performance may be materially
different from what we expect. In this article, statements of, or references to,
our intentions or those of any of our Directors or our Company are made as of the
date of this article. Any of these intentions may alter in light of future development.
For a further discussion of these and other factors that could cause future results
to differ materially from any forward-looking statement, please see the other risks
and uncertainties described in the Company’s Annual Report for the year ended December
31, 2025, and the documents subsequently submitted to the Hong Kong Stock Exchange.

For more information, please contact:

Investor Contacts: 
Donald LungE-mail: [donald.lung@antengene.com](https://www.thailand-business-news.com/pr-news/donald.lung@antengene.com)

BD Contacts:
Ariel GuoE-mail: [ariel.guo@antengene.com](https://www.thailand-business-news.com/pr-news/ariel.guo@antengene.com)

 

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