Opps,der var vi på rødt - igjen,og den lille effekten av TM støttekjøp er borte - igjen....

Det var et kort besøk opp mot 33 kr. Som alle andre oppturer ender også denne i en nedtur.

Svake sjeler kaster kortene.

Vi andre ser på Sk VM i Oberstdorf og gleder oss over gode resultater fra både BerGenBio og norske skiløpere.

La nå meglere og Market Makere «røre» i aksjekursen til BerGenBio så lenge de orker. «Ses på den andre siden av 100 lappen snart» ....

Jeg mener å begynne å se et mønster her.. mulig jeg er helt på jordet.. men jeg ser ikke på kjøpene til TM som støttekjøp. For meg virker det nesten som om han har et type samarbeid med de som shorter aksjen... For det er rart hvordan han alltid kommer inn å handler når den er på det laveste i en type dip.. Kanskje det er slik at når han har handlet trekker shorten seg ut, og kursen stiger.. og når TM har kapital til å handle flere aksjer kjøper shorten seg inn igjen og får kursen ned.. En vinn-vinn situasjon for begge.. og vi sitter igjen og klør oss i hode hvorfor ikke denne befinner seg på kursmålene som er satt for snart et år siden på kr. 60,-.. Ja, nei.. ikke vet jeg, men noe rart er det.. Jeg har også lagt merke til at det er rart hvordan BergenBio og Akso følger hverandre på opp og nedturer.. Det er jo helt forskjellige bransjer, men kan kanskje ha noen felles store investorer og shortere.. rart er det ihvertfall i min verden..

Merkel: - Vi må forberede oss på kontinuerlig vaksinering i flere år.......

https://direkte.vg.no/nyhetsdognet/news/merkel-vi-maa-forberede-oss-paa-kontinuerlig-vaksinering-i-flere-aar.8MHPWB42G?utm_source=vgfront&utm_content=row-1

Full speed ahead ! 👏👏👏
Årsrapport fra BGBIO :

Chairman’s Statement:


A YEAR OF CLINICAL PROGRESS IN ONCOLOGY AND COVID-19

Dear Shareholders

2020 was a challenging year on many levels, with the impact of the COVID-19 pandemic affecting the lives of millions around the world. For the healthcare sector, the challenge was particularly profound, as we and many of our
peers found ourselves operating
in an environment inhospitable to the continuation of the research
and clinical activities central to the progression of our work, as well as having to spearhead the response to the biggest global healthcare crisis in recent memory.
We were aware of pre-clinical studies that have shown the potential of AXL inhibition in the treatment of viruses.
This potential was validated by the decision of the UK government in April to select bemcentinib as the
first candidate in the ACCORD study, a multicentre, seamless, Phase II adaptive randomisation platform
trial to assess the efficacy and safety of multiple candidate agents for the treatment of COVID-19 in hospitalised UK NHS patients. Whilst funding was suspended by UKRI in July due to
the falling number of hospitalised COVID-19 patients, this was reinstated in September following a rise in
UK cases, and the trial recruitment resumed in December. In addition,
we have initiated our own sponsored studies in South Africa and India, countries of high COVID-19 incidence,
to continue obtaining the necessary data to determine the potential efficacy of bemcentinib in COVID-19 patients.
We are hopeful that bemcentinib can play a significant role in the global effort to find suitable treatment options for COVID-19 patients, which has had such serious implications for so many people and thereby ease pressures
on hospital intensive care units, and ultimately treat thousands
of patients.
The central focus of our efforts, oncology, remains unchanged. Throughout the year, and despite
the pandemic, we have continued
our work to explore the potential of bemcentinib as a first and second-line
Reflecting on the events of the past year, as Chairman of BerGenBio I am very proud of the way in which our company and staff have adapted, ensuring the continuation of our important work in oncology, where we hope to establish our AXL targeting therapies as a cornerstone treatment for cancer, but also in utilising our expertise to directly address the effort in combatting the virus.

cancer treatment, with specific focus on non-small cell lung cancer (NSCLC), the largest cancer killer worldwide,
and leukemia (AML and MDS). These diseases remain areas of high unmet need, with low survival rates amongst those who fail to respond to now well- established immunotherapy treatments such as checkpoint inhibitors, or who are too weak to undergo additional courses of chemotherapy.
Finally, I would like to thank the staff and management of BerGenBio, on behalf of the Board, for their dedication throughout this extraordinary year. We also extend our thanks to patients who have placed their trust in us and both new and established shareholders
for their support as we continue our progress.
Sveinung Hole
Chairman of the Board
Looking forward we will build on
the progress we have made into the coming year, with the aim of advancing bemcentinib into late-stage trials
in NSCLC and AML. The company remains well funded to achieve this goal, securing a NOK 520 million fundraising in May 2020 and
having maintained tight cost
controls throughout.
As a responsible corporate citizen,
we have a commitment to pursuing our business activities sustainably and support the Sustainable Development Goals outlined by the United Nations, in particular SDG 3, which aims to ensure healthy lives and promote well- being for all at all ages. Further details of BerGenBio’s corporate governance and sustainability policies can be found later in this report and I urge shareholders to familiarise themselves with these.

Finally, I would like to thank the staff and management of BerGenBio, on behalf of the Board, for their dedication throughout this extraordinary year. We also extend our thanks to patients who have placed their trust in us and both new and established shareholders
for their support as we continue our progress.


Sveinung Hole
Chairman of the Board

Re: "...og når TM har kapital til å handle flere aksjer..."

Er det slik at TM venter spent på ukelønnen sin slik som mange av oss andre, og bråhandler aksjer så fort han noen kroner igjen etter utgifter til godteposen, mon tro.

mvh

For TM så betyr det nada om han kjøper en pott aksjer i ny og ne.
Det er nok andre signaler han jevnlig vil sende ut,som : "Se,jeg har troen,det bør dere også ha" !

Kjøper du aksjer da?

Enig - stående klap klap klap - jeg skal love for chairman for formuleret sig TUNGT her. Jeg ved godt vi ved det, men hold da op:

..with specific focus on non-small cell lung cancer (NSCLC), the largest cancer killer worldwide, and leukemia (AML and MDS)
...Looking forward ....into the coming year, with the aim of advancing bemcentinib into late-stage trials in NSCLC and AML.
...hopeful that bemcentinib can play a significant role in the global effort to find suitable treatment options for COVID-19 patients.....and thereby ease pressures
on hospital intensive care units, and ultimately treat thousands of patients.

Blir nesten for.mye det her🎲

Ja ha - det er næsten uhyggeligt. Der er royalties imod Rigel der udvilkede bemcentinib for BGBIO. MEN, MEN, MEN:

While both tilvestamab and bemcentinib block the AXL signal, they will be strategically developed in different indications.

wupsa, der er to kort på hånden til at kaste sig ind med...ho ho ho...det er altså sygt overbevisende det de har gang i ! ! !

tidslinien i årsrapporten er også fin læsning....

De scanner markedet og researcher og laver gennembrud på mindre indikationer og så skal der rammes og tjenes BIG BIG MONEY med tilvestamab....

Global oncology sales i 2026 = 300.000.000.000 $
Og står med forecast til 50% forøgelse i 2040 fordi der bliver flere ældre og cancer er et stigende problem.
Så hvis man får en rimelig Jacpot her på 3-5år, kan den så kigge ind i et marked i vækst i 15år.

From the Annual report 2020. 👍

CEO Richard Godfrey:

I am pleased to report that our business operations and clinical trials have all been able to maintain high levels of activity throughout the year and our mitigation plans have been successful in limiting the impact of the pandemic.


This research leadership was showcased in a virtual R&D day we hosted in November 2020, which featured independent key opinion leaders from the US and Europe sharing their latest research findings on AXL and clinical experience with bemcentinib in a range of disease settings. I would like to extend my thanks to all of those who participated in and attended this event.
Throughout the year we have continued to make progress with our clinical
trials and data read outs, presenting updated clinical data and translational research findings to the scientific and medical community at several leading international congresses, albeit virtual. We remain committed to reporting our research findings and data at similar forums at regular intervals, and plan to present further data from our ongoing phase II trials in 2021.
In November 2020 we were pleased to be invited to make an oral presentation at the prestigious The Society for Immunotherapy of Cancer (SITC) conference, where we provided an update on clinical and translational
data from our Phase II bemcentinib and pembrolizumab combination study in refractory NSCLC patients previously treated with a PD-L1 or PD-1 checkpoint inhibitor (CPI) as a monotherapy. These patients have very limited treatment options available to them and their survival outlook is dismal.
Looking back on 2020, I reflect on what has been a challenging year, with the COVID-19 pandemic impacting communities and business around
the world with tragic consequences.
I am also extremely proud of the
way that the healthcare sector has responded to the challenge we are facing; with collaborations between academic institutions, governments and companies proving that the industry can be mobilised effectively to address a common good.

BerGenBio has been playing its own role in the effort to tackle COVID-19, about which I will go into some detail later, but our principal focus has remained unchanged: progressing the Phase II clinical development programme investigating our lead product candidate bemcentinib.
I am pleased to report that we
have made good progress towards meeting our clinical and operational milestones over the year despite COVID-19 related disruption. This global crisis has affected BerGenBio, along with many other companies across the sector, by extending the anticipated development timelines due to restrictions at clinical trial sites and lengthening patient recruitment processes. However, I am pleased to report that our operations and trials have all been able to remain active throughout the year and our mitigation plans have been successful in limiting the impact of the pandemic.
Bemcentinib is a first-in-class, highly selective, potent, once-a-day oral inhibitor of AXL kinase, and is currently undergoing trials as a monotherapy and in combination with other drug treatments against aggressive diseases, including non-small cell
lung cancer, acute myeloid leukaemia, myelodysplastic syndrome and COVID-19.
As a company, we remain world leaders in understanding the role
and function of AXL biology. AXL
is increasingly validated as a key mediator of aggressive disease, fostering immune evasion and therapy resistance and as a driver of metastasis, fibrosis and viral infection. BerGenBio’s development strategies are based on the hypothesis that selective inhibition of AXL has the potential to underpin the successful treatment of many serious diseases, including those where options for patients are limited.

(Cont.)

This research leadership was showcased in a virtual R&D day we hosted in November 2020, which featured independent key opinion leaders from the US and Europe sharing their latest research findings on AXL and clinical experience with bemcentinib in a range of disease settings. I would like to extend my thanks to all of those who participated in and attended this event.
Throughout the year we have continued to make progress with our clinical trials and data read outs, presenting updated clinical data and translational research findings to the scientific and medical community at several leading international congresses, albeit virtual. We remain committed to reporting our research findings and data at similar forums at regular intervals, and plan to present further data from our ongoing phase II trials in 2021.

In November 2020 we were pleased to be invited to make an oral presentation at the prestigious The Society for Immunotherapy of Cancer (SITC) conference, where we provided an update on clinical and translational
data from our Phase II bemcentinib and pembrolizumab combination study in refractory NSCLC patients previously treated with a PD-L1 or PD-1 checkpoint inhibitor (CPI) as a monotherapy. These patients have very limited treatment options available to them and their survival outlook is dismal.

The combination of bemcentinib and checkpoint inhibitor pembrolizumab continued to report promising clinical benefit and in June we presented an interim data read out from an ongoing study reporting the median progression-free survival is 2.5 times greater for cAXL-positive, checkpoint refractory, NSCLC patients. AXL expression is associated with resistance to immunotherapy, and the interim translational analysis of these data suggests that bemcentinib has the potential to reverse acquired resistance to checkpoint inhibitors among previously treated NSCLC patients by targeting AXL-expressing immune cells in the tumour. This finding was well received by the scientific community as it reinforces the belief that bemcentinib has the potential to improve the clinical benefit of existing immuno-oncology drugs.

At the American Society of Hematology conference (ASH) in December, we were pleased to share updated interim clinical data from two Phase II studies of bemcentinib in AML and MDS; reporting a clinical benefit rate of over 70% in relapsed AML patients. The prognosis for relapsed AML patients under current standards of care is very bleak, so we are pleased to see such an encouraging clinical benefit, with many of these seriously ill patients remaining on the drug for extended durations of time. Collectively, these continuing positive data readouts strengthenour confidence in bemcentinib as a therapy in these relapsed haematological cancer indications.

In addition, during 2020 togetherwith highly respected international research collaborators we announced several new clinical trial initiations and data being read out from investigator lead studies exploring bemcentinib’s potential in:
High Risk Myelodysplastic Syndromes (HR-MDS) or Acute Myeloid Leukaemia (AML),
Glioblastoma (GBM),
relapsed malignant mesothelioma,
and COVID-19.

(Cont.)

Alongside this core oncology-focused pipeline, 2020 saw BerGenBio respond to the global pandemic with the initiation of two trials to evaluate bemcentinib’s potential as a treatment for COVID-19. The rationale for these studies was based on consecutive research findings suggesting that AXL plays an important role facilitating enveloped viruses (SARS-CoV-2, Ebola, Zika, etc) entering host cells and dampening the anti-viral immune response, and bemcentinib has been shown to demonstrate promising anti-viral activity in pre-clinical models. With the continued emergence of
new strains of COVID-19, we remain confident that bemcentinib could play an important role in the global effort to combat the disease.
Two COVID-19 bemcentinib
studies are currently ongoing.
Patient recruitment for BGBC020,
a BerGenBio sponsored trial being conducted in South Africa and
India, was initiated in October. Post period-end, the trial’s independent Data Monitoring Committee twice confirmed that no safety concerns
had emerged, and recruitment of the target 120 patients could continue.
In the UK, in December 2020, we announced dosing had resumed in the Investigator Sponsored ACCORD trial funded by UK Research and Innovation (UKRI). We look forward to providing further updates on the progress in
this trial.
Looking ahead to 2021, we look forward to updating the market with further data from our AML, MDS
and NSCLC studies, in particular, we anticipate important data from AML and MDS studies to be reported during the first half of the year and NSCLC data later in the year as the survival data needs to mature and expect the first data readout from our COVID-19 studies in South Africa and India in Q1.

(Cont.)

During 2020 our organisation successfully adopted new working patterns ensuring the safety and wellbeing of our staff, collaborators and patients. We continued to build our organisation as we prepare for
the demands of late-stage clinical development. During the year we successfully completed two capital raises and we remain well-funded with a strong cash position and tight cost control, and as such BerGenBio is well positioned for continued success in 2021.
Going forward, we will continue to develop our sustainability management and report on the progress we make.
We are committed to building our business in line with international best practice on Environmental and Social Governance, in particular the Sustainable Development Goals identified by the United Nations. Through our vision to develop innovative drugs for aggressive diseases, we directly contribute
to SDG 3 – health and wellbeing. Through our work, we are also contributing to SDG 8 - decent work and economic growth, 9 - industry, innovation and infrastructure, and 17 – partnerships for the goals.
I am extremely proud and grateful
to our staff of the way our company has responded to challenges the past year has posed. I am also grateful
for the trust placed in us by patients, collaborators, and our shareholders as we have adapted to the rapidly changing landscape. We remain focused on delivering the best outcomes for all our stakeholders and look forward to providing updates from our oncology and COVID-19 trials in the coming months.

Richard Godfrey
CEO

BerGenBio is the future of medicine

Annual Report 2020:
https://www.bergenbio.com/wp-content/uploads/2021/02/BerGenBio-Annual-Report-2020.pdf


Årsrapporten til BGBIO burde vært kopiert av Moderna.

BerGenBio har en bedre PipeLine enn de fleste innen BigPharma( BP) og er mye mer informativ og spennende enn de fleste.

https://www.modernatx.com/pipeline

Q4 + 2020: https://investors.modernatx.com/node/11136/pdf

MODERNA :
150 Milliarder NOK
Moderna venter å få en inntjening på 18,4 milliarder dollar på sin koronavaksine i 2021. Det tilsvarer rundt 154 milliarder norske kroner. Dermed kan koronavaksinen bli svært innbringende for det amerikanske selskapet, viser selskapets regnskap som ble offentliggjort torsdag. Det har tidligere blitt dokumentert at deres vaksine er den dyreste blant de seks produsentene som EU har inngått avtaler med. (NTB)

🌴Oasen🌱🌿 i ørkenen heter Bemcentinib !
De to andre er luft speiling...

Ny oppdatering : https://www.edisongroup.com/publication/axleration-of-data-catalysts-in-2021/28906

BerGenBio (BGBIO) has made steady progress during 2020. Lead asset bemcentinib (oral, once a day, highly selective AXL inhibitor) reported encouraging efficacy data from ongoing Phase II trials. Multiple catalysts expected in 2021 will define BGBIO’s clinical trial strategy in AML/MDS and/or NSCLC. The FY20 operating loss was significantly higher than in FY19 (NOK261.1m vs NOK204.4m) due to higher set-up costs and increased investment in programme expenses. We expect operating expenses to increase significantly across 2021/22 as BGBIO further progresses its innovative AXL-centred pipeline, which includes bemcentinib in oncology (and COVID-19 potential) and the initiation of a Phase Ib/IIa trial to evaluate its AXL antibody tilvestamab in an undisclosed indication. BGBIO remains well funded following net c NOK700m raised in 2020. We value the company at NOK4.72bn or NOK54.1 per share.

Dual approach to AXL inhibition
We expect a plethora of bemcentinib efficacy data in 2021 to define its pivotal clinical trial strategy. This includes median overall survival data in relapsed AML and top-line data in NSCLC in combination with Keytruda. We believe BGBIO will focus on the relapsed AML/MDS setting (Phase III study of bemcentinib plus LDAC in relapsed elderly AML patients could start in 2021). We forecast the NDA submission for this indication in 2023 (FDA has granted fast-track status). BGBIO’s second clinical asset, tilvestamab (first-in-class AXL-targeting antibody), developed in-house and wholly owned by BGBIO, is set to start a Phase Ib/IIa trial shortly.
Eyes on COVID-19 trial readout
COVID-19 represents an additional opportunity that could expediate bemcentinib’s route to market in 2022. Bemcentinib has presented a unique dual mechanism of action in the potential treatment of COVID-19. Given the numerous emerging variants of COVID-19, we believe innovative therapies will be required alongside global vaccination strategies. Two Phase II trials are exploring bemcentinib efficacy (in combination with SOC) in hospitalised patients (the IDMC has confirmed safety). Top-line clinical data are expected in Q121 and will define the route to approval.
Valuation: NOK4.72bn or NOK54.1 per share
We value BGBIO at NOK4.72bn or NOK54.1/share (NOK5.16bn or NOK59.1/share previously). Our forecasts remain unchanged, but our valuation has been affected by FX. The key value drivers are bemcentinib in second-line NSCLC (peak sales $1.2bn, NOK37.4/share) and AML (peak sales $598m, NOK12.3/share) plus the COVID-19 opportunity (peak sales $300m, NOK5.4/share). We do not include tilvestamab in our valuation, but will revisit this when we have clarity on the indications prioritised for development.

The key value drivers are bemcentinib in second-line NSCLC (peak sales $1.2bn, NOK37.4/share) and AML (peak sales $598m, NOK12.3/share).
Må bare spørre, er dette realistisk med peak sales på 1.2 milliarder USD som tilsvarer omtrent 10 milliarder NOK og bare 37.4 NOK/aksje + de andre tallene

Ikke glem at dette tallet (37,4) er antatt med en 'Probability of success' på 35%.

mvh

Hoved oppslag i nyhetene nå var en Amerikansk medisin,Ivermektin,som visstnok skal ha god effekt som medisin mot Covid-19.
Noen som kjenner denne - og Ivermektin vs.Bemcentinib ?

10 øre under siste emisjon??????

Vi VET vel lite om Bem sin Covid virkning enda, men ett bredt studie med nesten 7500 deltagere viste liten virkning av Ivermectin både på overlevelsesgrad og sykehusdøgn. https://www.medrxiv.org/content/10.1101/2021.01.26.21250420v1

Ikke glem at covid-19 kun er en bonus mhp Bemcentinib. Hovedvekten i en verdivurdering av BgBio vil alltid være med fokus på kreftbehandling.

Afhængig af resultater og hvordan pandemien udvikler sig kan covid19 indikationen efter min mening være kandidat til at være uhyggeligt meget værd.
Hvis/når vi får op-blusning med nye mutationer så vil bemcentinib kunne være i frontlinien inden der så er nye vacciner klar. Her snakker folk om et muligt 10 årig marked.
Ud over dette så vil Covid19 indtjening kunne løfte BGBIO videre uden behov for yderligere kapital indsprøjtning. Hvis de skal klare sig med det vil deres tempo måske ikke være super højt, men de kan.
CEO har ydermere meldt meget sikkert ud omkring hvordan de ser opbakning fra aktionærerne. Han er fremstået med en uhyggelig selvtillid her. Jeg tænker Trond Mohn har givet ham noget selvtillid her.

Men ja, cancer er det som BGBIO virkelig kan få uhyggelig flyvehøjde af. Her vil Covid19 være peanuts. Oncology marked i cancer er 300 milliarder dollars og med gennemsnitlig årlig vækst på ca. 8%. BIG BIG BIG money.

Covid19 kan gøre BGBIO meget berømt. De behøves ikke bruge ret meget krudt på at gøre opmærksom på sig selv hvis der kommer stærke resultater. Reklame værdien er enorm. Hvem kender ikke de firmaer der laver vacciner til covid19.

Nye innside regler :

https://e24.no/boers-og-finans/i/VqG0ll/nye-innsideregler-for-boersselskapene-langt-fra-alle-har-rutinene-paa-plass

Skjerpings Folkens !

La oss tro og håpe at det ikke blir lekkasjer og ulovlig innside handel når COVID-19 de positive COVID-19 test resultatene fra BerGenBio kommer nå i mars.

Da Accord nyheten kom i 28.04.2020 Kl 23:43 var det merkelige transaksjoner i forkant av nyhetene samme dag, men Oslo Børs og Finanstilsynet ga blaffen i mine antydninger om mulig innside handel i BGBIO 28.04.2020 mellom Kl 10-12. Kursen spratt opp fra 19 til 22 kr på uvanlig høyt volum i forhold til tidligere.
29.04.2020 gikk kursen opp til 54kr før den falt tilbake. At ikke Finanstilsynet og Oslo Børs har i funnet noe kritikkverdig, - er helt utrolig.

https://www.bergenbio.com/bergenbios-bemcentinib-selected-to-be-fast-tracked-as-potential-treatment-for-covid-19-through-new-national-uk-government-clinical-trial-initiative/


Etter dette kom emisjonen og jeg stilte også flg nye spørmål til Finanstilsynet og Oslo Børs uten å få svar..

« Det har i ettertid også vært tildels betydelige negative svingninger i BGBIO aksjen etter at selskapet annonserte en 500 millioner kroners emisjon til eksisterende aksjonærer med innbetaling i dag.
Aksjen falt fra over 40kr til under 33kr på 2 dager etter at emisjonskurs på 37,5kr ble kjent 04.05.2020. Jeg ville derfor også undersøkt omsetning i aksjen noen dager i forkant av denne nyheten».


Nå er det enklere å følge med på brudd av innside regler :

https://www.trapets.com/wp-content/uploads/2019/11/Trapets-InstantWatch-Market-Product-Description.pdf

Hvordan vet du at resultatene blir posetive?

Det er ingen ting som tilsier at det blir positive resultater når du ser på aksjekursen. Resultatene kommer når dem er klare.

Talent, hvis vi ser isolert sett på dagens kurs så indikerer den en nøytral tilnærming/resultat til kommende trigger. Ser vi inn i det store bildet, hvor selskapet er ledende kandidat i Accord studie hvor antall deltakere er redusert og til eget studie i India og Afrika hvor vi har ett uavhengig organ som overvåker bivirkninger og effekt så heller resultatet av covid19 resultater i posetiv terreng..

Jeg håper og tror at resultatene blir positive. Ledelsen i BerGenBio og forsker Wendy M. er rimelig skråsikre i sine uttalelser om Bemcentinib og COVID-19.

Hvis du ikke kan / vil lese nyheter her eller på websidene om BGBIO ville jeg anbefalt å lytte til siste web cast siden du sliter med grammatikken...

Få noen til å klikke på denne web linken og skru på lyden :

https://www.bergenbio.com/radium-podcast-interview-with-bergenbio-ceo-richard-godfrey-hosted-by-radforsk/



Hvis du fortsatt etter dette er så pessimistisk ville jeg anbefalt å selge / shorte aksjen.

No Guts No Glory.... 😇

Hilsen BioBull

«I beg to differ» / Helt uenig med deg....
2. Mars 2020 lå aksjekursen på 16 NOK - nå er den 32 NOK. 100 % opp. Ta frem kuleramma og få på deg briller...

Er jeg pessimistisk på vegne av BERGENBIO? Ironi ?

Desember i 2019 så var kursen 23-25kr. Alle aksjer stupte vel i Mars hvis jeg ikke husker helt feil. Du får ta på deg brillene selv tror jeg.

Det er utrolig hvor dårlig utvikling det har vært på BGBIO aksjen fra børsinntreden til nå.
I dag igjen ser vi at etter en opptur kommer der en nedtur. Dette har vært signaturen til aksjen i laaaaang tid.
Aksjen er opp 5-6 kr på 4 år. En stor emmisjon innimellom, men det er utrolig dårlig avkastning så langt.

Biobull skrev:
"Jeg håper og tror at resultatene blir positive. Ledelsen i BerGenBio og forsker Wendy M. er rimelig skråsikre i sine uttalelser om Bemcentinib og COVID-19."

Javel, da er vi enige da jo, men ikke overdriv da. Godfrey sa bare 80%. "Skråsikker" da er du 100%. Selv tillegger jeg ikke Godfreys uttalelser særlig vekt.

Richard Godfrey 80% + Wendy M. 80% = skråsikker (- du sier skråsikker er 100% - ikke jeg ... )

Ja da får vi se da om den klarer å holde seg over 30kr. Jeg ble jo nesten dømt som talentløs når jeg sa det for noen måneder siden.

Akkurat samme mønster i dag som så mange dager tidligere. Åpner på ok nivå for deretter å sige nedover hele dagen. Aksjen er et trist skue og jeg håper at dere andre som har aksjer i selskapet ikke er all in, men har aksjer i andre selskaper også. Trist å ikke være med når nesten alt annet stiger...

Volumet er også størst på røde dager. Kommer det ikke nyheter snart så blir det fullstendig kollaps.

Er det Yngling som selger seg ut? Eller er det shortere som herjer i aksjen?

BGBIO har vel fått noen indikasjoner på hvordan Bemcentinib virker mot Covid19. Forhåpentligvis positive, Hvis ikke hadde de vel stoppet forsøkene i SA og India og meddelt dette til børsen? I stedet for å bruke penger på noe som ikke fungerer. En annen bra ting er jo at TM stadig kjøper aksjer. Blir færre og færre aksjer i omløp.

Ja, uten effekt hadde Bemcentintinib blitt kastet ut av både Accord studie og India/Afrika studie..

Alfred Berg fond har solgt over en periode nå og er nesten tomme for aksjer.

Når det gjelder vurdering av selskap og ledelse så pleier jeg å få rett til slutt. Håper jeg ikke får rett denne gangen. Småpenger riktignok, men det er penger det også.

Det som gjør at det er så fantastisk lønnsomt å investere i aksjer er at man er i et marked hvor det er så utrolig mange som ikke kan regne. Spetalen kunne neppe sagt det bedre. Men til dere som har trua og som synes Godfrey er fantastisk. Lykke til.