Adagene’s Muzastotug (ADG126) to be Highlighted in Two Presentations at the 2026 American Association for Cancer Research (AACR) Annual Meeting in San Diego, CA
Rhea-AI Summary
Adagene (Nasdaq: ADAG) announced that muzastotug (ADG126), a masked anti-CTLA-4 antibody, will be highlighted in two poster presentations at the AACR Annual Meeting in San Diego, April 17-22, 2026.
Presentations are scheduled April 20, 2026 at 9:00 AM PT in Poster Sections 50 and 51 (Poster Board 14), covering a Ph1b evaluation in MSS colorectal cancer and phase 1b/2 Morpheus Liver study results in unresectable or metastatic HCC.
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Key Figures
Market Reality Check
Peers on Argus
ADAG fell 3.39% while momentum-screened biotech peers like FATE, BMEA, and TCRX moved up. One close peer, ZNTL, also issued AACR poster news, suggesting company-specific reactions rather than a uniform sector move.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Feb 17 | Investor conferences | Neutral | +1.2% | Planned participation in two healthcare investor conferences with webcasts. |
| Jan 23 | Business update | Positive | +22.7% | Cash position of $74.5M and 2026 objectives focused on muzastotug. |
| Dec 16 | Fast Track status | Positive | +13.8% | FDA Fast Track designation for muzastotug plus pembrolizumab in MSS CRC. |
| Nov 13 | Licensing deal | Positive | +1.7% | Licensing agreement with Third Arc Bio for two masked CD3 T cell engagers. |
| Oct 31 | Clinical milestone | Positive | -7.3% | First patient dosed in randomized Phase 2 dose-optimization study of muzastotug. |
ADAG has typically shown positive price reactions to regulatory, partnership, and strategic updates, with occasional divergence on clinical trial milestone news.
Over the last six months, Adagene highlighted investor conference participation on Feb 25, 2026 and Mar 9, 2026, a business update on Jan 23, 2026 citing $74.5M in cash and 2026 objectives centered on muzastotug, and an FDA Fast Track designation for muzastotug on Dec 16, 2025. It also signed a Third Arc Bio licensing deal on Nov 13, 2025 and dosed the first patient in a randomized Phase 2 muzastotug study on Oct 31, 2025. Today’s AACR posters fit into this ongoing clinical and regulatory story for muzastotug.
Regulatory & Risk Context
Adagene has an effective Form F-3 resale registration filed on Oct 31, 2025 covering up to 10,625,000 ordinary shares or 8,500,000 ADSs issuable upon conversion of 1,062,500 Series A Non-Voting Redeemable Convertible Preferred Shares. The company is not selling securities under this prospectus and will receive no proceeds; sales would be by a selling shareholder.
Market Pulse Summary
This announcement highlights two AACR 2026 poster presentations for muzastotug, covering a Phase 1b MSS colorectal cancer combination regimen and Phase 1b/2 results in unresectable or metastatic hepatocellular carcinoma. These updates build on prior milestones, including FDA Fast Track designation and initiation of a randomized Phase 2 study. Investors may watch for depth of efficacy and safety data, as well as how these results support the broader development path previously outlined for muzastotug.
Key Terms
hepatocellular carcinoma medical
phase 1b/2 medical
first-in-human medical
AI-generated analysis. Not financial advice.
SAN DIEGO and SUZHOU, China, March 17, 2026 (GLOBE NEWSWIRE) -- Adagene Inc. (“Adagene or the Company”) (Nasdaq: ADAG), a company transforming the discovery and development of novel antibody-based therapies, today announced that muzastotug will be highlighted in two poster presentations at this year’s AACR Meeting, taking place April 17-22 in San Diego, CA.
The following abstracts have been selected for presentation at AACR 2026:
Title: Ph1b evaluation of ADG126 (muzastotug, an anti-CTLA-4 masking antibody) pembrolizumab (Pembro) IO doublet in combination with fruquintinib (Fruq) in advanced and metastatic microsatellite stable colorectal cancer
Session Title: Phase I Clinical Trials in Progress
Session Start: April 20, 2026, 9:00 AM - 12:00 PM Pacific Time
Location: Poster Section 51
Poster Board Number: 14
Abstract Presentation Number: CT083
Title: Results from the phase 1b/2 Morpheus Liver study in patients with unresectable locally advanced or metastatic hepatocellular carcinoma (HCC): Muzastotug (ADG126: masked anti-CTLA-4 Ab) combination arm
Session Title: First-in-Human Phase I Clinical Trials
Session Start: April 20, 2026, 9:00 AM - 12:00 PM Pacific Time
Location: Poster Section 50
Poster Board Number: 14
Abstract Presentation Number: CT054
About Adagene
Adagene Inc. (Nasdaq: ADAG) is a platform-driven, clinical-stage biotechnology company committed to transforming the discovery and development of novel antibody-based cancer immunotherapies. Adagene combines computational biology and artificial intelligence to design novel antibodies that address globally unmet patient needs. The company has forged strategic collaborations with reputable global partners that leverage its SAFEbody precision masking technology in multiple approaches at the vanguard of science.
Powered by its proprietary Dynamic Precision Library (DPL) platform, composed of NEObody™, SAFEbody, and POWERbody™ technologies, Adagene’s highly differentiated pipeline features novel immunotherapy programs. The company’s SAFEbody technology is designed to address safety and tolerability challenges associated with many antibody therapeutics by using precision masking technology to shield the binding domain of the biologic therapy. Through activation in the tumor microenvironment, this allows for tumor-specific targeting of antibodies, while minimizing on-target off-tumor toxicity in healthy tissues.
Adagene’s lead clinical program, muzastotug (ADG126), is a masked, anti-CTLA-4 SAFEbody with FDA Fast Track designation that targets a unique epitope of CTLA-4 in regulatory T cells (Tregs) in the tumor microenvironment. Muzastotug is currently in Phase 1b/2 and Phase 2 clinical studies in combination with anti-PD-1 therapy, particularly focused on microsatellite stable (MSS) metastatic colorectal cancer (CRC). Validated by ongoing clinical research, the SAFEbody platform can be applied to a wide variety of antibody-based therapeutic modalities, including Fc empowered antibodies, antibody-drug conjugates, and bi/multi-specific T-cell engagers.
For more information, please visit: https://investor.adagene.com.
Follow Adagene on WeChat, LinkedIn and X.
SAFEbody® is a registered trademark in the United States, China, Australia, Japan, Singapore, and the European Union.
Investor Contacts:
Raymond Tam
raymond_tam@adagene.com
Corey Davis
LifeSci Advisors
cdavis@lifesciadvisors.com
FAQ
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