# NORROY BIOSCIENCE Granted FDA Breakthrough Therapy and Fast Track Designations for Kidney Cancer Imaging Product

- Link: https://www.thailand-business-news.com/pr-news/norroy-bioscience-granted-fda-breakthrough-therapy-and-fast-track-designations-for-kidney-cancer-imaging-product
- Published: 2026-08-19T16:00:00+07:00
- Author: PR Newswire

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WUXI, China, Aug. 19, 2026 /PRNewswire/ — **NORROY BIOSCIENCE (NORROY)**, a clinical-
stage biotechnology company focused on innovative targeted radiopharmaceuticals,
announced that the U.S. Food and Drug Administration (FDA) has granted both Breakthrough
Therapy and Fast Track designations to NORROY’s ^(68)Ga-NYM096, a potential radiopharmaceutical
imaging agent targeting carbonic anhydrase Ⅸ (CAⅨ) for PET imaging of clear cell
renal cell carcinoma (ccRCC).

^(68)Ga-NYM096 is the first China-originated innovative radiopharmaceutical to receive
FDA Breakthrough Therapy Designation. It is being developed as a non-invasive PET
imaging agent to enable the characterization of indeterminate renal masses identified
by Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) and support the 
differentiation of ccRCC from non-ccRCC lesions.

The granting of this Breakthrough Therapy designation recognizes the potential of
^(68)Ga-NYM096 to provide meaningful clinical advantages over current diagnostic
approaches based on preliminary clinical data, while addressing significant unmet
clinical needs in the diagnosis and management of patients with ccRCC. The Fast 
Track designation is designed to facilitate the development and expedite the review
of ^(68)Ga-NYM096 by enabling more frequent interactions with the FDA, enhanced 
regulatory guidance throughout the clinical development process, and potential eligibility
for rolling review of a New Drug Application (NDA).

Clear cell renal cell carcinoma is the most common subtype of renal cell carcinoma(
RCC), accounting for approximately 70%–80% of RCC cases. According to the American
Cancer Society, in 2026, an estimated 80,450 new cases of kidney (renal) cancer 
will be diagnosed in the US, and 15,160 people will die from the disease.

NORROY Founder and CEO, Mr. Peng Fang, said: "We have seen promising clinical data
from the ongoing development of ^(68)Ga-NYM096, supporting its potential to advance
the diagnosis and management of patients with ccRCC. Additional clinical data of
^(68)Ga-NYM096 will be presented at the 2026 EANM Annual Congress. We plan to initiate
Phase I clinical trials evaluating ^(68)Ga-NYM096 in both China and the United States,
and will continue to work closely with the FDA to advance its clinical development.
We believe this innovative imaging agent has the potential to reshape the diagnosis
and management of ccRCC and ultimately benefit more patients worldwide."

**About NORROY BIOSCIENCE**

NORROY is a clinical-stage biotechnology company focused on the development and 
commercialization of innovative therapeutic and diagnostic radiopharmaceuticals,
as well as automated synthesis systems and functional modules for radiopharmaceutical
manufacturing in both R&D and GMP environments.

Founded in July 2021, NORROY has radiopharmaceutical candidates currently under 
clinical investigation in more than 10 disease targets across multiple therapeutic
areas, including urological oncology, gastrointestinal oncology, and other oncology
and non-oncology indications. Beyond innovative radiopharmaceuticals and automated
manufacturing solutions, NORROY continues to establish a reliable global supply 
chain for multiple radioisotopes, build commercial GMP manufacturing facilities,
and develop a global distribution network with international partners.

To date, NORROY has received six (6) IND clearances from the FDA and six (6) IND
approvals from the National Medical Products Administration (NMPA). The Company 
is actively working with global regulatory agencies to advance its late-stage programs
through internationally registered clinical trials.

To learn more about NORROY, visit [https://www.norroybiopharm.com/](https://www.norroybiopharm.com/)

and follow us on LinkedIn: [https://www.linkedin.com/company/norroybiopharm/](https://www.linkedin.com/company/norroybiopharm/)

**NORROY ContactsMedia: [BD@norroybioscience.com](https://www.thailand-business-news.com/pr-news/BD@norroybioscience.com)

**Important Information**

^(68)Ga-NYM096 is an investigational product and has not been approved for marketing
by the United States Food and Drug Administration (FDA) or any other regulatory 
authority. Its safety and efficacy have not been fully established.

FDA Breakthrough Therapy and Fast Track designations are intended to facilitate 
and expedite the development and review of certain investigational products to treat
serious conditions and fill an unmet medical need. Such designations do not constitute
marketing approval and do not guarantee that ^(68)Ga-NYM096 will receive regulatory
approval.

**Forward-Looking Statements**

This press release contains forward-looking statements, including statements regarding
the clinical development and regulatory progress of ^(68)Ga-NYM096; the presentation
of additional clinical data; the planned initiation, timing, progress and results
of clinical trials; interactions with regulatory authorities; potential regulatory
submissions and approvals; manufacturing activities; and the potential commercialization
of NORROY’s product candidates in China and/or in the United States.

These forward-looking statements are based on NORROY’s current expectations and 
assumptions and are subject to known and unknown risks, uncertainties and other 
factors that could cause actual results, performance or achievements to differ materially
from those expressed or implied by such statements. There can be no assurance that
planned clinical trials will be initiated or completed as anticipated, that clinical
results will support further development or regulatory submissions, or that any 
of NORROY’s product candidates will receive regulatory approval or achieve commercial
success.

Except as required by applicable law, NORROY undertakes no obligation to publicly
update or revise any forward-looking statements contained in this press release 
as a result of new information, future events or otherwise.

 

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