BIOCONJUGATES

Accelerate Your ADC Program

Altruist Biologics provides end-to-end development and manufacturing for antibody drug conjugates (ADCs) and other novel bioconjugates. Through our integrated capabilities for ADC clinical to commercial manufacturing, we can accelerate your timelines, de-risk and reduce complexities, and meet all product quality requirements.

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Scientist in protective gear operating equipment in a clean laboratory environment.

Our Integrated Capabilities

Our comprehensive services span every critical component of your ADC program – from linker-payload intermediates and antibodies through to the final bioconjugate drug substance and drug product. 
 
Explore Our Capabilities: 

Our Platforms

  • ADC – Antibody Drug Conjugate 
  • APC – Antibody Peptide Conjugate 
  • ACC – Antibody Chelator Conjugate 
  • DAC – Degrader Antibody Conjugate 
  • PEG – PEGylation-Based Conjugate 
  • ISAC – Immuno-Stimulant Antibody Conjugate 
  • AOC – Antibody Oligonucleotide Conjugate 
  • Dual Payload – Dual Payload Antibody Conjugate 
  • BsADC – Bispecific Antibody Drug Conjugate 
3D rendering of antibodies floating in a blue background, illustrating immune system and molecular biology research concepts.

Parallel Development of mAb and ADC 

Our Value Chain From DNA to ADC

Bridging the gap between drug discovery and commercial supply, we offer tailored CMC development for bioconjugation and antibody drug conjugates. 

Timeline of ADC platform development: From DNA to IND in 11-14 months and late-stage development to sBLA in 24 months.

Our Track Record

35+ ADC & AXC Projects

15+

Pre-IND ADC & AXC

8+

IND Enabling 
(FDA, NMPA)

10+

Phase I & II 
(2 FTD)

2

Phase III & PPQ
(FDA, EMA, PMDA, NMPA)

DEDICATED GMP FACILITIES

State-of-the-Art Equipment and Flexible Design

We provide synergy with existing systems and procedures for both mAbs and ADCs to accelerate timelines. 

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Hangzhou Site

Our dedicated ADC facility in Hangzhou features single-use reactor systems supporting conjugation scales of up to 500 L (1000L-5,000L are under construction), providing the flexibility and capacity required for scalable ADC manufacturing. The site includes fully integrated laboratories dedicated to ADC process development, quality control (QC), and MSAT to support seamless progression from development through manufacturing. 

The facility is designed for the safe handling of high-potency APIs (HPAPIs) and incorporates stringent high-containment systems with an Occupational Exposure Limit (OEL) capability of 5 ng/m³, ensuring the highest standards of safety, regulatory compliance, and operational control.

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Manufacturing Capacities Across the Entire Value Chain

Suzhou AXC Pilot Plant-Bioconjugation Drug Substance: 1g–1,500g/batch
-Dedicated AXC Pilot Plant
-Scale Up Experience: 100g, 150g, 500g, 5,000g
Hangzhou AXC Commercial Facility-ADC Drug Substance Plant: 20L–100L
-Commercial Drug Substance: 100L–500L, 500L–5,000L*
-Commercial Drug Product: 2 x 7.5m² lyophilizer, 2 x 35m² lyophilizer*

(*Under construction)

Contact

Let’s Move Medicine Forward

Leverage our end-to-end ADC expertise to quickly bring your life-changing drug to patients in need.