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ADC Therapeutics Accelerates R&D with Genedata Biologics


News provided by

Genedata Biologics

Apr 16, 2024, 08:30 ET

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Digitalizing Biopharma R&D: The Genedata Biopharma Platform is the #1 enterprise software system for achieving operational excellence in biopharma R&D.
Digitalizing Biopharma R&D: The Genedata Biopharma Platform is the #1 enterprise software system for achieving operational excellence in biopharma R&D.

Enterprise software solution streamlines development of breakthrough antibody drug conjugate (ADC) therapies for cancer treatment

BASEL, Switzerland, April 16, 2024 /PRNewswire-PRWeb/ -- Genedata, the leading provider of enterprise software solutions for biopharmaceutical R&D, announced today that ADC Therapeutics, a commercial-stage biotechnology company and pioneer in the field of antibody drug conjugates (ADCs), has successfully deployed Genedata Biologics® to streamline the development of next-generation ADCs for the treatment of hematological malignancies and solid tumors. 

"We are pleased that ADC Therapeutics has chosen Genedata Biologics to automate and digitalize their antibody drug conjugates research operations," said Othmar Pfannes, Ph.D., CEO of Genedata. "The implementation of the Genedata platform by yet another leading ADC company underscores the quality of our software for innovative conjugate-based drugs such as antibody, RNA, or peptide conjugates. Our ongoing commitment involves further investment in the Genedata Biopharma Platform to support global customers in advancing new drug modalities with intricate designs and unique properties, so they can accelerate therapeutic progress and deliver novel treatments to patients more efficiently."

When exploring the market, we were thrilled to find a commercial digital platform that is not only purpose-built for ADC workflows but can even support our proprietary conjugation and linker technologies out-of-the-box. Patrick van Berkel, Ph.D., Chief Scientific Officer at ADC Therapeutics

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Genedata Biologics, the market-leading R&D workflow platform, supports ADC Therapeutics in building and progressing a pipeline of proprietary ADC candidates for cancer treatment. The regulatory approval of ADC Therapeutics' first drug, ZYNLONTA®, just 10 years after the company's founding, has validated the success of the ADC Therapeutic proprietary technology. Since then, ADC Therapeutics has diversified their product portfolio to include alternative formats and linker-payload technology. This expansion of technologies and growth of research capabilities led them to choose Genedata Biologics as their enterprise research data management solution to streamline increasingly complex ADC development workflows and protect their intellectual property. Genedata Biologics is used for tracking and analyzing production of candidate molecules, including expression, purification, conjugation, and assay analytics. The platform is fully integrated with ADC Therapeutics' laboratory instruments and IT infrastructure, such as their ELN, to ensure full data traceability and integrity.

"As we scaled up our ADC discovery and development operations, we realized that a robust structured data management system such as Genedata Biologics was essential," said Patrick van Berkel, Ph.D., Chief Scientific Officer of ADC Therapeutics. "When exploring the market, we were thrilled to find a commercial digital platform that is not only purpose-built for ADC workflows but can even support our proprietary conjugation and linker technologies out-of-the-box. After a smooth deployment, our scientists now have real-time access to all critical data, which enables fully informed decision-making. Today, all our novel ADCs are registered in Genedata, and the platform's end-to-end capabilities have transformed our research operations, enabling us to systematically advance our next-generation ADC candidates to the clinic."

About ADC Therapeutics
ADC Therapeutics (NYSE: ADCT) is a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs). The Company is advancing its proprietary ADC technology to transform the treatment paradigm for patients with hematologic malignancies and solid tumors.

ADC Therapeutics' CD19-directed ADC ZYNLONTA (loncastuximab tesirine-lpyl) received accelerated approval by the FDA and conditional approval from the European Commission for the treatment of relapsed or refractory diffuse large B-cell lymphoma after two or more lines of systemic therapy. ZYNLONTA is also in development in combination with other agents and in earlier lines of therapy. In addition to ZYNLONTA, ADC Therapeutics has multiple ADCs in ongoing clinical and preclinical development.

ADC Therapeutics is based in Lausanne (Biopôle), Switzerland and has operations in London, the San Francisco Bay Area and New Jersey. For more information, please visit http://www.adctherapeutics.com and follow the Company on LinkedIn.

ZYNLONTA® is a registered trademark of ADC Therapeutics SA.

About Genedata
Genedata transforms data into intelligence with innovative software solutions that incorporate extensive biopharma R&D domain knowledge. Multinational biopharmaceutical organizations and cutting-edge biotechs around the globe rely on Genedata to digitalize and automate data-rich and complex R&D processes. From early discovery all the way to the clinic, Genedata solutions help maximize the ROI in R&D expenditure. Founded in 1997, Genedata is headquartered in Basel, Switzerland with additional offices in Boston, London, Munich, San Francisco, Singapore, and Tokyo.
http://www.genedata.com
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Contact
Allison Kurz
Genedata
Public Relations
[email protected] 

Disclaimer
The statements in this press release that relate to future plans, events or performance are forward-looking statements that involve risks and uncertainties, including risks associated with uncertainties related to contract cancellations, developing risks, competitive factors, uncertainties pertaining to customer orders, demand for products and services, development of markets for the Company's products and services. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. The Company undertakes no obligation to release publicly the result of any revisions to these forward-looking statements that may be made to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

All product and service names mentioned are the trademarks of their respective companies.

Media Contact

Allison Kurz, www.genedata.com, +41615118400, [email protected], www.genedata.com

SOURCE Genedata Biologics

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