Abpro's ABP-102 program was highlighted by Celltrion at the J.P. Morgan Healthcare Conference following FDA IND approval for clinical trials.
Quiver AI Summary
Abpro Holdings, Inc. announced that its lead oncology program, ABP-102 / CT-P72, was highlighted by its partner Celltrion at the 2026 J.P. Morgan Healthcare Conference. This presentation showcased Celltrion's ongoing drug development efforts and included news that ABP-102 has received FDA Investigational New Drug (IND) clearance, allowing for a global Phase 1 clinical trial for patients with HER2-positive solid tumors to begin in the first half of 2026. Abpro's CEO, Miles Suk, emphasized the significance of this exposure at such a major conference, reflecting the program's validation and potential. ABP-102 is designed as a multispecific T-cell engager to selectively target cancer cells while minimizing safety risks. The company's mission is to create next-generation antibody therapies for life-threatening diseases, leveraging its proprietary DiversImmune® platform.
Potential Positives
- ABP-102 / CT-P72 received FDA Investigational New Drug clearance, allowing the initiation of a global Phase 1 clinical trial for patients with HER2-positive solid tumors.
- The inclusion of ABP-102 in a presentation at the prestigious J.P. Morgan Healthcare Conference enhances visibility and credibility for Abpro's oncology program, showcasing its potential within the pharmaceutical community.
- The collaboration with Celltrion is highlighted as a strategic partnership that strengthens Abpro’s position and enhances the momentum following the recent IND clearance.
Potential Negatives
- While the IND clearance for ABP-102 is a positive development, the press release highlights significant dependency on the collaboration with Celltrion, raising concerns about Abpro's independent capabilities in progressing its oncology pipeline.
- The extensive forward-looking statements and risk disclosures indicate potential uncertainties surrounding the development timeline and regulatory approvals, which could negatively impact investor confidence.
- The mention of Abpro’s need to comply with Nasdaq listing standards could signal financial instability or operational challenges within the company.
FAQ
What is Abpro Holdings, Inc. known for?
Abpro Holdings, Inc. develops next-generation antibody therapeutics, primarily targeting solid tumors.
What program was highlighted at the J.P. Morgan Healthcare Conference?
ABP-102 / CT-P72, a multispecific antibody oncology program, was featured in a presentation by Celltrion.
What recent approval did ABP-102 / CT-P72 receive?
ABP-102 / CT-P72 received FDA Investigational New Drug (IND) clearance for a global Phase 1 clinical trial.
When is the clinical trial for ABP-102 expected to start?
The clinical trial for ABP-102 is anticipated to commence in the first half of 2026.
What therapeutic approach does ABP-102 utilize?
ABP-102 is engineered as a HER2 × CD3 T-cell engager to selectively target HER2-overexpressing tumor cells.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$ABP Insider Trading Activity
$ABP insiders have traded $ABP stock on the open market 1 times in the past 6 months. Of those trades, 1 have been purchases and 0 have been sales.
Here’s a breakdown of recent trading of $ABP stock by insiders over the last 6 months:
- JIN WOOK (MILES) SUK (CEO and Chairman) purchased 72,035 shares for an estimated $20,169
To track insider transactions, check out Quiver Quantitative's insider trading dashboard.
$ABP Hedge Fund Activity
We have seen 9 institutional investors add shares of $ABP stock to their portfolio, and 11 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- CANTOR FITZGERALD, L. P. removed 600,000 shares (-100.0%) from their portfolio in Q3 2025, for an estimated $134,520
- GEODE CAPITAL MANAGEMENT, LLC removed 189,702 shares (-96.5%) from their portfolio in Q3 2025, for an estimated $42,531
- POLAR ASSET MANAGEMENT PARTNERS INC. added 87,500 shares (+inf%) to their portfolio in Q3 2025, for an estimated $588,525
- ATLAS MERCHANT CAPITAL LLC removed 84,583 shares (-96.7%) from their portfolio in Q3 2025, for an estimated $18,963
- AQR ARBITRAGE LLC added 84,583 shares (+2899.7%) to their portfolio in Q3 2025, for an estimated $568,905
- VIRTU FINANCIAL LLC removed 77,467 shares (-100.0%) from their portfolio in Q3 2025, for an estimated $17,368
- LMR PARTNERS LLP removed 60,417 shares (-96.7%) from their portfolio in Q3 2025, for an estimated $13,545
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
Full Release
BURLINGTON, Mass., Jan. 15, 2026 (GLOBE NEWSWIRE) -- Abpro Holdings, Inc. (Nasdaq: ABP), a clinical-stage biotechnology company developing next-generation antibody therapeutics for solid tumors, today announced that its lead multispecific antibody oncology program, ABP-102 / CT-P72, was featured in a presentation by its global collaboration partner, Celltrion, at the 2026 J.P. Morgan Healthcare Conference.
Celltrion’s senior executives attended the conference to present the company’s latest progress in new drug development and long-term growth strategy. The presentation took place on Tuesday, January 13, 2026 at the conference venue. The Celltrion team highlighted its oncology pipeline and partnered programs, including ABP-102 / CT-P72.
ABP-102 / CT-P72 recently received U.S. Food and Drug Administration (FDA) Investigational New Drug (IND) clearance , enabling the initiation of a global Phase 1 clinical trial evaluating the candidate in patients with HER2-positive solid tumors. The study is anticipated to commence in the first half of 2026 through Abpro’s strategic collaboration with Celltrion.
“The inclusion of ABP-102 in Celltrion’s presentation at the J.P. Morgan Healthcare Conference represents a meaningful validation of the program and its potential,” said Miles Suk, Chief Executive Officer of Abpro. “JPM remains the most influential healthcare investment forum globally, and having ABP-102 highlighted by a leading global biopharmaceutical partner underscores the strength of our science, our collaboration with Celltrion, and the momentum we are building following recent IND clearance.”
The J.P. Morgan Healthcare Conference is the world’s largest annual healthcare investment conference, bringing together global pharmaceutical and biotechnology companies alongside institutional investors and partners.
ABP-102 / CT-P72 is a multispecific HER2 × CD3 T-cell engager engineered to selectively target HER2-overexpressing tumor cells while engaging cytotoxic T cells, with optimized binding designed to enhance tumor selectivity and mitigate safety risks that have historically limited the use of T-cell engagers in solid tumors. Preclinical data supporting the program were presented at major international scientific meetings in 2025, including the Annual Meetings of the American Association for Cancer Research (AACR) and the Society for Immunotherapy of Cancer (SITC).
About Abpro
Abpro’s mission is to improve the lives of mankind facing severe and life-threatening diseases with next-generation antibody therapies. Abpro is advancing a pipeline of next-generation antibody therapies, for HER2+ cancers, non-HER2+ gastric and liver cancer, and wet age-related macular degeneration (AMD) and diabetic macular edema (DME). These antibodies are developed using Abpro's proprietary DiversImmune
®
platform. Abpro is located in Burlington, Massachusetts. For more information, please visit
www.abpro.co
.
Forward-Looking Statements
This press release includes certain disclosures that contain “forward-looking statements,” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, express or implied statements regarding the timing and advancement of development programs, including the timing and availability of additional data, and expectations regarding the therapeutic benefit of Abpro’s programs, as well as strategic partnerships. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, those risks and uncertainties related to the timing and advancement of development programs; Abpro’s ability to continue as a going concern; Abpro’s ability to achieve compliance with Nasdaq listing standards; expectations regarding the therapeutic benefit of Abpro’s programs; that final data from Abpro’s preclinical studies and completed clinical trials may differ materially from reported interim data from ongoing studies and trials; Abpro’s ability to efficiently discover and develop product candidates; Abpro’s ability to obtain and maintain regulatory approval of product candidates; Abpro’s ability to maintain its intellectual property; the implementation of Abpro’s business model, including strategic plans for Abpro’s business and product candidates; and other risks identified in Abpro’s filings with the U.S. Securities and Exchange Commission (SEC) including Abpro’s most recent Annual Report on Form 10-K filed with the SEC and subsequent filings with the SEC. Abpro cautions you not to place undue reliance on any forward-looking statements, which speak only as of the date they are made. Abpro disclaims any obligation to publicly update or revise any such statements to reflect any change in expectations or in events, conditions, or circumstances on which any such statements may be based, or that may affect the likelihood that actual results will differ from those set forth in the forward-looking statements. Any forward-looking statements contained in this press release represent Abpro’s views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date.
About Celltrion
Celltrion is a leading biopharmaceutical company based in Incheon, South Korea, that specializes in researching, developing, and manufacturing innovative therapeutics that improve people's lives worldwide. Celltrion pursues sustainable growth by leveraging its experience and assets in the successful biosimilar business to develop new medicines and healthcare platform technologies. The company works with a sense of duty to advance patients' wellness and provide them with enhanced access to reliable healthcare. To accomplish this, Celltrion adheres to strong internal ethical standards in its daily operations. To learn more, please visit
www.celltrion.com.
Investor and Media Contact:
Daniel Kontoh-Boateng
DKB Partners, LLC
Tel: +1-862-213-1398
[email protected]