The Medicine Maker
  • Explore

    Explore

    • Latest
    • Features
    • Interviews
    • Business & Trends
    • Technology & Manufacturing
    • Product Profiles
    • White Papers

    Featured Topics

    • Biopharma
    • Small Molecules
    • Cell & Gene
    • Future of Pharma

    Issues

    • Latest Issue
    • Archive
    • Cell and Gene Therapy Supplement
  • Topics

    Topics

    • Cell & Gene
    • Bioprocessing
    • Drug Delivery
    • Drug Discovery
    • Development & Clinical
    • Formulation
    • Facilities & Equipment
    • Outsourcing
    • Packaging
    • Regulation & Standards
    • Small Molecules
    • Supply Chain
  • News & Blogs

    News & Blogs

    • Industry News
    • Research News
    • Blogs
  • Events
    • Live Events
    • Webinars
  • Community & Awards

    Community & Awards

    • Power List
    • Sitting Down With
    • Innovation Awards
    • Company of the Year Awards
    • Authors & Contributors
  • Multimedia
    • Video
    • eBooks
    • Content Hubs
Subscribe
Subscribe
The Medicine Maker / Issues / 2019 / Oct / Delivering the ADC Promise
Manufacture Outsourcing Technology & Manufacturing Sponsored

Delivering the ADC Promise

What challenges do CDMOs face when manufacturing antibody-drug conjugates?

By Maryam Mahdi, John Fowler 10/22/2019 0 min read Quick Read (pre 2022)

Share

With companies seeking external support for antibody-drug conjugate development and manufacturing, CDMOs are playing an increasingly integral role in their success story. Piramal Pharma Solutions – an early adopter of ADC manufacturing capabilities – is one such actor. Here, John Fowler, COO at Piramal Pharma Solutions, discusses the promise  – and the challenges – of ADCs.

“With 40 ADCs in clinical trials, there’s a great deal to be excited about when it comes to this class of drugs,” says Fowler. “They have the potential to change not only the way we treat cancer, but a variety of disease indications. And that’s why three of our clients have been able to skip phase III and are ready to apply for INDs.”

Five ADCs have now been approved – certainly “wins” for the field, but what challenges do CDMOs specifically encounter when it comes to ADCs? 

  • Scale up. “The sticking point for companies is that an ADC has three elements: antibody, linker and a cytotoxic agent. All three pose different challenges and linkers can have varying levels of sophistication, so developing expertise to handle these challenges is essential,” says Fowler.
  • Cost. A single batch of product may cost  “several million dollars” according to Fowler. But he argues that the cost burden is outweighed by the market potential of ADCs.
  • Supply chain.
    Dealing with multiple vendors and quality systems can often slow down the development cycle of ADCs. Fowler, therefore, recommends that suppliers adopt an integrated approach to enhance their capability for managing the production of high potent APIs, payloads and linkers to help “de-risk” the process. Fowler explains that having direct control of an entire supply chain brings adds value to a company as they are able to prioritize and control timelines to include accelerated quality release under a common system.

Despite the development and manufacturing challenges presented by ADCs, Fowler is optimistic about the future – with the approvals to date proving the concept. “ADCs are improving clinical outcomes for cancer, and so we’re seeing the field open up. I expect to see more companies pursuing innovative solutions for patients – and, therefore, a diverse range of products entering the market. Ultimately, we cannot ignore the therapeutic benefits offered by ADCs – they more than make up for the challenges of their manufacture.”

John Fowler, COO at Piramal Pharma Solutions.

Newsletters

Receive the latest pharmaceutical news, personalities, education, and career development – weekly to your inbox.

Newsletter Signup Image

About the Author(s)

Maryam Mahdi

After finishing my degree, I envisioned a career in science communications. However, life took an unexpected turn and I ended up teaching abroad. Though the experience was amazing and I learned a great deal from it, I jumped at the opportunity to work for Texere. I'm excited to see where this new journey takes me!

More Articles by Maryam Mahdi

John Fowler

More Articles by John Fowler

Recommended

Related Content

The Mindset for Success in Biopharma's New Multipolar World
Biopharma Development & Clinical Outsourcing
The Mindset for Success in Biopharma's New Multipolar World

August 18, 2026

10 min read

From collapsing legacy models to the rise of Chinese biotech, industry leaders are being forced to rethink how drugs are developed, funded, and brought to market

Musings from The Power List: Ali Pashazadeh
Outsourcing Biopharma Business & Trends
Musings from The Power List: Ali Pashazadeh

August 7, 2026

7 min read

Ali Pashazadeh argues that management failures sink too many clinical programs – and explains why commercial discipline must start much earlier

The Confidentiality Barrier to AI-Enabled Drug Development
Small Molecules Small Molecules Formulation
The Confidentiality Barrier to AI-Enabled Drug Development

July 27, 2026

3 min read

AI can help formulation teams better predict performance and allocate resources, but proprietary data protections remain a critical bottleneck

The Rise of China: From Science Cities to Global Ambition
Outsourcing Regulation & Standards Biopharma
The Rise of China: From Science Cities to Global Ambition

July 15, 2026

8 min read

Daphne Smyth of Veristat on the rise of Chinese biopharma, regulatory realities, and what comes next

The Medicine Maker
Subscribe

About

  • About Us
  • Work at Conexiant Europe
  • Terms and Conditions
  • Privacy Policy
  • Advertise With Us
  • Contact Us

Copyright © 2026 Texere Publishing Limited (trading as Conexiant), with registered number 08113419 whose registered office is at Booths No. 1, Booths Park, Chelford Road, Knutsford, England, WA16 8GS.

Affiliations:

Specialties:

Areas of Expertise:

Contributions: