Da starer oppturen innen kreft, etter gode resultat i går.
Verrica’s presentation is titled “VP-315, an Investigational Non-surgical Immunotherapy in Subjects with Biopsy Proven Basal Cell Carcinoma” and will highlight the antitumor activity of LTX-315 - by Verrica designated as VP-315 - as determined by clinical and histological clearance of treated BCC lesions from the Verrica’s ongoing Phase II trial. The data will be presented at the 2023 American Academy of Dermatology 2023 Innovation Academy meeting, which is being held from August 10-13, 2023, in Tampa, Florida.
Oslo, 3 August 2023. Lytix Biopharma AS ("Lytix") (Euronext Growth Oslo: LYTIX),
a clinical stage immuno-oncology company, announces that an abstract from its
licensing partner Verrica Pharmaceuticals Inc ("Verrica") is accepted for
presentation at the American Academy of Dermatology Association's (AAD) 2023
Innovation Academy.
Verrica's presentation is titled "VP-315, an Investigational Non-surgical
Immunotherapy in Subjects with Biopsy Proven Basal Cell Carcinoma" and will
highlight the antitumor activity of LTX-315 - by Verrica designated as VP-315 -
as determined by clinical and histological clearance of treated BCC lesions from
the Verrica's ongoing Phase II trial. The data will be presented at the 2023
American Academy of Dermatology 2023 Innovation Academy meeting, which is being
held from August 10-13, 2023, in Tampa, Flori
Oslo, 3 August 2023. Lytix Biopharma AS ("Lytix") (Euronext Growth Oslo: LYTIX),
a clinical stage immuno-oncology company, announces that an abstract from its
licensing partner Verrica Pharmaceuticals Inc ("Verrica") is accepted for
presentation at the American Academy of Dermatology Association's (AAD) 2023
Innovation Academy.
Verrica's presentation is titled "VP-315, an Investigational Non-surgical
Immunotherapy in Subjects with Biopsy Proven Basal Cell Carcinoma" and will
highlight the antitumor activity of LTX-315 - by Verrica designated as VP-315 -
as determined by clinical and histological clearance of treated BCC lesions from
the Verrica's ongoing Phase II trial. The data will be presented at the 2023
American Academy of Dermatology 2023 Innovation Academy meeting, which is being
held from August 10-13, 2023, in Tampa, Flori
Redigert 11.08.2023 kl 14:21
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X-43 scramjet
11.08.2023 kl 19:35
4266
Kan komme mer nyheter etter presentasjonen i USA, varer til søndag. Sitter i ro
X-43 scramjet
11.08.2023 kl 21:59
4173
Kan komme nytt medisinsk samarbeid med nytt pharma selskap? Gjelder å ha is i magen til vi får mer nyheter. Er vi heldige ser vi 20 kr til høsten
X-43 scramjet
12.08.2023 kl 09:08
4049
The ESMO Congress is the most influential oncology platform for clinicians, researchers, patient advocates, journalists and healthcare industry representatives from all over the world.
ESMO 2023 will disseminate the latest cutting-edge data, provide high quality education and unparalleled networking opportunities for oncologists and other stakeholders from all around the world.
An abstract with clinical data from the ATLAS-IT-05 study is accepted for presentation at ESMO 2023.
In ATLAS-IT-05, a Phase II study, LTX-315 is given to patients with advanced melanoma in combination with the immune checkpoint inhibitor pembrolizumab (Keytruda), a market leading approved immunotherapeutic antibody. In the abstract, interim efficacy and safety data from the first patients enrolled in the Phase II study are presented.
20-24.Oktober, Madrid, her skal Lytix og delta. Noe å se frem til
ESMO 2023 will disseminate the latest cutting-edge data, provide high quality education and unparalleled networking opportunities for oncologists and other stakeholders from all around the world.
An abstract with clinical data from the ATLAS-IT-05 study is accepted for presentation at ESMO 2023.
In ATLAS-IT-05, a Phase II study, LTX-315 is given to patients with advanced melanoma in combination with the immune checkpoint inhibitor pembrolizumab (Keytruda), a market leading approved immunotherapeutic antibody. In the abstract, interim efficacy and safety data from the first patients enrolled in the Phase II study are presented.
20-24.Oktober, Madrid, her skal Lytix og delta. Noe å se frem til
Redigert 12.08.2023 kl 09:14
Du må logge inn for å svare
X-43 scramjet
13.08.2023 kl 14:56
3831
Er favoritt i aksje sladder, 1:09:13. Lytix kan gå veldig bra på gode resultater. Kan bli årets Biotech aksje
X-43 scramjet
14.08.2023 kl 10:05
3491
Nære 10 kr. Sluker snart rakettdrivstoff, skal opp til 30-40 kr med mirakel vaksine et steg videre utvikling
helloween
14.08.2023 kl 10:43
3411
Her er det bare å sitte stille I båten og vente på den store oppgangen 👌😎
Sabi
15.08.2023 kl 08:52
3119
Husk at med denne nyheten, er denne priset til 26kr under oppstart
Nå med slike resultater så skal kursen xxxkr
Nå med slike resultater så skal kursen xxxkr
Redigert 15.08.2023 kl 08:53
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helloween
15.08.2023 kl 15:56
2898
Noen som kan forklare historikken her?
Fikk milliardavtale med Nasdaq-notert selskap. – Ikke mulig uten inkubatorene
Det norske biotekselskapet Lytix Biopharma har inngått en lisensavtale som kan være verd mer enn 100 millioner dollar med amerikanske Verrica Pharmaceuticals Inc.
Publisert 27.08.2020
Brukt som illustrasjon i Lytix Biopharma
Avtalen gir Verrica Pharmaceuticals rett til å produsere og selge et kreft-legemiddel som Lytix Biopharma har utviklet
Fikk milliardavtale med Nasdaq-notert selskap. – Ikke mulig uten inkubatorene
Det norske biotekselskapet Lytix Biopharma har inngått en lisensavtale som kan være verd mer enn 100 millioner dollar med amerikanske Verrica Pharmaceuticals Inc.
Publisert 27.08.2020
Brukt som illustrasjon i Lytix Biopharma
Avtalen gir Verrica Pharmaceuticals rett til å produsere og selge et kreft-legemiddel som Lytix Biopharma har utviklet
BillVonka
15.08.2023 kl 16:06
2871
Na er hausegjengen helt desperat Na kommer de med ting fra 2020
Jeg solgte mine for 13,50 og vil gjerne kjøpe dem tilbake for kr 9
Jeg solgte mine for 13,50 og vil gjerne kjøpe dem tilbake for kr 9
helloween
15.08.2023 kl 16:30
2801
BillVonka
I går kl 11:36
2517
Denne er fra april
TDN Direkt
Lytix mottar milepælbetaling på en million dollar
Lytix Biopharma opplyser at den første pasienten har blitt dosert i Verrica Pharmaceuticals Inc. sin fase II-studie som evaluerer LTX-315 for behandling av hudkreft, utløser en milepælsbetaling på 1 million dollar til Lytix.
Det fremgår av en melding tirsdag.
LYTIX BIOPHARMA AS
Når de mottar 10 mil nok pr pasient så må vel dette bli en gullgruve BillVonka😆
I går kl 11:36
2517
Denne er fra april
TDN Direkt
Lytix mottar milepælbetaling på en million dollar
Lytix Biopharma opplyser at den første pasienten har blitt dosert i Verrica Pharmaceuticals Inc. sin fase II-studie som evaluerer LTX-315 for behandling av hudkreft, utløser en milepælsbetaling på 1 million dollar til Lytix.
Det fremgår av en melding tirsdag.
LYTIX BIOPHARMA AS
Når de mottar 10 mil nok pr pasient så må vel dette bli en gullgruve BillVonka😆
X-43 scramjet
15.08.2023 kl 16:37
2776
Smarte investorer kjøper aksjer billig, sitter long og gjerne har ekstra godt med aksjer som trades for rask gevinst. Lytix tar nok turen ned litt til før den går opp igjen
boreren
17.08.2023 kl 16:07
2404
Den nærmer seg kr. 6 igjen. Samme hvor gode utsikter Lytix har, blir den kjørt nedover.
Tobias
28.08.2023 kl 08:50
1815
Lytix har presentasjon i dag (kl.14:00) på ABG Sundal Collier's "Canser vaccine seminar".
Spennende case dette.
Spennende case dette.
bulleye
28.08.2023 kl 14:05
1716
Oslo, 28 August 2023. Lytix Biopharma – Lytix Biopharma AS (“Lytix”) (Euronext Growth Oslo: LYTIX), a clinical stage immuno-oncology company, announces that it has completed recruitment of 20 patients in the ATLAS-IT-05 trial - a trial evaluating LTX-315, Lytix’ lead drug candidate.
The ATLAS-IT-05 trial is designed to assess the efficacy of LTX-315 in patients with advanced melanoma, who are refractory to treatment with anti-PD-1/PD-L1 inhibitors. LTX-315 is being studied in combination with the immune checkpoint inhibitor pembrolizumab, which blocks tumor cells’ ability to prevent the body’s immune response. Results from earlier studies indicate that the combination of LTX-315 and pembrolizumab may work better than pembrolizumab alone.
***
Dr. Øystein Rekdal, CEO at Lytix Biopharma, commented: “We are confident that Lytix’ unique technology offers a solution to today’s cancer treatment challenges, through the direct killing of cancer cells and a broad activation of the body’s own immune system. The results from the study will help us understand the contribution of LTX-315 to the clinical response among patients and help us to advance LTX-315 further towards the market”.
***
The first patient in this trial was enrolled in December 2021, at MD Anderson Cancer Center in Houston, Texas - one of the world’s leading cancer hospitals. A total of 10 sites have been involved in this study - 4 in the US and 6 in Europe.
Enrolled patients receive treatment with LTX-315 for up to 5 weeks. Pembrolizumab therapy will continue until disease progression or 24 months after enrollment. (More information about the trial is available at https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fclinicaltrials.gov%2Fstudy%2FNCT04796194&data=05%7C01%7Cgunnar.oye%40nho.no%7C82d6e677a57f4da4f4a908dba7bd119b%7C21be13a8b92f4a809cf317026d4a8118%7C0%7C0%7C638288202708565782%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2BahgjXJp0SYODqplZdkwl3KenVTTei9h3K0u%2FnB3xAI%3D&reserved=0.)
The first interim results from the trial will be presented by the top recruiting investigator, Professor Stéphane Dalle (Centre Hospitalier Universitaire de Lyon, France), in a poster session at ESMO, taking place in Madrid, Spain, 20-24 October 2023. The poster title is: Intratumoral injection of LTX-315 in combination with pembrolizumab in patients with advanced melanoma refractory to prior PD-1/PD-L1 therapy: interim results from the ATLAS-IT-05 trial.
***
“We see a strong mechanistic rationale to explore the combination and treatment sequence of LTX-315 and an immune checkpoint inhibitor. Data from the ATLAS-IT-05 trial will help us understand the potential of LTX-315 to improve durability and response rates of patients treated in combination with existing immuno-oncology drugs. We look forward to presenting the first interim results of this trial at ESMO in October”, Dr. Graeme Currie, CDO in Lytix Biopharma, commented.
The ATLAS-IT-05 trial is designed to assess the efficacy of LTX-315 in patients with advanced melanoma, who are refractory to treatment with anti-PD-1/PD-L1 inhibitors. LTX-315 is being studied in combination with the immune checkpoint inhibitor pembrolizumab, which blocks tumor cells’ ability to prevent the body’s immune response. Results from earlier studies indicate that the combination of LTX-315 and pembrolizumab may work better than pembrolizumab alone.
***
Dr. Øystein Rekdal, CEO at Lytix Biopharma, commented: “We are confident that Lytix’ unique technology offers a solution to today’s cancer treatment challenges, through the direct killing of cancer cells and a broad activation of the body’s own immune system. The results from the study will help us understand the contribution of LTX-315 to the clinical response among patients and help us to advance LTX-315 further towards the market”.
***
The first patient in this trial was enrolled in December 2021, at MD Anderson Cancer Center in Houston, Texas - one of the world’s leading cancer hospitals. A total of 10 sites have been involved in this study - 4 in the US and 6 in Europe.
Enrolled patients receive treatment with LTX-315 for up to 5 weeks. Pembrolizumab therapy will continue until disease progression or 24 months after enrollment. (More information about the trial is available at https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fclinicaltrials.gov%2Fstudy%2FNCT04796194&data=05%7C01%7Cgunnar.oye%40nho.no%7C82d6e677a57f4da4f4a908dba7bd119b%7C21be13a8b92f4a809cf317026d4a8118%7C0%7C0%7C638288202708565782%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=%2BahgjXJp0SYODqplZdkwl3KenVTTei9h3K0u%2FnB3xAI%3D&reserved=0.)
The first interim results from the trial will be presented by the top recruiting investigator, Professor Stéphane Dalle (Centre Hospitalier Universitaire de Lyon, France), in a poster session at ESMO, taking place in Madrid, Spain, 20-24 October 2023. The poster title is: Intratumoral injection of LTX-315 in combination with pembrolizumab in patients with advanced melanoma refractory to prior PD-1/PD-L1 therapy: interim results from the ATLAS-IT-05 trial.
***
“We see a strong mechanistic rationale to explore the combination and treatment sequence of LTX-315 and an immune checkpoint inhibitor. Data from the ATLAS-IT-05 trial will help us understand the potential of LTX-315 to improve durability and response rates of patients treated in combination with existing immuno-oncology drugs. We look forward to presenting the first interim results of this trial at ESMO in October”, Dr. Graeme Currie, CDO in Lytix Biopharma, commented.
Tobias
25.01.2024 kl 11:38
797
Blir vel en ny Algeta dette.
Utrolig at man kan få kjøpt aksjen på dagens nivåer.
Utrolig at man kan få kjøpt aksjen på dagens nivåer.
Tobias
25.01.2024 kl 11:51
754
Tipper det er utlendinger som kjøper etter presentasjonene som ble holdt i går i Sverige.
Gullhaugen
06.02.2024 kl 11:00
306
Det gjelder å følge med på news fra USA også fra https://finance.yahoo.com/news/verrica-pharmaceuticals-announces-last-patient-123000649.html
https://www.nordnet.no/market/news/1008690712
https://www.nordnet.no/market/news/1008690712
Redigert 06.02.2024 kl 11:20
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