Medimmune Ltd v Novartis Pharmaceuticals UK Ltd & Anor
The patents are invalid as they are not entitled to priority from PD3, and the claimed inventions are obvious in light of Professor Smith's Banbury Conference disclosure. Even if valid, Novartis did not infringe because the process used to make ranibizumab did not fall within the claims, as it did not produce a population with a range of binding specificities as required. The claims are not invalid for insufficiency or added matter. If the process claims had been infringed, ranibizumab would have been a product obtained directly by the process under UK law, and the Biotech Directive would not have limited this protection.
- Parties
- Claimant: MedImmune Limited; First Defendant: Novartis Pharmaceuticals UK Limited; Second Defendant: Medical Research Council
- Jurisdiction
- England and Wales
- Judgment Date
- 05 July 2011
- Procedural Posture
- Patent Infringement and Revocation / Judgment After Full Trial
- Outcome
- Claims 5-8 of 511 and claim 1 of 777 are invalid for lack of priority and obviousness. No infringement by Novartis. If valid and infringed, ranibizumab would be a product obtained directly by the process, not excluded by the Biotech Directive.
- Legal Topics
- Patent Infringement, Patent Validity, Obviousness, Sufficiency, Added Matter, Priority Rights, Biotechnology Patents
Case Brief
Summary, issues, holding and outcome
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Parties
MedImmune Limited
Claimant
Novartis Pharmaceuticals UK Limited
First Defendant
Medical Research Council
Second Defendant
Procedural Posture
Patent Infringement and Revocation / Judgment After Full Trial
Legal Issues
- 1 Whether MedImmune's patents are valid over the prior art and entitled to priority from PD3
- 2 Whether Novartis infringed the patents by the sale of ranibizumab (Lucentis)
- 3 Whether the patents are invalid for obviousness, insufficiency, or added matter
Ratio Decidendi
The patents are invalid as they are not entitled to priority from PD3, and the claimed inventions are obvious in light of Professor Smith's Banbury Conference disclosure. Even if valid, Novartis did not infringe because the process used to make ranibizumab did not fall within the claims, as it did not produce a population with a range of binding specificities as required. The claims are not invalid for insufficiency or added matter. If the process claims had been infringed, ranibizumab would have been a product obtained directly by the process under UK law, and the Biotech Directive would not have limited this protection.
Court Disposition
Claims 5-8 of 511 and claim 1 of 777 are invalid for lack of priority and obviousness. No infringement by Novartis. If valid and infringed, ranibizumab would be a product obtained directly by the process, not excluded by the Biotech Directive.
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