Close
Novotech
Jabsco PureFlo 21 Single Use

Moderna to Acquire OriCiro Genomics for $85M

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

Smarter Trial Design Improves Drug Development Speed

Optimization of clinical trial protocols through innovative designs and strategic endpoint selection directly accelerates drug development speed and improves operational reliability.

Data Driven Decisions Improve Drug Development Outcomes

Integrating comprehensive analytics and real-world data into clinical planning allows pharmaceutical companies to optimize trial design and significantly improve patient outcomes.

Efficient Early Strategies Enable Faster Clinical Progress

Implementing optimized early-stage frameworks and enhancing trial readiness allows pharmaceutical sponsors to accelerate clinical timelines and maintain high R&D efficiency.
- Advertisement -

Moderna has announced it will acquire Japan-based DNA supplier OriCiro Genomics K.K (OriCiro) for $85m, marking the US company’s first acquisition since its 2010 launch.

Through the acquisition, Moderna will obtain OriCiro’s tools for cell-free synthesis and amplification of plasmid DNA, a type of DNA molecule for use in mRNA manufacturing.

“OriCiro’s technology strategically complements our manufacturing expertise and further accelerates our research and development engine,” said Stépahane Bancel, chief executive officer of Moderna. “We look forward to welcoming the OriCiro team to Moderna.”

Also commenting on the agreement, OriCiro’s chief executive officer, Nasir Kato Bashiruddin, said: “Moderna has demonstrated remarkable speed and ability to impact lives through their innovative platform and mRNA therapeutics. I am confident that our technology and talent will be a highly strategic fit with Moderna.”

OriCiro’s synthetic biology and enzyme technologies will support Moderna’s portfolio of therapeutics and vaccines, the company said.

In December 2022, a personalised mRNA cancer vaccine from Moderna and Merck & Co – known as MSD outside the US and Canada – was shown to benefit patients with high-risk melanoma.

Personalised cancer vaccines are designed to prime the immune system so that patients can generate tailored antitumour responses as part of their cancer treatment.

In October 2022, the companies announced that Merck had exercised its option to jointly develop and commercialise the vaccine in accordance with the terms of its existing collaboration and licence agreement.

“[The results are] highly encouraging for the field of cancer treatment,” Bancel said at the time of the announcement. “mRNA has been transformative for COVID-19 and now, for the first time ever, we have demonstrated the potential for mRNA to have an impact on outcomes in a randomised clinical trial in melanoma.”

He also outlined the companies’ plans to begin additional studies in melanoma and other forms of cancer “with the goal of bringing truly individualised cancer treatments to patients”.

Latest stories

Related stories

Smarter Trial Design Improves Drug Development Speed

Optimization of clinical trial protocols through innovative designs and strategic endpoint selection directly accelerates drug development speed and improves operational reliability.

Data Driven Decisions Improve Drug Development Outcomes

Integrating comprehensive analytics and real-world data into clinical planning allows pharmaceutical companies to optimize trial design and significantly improve patient outcomes.

Efficient Early Strategies Enable Faster Clinical Progress

Implementing optimized early-stage frameworks and enhancing trial readiness allows pharmaceutical sponsors to accelerate clinical timelines and maintain high R&D efficiency.

Early Insights Reduce Risk in Drug Development Programs

Leveraging early-stage data and translational research allows pharmaceutical companies to mitigate drug development risk and implement adaptive strategies for higher success.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »