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From vial to value: How GLP-1s are redefining injectable care for chronic conditions

October 3, 2025

The market for glucagon-like peptide-1 (GLP-1) therapies is growing rapidly, with a projected value of $186.6 billion by 2032. Originally developed for diabetes, these therapies are now widely used for obesity treatment, which has created a need for convenient and scalable delivery systems. This growth is reshaping the industry, creating new demands on manufacturing capacity and requiring innovative solutions for at-home care.

The shift to self-administration

GLP-1 therapies are changing patient expectations for injectable treatments. Patients now expect at-home administration, simple instructions, minimal pain and less frequent dosing. This has led to a significant shift from traditional vial-based delivery to more patient-friendly options like prefilled syringes and autoinjectors. These devices simplify dosing and are designed for ease of use, eliminating the need for clinical oversight.

As patients transition to at-home care, the manufacturing of these products becomes more complex. Devices must be intuitive, compatible with various formulations and meet strict standards for sterility and reliability. Manufacturers are challenged to act as both product developers and regulatory strategists to ensure these devices meet all necessary standards.

With the accelerated adoption of GLP-1s, contract development and manufacturing organizations (CDMOs) have become essential strategic partners for navigating the evolving landscape. They are critical for meeting the unprecedented demand for prefilled syringes and autoinjectors, which has outpaced market preparation and created a significant capacity shortfall.

By reading this comprehensive whitepaper, you will learn:

  • Why the shift from vial-based delivery to prefilled syringes and autoinjectors is creating new capacity demands
  • The details of the device formats, both approved and in development, that are best suited for self-administered chronic care
  • What combination product compliance looks like under evolving global regulations.

Ready to navigate the future of chronic care?
Download the full whitepaper to learn more about how GLP-1s are reshaping injectable manufacturing, device design and patient expectations.

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