PLUVIA AS
Organization number 916635559 · Aksjeselskap
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Facts
- organisasjonsnummer:
- 916635559
- navn:
- PLUVIA AS
- organisasjonsform:
- kode:
- AS
- beskrivelse:
- Aksjeselskap
- naeringskode1:
- kode:
- 72.100
- beskrivelse:
- Forskning og eksperimentell utvikling innenfor naturvitenskap og teknikk
- antallAnsatte:
- 5
- hjemmeside:
- www.pluviabiotech.com
- epostadresse:
- info@pluviabiotech.com
- telefon:
- not reported by source
- forretningsadresse:
- adresse:
- Thormøhlens gate 51
- poststed:
- BERGEN
- postnummer:
- 5006
- kommune:
- BERGEN
- stiftelsesdato:
- 2015-11-17
- registreringsdatoenhetsregisteret:
- 2016-02-11
- aktivitet:
- Medisin. Utvikle metode for medisinsk behandling av sykdom.
- vedtektsfestetFormaal:
- Utvikle human medisin og det som hermed hører til.
Board and other roles
Daglig leder
- Daglig leder: Torgeir Vaage
Regnskapsfører
- Regnskapsfører: ECIT SERVICES AS
Revisor
- Revisor: CEDRA NORGE MOMENTUM AS
Styre
- Styremedlem: Aurora Martinez
- Styremedlem: Randi Elisabeth Taxt
- Styremedlem: Birgitte Villmo
- Styremedlem: Maija Slaidina
- Styremedlem: Hilde Furberg
- Styrets leder: Sveinung Hole
- Varamedlem: Øivind Enger
Owners
- SARSIA SEED FOND II AS – 30.62 % (40903 shares, share class: Ordinære aksjer)
- TROND MOHN FORSKNINGSSTIFTELSE – 28.93 % (38645 shares, share class: Ordinære aksjer)
- VESTLANDETS INNOVASJONSSELSKAP AS – 16.11 % (21520 shares, share class: Ordinære aksjer)
- INVESTINOR DIREKTE AS – 12.89 % (17218 shares, share class: Ordinære aksjer)
- AURORA MARTINEZ – 4.01 % (5355 shares, share class: Ordinære aksjer)
- OSCAR AUBI CATEVILLA – 2.29 % (3060 shares, share class: Ordinære aksjer)
- JARL UNDERHAUG – 1.72 % (2295 shares, share class: Ordinære aksjer)
- LARS SKJÆRVEN – 1.72 % (2295 shares, share class: Ordinære aksjer)
- MING YING – 0.86 % (1148 shares, share class: Ordinære aksjer)
- KNUT TEIGEN – 0.86 % (1147 shares, share class: Ordinære aksjer)
Company holdings
No holdings found.
Grants and support
Innovasjon Norge (2)
2 results
- fylkesnavn:
- Hordaland
- kommunenavn:
- Bergen
- org_nr:
- 916635559
- bedriftsnavn:
- PLUVIA AS
- virkemiddelkategori:
- Oppstartstilskudd
- underkategori:
- Landsdekkende etablerertilskudd
- innvilget_belop:
- 100000
- innvilget_dato:
- 26.08.16
- beslutningsenhet:
- IN Kommersialisering og vekst
- naringshovedgruppe:
- N - Faglig, vitenskapelig og teknisk tjenesteyting
- naring:
- 72.100 Forskning og eksperimentell utvikling innenfor naturvitenskap og teknikk
- type_finansiering:
- Tilskudd
- fylkesnavn:
- Hordaland
- kommunenavn:
- Bergen
- org_nr:
- 916635559
- bedriftsnavn:
- PLUVIA AS
- virkemiddelkategori:
- Innovasjonstilskudd
- underkategori:
- Tilskudd til EU-rådgivning
- innvilget_belop:
- 454000
- innvilget_dato:
- 20.12.16
- beslutningsenhet:
- IN Hordaland
- naringshovedgruppe:
- N - Faglig, vitenskapelig og teknisk tjenesteyting
- naring:
- 72.100 Forskning og eksperimentell utvikling innenfor naturvitenskap og teknikk
- type_finansiering:
- Tilskudd
EU-tildelinger (0)
No registered grants.
Forskningsrådet (3)
3 results
- id:
- 48057
- prosjektnummer:
- 282238
- prosjekttittel:
- Development of innovative pharmacological chaperone therapy for phenylketonuria
- prosjektstart:
- 2018
- prosjektslutt:
- 2022
- prosjektansvarlig_navn:
- PLUVIA AS
- organisasjonsnummer:
- 916635559
- sokt_belop:
- Bioteknologi
- tildelt_belop:
- 0.0
- virkemiddel:
- Programmer
- aktivitet:
- Brukerstyrte innovasjonsprogrammer
- id:
- 51920
- prosjektnummer:
- 290886
- prosjekttittel:
- Phenylketonuria as a paradigm disease to understand protein instability in conformational disorders and to develop chaperoning therapies
- prosjektstart:
- 2018
- prosjektslutt:
- 2022
- prosjektansvarlig_navn:
- PLUVIA AS
- organisasjonsnummer:
- 916635559
- sokt_belop:
- Medisinsk biokjemi
- tildelt_belop:
- 3.66
- virkemiddel:
- Frittstående prosjekter
- aktivitet:
- Andre frittstående prosjekter
- id:
- 42768
- prosjektnummer:
- 270286
- prosjekttittel:
- Novel therapy for PKU: Candidate Drug Selection
- prosjektstart:
- 2016
- prosjektslutt:
- 2016
- prosjektansvarlig_navn:
- PLUVIA AS
- organisasjonsnummer:
- 916635559
- sokt_belop:
- Tverr/flerfaglig teknologi og andre fagområder
- tildelt_belop:
- 0.0
- virkemiddel:
- Nettverkstiltak
- aktivitet:
- Internasjonale nettverkstiltak
SkatteFUNN (3)
3 results
- id:
- 40293
- innsendt_dato:
- 2016-08-22
- prosjektnummer:
- 264506
- bedriftsnavn:
- PLUVIA AS
- prosjekttittel:
- Innovativ terapi for PKU pasienter - utvikling frem til legemiddelkandidat
- organisasjonsnummer:
- 916635559
- fylke:
- Vestland
- kommunenavn:
- Bergen
- poststed:
- BERGEN
- soknad_godkjent:
- JA
- soknad_avslatt:
- NEI
- vedtaksdato:
- 2016-09-19
- prosjekt_fra_ar:
- 2016
- prosjekt_til_ar:
- 2018
- sammendrag:
- not reported by source
- id:
- 54185
- innsendt_dato:
- 2019-08-21
- prosjektnummer:
- 305593
- bedriftsnavn:
- PLUVIA AS
- prosjekttittel:
- Innovativ terapi for PKU pasienter - utvikling frem til klinikk
- organisasjonsnummer:
- 916635559
- fylke:
- Vestland
- kommunenavn:
- Bergen
- poststed:
- BERGEN
- soknad_godkjent:
- JA
- soknad_avslatt:
- NEI
- vedtaksdato:
- 2019-09-12
- prosjekt_fra_ar:
- 2019
- prosjekt_til_ar:
- 2021
- sammendrag:
- Phenylketonuria (PKU) is an inborn genetic disease, affecting 1:10 000 children. Genetic diseases are caused by gene mutations that lead to destabilization, misfolding and loss of function of key proteins. In PKU, mutations affecting the enzyme phenylalanine hydroxylase (PAH) make the patients unable to process the amino acid phenylalanine - which is commonly found in food, such as meat, fish and dairy. There is no cure for the disease, and it is usually treated with a strict, lifelong diet. All PKU patients will need to follow a strict medical diet, avoiding food containing phenylalanine throughout their entire life and follow medical surveillance. The treatments available today are very burdensome for patients, often effective only for a limited proportion of patient and require maintenance of a medical diet. If the disease stays untreated, it might lead to severe physical and psychological disability, including seizures, behavioural problems and mental disorders. A research team from the University of Bergen has discovered small molecules that could be used to treat the PKU disease. These molecules, called pharmacological chaperones, are able to prevent and correct loss of function of PAH. Throughout the years, the research team has gained substantial knowledge and understanding on how mutations from PKU patients are affecting our molecular target PAH. The project is now developing a new pharmacological chaperone based therapy for PKU patients. In the next years, Pluvia hopes to develop a molecule that is advanced enough to be taken to the clinic. The potential of novel pharmacological chaperones-based therapies for the correction of the genetic disorders has also been proven for other diseases, such as cystic fibrosis, a life threatening disease affecting lung function, and Fabry disease, a rare genetic disorder.
- id:
- 65078
- innsendt_dato:
- 2022-08-07
- prosjektnummer:
- 338936
- bedriftsnavn:
- PLUVIA AS
- prosjekttittel:
- Innovativ terapi for PKU pasienter - utvikling frem til klinikk
- organisasjonsnummer:
- 916635559
- fylke:
- Vestland
- kommunenavn:
- Bergen
- poststed:
- BERGEN
- soknad_godkjent:
- JA
- soknad_avslatt:
- NEI
- vedtaksdato:
- 2022-11-21
- prosjekt_fra_ar:
- 2022
- prosjekt_til_ar:
- 2024
- sammendrag:
- Phenylketonuria (PKU) is an inborn genetic disease, affecting 1:10 000 children. Genetic diseases are caused by gene mutations that lead to destabilization, misfolding and loss of function of key proteins. In PKU, mutations affecting the enzyme phenylalanine hydroxylase (PAH) make the patients unable to process the amino acid phenylalanine - which is commonly found in food, such as meat, fish and dairy. There is no cure for the disease, and it is usually treated with a strict, lifelong diet. All PKU patients will need to follow a strict medical diet, avoiding food containing phenylalanine throughout their entire life and follow medical surveillance. The treatments available today are very burdensome for patients, often effective only for a limited proportion of patient and require maintenance of a medical diet. If the disease stays untreated, it might lead to severe physical and psychological disability, including seizures, behavioural problems and mental disorders. A research team from the University of Bergen has discovered small molecules that could be used to treat the PKU disease. These molecules, called pharmacological chaperones, are able to prevent and correct loss of function of PAH. Throughout the years, the research team has gained substantial knowledge and understanding on how mutations from PKU patients are affecting our molecular target PAH. The project is now developing a new pharmacological chaperone based therapy for PKU patients. In the next years, Pluvia hopes to develop a molecule that is advanced enough to be taken to the clinic. The potential of novel pharmacological chaperones-based therapies for the correction of the genetic disorders has also been proven for other diseases, such as cystic fibrosis, a life threatening disease affecting lung function, and Fabry disease, a rare genetic disorder.
Subunits
- PLUVIA AS (916727747)
Open positions
- count:
- 0
- stillinger:
No results.
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