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Aandeel RELIEF THERAPEUTICS N ZSE:RLF.CH, CH1251125998

Laatste koers (chf) Verschil Volume
5,300   -0,040   (-0,75%) Dagrange 5,000 - 5,880 124.131   Gem. (3M) 160,6K

Relief therapeutics Holding

9.105 Posts
Pagina: «« 1 ... 4 5 6 7 8 ... 456 »» | Laatste | Omlaag ↓
  1. forum rang 4 MisterBlues 16 juli 2020 15:59
    quote:

    Forecast2006 schreef op 16 juli 2020 15:30:

    Dat is echt goed nieuws.

    Koop er maar weer 100.000 bij nu ze nog laag staan.

    Kind regards,

    Forecast.
    Ik vind dat de markt lauw reageert op het goede nieuws. Nu ca. 10% erbij.

    Zou dat komen omdat beleggers een beetje suf zijn gebeukt door de markt voor dit aandeel, plus dat het van heel ver komt?:

    Laagste prijs CHF 0,0008 4.400,00 % 30-10-2019

    Iemand een idee?
  2. forum rang 4 MisterBlues 19 juli 2020 12:18
    quote:

    maikel85 schreef op 19 juli 2020 10:17:

    Beste allemaal,

    Graag jullie mening over de verrekening van schuld in aandelen. Wat denken jullie dat de invloed nu en op lange termijn gaat zijn.

    Groeten,

    Maikel
    Verrekening van schuld in aandelen lijkt me in deze situatie een win-win: Relief heeft weinig geld over en voor de investeerder is de aandelenoverdracht tegen deze prijs buitengewoon laag.

    Voor ons als beleggers wordt de situatie nog riskanter: stapt de investeerder er met grote delen uit dan kan de koers elk moment kelderen, alsof er een soort tijdbom in zit. Maar goed, dat was toch al zo.

    Het fonds is echter uit op een grote winst zo neem ik aan. Ze blijven nog wel even zitten…(?)
  3. forum rang 4 MisterBlues 20 juli 2020 16:10
    Een concurrent erbij die al wat verder is. Laat wel zien wat er kan gebeuren bij succes:

    SYNAIRGEN SHARE PRICE EXPLODES 400% ON POSITIVE COVID-19 TRIAL RESULTS
    UPDATED: 20 JULY 2020
    Shares of Synairgen PLC (LON: SNG) have exploded nearly 400% to 180p after the drugmaker revealed positive results from a clinical trial of its drug for the treatment of the severe symptoms of COVID-19 disease.

    The firm said that 79% of tested patients showed a “lower risk of developing severe disease compared to those given the placebo”.

    “Our efforts are now focused on working with the regulators and other key groups to progress this potential COVID-19 treatment as rapidly as possible,” chief executive Richard Marsden said.

    SNG001, a test drug developed to treat positive patients with more severe symptoms, has also proved successful in ramping up the recovery from the COVID-19 virus. Patients who received the drug were more than twice as likely to recover from the illness than those that received the placebo.

    Synairgen share price exploded almost 400% today on the news. Despite the rapid ascendance, analysts believe that the upside may be much higher for the stock.

    Synairgen share price erupts 400% on positive COVID-19 drug tests July 2020

    Mark Brewer, the analyst at finnCap, increased his target for Synairgen stock price to 360p. The set target price represents a premium of 886% from Friday’s close of 36.5p.

    www.asktraders.com/analysis/synairgen...

    > 500% momenteel:
    www.google.com/search?newwindow=1&...
  4. forum rang 4 MisterBlues 29 juli 2020 09:05
    quote:

    maikel85 schreef op 29 juli 2020 08:46:

    Hallo allemaal,

    Goed nieuws vandaag!

    www.prnewswire.com/news-releases/fda-...
    Thnx Maikel85! Ze lijken op goede voet te staan met de FDA en van onderstaande zinnen word je als belegger wel blij:

    The protocol makes treatment available to patients who have exhausted approved therapies and are not eligible for the current phase 2/3 trial of RLF-100 because of other medical conditions and specifically makes the treatment available to pregnant women. Although the drug remains under investigation, rapid recovery from respiratory failure in COVID-19 has been seen in patients treated under FDA Emergency Use authorization.1

    "By granting this Expanded Access protocol, FDA has made a potentially lifesaving drug immediately available to critically ill patients who have no other available treatment," said Dr. Jonathan C. Javitt, MD, MPH, NeuroRx's CEO. "We thank the FDA's pulmonary division for its rapid and proactive implementation of the Coronavirus Treatment Acceleration Program and we aspire to demonstrate broad safety and efficacy for RLF-100 in our ongoing clinical trial.
  5. Forecast2006 29 juli 2020 11:06

    FDA grants Expanded Access Protocol to RLF-100 (Aviptadil) for Respiratory Failure in COVID-19

    by Relief Therapeutics | Jul 29, 2020

    Expanded access protocol, including for pregnant women, is becoming available to patients who are ineligible for enrollment in the FDA clinical trial of RLF-100,
    RLF-100, a patented formulation of Aviptadil, is currently in development by NeuroRx and RELIEF THERAPEUTICS Holding AG under Fast Track Designation, and recently obtained positive safety opinion from the data monitoring committee.

    Geneva and Radnor, PA, July 29, 2020 – RELIEF THERAPEUTICS Holding AG (SIX:RLF, OTC:RLFTF) “Relief” and its U.S. partner, NeuroRx, Inc. today announced that FDA has granted an Expanded Access Protocol for treatment of Respiratory Failure in COVID-19 with RLF-100 (aviptadil), a synthetic form of Vasoactive Intestinal Peptide (VIP). The protocol makes treatment available to patients who have exhausted standard therapies and are not eligible for the current phase 2/3 trial of RLF-100 because of confounding medical conditions and specifically makes the treatment available to pregnant women. Although the drug remains under investigation, rapid recovery from respiratory failure in COVID-19 has been seen in patients treated under FDA Emergency Use authorization.[1]

    The expanded access protocol may be viewed on www.clinicaltrials.gov NCT04453839. Physicians who wish to enroll their patients in the protocol must submit the protocol to their local investigational review board and file FDA form 1572 with NeuroRx, Inc. Further information may be obtained from expandedaccess@neurorxpharma.com.

    “By granting this Expanded Access protocol, FDA has made a potentially lifesaving drug immediately available to critically ill patients who have no other available treatment,” said Dr. Jonathan C. Javitt, MD, MPH, NeuroRx’s CEO. “We thank the FDA’s pulmonary division for its rapid and proactive implementation of the Coronavirus Treatment Acceleration Program, and we aspire to demonstrate broad safety and efficacy for RLF-100 in our ongoing clinical trial.”

    The SARS-CoV-2 coronavirus that causes COVID-19 attacks the body by entering the small population of Alveolar Type II cells in the lung.[2] Without Type II cells, the lung cannot transmit oxygen, which why the coronavirus causes acute respiratory failure. 50 years of scientific research demonstrates that VIP binds specifically to the Type II cell and protects that cell against cytokines (inflammatory molecules) and a wide array of toxic and infectious injuries.”[3]



    About RELIEF THERAPEUTICS Holding AG

    Kind regards,

    Forecast
  6. forum rang 4 MisterBlues 29 juli 2020 11:08
    We moeten later kijken op o.a. clinical trials of de onderzoeksgroepen van Relief groter worden. Wellicht dat er PB's komen. Dit zou een buitengewoon goede aanwijzing zijn dat het een krachtig kandidaat-medicijn is.

    Even wat anders, kan Relief niet vinden op de Covid-19 tracker site:

    covid-19tracker.milkeninstitute.org/

  7. [verwijderd] 29 juli 2020 12:16
    Ze staan wel op die site mrblues ??

    NEURORX/ RELIEF THERAPEUTICS/ THOMAS JEFFERSON UNIVERSITY HOSPITAL/ NYU LANGONE HEALTH/ HOUSTON METHODIST HOSPITAL
    AVIPTADIL, SYNTHETIC FORM OF VASOACTIVE INTESTINAL POLYPEPTIDE (RLF-100)
    CLINICAL
    Phase II/III trial ongoing July 2020; FDA grants Fast Track Designation June 2020; Expanded access protocols

    Staan onder neurorx/relieftherapeutics bij others
  8. forum rang 4 MisterBlues 29 juli 2020 16:20
    quote:

    maikel85 schreef op 29 juli 2020 12:16:

    Ze staan wel op die site mrblues ??

    NEURORX/ RELIEF THERAPEUTICS/ THOMAS JEFFERSON UNIVERSITY HOSPITAL/ NYU LANGONE HEALTH/ HOUSTON METHODIST HOSPITAL
    AVIPTADIL, SYNTHETIC FORM OF VASOACTIVE INTESTINAL POLYPEPTIDE (RLF-100)
    CLINICAL
    Phase II/III trial ongoing July 2020; FDA grants Fast Track Designation June 2020; Expanded access protocols

    Staan onder neurorx/relieftherapeutics bij others
    Thnx.

    Wederom vind ik de reactie van beleggers wat tam:

    Relief Therapeutics Holding AG CHF 0,0326 0,0024 7,95 %
    Aan het einde is dat vermoedelijk nog 5%

    Uit die site wordt duidelijk hoeveel bedrijven wel niet actief zijn op Covid-19 gebied en vooral voor de severe & critical groep patiënten.

    Eerder hadden we het over de pijplijn. Er is meer en dat moet ook wel willen ze echt boven Jan komen. Iemand hier een mening over?
  9. forum rang 4 MisterBlues 29 juli 2020 16:41
    Het gaat om 1 molecuul – rlf 100 met 4 toepassingen, 2 binnen Covid en 2 binnen Sarcoidosis

    Acute respiratory distress syndrome:

    COVID-19 induced ARDS:

    Our goal for the treatment of COVID-19-induced ARDS, is to provide immunomodulation and anti-inflammatory properties as well as a protective action on AT-II cells at levels that will prevent hospitalization of patients and ARDS lethality.

    Sarcoidosis
    Sarcoidosis, also known as Besnier-Boeck-Schaumann disease, is an auto-aggressive systemic granulomatous disease that primarily affects the lungs, but can affect almost all organs of the body. The prevalence of sarcoidosis is between 1 and 60 people affected every 100’000 individuals, and presents a clear south-north gradient and racial variations. It is usually considered as a fairly mild disease as most cases of sarcoidosis disappear spontaneously. However 10 to 20% of sarcoidosis patients develop a chronic form that could even be life threatening.

    Meestal als een molekuul effectief is vinden ze vaak meer toepassingen. Kan niet goed begrijpen dat dit aandeel ooit op 80 euro stond of zoiets...
9.105 Posts
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