Skip to main content
Premium Trial:

Request an Annual Quote

Traversa Inks Deal to Evaluate siRNA Delivery Technology with Sanofi-Aventis

Premium

Traversa Therapeutics announced this week that it has signed a research agreement with Sanofi-Aventis for the development of the RNAi shop's delivery technology.

The technology, dubbed PTD-DRBD, comprises protein transduction domains linked with a double-stranded RNA binding domain.

According to Traversa, an siRNA coated with PTD-DRBD molecules binds to cell-surface proteoglycans, which stimulates macropinocytosis. The drug then enters the cell inside a macropinosome, at which point the pH inside the vesicle drops and the siRNA is released from the PTD-DRBD molecules into the cytoplasm.

Under the agreement, the companies will examine the ability of the PTD-DRBD technology to deliver siRNAs against undisclosed targets, with an eye toward developing RNAi therapeutics. Additional terms were not disclosed.

“This agreement will allow Sanofi-Aventis to select lead RNAi candidates and provide Traversa with a better understanding of the strengths of our RNAi delivery technology," Traversa President and CEO Hans Petersen said in a statement. "We are excited to be working with Sanofi-Aventis to conduct this research, and hope to advance the treatments selected during this collaboration into [investigational new drug application]-enabling studies and into the clinic.”

The Scan

Positive Framing of Genetic Studies Can Spark Mistrust Among Underrepresented Groups

Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants.

Small Study of Gene Editing to Treat Sickle Cell Disease

In a Novartis-sponsored study in the New England Journal of Medicine, researchers found that a CRISPR-Cas9-based treatment targeting promoters of genes encoding fetal hemoglobin could reduce disease symptoms.

Gut Microbiome Changes Appear in Infants Before They Develop Eczema, Study Finds

Researchers report in mSystems that infants experienced an enrichment in Clostridium sensu stricto 1 and Finegoldia and a depletion of Bacteroides before developing eczema.

Acute Myeloid Leukemia Treatment Specificity Enhanced With Stem Cell Editing

A study in Nature suggests epitope editing in donor stem cells prior to bone marrow transplants can stave off toxicity when targeting acute myeloid leukemia with immunotherapy.