
Developing a robust pipeline of biosimilar products
Biosimilar Products
We have a strong and sustainable pipeline of high value biosimilar programs with a primary focus on Oncology and Immunology therapeutic segments.
Bevqolva® (Bevacizumab biosimilar) has received MHRA approval.
Zefylti® (Filgrastim biosimilar) has received EC and MHRA approval.
Dyrupeg® (Pegfilgrastim biosimilar) has received EC and MHRA approval.
Dazublys® (Trastuzumab biosimilar) has received EC and CDSCO approval.
Stage Complete
In Progress
Next Stage
BP13 | Zefylti®
MOLECULE
FILGRASTIM
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Filing
Approval
EC and MHRA marketing authorization received.
Launch
Learn More
BP14 | Dyrupeg®
MOLECULE
PEGFILGRASTIM
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Filing
Approval
EC and MHRA marketing authorization received.
Launch
Learn More
BP01 | Bevqolva®
MOLECULE
BEVACIZUMAB
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Phase 3
Filing
Product filed with UK MHRA based on Phase I data.
Approval
UK MHRA approval received.
Launch
Learn More
BP02 | Dazublys®
MOLECULE
TRASTUZUMAB
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Phase 3
Filing
Approval
EC and CDSCO marketing authorization received.
Launch
Learn More
BP11 | Omazijev®
MOLECULE
OMALIZUMAB
Therapeutic Segment
RESPIRATORY AND DERMATOLOGY
Development
Phase 1
Phase 3
Filing
Approval
Launch
Learn More
BP16 | Fugevy® Filvizy®
MOLECULE
Denosumab
Therapeutic Segment
Orthopaedic
Development
Phase 1
Phase 3
Filing
Approval
Launch
Learn More
BP05
MOLECULE
RANIBIZUMAB
Therapeutic Segment
OPHTHALMOLOGY
Development
Phase 3
Filing
Approval
Launch
Learn More
BP08 | Iztalvys®
MOLECULE
Tocilizumab
Therapeutic Segment
Immunology
Development
Phase 1
Phase 3
Approval
Launch
Learn More
BP27
MOLECULE
Undisclosed
Therapeutic Segment
Oncology
Development
Phase 1
Phase 3
Filing
Approval
Launch
BP33
MOLECULE
Undisclosed
Therapeutic Segment
Haematology
Development
Phase 1
Phase 3
Filing
Approval
Launch