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Relief therapeutics Holding

9.106 Posts
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  1. Rotmeo 28 januari 2021 21:16
    Volgens mij timmeren ze al behoorlijk aan de weg.... kan toch enkel gebaseerd zijn op goede uitkomst?
  2. eric_k4 28 januari 2021 21:18
    Tribute no. xxx to DZR

    About RLF-100

    RLF-100 (Aviptadil) is a patented formulation of Vasoactive Intestinal Polypeptide (VIP) that was developed based on Dr. Said’s original work and was originally approved for human trials by the FDA in 2001 and the European Medicines Agency in 2005. VIP is known to be highly concentrated in the lungs and to inhibit a variety of inflammatory cytokines. Relief’s predecessor company, Mondo Biotech, was awarded Orphan Drug Designation in 2001 by the U.S. FDA for Aviptadil in the treatment of Acute Respiratory Distress Syndrome and in 2005 for treatment of Pulmonary Arterial Hypertension. Mondo was awarded Orphan Drug Designation by the European Medicines Agency in 2006 for the treatment of acute lung injury and in 2007 for the treatment of sarcoidosis. Both Mondo and Relief have worked on development of an inhaled formulation of Aviptadil for several years. Both the U.S. FDA and the EMEA have granted Investigational New Drug licenses for human trials of Aviptadil.
  3. evr68@hotmail.com 28 januari 2021 21:23
    quote:

    eric_k4 schreef op 28 januari 2021 21:18:

    Tribute no. xxx to DZR

    About RLF-100

    RLF-100 (Aviptadil) is a patented formulation of Vasoactive Intestinal Polypeptide (VIP) that was developed based on Dr. Said’s original work and was originally approved for human trials by the FDA in 2001 and the European Medicines Agency in 2005. VIP is known to be highly concentrated in the lungs and to inhibit a variety of inflammatory cytokines. Relief’s predecessor company, Mondo Biotech, was awarded Orphan Drug Designation in 2001 by the U.S. FDA for Aviptadil in the treatment of Acute Respiratory Distress Syndrome and in 2005 for treatment of Pulmonary Arterial Hypertension. Mondo was awarded Orphan Drug Designation by the European Medicines Agency in 2006 for the treatment of acute lung injury and in 2007 for the treatment of sarcoidosis. Both Mondo and Relief have worked on development of an inhaled formulation of Aviptadil for several years. Both the U.S. FDA and the EMEA have granted Investigational New Drug licenses for human trials of Aviptadil.
    Geweldig nieuws!
    MB had je ze ook in je bezit?
  4. Rotmeo 28 januari 2021 21:34
    Benieuwd waar hij op landt straks.... we hebben wel vaker een laatste moment dip gezien...
  5. [verwijderd] 28 januari 2021 21:57
    quote:

    Rotmeo schreef op 28 januari 2021 21:48:

    [...]
    Als we dat toch hadden geweten...pfffff
    Toch eens in de gaten gaan houden welke goedkope fondsen gaan stijgen zonder aanwijsbare oorzaak. Ik denk dat degene die dit begint stinkend rijk aan het worden is terwijl anderen met dure aandelen blijven zitten. Lijkt toch wel op strafbaar handelen wat mij betreft.
  6. [verwijderd] 28 januari 2021 23:10
    [quote alias=MisterBlues id=13137663 date=202101281616]
    [...]

    Dat moet je eens aan de Afro-Amerikanen, Zuid-Afrikanen, andere Afrikanen, Indiërs, andere Aziaten etc. etc. vragen...
    [/quote
    Geen geld voor een Vaccin = Geen geld voor andere middelen vrees ik.
    Echter toelating voor deze indicatie opent enorm veel andere deuren...
    Ik zie het niet zo heel somber in :-) Integendeel...
  7. M c M 28 januari 2021 23:20
    quote:

    eric_k4 schreef op 28 januari 2021 21:18:

    Tribute no. xxx to DZR

    About RLF-100

    RLF-100 (Aviptadil) is a patented formulation of Vasoactive Intestinal Polypeptide (VIP) that was developed based on Dr. Said’s original work and was originally approved for human trials by the FDA in 2001 and the European Medicines Agency in 2005. VIP is known to be highly concentrated in the lungs and to inhibit a variety of inflammatory cytokines. Relief’s predecessor company, Mondo Biotech, was awarded Orphan Drug Designation in 2001 by the U.S. FDA for Aviptadil in the treatment of Acute Respiratory Distress Syndrome and in 2005 for treatment of Pulmonary Arterial Hypertension. Mondo was awarded Orphan Drug Designation by the European Medicines Agency in 2006 for the treatment of acute lung injury and in 2007 for the treatment of sarcoidosis. Both Mondo and Relief have worked on development of an inhaled formulation of Aviptadil for several years. Both the U.S. FDA and the EMEA have granted Investigational New Drug licenses for human trials of Aviptadil.
    Officieel PB? Ik zie het nog niet. Koers van 0.75 naar 0.57 dollar (al is dat ook niet slecht natuurlijk)
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