Skip to main content
Premium Trial:

Request an Annual Quote

In Brief This Week: Enzo Biochem, Epigenomics, OpGen, Precipio, Agilent Technologies, More

NEW YORK – Enzo Biochem said this week that total revenues for its fiscal third quarter were down 39 percent year over year to $16.1 million from $26.2 million as COVID-19 testing declined and a ransomware attack reduced volumes. Enzo Life Sciences revenues dipped 1 percent to $7.5 million compared to $7.6 million a year ago, the Farmingdale, New York-based firm said, while Enzo Clinical Lab revenues decreased 54 percent to $8.6 million from $18.6 million a year ago. Laboratory Corporation of America in March said it is buying Enzo's clinical lab assets for $146 million in cash. Enzo's shareholders have approved the deal, and the firm has met all regulatory requirements for the deal, it said. 


Epigenomics said this week that it is in advanced negotiations with an unnamed US-based strategic investor about the acquisition of almost all of its assets. If the deal comes through, it will include all patents and other intellectual property rights relating to the German company's Epi proColon and Epi proColon "NextGen" tests as well as all blood samples owned by the firm. The anticipated purchase price is just over $11.5 million, consisting of $1.5 million in cash at closing and in December of this year, as well as milestone payments relating to Epi proColon and Epi proColon "NextGen," and shares of the acquiring company. The agreement would also include royalties and earn-out payments that Epigenomics would receive if the Epi proColon "NextGen" assay is commercialized. 


OpGen said last week that Nasdaq has told the company it is not in compliance with a requirement calling for a minimum bid price of $1.00 per share over the prior 30 consecutive business days. As a result, OpGen's shares could face delisting action. The firm has 180 calendar days to regain compliance. If it does not, it may seek an additional 180 calendar days to regain compliance. 


Precipio announced this week a deal with an unnamed New York-based academic healthcare institution to jointly develop a panel for glioblastoma using the company's HemeScreen technology. Precipio will design and develop the genetic panel, which provides prognostic and therapeutic markers for the brain cancer. The institution will provide patient samples as well as clinical expertise. It intends to be the first to use the panel upon completion of its development. New Haven, Connecticut-based Precipio said it anticipates the development process will last four months and cost less than $50,000.  


Agilent Technologies said this week in a document filed with the US Securities and Exchange Commission that it has entered into an agreement for a new $1.5 billion five-year unsecured credit agreement that it will use for general corporate purposes. The agreement runs through June 7, 2028. BNP Paribas is the administrative agent, swingline lender, and one of the issuers of lines of credit, and the other lenders included Citibank, Bank of America, JP Morgan Chase Bank, and Wells Fargo Bank. 


NeoGenomics said this week that it has obtained its first commercial payor coverage for its Radar minimal residual disease assay. Effective Aug. 1, Blue Shield of California will cover the test for its plan members, approximately 4.7 million covered lives. The policy considers the test medically necessary for patients with stage I-IV cancer after surgical intervention for adjuvant or targeted therapy and/or monitoring for relapse or progression. 


Molecular diagnostics developer Gencurix said this week that it has gained Korean Ministry of Food and Drug Safety approval for a PCR test used to identify EGFR mutations that are common in non-small cell lung cancer patients and can guide therapy selection. The Seoul-based firm said its Droplex EGFR Mutation Test V2 can detect up to 107 mutations, including exon 20 insertion, and can be run on Bio-Rad Laboratories' Droplet Digital PCR instrument. The firm noted it secured CE marking for the test last year. 


The Department of Health of Abu Dhabi said this week that it has signed a declaration of collaboration with Mass General Brigham's International Center for Genetic Disease (iCGD). The goal of the collaboration, financial terms of which were not disclosed, is to promote clinical and translational research, build capacity, and commercialize technology in the life sciences. The partners will use the Emirate's genomics capabilities to expand research into genomic medicine and genetic diseases including rare diseases, oncology, neurology, cardiovascular disease, and metabolic disease. The collaboration aims to enhance access to treatments for patients in the United Arab Emirates and beyond. Specifically, it will focus on analyzing whole-genome sequencing data from the Emirati Genome Program and on translational studies to develop novel therapies including gene therapies. The partners will also explore opportunities to establish joint laboratories and genetic screening programs in Abu Dhabi. 


BC Platforms said this week that it has added Hospital do Coração in São Paulo, Brazil, to its BCRquest.com global biobank analytics platform. The cardiology center, known as HCor, will contribute de-identified longitudinal patient data on conditions including atrial fibrillation, heart failure, and stroke to the BCRquest.com network. HCor sees nearly 80,000 patients per day. 


In Brief This Week is a selection of news items that may be of interest to our readers but had not previously appeared on GenomeWeb. 

The Scan

Cystatin C Plays Role in Immunosuppression, Cancer Immunotherapy Failure, Study Finds

A study in Cell Genomics provides insight into how glucocorticoids can lead to cancer immunotherapy failure via cystatin C production.

Aging, Species Lifespan Gene Expression Signatures Overlap

An Osaka Metropolitan University team reports in Nucleic Acids Research that transcriptional signatures of aging and maximum lifespan have similarities.

Splicing Subgroup Provides Protocols for Evaluating Splicing Variant Data

The group presents their approach on how to apply evidence codes to splicing predictions and other data in the American Journal of Human Genetics.

Single-Cell Transcriptomic Atlas of Mouse Cochlea to Aid Treatment Development

Researchers in PNAS conducted single-cell and single-nuclear sequencing of about 120,000 cells at three key timepoints in cochlear development to generate a transcriptomic atlas.