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2025 Q4 -tulosraportti
56 päivää sitten
1,00 NOK/osake
Viimeisin osinko
28,65%Tuotto/v

Tarjoustasot

NorwayOslo Børs
Määrä
Osto
-
Myynti
Määrä
-

Viimeisimmät kaupat

AikaHintaMääräOstajaMyyjä
3 221--
5 854--
3 196--
810--
1 714--

Huomioi, että vaikka osakkeisiin säästäminen on pitkällä aikavälillä tuottanut hyvin, tulevasta tuotosta ei ole takeita. On olemassa riski, että et saa sijoittamiasi varoja takaisin.

Välittäjätilasto

Dataa ei löytynyt

Yhtiötapahtumat

Datan lähde: FactSet, Quartr
Seuraava tapahtuma
2026 Q1 -tulosraportti
27.5.
Menneet tapahtumat
2025 Q4 -tulosraportti
25.2.
2025 Q3 -tulosraportti
24.11.2025
2025 Q2 -tulosraportti
27.8.2025
2025 Q1 -tulosraportti
28.5.2025
2024 Q4 -tulosraportti
26.2.2025

Shareville

Liity keskusteluun SharevillessäShareville on aktiivisten yksityissijoittajien yhteisö, jossa voit seurata muiden asiakkaiden kaupankäyntiä ja omistuksia.
Kirjaudu
  • 11 t sitten
    11 t sitten
    ◦ Today at #AACR2026, our senior scientist, Ingvild Sørum Leikfoss presented additional immunogenicity data from our VB-C-03 trial and the results are compelling. 100% of evaluable patients in the 6 mg and 9 mg dose groups showed HPV16-specific T-cell immune responses to abi-suva in combination with pembrolizumab. Responses were rapid, robust and durable, with a demonstrated persistence into the last analyzed timepoint at the completed end-of-treatment. Our VB-C-03 trial demonstrated a confirmed objective response rate of 38.5% in patients with HPV16+ recurrent or metastatic head and neck cancer, where standard of care achieves an obiective response rate of only ~19% and we believe abi-suva can make a real difference for these patients., These data give us strong confidence as we move into the Abili-T Phase Il randomized trial G The poster is available for viewing in the "R&D" section of Nykode's website https://lnkd.in/eh4Nrx76 #Nykode #abisuva #HNSCC #HPV16 #CancerVaccine #lmmunotherapy #AACR2026 https://www.linkedin.com/posts/nykode_scientific-papers-and-presentations-nykode-activity-7452434758468456448-V-cn?utm_source=share&utm_medium=member_android&rcm=ACoAAGGSC24B2EXoI8xUZIcaQ9SFwUPmSQJHIyU
    11 t sitten
    ·
    11 t sitten
    ·
    Anything new since yesterday?
    10 t sitten
    ·
    10 t sitten
    ·
    Tonight, the actual data was presented at the AACR conference. Here's the most important: Double effect: The data confirms an objective response rate (ORR) of 38.5%. In comparison, today's standard treatment only yields ~19%. Nykode thus doubles the effect. Dose selection: They have now locked the dosage to 6 mg and 9 mg. The data showed that 100% of patients in these groups achieved a strong and lasting immune response. T-cell proof: New graphs (TCR sequencing) prove that the vaccine creates many different types of 'soldiers' that survive in the blood throughout the entire treatment. This is technically impressive and distinguishes them from competitors. Operational status: They confirmed tonight that the study centers are now open, and they maintain the goal of the first patient dosed now in Q2 2026. Yesterday we learned that things were going well – tonight we received the scientific evidence for why things are going so well!
  • 19 t sitten
    ·
    19 t sitten
    ·
    For what it's worth - Claude's interpretation of the Nykode presentation at AACR Objections are welcome as I am not a specialist in this This VB-C-016 AACR 2026 presentation from Nykode delivers strong data supporting partnership potential with MSD. Here's why: 🎯 DIRECT VALIDATION OF PEMBROLIZUMAB COMPATIBILITY Proven synergy with Keytruda The study shows that the VB10.16 + pembrolizumab combination: Induced HPV16-specific immune responses in 10/11 OPC patients Showed strong and durable T-cell expansion Demonstrated both amplified and de novo T-cell responses This proves that Nykode's technology works synergistically with MSD's flagship molecule. 📊 KEY DATA SUPPORTING PARTNERSHIP 1. Robust immune activation 100% response in the high-dose group (9 mg, n=5) 91% response in the total population (10/11 patients) Strong HPV16 E6/E7-specific T-cell responses were observed 2. Durable immune memory T-cell responses were long-lasting and demonstrated at high magnitude Individual case studies show persistent expansion of specific clones Months of sustained response 3. Safety profile The combination was well tolerated without unexpected safety signals - critical for future development. 🤝 STRATEGIC VALUE FOR MSD A. Differentiation in a competitive market While MSD is concerned about ivonescimab competition, VB10.16 + pembrolizumab offers a completely unique mechanism Personalized neoantigen approach that MSD has not internalized HPV+ tumors represent a large market (oropharyngeal, cervical, anal cancer) B. Expansion of pembrolizumab franchise Adjuvant setting - where MSD is increasing focus Combination data that can support new indications Proof-of-concept for vaccine + checkpoint inhibitor synergy C. Pipeline validation This data shows that Nykode's platform can deliver, making VB10.NEO (personalized neoantigens) even more attractive for MSD's broader oncology portfolio. 🎯 PRACTICAL NEXT STEPS Immediate opportunities: VB10.16 + pembrolizumab phase 2 in HPV+ cancer VB10.NEO combinations in adjuvant setting Platform evaluation for other Keytruda combinations Strategic positioning: Nykode can offer MSD what they need: innovative differentiation MSD can offer Nykode what they need: global reach and regulatory expertise 🔥 CONCLUSION This presentation is golden for potential MSD discussions because it: ✅ Proves Keytruda compatibility ✅ Shows robust clinical efficacy ✅ Demonstrates platform potential ✅ Addresses MSD's need for differentiation Timing is perfect - MSD's AACR focus on combinations + Nykode's proven data = natural conversation about partnership.
Yllä olevat kommentit ovat peräisin Nordnetin sosiaalisen verkoston Sharevillen käyttäjiltä, ​​eikä niitä ole muokattu eikä Nordnet ole tarkastanut niitä etukäteen. Ne eivät tarkoita, että Nordnet tarjoaisi sijoitusneuvoja tai sijoitussuosituksia. Nordnet ei ota vastuuta kommenteista.

Uutiset

Tämän sivun uutiset ja/tai sijoitussuositukset tai otteet niistä sekä niihin liittyvät linkit ovat mainitun tahon tuottamia ja toimittamia. Nordnet ei ole osallistunut materiaalin laatimiseen, eikä ole tarkistanut sen sisältöä tai tehnyt sisältöön muutoksia. Lue lisää sijoitussuosituksista.

Tuotteita joiden kohde-etuutena tämä arvopaperi

2025 Q4 -tulosraportti
56 päivää sitten
1,00 NOK/osake
Viimeisin osinko
28,65%Tuotto/v

Uutiset

Tämän sivun uutiset ja/tai sijoitussuositukset tai otteet niistä sekä niihin liittyvät linkit ovat mainitun tahon tuottamia ja toimittamia. Nordnet ei ole osallistunut materiaalin laatimiseen, eikä ole tarkistanut sen sisältöä tai tehnyt sisältöön muutoksia. Lue lisää sijoitussuosituksista.

Shareville

Liity keskusteluun SharevillessäShareville on aktiivisten yksityissijoittajien yhteisö, jossa voit seurata muiden asiakkaiden kaupankäyntiä ja omistuksia.
Kirjaudu
  • 11 t sitten
    11 t sitten
    ◦ Today at #AACR2026, our senior scientist, Ingvild Sørum Leikfoss presented additional immunogenicity data from our VB-C-03 trial and the results are compelling. 100% of evaluable patients in the 6 mg and 9 mg dose groups showed HPV16-specific T-cell immune responses to abi-suva in combination with pembrolizumab. Responses were rapid, robust and durable, with a demonstrated persistence into the last analyzed timepoint at the completed end-of-treatment. Our VB-C-03 trial demonstrated a confirmed objective response rate of 38.5% in patients with HPV16+ recurrent or metastatic head and neck cancer, where standard of care achieves an obiective response rate of only ~19% and we believe abi-suva can make a real difference for these patients., These data give us strong confidence as we move into the Abili-T Phase Il randomized trial G The poster is available for viewing in the "R&D" section of Nykode's website https://lnkd.in/eh4Nrx76 #Nykode #abisuva #HNSCC #HPV16 #CancerVaccine #lmmunotherapy #AACR2026 https://www.linkedin.com/posts/nykode_scientific-papers-and-presentations-nykode-activity-7452434758468456448-V-cn?utm_source=share&utm_medium=member_android&rcm=ACoAAGGSC24B2EXoI8xUZIcaQ9SFwUPmSQJHIyU
    11 t sitten
    ·
    11 t sitten
    ·
    Anything new since yesterday?
    10 t sitten
    ·
    10 t sitten
    ·
    Tonight, the actual data was presented at the AACR conference. Here's the most important: Double effect: The data confirms an objective response rate (ORR) of 38.5%. In comparison, today's standard treatment only yields ~19%. Nykode thus doubles the effect. Dose selection: They have now locked the dosage to 6 mg and 9 mg. The data showed that 100% of patients in these groups achieved a strong and lasting immune response. T-cell proof: New graphs (TCR sequencing) prove that the vaccine creates many different types of 'soldiers' that survive in the blood throughout the entire treatment. This is technically impressive and distinguishes them from competitors. Operational status: They confirmed tonight that the study centers are now open, and they maintain the goal of the first patient dosed now in Q2 2026. Yesterday we learned that things were going well – tonight we received the scientific evidence for why things are going so well!
  • 19 t sitten
    ·
    19 t sitten
    ·
    For what it's worth - Claude's interpretation of the Nykode presentation at AACR Objections are welcome as I am not a specialist in this This VB-C-016 AACR 2026 presentation from Nykode delivers strong data supporting partnership potential with MSD. Here's why: 🎯 DIRECT VALIDATION OF PEMBROLIZUMAB COMPATIBILITY Proven synergy with Keytruda The study shows that the VB10.16 + pembrolizumab combination: Induced HPV16-specific immune responses in 10/11 OPC patients Showed strong and durable T-cell expansion Demonstrated both amplified and de novo T-cell responses This proves that Nykode's technology works synergistically with MSD's flagship molecule. 📊 KEY DATA SUPPORTING PARTNERSHIP 1. Robust immune activation 100% response in the high-dose group (9 mg, n=5) 91% response in the total population (10/11 patients) Strong HPV16 E6/E7-specific T-cell responses were observed 2. Durable immune memory T-cell responses were long-lasting and demonstrated at high magnitude Individual case studies show persistent expansion of specific clones Months of sustained response 3. Safety profile The combination was well tolerated without unexpected safety signals - critical for future development. 🤝 STRATEGIC VALUE FOR MSD A. Differentiation in a competitive market While MSD is concerned about ivonescimab competition, VB10.16 + pembrolizumab offers a completely unique mechanism Personalized neoantigen approach that MSD has not internalized HPV+ tumors represent a large market (oropharyngeal, cervical, anal cancer) B. Expansion of pembrolizumab franchise Adjuvant setting - where MSD is increasing focus Combination data that can support new indications Proof-of-concept for vaccine + checkpoint inhibitor synergy C. Pipeline validation This data shows that Nykode's platform can deliver, making VB10.NEO (personalized neoantigens) even more attractive for MSD's broader oncology portfolio. 🎯 PRACTICAL NEXT STEPS Immediate opportunities: VB10.16 + pembrolizumab phase 2 in HPV+ cancer VB10.NEO combinations in adjuvant setting Platform evaluation for other Keytruda combinations Strategic positioning: Nykode can offer MSD what they need: innovative differentiation MSD can offer Nykode what they need: global reach and regulatory expertise 🔥 CONCLUSION This presentation is golden for potential MSD discussions because it: ✅ Proves Keytruda compatibility ✅ Shows robust clinical efficacy ✅ Demonstrates platform potential ✅ Addresses MSD's need for differentiation Timing is perfect - MSD's AACR focus on combinations + Nykode's proven data = natural conversation about partnership.
Yllä olevat kommentit ovat peräisin Nordnetin sosiaalisen verkoston Sharevillen käyttäjiltä, ​​eikä niitä ole muokattu eikä Nordnet ole tarkastanut niitä etukäteen. Ne eivät tarkoita, että Nordnet tarjoaisi sijoitusneuvoja tai sijoitussuosituksia. Nordnet ei ota vastuuta kommenteista.

Tarjoustasot

NorwayOslo Børs
Määrä
Osto
-
Myynti
Määrä
-

Viimeisimmät kaupat

AikaHintaMääräOstajaMyyjä
3 221--
5 854--
3 196--
810--
1 714--

Huomioi, että vaikka osakkeisiin säästäminen on pitkällä aikavälillä tuottanut hyvin, tulevasta tuotosta ei ole takeita. On olemassa riski, että et saa sijoittamiasi varoja takaisin.

Välittäjätilasto

Dataa ei löytynyt

Yhtiötapahtumat

Datan lähde: FactSet, Quartr
Seuraava tapahtuma
2026 Q1 -tulosraportti
27.5.
Menneet tapahtumat
2025 Q4 -tulosraportti
25.2.
2025 Q3 -tulosraportti
24.11.2025
2025 Q2 -tulosraportti
27.8.2025
2025 Q1 -tulosraportti
28.5.2025
2024 Q4 -tulosraportti
26.2.2025

Tuotteita joiden kohde-etuutena tämä arvopaperi

2025 Q4 -tulosraportti
56 päivää sitten

Uutiset

Tämän sivun uutiset ja/tai sijoitussuositukset tai otteet niistä sekä niihin liittyvät linkit ovat mainitun tahon tuottamia ja toimittamia. Nordnet ei ole osallistunut materiaalin laatimiseen, eikä ole tarkistanut sen sisältöä tai tehnyt sisältöön muutoksia. Lue lisää sijoitussuosituksista.

Yhtiötapahtumat

Datan lähde: FactSet, Quartr
Seuraava tapahtuma
2026 Q1 -tulosraportti
27.5.
Menneet tapahtumat
2025 Q4 -tulosraportti
25.2.
2025 Q3 -tulosraportti
24.11.2025
2025 Q2 -tulosraportti
27.8.2025
2025 Q1 -tulosraportti
28.5.2025
2024 Q4 -tulosraportti
26.2.2025

Tuotteita joiden kohde-etuutena tämä arvopaperi

1,00 NOK/osake
Viimeisin osinko
28,65%Tuotto/v

Shareville

Liity keskusteluun SharevillessäShareville on aktiivisten yksityissijoittajien yhteisö, jossa voit seurata muiden asiakkaiden kaupankäyntiä ja omistuksia.
Kirjaudu
  • 11 t sitten
    11 t sitten
    ◦ Today at #AACR2026, our senior scientist, Ingvild Sørum Leikfoss presented additional immunogenicity data from our VB-C-03 trial and the results are compelling. 100% of evaluable patients in the 6 mg and 9 mg dose groups showed HPV16-specific T-cell immune responses to abi-suva in combination with pembrolizumab. Responses were rapid, robust and durable, with a demonstrated persistence into the last analyzed timepoint at the completed end-of-treatment. Our VB-C-03 trial demonstrated a confirmed objective response rate of 38.5% in patients with HPV16+ recurrent or metastatic head and neck cancer, where standard of care achieves an obiective response rate of only ~19% and we believe abi-suva can make a real difference for these patients., These data give us strong confidence as we move into the Abili-T Phase Il randomized trial G The poster is available for viewing in the "R&D" section of Nykode's website https://lnkd.in/eh4Nrx76 #Nykode #abisuva #HNSCC #HPV16 #CancerVaccine #lmmunotherapy #AACR2026 https://www.linkedin.com/posts/nykode_scientific-papers-and-presentations-nykode-activity-7452434758468456448-V-cn?utm_source=share&utm_medium=member_android&rcm=ACoAAGGSC24B2EXoI8xUZIcaQ9SFwUPmSQJHIyU
    11 t sitten
    ·
    11 t sitten
    ·
    Anything new since yesterday?
    10 t sitten
    ·
    10 t sitten
    ·
    Tonight, the actual data was presented at the AACR conference. Here's the most important: Double effect: The data confirms an objective response rate (ORR) of 38.5%. In comparison, today's standard treatment only yields ~19%. Nykode thus doubles the effect. Dose selection: They have now locked the dosage to 6 mg and 9 mg. The data showed that 100% of patients in these groups achieved a strong and lasting immune response. T-cell proof: New graphs (TCR sequencing) prove that the vaccine creates many different types of 'soldiers' that survive in the blood throughout the entire treatment. This is technically impressive and distinguishes them from competitors. Operational status: They confirmed tonight that the study centers are now open, and they maintain the goal of the first patient dosed now in Q2 2026. Yesterday we learned that things were going well – tonight we received the scientific evidence for why things are going so well!
  • 19 t sitten
    ·
    19 t sitten
    ·
    For what it's worth - Claude's interpretation of the Nykode presentation at AACR Objections are welcome as I am not a specialist in this This VB-C-016 AACR 2026 presentation from Nykode delivers strong data supporting partnership potential with MSD. Here's why: 🎯 DIRECT VALIDATION OF PEMBROLIZUMAB COMPATIBILITY Proven synergy with Keytruda The study shows that the VB10.16 + pembrolizumab combination: Induced HPV16-specific immune responses in 10/11 OPC patients Showed strong and durable T-cell expansion Demonstrated both amplified and de novo T-cell responses This proves that Nykode's technology works synergistically with MSD's flagship molecule. 📊 KEY DATA SUPPORTING PARTNERSHIP 1. Robust immune activation 100% response in the high-dose group (9 mg, n=5) 91% response in the total population (10/11 patients) Strong HPV16 E6/E7-specific T-cell responses were observed 2. Durable immune memory T-cell responses were long-lasting and demonstrated at high magnitude Individual case studies show persistent expansion of specific clones Months of sustained response 3. Safety profile The combination was well tolerated without unexpected safety signals - critical for future development. 🤝 STRATEGIC VALUE FOR MSD A. Differentiation in a competitive market While MSD is concerned about ivonescimab competition, VB10.16 + pembrolizumab offers a completely unique mechanism Personalized neoantigen approach that MSD has not internalized HPV+ tumors represent a large market (oropharyngeal, cervical, anal cancer) B. Expansion of pembrolizumab franchise Adjuvant setting - where MSD is increasing focus Combination data that can support new indications Proof-of-concept for vaccine + checkpoint inhibitor synergy C. Pipeline validation This data shows that Nykode's platform can deliver, making VB10.NEO (personalized neoantigens) even more attractive for MSD's broader oncology portfolio. 🎯 PRACTICAL NEXT STEPS Immediate opportunities: VB10.16 + pembrolizumab phase 2 in HPV+ cancer VB10.NEO combinations in adjuvant setting Platform evaluation for other Keytruda combinations Strategic positioning: Nykode can offer MSD what they need: innovative differentiation MSD can offer Nykode what they need: global reach and regulatory expertise 🔥 CONCLUSION This presentation is golden for potential MSD discussions because it: ✅ Proves Keytruda compatibility ✅ Shows robust clinical efficacy ✅ Demonstrates platform potential ✅ Addresses MSD's need for differentiation Timing is perfect - MSD's AACR focus on combinations + Nykode's proven data = natural conversation about partnership.
Yllä olevat kommentit ovat peräisin Nordnetin sosiaalisen verkoston Sharevillen käyttäjiltä, ​​eikä niitä ole muokattu eikä Nordnet ole tarkastanut niitä etukäteen. Ne eivät tarkoita, että Nordnet tarjoaisi sijoitusneuvoja tai sijoitussuosituksia. Nordnet ei ota vastuuta kommenteista.

Tarjoustasot

NorwayOslo Børs
Määrä
Osto
-
Myynti
Määrä
-

Viimeisimmät kaupat

AikaHintaMääräOstajaMyyjä
3 221--
5 854--
3 196--
810--
1 714--

Huomioi, että vaikka osakkeisiin säästäminen on pitkällä aikavälillä tuottanut hyvin, tulevasta tuotosta ei ole takeita. On olemassa riski, että et saa sijoittamiasi varoja takaisin.

Välittäjätilasto

Dataa ei löytynyt
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