Summary
Cancer is one of the most dangerous life-threatening disorders for humanity of which melanoma is considered to be one of
the most dangerous and aggressive. There are a number of therapies available to treat melanoma. However, these
treatments are generally marginally effective and very expensive.
Latima SIA develops and produces Rigvir® for virotherapy. Rigvir® is a unique anti-cancer medicine using non-pathogenic
virus. It has been demonstrated to be very effective in treating various cancers, and has a promising medical future .
RIGVIR is commercialised in Latvia, Georgia and Armenia. Rigvir® was approved and registered in Latvia in 2004 and has since been a front-line treatment for melanoma in Latvia. However,further use and commercialisation in the EU is prevented as EU regulations require cancer medicines to be registered centrally through the European Medicine Agency (EMA). National registrations are not considered. Therefore, the process for European Union registration must be started de novo.
Registration of a medicinal product requires significant costs and resources. The purpose of this H2020-SMEInst-2016-2017
application is to secure the financial support for an initial feasibility study that would provide the basis for subsequent clinical
trials necessary for the registration of Rigvir® with the EMA.
It is expected that after feasibility study we would continue with next phase of H2020-SMEInst-2016-2017 and perform the
clinical trials necessary for registration in EMA.
the most dangerous and aggressive. There are a number of therapies available to treat melanoma. However, these
treatments are generally marginally effective and very expensive.
Latima SIA develops and produces Rigvir® for virotherapy. Rigvir® is a unique anti-cancer medicine using non-pathogenic
virus. It has been demonstrated to be very effective in treating various cancers, and has a promising medical future .
RIGVIR is commercialised in Latvia, Georgia and Armenia. Rigvir® was approved and registered in Latvia in 2004 and has since been a front-line treatment for melanoma in Latvia. However,further use and commercialisation in the EU is prevented as EU regulations require cancer medicines to be registered centrally through the European Medicine Agency (EMA). National registrations are not considered. Therefore, the process for European Union registration must be started de novo.
Registration of a medicinal product requires significant costs and resources. The purpose of this H2020-SMEInst-2016-2017
application is to secure the financial support for an initial feasibility study that would provide the basis for subsequent clinical
trials necessary for the registration of Rigvir® with the EMA.
It is expected that after feasibility study we would continue with next phase of H2020-SMEInst-2016-2017 and perform the
clinical trials necessary for registration in EMA.
Unfold all
/
Fold all
More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/736051 |
| Start date: | 01-08-2016 |
| End date: | 31-01-2017 |
| Total budget - Public funding: | 71 429,00 Euro - 50 000,00 Euro |
Cordis data
Original description
Cancer is one of the most dangerous life-threatening disorders for humanity of which melanoma is considered to be one ofthe most dangerous and aggressive. There are a number of therapies available to treat melanoma. However, these
treatments are generally marginally effective and very expensive.
Latima SIA develops and produces Rigvir® for virotherapy. Rigvir® is a unique anti-cancer medicine using non-pathogenic
virus. It has been demonstrated to be very effective in treating various cancers, and has a promising medical future .
RIGVIR is commercialised in Latvia, Georgia and Armenia. Rigvir® was approved and registered in Latvia in 2004 and has since been a front-line treatment for melanoma in Latvia. However,further use and commercialisation in the EU is prevented as EU regulations require cancer medicines to be registered centrally through the European Medicine Agency (EMA). National registrations are not considered. Therefore, the process for European Union registration must be started de novo.
Registration of a medicinal product requires significant costs and resources. The purpose of this H2020-SMEInst-2016-2017
application is to secure the financial support for an initial feasibility study that would provide the basis for subsequent clinical
trials necessary for the registration of Rigvir® with the EMA.
It is expected that after feasibility study we would continue with next phase of H2020-SMEInst-2016-2017 and perform the
clinical trials necessary for registration in EMA.
Status
CLOSEDCall topic
SMEInst-03-2016-2017Update Date
27-10-2022
Images
No images available.
Geographical location(s)
Structured mapping
Unfold all
/
Fold all
H2020-EU.2.1.4. INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies – Biotechnology
