Javascript must be enabled for the correct page display
Skip to Content
Press Releases

Bora Group to Acquire MacroGenics’ GMP Manufacturing Operations

Bora Group has announced a definitive agreement to acquire the GMP manufacturing operations of MacroGenics, Inc. for $122.5 million, including a biologics drug substance facility in Rockville, Maryland.

This strategic acquisition significantly expands Bora Biologics’ U.S. drug substance capacity and strengthens our integrated end‑to‑end biologics platform. The Rockville site adds five 2,000‑liter and two 500‑liter single‑use bioreactors, fully integrated QC and analytical laboratories, and an established commercial and clinical manufacturing backlog. Upon closing, Bora Biologics’ total drug substance capacity will reach 20,000 liters (SUB), further enhancing our ability to support programs from development through commercial supply.

The transaction also includes a long‑term CDMO service agreement and existing commercial-stage monoclonal antibody programs, reinforcing Bora’s position as a trusted U.S.-based biologics manufacturing partner.

Read Full Press Release

Bora Biologics

the logical choice

Join the ranks of biopharma pioneers who trust us.
Explore how we minimize risks and accelerate your success.

Partner with us

Client-Centric

100% commitment to supporting your success

We have been the client, bringing multiple biologics from IND to BLA. Your needs and goals are at the forefront of our approach. By involving you in every step of the process, we ensure transparency and alignment, reducing the likelihood of misunderstandings and ensuring the outcome meets your expectations.

Experience

14 years developing & manufacturing biologics

We have honed our ability to navigate complexities. Our track record from concept to commercialization means we can apply best practices and lessons learned, ensuring smoother project execution.

Expertise

125 seasoned scientists & regulatory professionals

Our team exudes deep knowledge and specialized skills. This expertise allows us to foresee potential challenges and implement proactive solutions, reducing the likelihood of setbacks.

Commercial-Ready

US FDA registered GMP manufacturing facility

We focus on delivering solutions that are ready for market. With clinical to commercial scale facilities consistently meeting compliance standards, we ensure your project is primed for success, minimizing the risk of costly revisions or delays.

Allied

access to global CDMO resources

Our partnership with Bora Pharmaceuticals provides additional resources and insights. This network enables us to leverage shared knowledge and expertise, further mitigating risks and accelerating the overall success of your project.