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 UK MHRA approval.
Dazublys™, (Trastuzumab biosimilar), has received CDSCO approval in India, and is under review with EMA.
Stage Complete
In Progress
Next Stage
BP13
MOLECULE
FILGRASTIM
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Filing
Approval
CHMP (EMA) positive opinion received.
Launch
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BP14
MOLECULE
PEGFILGRASTIM
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Filing
Approval
Launch
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BP01
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
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BP02
MOLECULE
TRASTUZUMAB
Therapeutic Segment
ONCOLOGY
Development
Phase 1
Phase 3
Filing
Approval
Marketing authorization received from CDSCO – India.
Launch
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BP05
MOLECULE
RANIBIZUMAB
Therapeutic Segment
OPHTHALMOLOGY
Development
Phase 3
Filing
Approval
Launch
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BP11
MOLECULE
OMALIZUMAB
Therapeutic Segment
RESPIRATORY AND DERMATOLOGY
Development
Phase 1
Phase 3
Filing
Approval
Launch
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BP16
MOLECULE
Denosumab
Therapeutic Segment
Orthopaedic
Development
Phase 1
Phase 3
Filing
Approval
Launch
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BP08
MOLECULE
Tocilizumab
Therapeutic Segment
Immunology
Development
Phase 1
Phase 3
Approval
Launch
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BP38
MOLECULE
Ustekinumab
Therapeutic Segment
Immunology
Development
Phase 1
Phase 3
Filing
Approval
Launch
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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