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IQVIA and Kexing Biopharm Expand Strategic Collaboration to Accelerate Global Biosimilar Development using AI-Enabled Capabilities

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Key Terms

biosimilar medical
A biosimilar is a medicine created to be highly similar to an existing complex drug made from living cells, matching its safety and effectiveness while allowing for small, natural variations. For investors, biosimilars matter because they introduce lower-cost competition when patents end, which can cut prices, shift market share, and change revenue forecasts for companies selling the original drugs, much like a generic version does for simpler chemical medicines.
clinical trial medical
A clinical trial is a carefully controlled study in which a new medicine, medical device, or treatment is tested on people to see if it is safe and effective. For investors it matters because trial results determine whether a product can win regulatory approval and reach patients, much like a road test decides if a new car can be sold; positive or negative results can sharply change a company’s prospects and stock value.
regulatory strategy regulatory
A regulatory strategy is a company’s plan for getting products, services, or operations approved and kept in compliance with government rules; think of it as a roadmap and playbook for dealing with regulators. It matters to investors because the plan determines how quickly a product can reach the market, how much it will cost to meet legal requirements, and how likely the company is to face fines or delays — all of which affect future revenue and risk.
commercialization technical
Commercialization is the process of bringing a new product, service, or idea to the market so that people can buy and use it. It involves turning an invention or development into something that is widely available and profitable. For investors, commercialization matters because it signals the transition from development to generating revenue, indicating potential growth and the likelihood of a return on investment.
microecological preparations medical
Microecological preparations are products that introduce or support beneficial microscopic organisms to restore or maintain a healthy balance of microbes in the body, most often the gut. Think of them like a targeted gardening kit that helps desirable plants flourish and crowds out weeds; their effectiveness, safety and manufacturing quality determine customer demand, regulatory approval, and pricing. Investors watch them because clinical evidence, regulatory status and scalable production directly affect sales potential, competitive advantage and risk.
AI‑enabled technical
ai‑enabled describes products, services, or processes that use artificial intelligence to add automation, prediction, or decision support to tasks that were once done entirely by humans or simple rules. For investors, ai‑enabled offerings can mean faster work, lower costs, new features, or competitive differentiation, but they also bring questions about accuracy, ongoing training costs, regulatory oversight and how reliably the technology performs in real-world conditions.
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RESEARCH TRIANGLE PARK, N.C.--(BUSINESS WIRE)-- IQVIA (NYSE:IQV), a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries, is advancing its strategic collaboration with Kexing Biopharm to support a global, multi-product biosimilar development and commercialization program. Kexing Biopharm (Stock Code: 688136.SH) is an innovative biopharmaceutical enterprise mainly engaged in the R&D, production and sales of recombinant protein drugs and microecological preparations.

The collaboration is designed to support Kexing’s global expansion by bringing together IQVIA’s end-to-end capabilities across the development lifecycle. By aligning clinical development, regulatory strategy, advanced analytics and commercialization under a coordinated global approach, the program aims to accelerate biosimilar development for international markets while upholding rigorous standards for quality and scientific integrity.

In parallel, the collaboration integrates IQVIA’s AI‑enabled clinical trial capabilities to enhance speed, efficiency and confidence in decision-making throughout development. The use of AI across key activities — from protocol design to site identification and study conduct — will help streamline execution and improve overall trial performance.

“Through this collaboration, we are supporting Kexing as it progresses its global biosimilar development efforts,” said Brian Mi, President, Asia Pacific, IQVIA. “IQVIA brings deep biosimilar expertise, global execution capabilities and AI-powered solutions to accelerate Kexing’s global expansion strategy."

The collaboration reflects IQVIA’s ability to integrate science, insight and execution to help biosimilar developers navigate global complexity with confidence.

“This strategic collaboration will accelerate Kexing’s internationalization strategy and we are highly confident in its prospects,” said Yanqing Zhao, General Manager, Kexing Biopharm. “IQVIA’s scale, global data resources, AI capabilities, patient insights and clinical expertise will support the optimization of trial design, mitigation of regulatory risk and improvement of overseas registration efficiency.”

For more information, visit IQVIA.com.

About IQVIA

IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high‑quality health data, Healthcare‑grade AI®, advanced analytics, the latest technologies and extensive domain expertise. IQVIA is committed to using AI responsibly, with AI‑powered capabilities built on best‑in‑class approaches to privacy, regulatory compliance and patient safety, and delivering AI to the high standards of trust, scalability and precision demanded by the industry. With approximately 93,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy‑enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

About Kexing Biopharm

Kexing Biopharm (Stock Code: 688136.SH) is a leading Internationalization biopharmaceutical company specializing in the research, manufacture, and commercialization of innovative medicines combining recombinant proteins, antibodies, and targeted delivery therapies, etc. Harnessing proprietary technology platforms, Kexing pioneers novel targeted biological therapies and advanced drug delivery systems to address critical unmet needs in oncology, autoimmune and infectious diseases, making transformative impact on patients. Driven by a dual strategic focus on breakthrough innovation and global outreach, Kexing is committed to becoming a world-class leader in bringing high-quality pharmaceutical solutions to patients worldwide.

IQVIAFIN

Kerri Joseph, IQVIA Investor Relations
kerri.joseph@iqvia.com
+1.973.541.3558

Alissa Maupin, IQVIA Media Relations
alissa.maupin1@iqvia.com
+1.919.923.6785

Source: IQVIA