Van beleggers
voor beleggers
desktop iconMarkt Monitor
  • Word abonnee
  • Inloggen

    Inloggen

    • Geen account? Registreren

    Wachtwoord vergeten?

Ontvang nu dagelijks onze kooptips!

word abonnee

Aandeel RELIEF THERAPEUTICS N ZSE:RLF.CH, CH1251125998

  • 1,310 19 apr 2024 17:30
  • +0,050 (+3,97%) Dagrange 1,200 - 1,325
  • 27.123 Gem. (3M) 15,2K

Relief therapeutics Holding

9.103 Posts
Pagina: «« 1 ... 283 284 285 286 287 ... 456 »» | Laatste | Omlaag ↓
  1. [verwijderd] 25 januari 2021 10:16
    quote:

    DeZwarteRidder schreef op 25 januari 2021 08:54:

    [...]

    Relief ziet de bui al hangen dat Aviptadil geen succes gaat opleveren en dekt zich in.
    Ik heb juist de indruk dat ze al verder zijn en uitgaan van een succes. Als aviptadil geen succes wordt zijn deze investeringen ook moeilijk te verklaren. Dan kan GEM de deal met ACER ook wel zelf maken.
  2. forum rang 5 MisterBlues 25 januari 2021 10:22
    quote:

    Kleintje66 schreef op 25 januari 2021 10:16:

    [...]

    Ik heb juist de indruk dat ze al verder zijn en uitgaan van een succes. Als aviptadil geen succes wordt zijn deze investeringen ook moeilijk te verklaren. Dan kan GEM de deal met ACER ook wel zelf maken.
    Bovendien gaat de deal Relief echt niet redden als ze geen goedkeuring krijgen. Dat snapt een kind.
  3. Vollebeurs 25 januari 2021 10:56
    quote:

    Kleintje66 schreef op 25 januari 2021 10:16:

    [...]

    Ik heb juist de indruk dat ze al verder zijn en uitgaan van een succes. Als aviptadil geen succes wordt zijn deze investeringen ook moeilijk te verklaren. Dan kan GEM de deal met ACER ook wel zelf maken.
    U trekt me de woorden uit het toetsenbord. Natuurlijk zitten er de nodige mitsen en maren aan deze deal, maar het eerste miljoen wordt gelijk overgemaakt. Die pieken geef je alleen uit als je ze niet direct nodig hebt - een motivatie kan zijn dat je op korte termijn verwacht dat er inkomsten komen...
  4. forum rang 10 DeZwarteRidder 25 januari 2021 13:53
    Israel sees 60% drop in hospitalizations for age 60-plus 3 weeks after 1st shot
    Full effects of Pfizer’s shots only kick in around a month after inoculation, but data from Israel shows there is a stark drop in infections even before that point
    By Nathan Jeffay 24 January 2021, 4:31 pm 12

    Vaccines are quickly averting serious cases of COVID-19 among the most vulnerable members of society, an Israeli healthcare provider has indicated.

    The full effects of Pfizer’s vaccine are only slated to kick in around a month after the first shot, but data from Israel, home to the world’s fastest vaccination drive, has already shown that there is a stark drop in infections even before this point.

    Attracting widespread international interest by sharing early data, Maccabi Healthcare Services reported earlier this month that it has seen a 60 percent reduction in coronavirus infections three weeks after the first shot is administered.

    But it wasn’t clear if the benefits were being felt equally by those who have a propensity to mild infection and those who would be likely to take COVID-19 badly.
    An Israeli man receives a coronavirus vaccine at a Clalit vaccination center in Jerusalem on January 4, 2021. (Olivier Fitoussi/Flash90)

    Now, Maccabi is starting to answer the question that hospitals and health ministers around the world are anxiously asking, amid fears of health service meltdowns: How quickly will COVID-19 wards start to see the benefits of vaccination?

    The decrease in hospital admissions is swift after vaccination, Maccabi suggests in its latest data, finding that hospitalizations start to fall sharply from Day 18 after people receive the first shot. Galia Rahav, head of infectious diseases at Israel’s largest hospital, Sheba Medical Center, described the data as “very important.”

    By Day 23, which is 2 days after the second shot, there is a 60% drop in hospitalizations among vaccinated people aged 60-plus, Maccabi revealed after monitoring 50,777 patients. It compared their hospitalization rate at that point with their hospitalization rate soon after receiving the vaccine, using 7-day moving averages.
    Israeli Prof. Galia Rahav in Tel Aviv on June 22, 2020.(Yossi Aloni/Flash90)

    “This is very important data,” Rahav, who is unconnected to the study, told The Times of Israel. “It has an impact because amid high infection rates and the spread of variants it’s hard to see from general figures how vaccination is influencing things.

    “By giving an insight into hospitalizations among just those elderly people who were vaccinated, this data is valuable.”

    However, she cautioned that some of the drop may be due to a tendency of newly vaccinated people to adhere to lockdown rules, which causes a drop in infection and hospitalization.

    The new data also supports Maccabi’s earlier claim of a 60% infection rate drop after three weeks, reporting that it saw the same drop with a new sample comprising only the 60-plus age group.

    Maccabi’s graph gives a real picture of infection in Israel, showing that until Day 13, vaccinated over-60s had similar infection rates as the overall 60-plus population. Then, a gap opens, and by Day 23, there were 18 daily infections among the 50,777 overall, but just six among the vaccinated.
  5. Reader 25 januari 2021 16:06
    quote:

    Frank312 schreef op 25 januari 2021 15:16:

    Super nieuws!!

    MAAR. dát gaat natuurlijk voor de rest van de wereld nog wel even ( lees: t*ring lang ) duren....dus nog steeds heel positief over RLF. Maar wel aardig dat je positief nieuws deelt.
    Dat doet "ie" gelukkig altijd. Het lijkt een vreemde vent maar hij heeft goede info lijnen en deelt ze.

    Hij wil natuurlijk feedback hebben als ie weer eens in de contramine is want hij heeft ze ook, geloof mij maar...toch ridder?

    Mvgr,

    Reader
  6. forum rang 5 MisterBlues 25 januari 2021 18:25
    Sommige posters beweren dat er een merger komt met Acer die al op de Nasdaq zit.

    Acer is on Nasdaq.
    $51M market cap.
    14M shares
    Their UCD drug is in phase 3.
    Their MSUD drug is phase 1 and website says additional funding needed.
    Last year losses $21M.

    PR also says Relief will pay up to ~$35M to bring UCD and MSUD to market.
    A little confusing as it leaves investors to speculate and read the tea leafs!
    Perhaps how Relief gets on Nasdaq?
  7. Geweren_Gerrit 25 januari 2021 22:03
    Het blijkt dat in India ook het eea gaat gebeuren via Dr Reddys

    wap.business-standard.com/article/com...

    Dr Reddy's, Zuventus get nod to conduct Covid-19 trials on repurposed drugs

    The subject expert committee (SEC) has given the go-ahead to a clutch of firms, including Dr Reddy’s Laboratories (DRL) and Zuventus Healthcare, to conduct clinical trials on repurposed drugs for Covid-19.

    Mumbai’s Zuventus and Hyderabad’s DRL have got the nod to conduct Phase 3 clinical trials of Aviptadil injectable formulation. Aviptadil — a vasoactive intestinal polypetide used to treat erectile dysfunction — has been found to be useful in treating respiratory distress in Covid-19 patients. The US Food and Drug Administration has allowed emergency-use of the drug for treating Covid-19 patients.

    NeuroRx and Relief Therapeutics have partnered to develop a drug called RLF-100 that has anti-inflammatory and anti-cytokine activity properties.

    The SEC noted that Zuventus had presented revised Phase 3 clinical trial protocol before the committee, and after “detailed deliberation”, it recommended grant of permission of Phase 3 trials with the drug, “subject to condition that criteria for discharge of patients from intensive care unit should be defined clearly in the protocol”.

    As for DRL, the SEC has noted that the trial should be termed Phase 3 clinical trial instead of Phase 2/3 trial.

    Another drug Colchicine, used to treat gout, is also going to be tested for treating Covid patients. Telangana-based LAXAI Life Sciences has been recommended a grant of permission for Phase 2 trial with some conditions like blood pressure should be measured for inclusion of patients, discharge criteria should be specified, etc. Canadian researchers have said the use of Colchicine can reduce the risk of death or hospitalisation in Covid patients by 21 per cent.

    SEC seeks data on SII, Bharat Biotech jabs

    Pune’s Serum Institute of India (SII) has been asked to submit a revised clinical trial protocol before the SEC for conducting trial on Covovax vaccine. Developed by Novavax, the vaccine will undergo clinical trials in India and Serum is the partner here.

    Meanwhile, Bharat Biotech has been asked to submit the data for consideration again to proceed to Phase 2 clinical trial for its chimpanzee adenovirus vectored Covid-19 vaccine code-named BBV154. Bharat Biotech has to submit revised clinical trial protocol for consideration of the committee.
  8. forum rang 5 MisterBlues 26 januari 2021 08:00
    quote:

    Geweren_Gerrit schreef op 25 januari 2021 22:03:

    Het blijkt dat in India ook het eea gaat gebeuren via Dr Reddys

    wap.business-standard.com/article/com...

    Dr Reddy's, Zuventus get nod to conduct Covid-19 trials on repurposed drugs

    The subject expert committee (SEC) has given the go-ahead to a clutch of firms, including Dr Reddy’s Laboratories (DRL) and Zuventus Healthcare, to conduct clinical trials on repurposed drugs for Covid-19.

    Mumbai’s Zuventus and Hyderabad’s DRL have got the nod to conduct Phase 3 clinical trials of Aviptadil injectable formulation. Aviptadil — a vasoactive intestinal polypetide used to treat erectile dysfunction — has been found to be useful in treating respiratory distress in Covid-19 patients. The US Food and Drug Administration has allowed emergency-use of the drug for treating Covid-19 patients.

    NeuroRx and Relief Therapeutics have partnered to develop a drug called RLF-100 that has anti-inflammatory and anti-cytokine activity properties.

    The SEC noted that Zuventus had presented revised Phase 3 clinical trial protocol before the committee, and after “detailed deliberation”, it recommended grant of permission of Phase 3 trials with the drug, “subject to condition that criteria for discharge of patients from intensive care unit should be defined clearly in the protocol”.

    As for DRL, the SEC has noted that the trial should be termed Phase 3 clinical trial instead of Phase 2/3 trial.

    Another drug Colchicine, used to treat gout, is also going to be tested for treating Covid patients. Telangana-based LAXAI Life Sciences has been recommended a grant of permission for Phase 2 trial with some conditions like blood pressure should be measured for inclusion of patients, discharge criteria should be specified, etc. Canadian researchers have said the use of Colchicine can reduce the risk of death or hospitalisation in Covid patients by 21 per cent.

    SEC seeks data on SII, Bharat Biotech jabs

    Pune’s Serum Institute of India (SII) has been asked to submit a revised clinical trial protocol before the SEC for conducting trial on Covovax vaccine. Developed by Novavax, the vaccine will undergo clinical trials in India and Serum is the partner here.

    Meanwhile, Bharat Biotech has been asked to submit the data for consideration again to proceed to Phase 2 clinical trial for its chimpanzee adenovirus vectored Covid-19 vaccine code-named BBV154. Bharat Biotech has to submit revised clinical trial protocol for consideration of the committee.

    Goed nieuws wederom. Voor Relief en Novavax.
  9. Beso 26 januari 2021 08:20
    Diverse partijen die hun aandeel recent verhoogd hebben wat toch een goed teken moet zijn :

    Stans (awp) - Die Relief Therapeutics Holding AG meldet im Rahmen einer Pflichtmitteilung folgende Beteiligungen bzw. Beteiligungsveränderungen (Publikationsdatum 26.01.2021):

    Aktionär Entstehung zuvor
    aktuell Meldepflicht gemeldeter Wert

    Yves Sagot, FR 2,63%* 22.01.2021 3,382%
    * davon 2,322% in Namenaktien
    Meldegrund: Kapitalerhöhung

    Relief Therapeutics
    - Veräusserungspositionen 7,372% 22.01.2021 9,676%
    Meldegrund: Kapitalerhöhung

    BG Consulter GmbH, DE <3% 22.01.2021 3,198%
    Meldegrund: Kapitalerhöhung

    Yves Sagot, FR 3,382%* 20.01.2021 4,528%
    * davon 2,987% in Namenaktien
    Meldegrund: Verkauf

    Relief Therapeutics
    - Veräusserungspositionen 9,676% 20.01.2021 4,151%
    Meldegrund: Unterzeichnung einer Aktienzeichnungsanlage

    BG Consulter GmbH, DE 3,198% 19.01.2021 k.A.
    Meldegrund: Erwerb

    Relief Therapeutics
    - Veräusserungspositionen 4,151% 19.01.2021 0,952%
    Meldegrund: Ausübung, Nichtausübung oder Verfall von Derivatbeständen; Verkauf
  10. GoGo68 26 januari 2021 10:02
    quote:

    User133 schreef op 26 januari 2021 09:57:

    Netto verhoging van holdings maar iedereen is behoorlijk angstig omdat Yves Sagot - Chief Scientific Officer zijn positie verlaagde van 90M naar 75M aandelen.
    Voor de duidelijkheid: Yves Sagot heeft zijn aandeel niet verkocht, het percentage van zijn aandelen is verlaagd en je kunt op Swissquote zien dat de reden daarvoor een kapitaalverhoging is. Hij bezit nog steeds hetzelfde aantal aandelen.
  11. TraceyH 26 januari 2021 10:02
    quote:

    User133 schreef op 26 januari 2021 09:57:

    Netto verhoging van holdings maar iedereen is behoorlijk angstig omdat Yves Sagot - Chief Scientific Officer zijn positie verlaagde van 90M naar 75M aandelen.
    Hij had vast geld nodig! Als hij echt ' bang is ' voor het ongewisse had hij vast meer gedumpt.
9.103 Posts
Pagina: «« 1 ... 283 284 285 286 287 ... 456 »» | Laatste |Omhoog ↑

Meedoen aan de discussie?

Word nu gratis lid of log in met je emailadres en wachtwoord.

Direct naar Forum

Premium drie voorbeelden van IEX Premium: de exclusieve content op de site, de app op een smartphone en IEX Magazine.

Benieuwd naar onze analyses en kooptips?

Word nu abonnee van IEX en krijg onbeperkt toegang tot onze (koop)tips en succesvolle modelportefeuilles. Nu 3 maanden voor slechts €19,95! Profiteer van 58% korting!

Word abonnee

Lees verder op het IEX netwerk Let op: Artikelen linken naar andere sites

Gesponsorde links