Om denne utviklingen fortsetter så blir Ultimovacs svensk.

Fornybar / Biotekprofeten
Professor LOLcat @ProfessorLOLca7
Næringsminister Iselin Nybø har skrevet et innlegg i Vesterålen Online, og nevner Ultimovacs og Targovax.
ASCO
The poster presentation will be available on the Ultimovacs website on 4 June 2021 at 15:00 CEST.
Klokken 15 på fredag slippes ASCO-posteren med de komplette dataene fra kohort 1. Her får vi sannsynligvis et innblikk i følgende datapunkter som er veldig relevante ifht generell sammenlikning av populasjoner:
I tillegg så har jeg et ørlite håp om at de har tatt med 6 mnd ORR fra kohort 2 og bare unnlatt å nevne det…
Dagens morgenbrev - torsdag
Neste milepæl å fortelle om angående svenskene blir når Avanza når 1000 eiere. Det er tydelig at Ultimovacs er oppdaget over der nå. Synd for oss og Ultimovacs at Inven2 og Fidelityfondet har dumpet 600 000 aksjer rett i fangene på de mens kjøpsviljen var som størst.
~30% av alt salg i perioden utført med relativt store dumper må sies å ha hatt en stor impact en så lite likvid aksje
Anyways - Svenskene stopper nok ikke å kjøpe med det første, men Inven2 har stoppet å selge og FIL blir fri til slutt eller stopper de og. Jeg vil tro kurseffekten og ekstra omsetning vil fortsette i tiden fremover og at nye øyne på selskapet vil gjøre veldig godt ved fremtidige positive meldinger. Vi vet de sier de ikke har gjort jobben sin om de ikke snakker med regulatoriske myndigheter om Fast Track og Breakthrough Therapy Designation på bakgrunn av de gode dataene.
Om ORR på 30 pasienter og 21mnd median oppfølging er nok eller om de venter til etter 2års-readouten vet jeg ikke, men det gir i hvert fall mening at de har startet dialogen nå.
Som investor vil det være verdifullt på flere måter, både langsiktig og kortsiktig. For det første så vil det gi stor blest om selskapet enda en gang, og de vil nå ut til enda flere kjøpere. For det andre så vil Fast Track og BTD korte ned utviklingstiden av UV1 ved at de får raskere saksbehandling og tilgang på mer erfarent personell hos myndighetene. I tillegg vil det fungere som et kvalitetsstempel for nye investorer når de vurderer caset.
Mon tro om det er denne karen som skal ta over for Gjelsten, han har har en børsverdi på ~5000 milliarder SEK og 1300 livvakter:
Jepp, og det får de gjort til marginalt økende priser. Sousa &co har vært ute å fortalt at besøkelses tiden er nå, men oladunk drar nisselua nedover ørene og sender aksjene over grensen i mangel av normal harryhandel.
Haha. Det er nedsalgene på topp 10 som har skylden for det, ikke Ola Dunk Dessuten er det ikke over enda, OG vi er opp 10% siden nyheten!
Fint diagram Svensken ska ikke miste oljan denne gången! Biotec är den nya oljan
DNB Markets: Tre nordiske biotekselskap skal i dag og de neste dagene presentere sine siste studier på den årlige amerikanske ASCO-konferansen for onkologi. Etter det vi forstår er dette et av årets viktigste arrangementer for bransjen og gir både større etablerte selskap og investorer innen sektoren god anledning til å vurdere fremdriften for mindre aktører. Alligator Bioscience, Oncopeptides og Ultimovacs skal i løpet av konferansen legge frem sine studier. Vi har kjøpsanbefalinger på alle disse tre med kursmål på henholdsvis SEK 14, SEK 290 og NOK 125 pr aksje. Vi minner samtidig om at risikoen innen denne sektoren kan være høy.
DNB får ta morgenbrevet i dag, jeg vil ha posteren.
«Etter det vi forstår er dette et av årets viktigste arrangementer for bransjen…»
Høres ikke dette i overkant amatørmessig ut? Burde ikke noen som påstår å faktisk kunne sette «riktig» verdi på kreftforsknings-selskapene vite om ASCO er et viktig arrangement eller ikke??
Ikke et dumt poeng. Og i tillegg er det (minst) FIRE nordiske, for BerGenBio, som DNB har dekning på… skal også presentere på ASCO.
Det må være sommerferievikaren som står bak denne meldingen, tenker jeg.
Haha, det gjorde det ikke bedre, nei…
Professor LOLcat @ProfessorLOLca7
Lik og retweet
Litt #hauss fra graveren vår!
DNB Markets venter kursoppgang i Alligator Bioscience, Oncopeptides og Ultimovacs. Samtidig advares det mot høy risiko i bioteknologisektoren.
De bryr seg så lite om Norge at de ikke gidder å melde det her engang…
En spøk, om man ikke tok den
• UV1/pembrolizumab results in 30% complete responses plus 30% partial responses
• Good safety and tolerability profile supports expanded Phase II combination program
• Data highlighted at ASCO in poster presentation
…Vis børsmeldingen
Oslo, 4 June 2021: Ultimovacs ASA (“Ultimovacs”) (OSE ULTI), a clinical stage leader in immune stimulatory vaccines for cancer, announced that data on its universal cancer vaccine, UV1, in combination with the checkpoint inhibitor pembrolizumab will be presented as a poster presentation at the American Society of Clinical Oncology (ASCO) 2021 Annual Meeting and available today at 9:00 am ET / 15:00 CEST.
In a twenty patient cohort of patients with advanced melanoma, the combination of UV1 with pembrolizumab as a first-line treatment demonstrated an objective response rate (ORR) of 60% after a minimum of 18 months. Median observation time was 21 months. In addition, 30% of treated patients achieved a complete response (CR), with no signs of tumor detected. These response rates clearly exceed those seen in previous studies for pembrolizumab alone in advanced melanoma of 33-37% ORR and 5-12% CR*.
The median progression-free survival for the UV1/pembrolizumab combination in the study was 18.9 months compared with the range of 5.5-11.6 months for pembrolizumab alone*. The overall survival was 80%, with the median overall survival yet to be reached after 21 months of follow-up.
The data also shows that the UV1/pembrolizumab combination is safe and well tolerated, with adverse events largely restricted to low grade effects, mainly injection site reactions.
Principal investigator and presenter of the ASCO data, Yousef Zakharia, MD, Associate Professor of Medicine and Medical Oncologist at the University of Iowa, commented: “These results are encouraging and warrant further investigation. The trial gives a preliminary signal that UV1 vaccine has the potential to increase efficacy and promote durable responses when combined with checkpoint inhibitors and, more importantly, the combination seems to be safe and well tolerable.”Ultimovacs continues to build on the safety and tolerability profile of UV1 with several ongoing Phase I and Phase II clinical studies of UV1 in combination with checkpoint inhibitors. In the Phase I UV1/pembrolizumab trial, data on a second cohort of 10 patients (given a standard GM-CSF adjuvant dose of 75 µg, twice that for cohort 1) will be reported when one year follow-up is complete in Q4 2021. Two year follow up on the first cohort will also be reported in Q4 2021. Meanwhile, recruitment continues in Ultimovacs’ expanding Phase II program of randomized multinational trials of UV1 with checkpoint inhibitors in malignant melanoma, malignant pleural mesothelioma, ovarian cancer and metastatic head-and-neck cancer.
“These ASCO data from our Phase I trial in malignant melanoma represent the moving edge of a much broader Ultimovacs clinical program on the safety and effectiveness of UV1 used in combination with checkpoint inhibitors and other therapeutic classes” said Carlos de Sousa, CEO of Ultimovacs. “Across a variety of cancer types and with several different checkpoint inhibitors, we are accumulating a growing body of evidence underpinning our conviction that UV1 can mobilize the immune system and play a transformative role in the treatment of solid tumors.”
Poster Presentation and Webcast
Title: “A Phase I Clinical Trial Investigating the Telomerase Vaccine UV1 in Combination with Pembrolizumab in Patients with Advanced Melanoma” ; ASCO abstract 2620.The oral presentation can be accessed on the ASCO website on June 4 at 9.00 a.m ET (15.00 CEST). The ASCO presentation is also available on the Ultimovacs website from 4 June 2021 at 15:00 CEST: at https://ultimovacs.com/
*Range reported in authoritative sources: FDA pembrolizumab packet insert; EMA pembrolizumab product information; Robert, C. et al (2019) Lancet Oncology 20, 1239-1251
About UV1
UV1 is a peptide-based vaccine inducing a specific T cell response against the universal cancer antigen telomerase. UV1 is being developed as an “off-the-shelf” therapeutic cancer vaccine which may serve as a platform for use in combination with other immunotherapy which requires an ongoing T cell response for their mode of action. To date, UV1 has been tested in four phase I clinical trials in a total of 82 patients and maintained a positive safety and tolerability profile as well as encouraging signals of efficacy.About UV1 Clinical Programs
As a universal cancer vaccine, UV1’s unique mechanism of action has the potential to be applicable across most cancer types. The clinical development of the UV1 vaccine includes four randomized, multinational, Phase II combination trials: INITIUM, NIPU, DOVACC and FOCUS, recruiting over 500 patients in total. Ultimovacs anticipates announcing data on the primary endpoints for the NIPU and INITIUM studies in 2H2022 and for the DOVACC and FOCUS studies in 2023.• The INITIUM trial is an Ultimovacs-sponsored clinical trial recruiting 154 patients with metastatic malignant melanoma to evaluate UV1 in combination with ipilimumab and nivolumab as first-line treatment.
• The NIPU study is testing UV1 in combination with checkpoint inhibitors ipilimumab and nivolumab as second-line treatment in 118 patients with advanced malignant pleural mesothelioma, a rare lung cancer. The study is sponsored by Oslo University Hospital and Bristol-Myers Squibb is providing the checkpoint inhibitors for this study.
• The DOVACC study is sponsored by the Nordic Society of Gynecological Oncology. In total, 184 patients with high-grade ovarian cancer will be enrolled to evaluate UV1 in combination with durvalumab and olaparib, both provided by AstraZeneca.
• FOCUS is an investigator-sponsored, randomized clinical trial enrolling 75 patients with metastatic head and neck cancer receiving pembrolizumab as standard of care, and will evaluate the impact of adding UV1 to this regimen.About Ultimovacs
Ultimovacs seeks to become a leader in developing immune-stimulatory vaccines to treat a broad range of cancers. Ultimovacs’ lead universal cancer vaccine candidate UV1 leverages the high prevalence of the human telomerase (hTERT) to be effective across the dynamic stages of the tumor’s growth and its microenvironment. By directing the immune system to hTERT antigens that are present in over 80% of all cancers, UV1 drives CD4 helper T cells to the tumor with the goal of activating an immune system cascade to increase anti-tumor responses. Ultimovacs’ strategy is to clinically demonstrate UV1’s impact in many cancer types and in combination with other immunotherapies. The Company will expand its pipeline using its novel TET-platform, which is an innovative vaccine technology that can generate multiple vaccine candidates designed to achieve increased T cell responses to a broad range of target antigens.For further information, please see www.ultimovacs.com or contact:
Carlos de Sousa, CEO
Email: carlos.desousa@ultimovacs.com
Phone: +47 908 92507
Hans Vassgård Eid, CFO
Email: hans.eid@ultimovacs.com
Phone: +47 482 48632
Mary-Ann Chang, LifeSci Advisors
Email: mchang@lifesciadvisors.com
Phone: +44 7483 284 853
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