We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

FDA-Cleared Genomic Profiling Assay Guides Treatment Selection in Solid Tumors

By LabMedica International staff writers
Posted on 19 May 2026

Datar Cancer Genetics (DCG; Nashik, India), a global precision oncology company, has announced that its tissue-based comprehensive genomic profiling (CGP) assay for all solid tumors, CellDx-Tissue, has received U.S. Food and Drug Administration (FDA) clearance. The assay is intended to support personalized clinical management decisions in accordance with professional guidelines and is performed as a single-site test at a CAP- and CLIA-accredited laboratory.

The technology employs targeted next‑generation sequencing of DNA and RNA isolated from formalin‑fixed paraffin‑embedded (FFPE) tumor tissue. It analyzes 517 cancer‑associated genes and reports somatic single nucleotide variants, small insertions and deletions, ERBB2 gene amplification, and gene fusions involving ALK, RET, and ROS1. Fusion calls are based on RNA‑level evidence within a dual‑analyte DNA/RNA workflow.


Image: CellDx-Tissue is a qualitative IVD test that uses targeted NGS of DNA and RNA isolated from FFPE solid tumor tissue to analyze 517 cancer-associated genes (image credit: Adobe Stock)
Image: CellDx-Tissue is a qualitative IVD test that uses targeted NGS of DNA and RNA isolated from FFPE solid tumor tissue to analyze 517 cancer-associated genes (image credit: Adobe Stock)

The FDA clearance process spans analytical, clinical, and information technology domains. The clearance recognizes the assay’s dual‑analyte design and complements earlier FDA Breakthrough Device Designations received for the company’s liquid biopsy platforms. The platform is intended for use by oncologists globally to aid personalized clinical decision‑making.

“This US FDA clearance for CellDx-Tissue adds gold-standard regulatory endorsement to an important solution offered by DCG. CellDx-Tissue bridges the gap between genomic complexity and clinical decision-making, offering patients wider options in an era of rapidly evolving therapies. We're proud to bring this technology to oncologists worldwide,” said Dr. Vineet Datta, Senior Director, Global Strategy and Business Development.

“US FDA clearance of our tissue-based genomic panel is a substantive validation of our science and quality systems. It enables us to support oncologists with robust, standardized genomic information to guide complex treatment decisions, and reinforces our commitment to combining advanced genomics, rigorous science, and real-world clinical relevance in service of cancer patients,” said Dr. Darshana Patil, Senior Director, Group Medical Affairs.

Related Links
Datar Cancer Genetics


Gold Member
Automatic Hematology Analyzer
CF9600
Online QC Software
Acusera 24•7
Steam Sterilizer
Hi Vac II Line
Electrolyte Analyzer
BKE-B

Latest Molecular Diagnostics News

Plasma Protein Signature Predicts Lung Cancer Risk Up to Five Years Ahead
19 May 2026  |   Molecular Diagnostics

Circulating Tumor DNA Testing Guides Chemotherapy, Reduces Relapse in Colon Cancer
19 May 2026  |   Molecular Diagnostics

Researchers Uncover Distinct Chromosome Signature in Aggresive ALT Cancers
19 May 2026  |   Molecular Diagnostics



ADLM