No Data Yet, But Homology Upsizes IPO and Raises $144M

[Note - This is a left-handed helix, don't use - SdC] DNA Double Helix

Homology Medicines, a company trying to leapfrog existing gene editing developers, has raised $144 million in an IPO that will help fund its first clinical trials.

Bedford, MA-based Homology (NASDAQ: [[ticker:FIXX]]) priced its offering and sold 9 million shares at $16 apiece. Homology had planned to sell 7.6 million shares at $14 to $16 each. The company’s shares are expected to begin trading later today.

Homology is trying to prove that it owns a better version of existing gene editing methods, among them CRISPR-Cas9, by harnessing a natural biological process known as “homologous recombination,” which cells in humans and other species do to repair DNA damage. But Homology is developing gene therapies as well that utilize adeno-associated viruses—commonly used gene therapy delivery tools—the company has developed in-house. The startup doesn’t yet have human clinical data for its drugs.

Homology’s first target is phenylketonuria, a genetic disorder that leads to the buildup of an amino acid called phenylalanine. With the IPO proceeds, Homology will run an early stage test of a gene therapy candidate, HMI-102, in PKU in adults. Homology aims to follow up by identifying a gene editing treatment for PKU in children later this year.

Here’s more on Homology’s approach to developing drugs for genetic disorders.

Image by Depositphotos.

Author: Frank Vinluan

Xconomy Editor Frank Vinluan is a business journalist with experience covering technology and life sciences. Based in Raleigh, he was a staff writer at the Triangle Business Journal covering technology, biotechnology and energy before joining MedCityNews.com as North Carolina bureau chief. Prior to moving to North Carolina’s Research Triangle in 2007 he held business reporting positions at The Des Moines Register and The Seattle Times.