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AcroCyte Therapeutics Awarded ARPA ‑H Funding to Advance Scalable Human Organoid Technologies


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AcroCyte Therapeutics Inc.

Jul 23, 2026, 09:05 ET

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TAIPEI and SAN CARLOS, Calif., July 23, 2026 /PRNewswire/ -- AcroCyte Therapeutics Inc. announced today that it has been selected to receive funding from the Advanced Research Projects Agency for Health (ARPA‑H) to advance scalable human organoid technologies for regenerative medicine applications.

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AcroCyte Therapeutics announces ARPA-H funding during a press conference in Taipei, Taiwan, on July 23, 2026.
AcroCyte Therapeutics announces ARPA-H funding during a press conference in Taipei, Taiwan, on July 23, 2026.

Established by the U.S. government in 2022, ARPA‑H was modeled after the Defense Advanced Research Projects Agency (DARPA) to support high‑risk, high‑reward research programs with the potential to transform human health. Rather than funding incremental advances, ARPA‑H focuses on enabling disruptive technologies capable of addressing major unmet medical and societal challenges.

Among ARPA‑H's priority focus areas is regenerative medicine, including flagship programs aimed at addressing the global shortage of transplantable organs through the development of bioengineered, clinically functional replacement tissues and organs. AcroCyte's selection reflects recognition of its original cell expansion technology as a critical enabling platform for these ambitious efforts.

Core Technology: R3CE® Platform Enables Standardized, Scalable Organoid Production

Human organoids represent one of the most promising frontiers in biomedical science; however, their translation into clinical and translational applications has been limited by long‑standing challenges, including scalability, reproducibility, and manufacturing standardization.

AcroCyte has addressed these challenges through its proprietary R3CE® (Rapid Reproducible Rare Cell 3D Expansion) platform, which enables highly reproducible and standardized three‑dimensional expansion of rare human cells. The R3CE® platform is currently FDA‑registered as a Class I medical device, making it the first standardized organoid expansion system to obtain this regulatory designation.

Using minimally invasive procedures, autologous kidney cells can be obtained from patients and expanded within weeks into physiologically relevant renal organoid modules. This capability supports new pathways for regenerative research and translational development beyond conventional organ transplantation.

International Clinical Strategy: Parallel Development in the U.S. and Taiwan

The ARPA‑H–supported project will be executed through a binational clinical and translational strategy, integrating clinical expertise in both the United States and Taiwan. AcroCyte will collaborate with the University of Chicago Medicine in the U.S. and National Taiwan University Hospital (NTUH), together with the National Center for Biomodels (NCB), to pursue parallel development efforts across both regions.

This coordinated approach is designed to support early alignment with international regulatory standards and facilitate efficient translation toward global clinical applications.

AcroCyte's CEO Statement

"Being selected for support by ARPA‑H is a strong validation of our team's long‑term commitment to advancing three‑dimensional cell technologies," said Dr. Ying C. Chang, Co‑Founder and Chief Executive Officer of AcroCyte Therapeutics. "Following our recognition at MEDICA 2025, where AcroCyte became the first biotechnology company from Taiwan to secure second place in the MEDICA Start-up Competition, this milestone underscores AcroCyte's role in advancing organoid technologies across borders. Our focus is on translating organoid platforms from the laboratory into standardized systems that support regenerative and translational medicine."

NTUH's Vice Superintendent Statement

"NTUH participation as a clinical partner alongside the University of Chicago Medicine in this ARPA-H project reflects international recognition of our clinical and research excellence in regenerative medicine," stated Professor Jia-Horng Kao, Vice Superintendent of NTUH. "Kidney disease remains a significant health concern in Taiwan. Through this collaboration, we hope to integrate global research resources and clinical expertise to advance regenerative medicine for patients with chronic kidney disease."

About AcroCyte Therapeutics Inc.

AcroCyte Therapeutics Inc. is a biotechnology company dedicated to addressing key challenges in New Approach Methodologies (NAMs) by enabling reproducible, robust, and scalable human‑relevant model systems. Through its organoid platforms, the company is advancing animal‑free, high‑throughput alternatives for drug discovery and safety assessment, while enhancing translational relevance across drug development and regenerative medicine.

AcroCyte maintains research and development operations in Silicon Valley, California, and continues to advance high‑quality, scalable cell‑based technologies toward global clinical use.

This research was funded, in part, by the Advanced Research Projects Agency for Health (ARPA-H). The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed or implied, of the U.S. Government.

SOURCE AcroCyte Therapeutics Inc.

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