PLUVIA AS

Organization number 916635559 · Aksjeselskap

Programmatic access to company data (JSON)

Source: Firmafakta. Data read and page generated 2026-09-19T06:20:09Z. HTML cache: no-store (TTL 0 seconds). Default TTL for Firmafakta JSON/API responses: 60 seconds.

Facts

Source: Firmafakta, with business data from public registers.

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.

View the address in Geonorge

Board and other roles

Source: Firmafakta. Also see the separate Brønnøysund lookup under related lookups.

Daglig leder

Regnskapsfører

Revisor

Styre

Owners

Source: Firmafakta shareholder dataset.

  1. SARSIA SEED FOND II AS – 30.62 % (40903 shares, share class: Ordinære aksjer)
  2. TROND MOHN FORSKNINGSSTIFTELSE – 28.93 % (38645 shares, share class: Ordinære aksjer)
  3. VESTLANDETS INNOVASJONSSELSKAP AS – 16.11 % (21520 shares, share class: Ordinære aksjer)
  4. INVESTINOR DIREKTE AS – 12.89 % (17218 shares, share class: Ordinære aksjer)
  5. AURORA MARTINEZ – 4.01 % (5355 shares, share class: Ordinære aksjer)
  6. OSCAR AUBI CATEVILLA – 2.29 % (3060 shares, share class: Ordinære aksjer)
  7. JARL UNDERHAUG – 1.72 % (2295 shares, share class: Ordinære aksjer)
  8. LARS SKJÆRVEN – 1.72 % (2295 shares, share class: Ordinære aksjer)
  9. MING YING – 0.86 % (1148 shares, share class: Ordinære aksjer)
  10. KNUT TEIGEN – 0.86 % (1147 shares, share class: Ordinære aksjer)

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Company holdings

No holdings found.

Grants and support

Sources provided through Firmafakta: Innovation Norway, the EU, the Research Council of Norway and SkatteFUNN.

Innovasjon Norge (2)

2 results

  1. 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
  2. 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

  1. 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
  2. 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
  3. 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

  1. 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
  2. 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.
  3. 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.

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