LOPINAVIR, RITONAVIR (LPV/r) PAEDIATRICS
In November 2014, the Medicines Patent Pool (MPP) signed a licensing agreement with AbbVie for lopinavir (LPV) and ritonavir (r) for paediatric use. The agreement permits generic manufacturers to produce low-cost versions of LPV/r for paediatric use for at least 102 countries.
For more information see MedsPaL
Eligibility for sublicences | Sublicences can be issued to any qualified entity worldwide. |
Manufacturing | Allows manufacturing of the active pharmaceutical ingredient and the finished formulation of LPV/r and RTV anywhere in the world. |
Geographical scope for sale | Allows for sale of LPV/r and RTV in at least 102 countries (see âSales outside the licensed territoryâ). |
Sales outside the licensed territory | Sales outside the 102 countries are permitted if no granted patent is being infringed. This includes cases in which a compulsory licence is issued. It is estimated that licensees can thus sell the product in 125 countries where 98.8% of children living with HIV reside. |
Royalties | The license is royalty free. |
Quality assurance | Licensees must obtain approval from WHO Pre-qualification, or a Stringent Regulatory Authority. Where such approval is not yet available, temporary approval from a WHO Expert Review Panel may be obtained. |
Combinations | Sublicensees have the right to combine LPV or RTV with other ARVs and to develop suitable new fixed-dose combinations. |
Data exclusivity | Data exclusivity is waived in countries with such form of protection, thus facilitating regulatory approval of generics. |
Patent disclosure | The licence discloses the list of pending and granted patents on LPV/r and RTV worldwide at the time of licence signing. |
Additional flexibilities for licensees: | Licensees have the right to challenge any of the licensed patents. |
LOPINAVIR, RITONAVIR (LPV/r) PAEDIATRICS