geht hier was
allen Anderen natürlich auch . Anbei noch die Ankündigung von Acer ein
neues Medikament erproben zu wollen ! Es tut sich gewaltiges im Hintergrund !!
https://ownsnap.com/...f-stock-is-on-the-verge-of-breakout-what-next/
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Go go go
PRESS RELEASE1ReliefTherapeutics Reports that its Collaboration Partner, NRx Pharmaceuticals, has Submitted an Application for Emergency Use Authorization for Aviptadil to the U.S. Food & Drug AdministrationGeneva, Switzerland, June 2, 2021RELIEF THERAPEUTICS Holding AG (SIX: RLF, OTCQB: RLFTF)(Relief), a biopharmaceutical company with its lead compound RLF-100 (aviptadil) in advanced clinical development to treat COVID-19-induced respiratory disorders, reported today that its collaboration partner,NRx Pharmaceuticals, Inc. (formerly known as: NeuroRx Pharmaceuticals, Inc.), has announced that it has submitted an application to the U.S. Food and Drug Administration (FDA) seekingEmergency Use Authorization(EUA)forthe use ofaviptadil in the treatment of critical COVID-19 in patients with respiratory failure.NRxs press release announcing its EUA submission can be accessed through the following link. We are delighted that our partner has submitted aviptadil forEUAand look forward to a decision by the Agency, said Raghuram (Ram) Selvaraju, Chairman of the Board of Relief. Despite the increase in the number of people being fully vaccinated against COVID-19, with emerging variants and disparities in vaccination rates, there remains a major need for effective therapeutic optionsfor patients with respiratory failure. We are excited about the potential aviptadil holds in helping critical COVID-19 patients and are hopeful that the drug candidate will soon be available to those who remain inneedof bettertreatments.Dr. Selvaraju continued: We would also like to take this opportunity to not only congratulate our partner on completing theEUAsubmission but also on their recent listing on Nasdaq.The EUA submission is based on the results of a COVID-19 IVrandomized, placebo-controlled phase 2b/3clinical trialconducted by NRx in the United States. Relief also confirms that it has received a copy of the clinical study report from this trial from NRx and looks forward topursuingthe best path forward for the development ofIV RLF-100 in Europeand other territories.FDAs guidance to industry identifies the criteria for EUA as safe and may be effective, in contrast to the far more stringent requirement of safe and effective required for traditional drug approval. EUA may only be granted in circumstances where the Secretary of Health and Human Services has declared a Public Health Emergency, as is trueforthe COVID-19 pandemic.There is no guidance or regulation regarding how quickly FDA will review EUA applications.###
PRESS RELEASE2ABOUT RELIEFRelief focuses primarily on clinical-stage programs based on molecules with a history of clinical testing and use in human patients or a strong scientific rationale. Reliefs lead drug candidate RLF-100TM(aviptadil), a synthetic form of Vasoactive Intestinal Peptide (VIP), is in late-stage clinical developmentin the U.S. for the treatment of respiratory deficiency due to COVID-19. As part of its pipeline diversification strategy, in March 2021, Relief entered into a Collaboration and License Agreement with Acer Therapeutics for the worldwide development and commercialization of ACER-001. ACER-001 is a taste-masked and immediate release proprietary powder formulation of sodium phenylbutyrate (NaPB) for the treatment of Urea Cycle Disorders and Maple Syrup Urine Disease. RELIEF THERAPEUTICS Holding AG is listed on the SIX Swiss Exchange under the symbol RLF and quoted in the U.S. on OTCQB under the symbol RLFTF. For more information, visitwww.relieftherapeutics.com.Follow us on LinkedIn.CONTACT:RELIEF THERAPEUTICS Holding AGJack WeinsteinChief Financial Officer and Treasurer Mail: contact@relieftherapeutics.comFOR MEDIA/INVESTOR INQUIRIES: MC Services AGAnne HenneckeTel.: +49 (0) 211-529-252-22Mail:relief@mc-services.euDisclaimer:This communication expressly or implicitly contains certain forward-looking statements concerning RELIEF THERAPEUTICS Holding AG, and there can be no assurance that NRx's application for EUA will be approved by the FDA or that Relief will be successful in obtaining approval for the product in Europe or other territories. Such statements involve certain known and unknown risks, uncertainties and other factors, which could cause the actual results, financial condition, performance or achievements of RELIEF THERAPEUTICS Holding AG to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. RELIEF THERAPEUTICS Holding AG is providing this communication as of this date and do not undertake to update any forward-looking statements contained herein as a result of new information, future events or otherwise.
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deaktivieren !! :-) Wünsche euch allen einen grünen Mittwoch ! :-)
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Briefkurs (ask) Vol. Brief Zeit
0.224 26'217 (2) 07:40:00
0.223 66'637 (2) 07:00:05
0.222 1'264'000 (6) 07:40:00
0.22 386'092 (12) 08:00:03
0.219 143'576 (5) 07:40:00
0.218 100'000 (1) 05:55:02
0.217 4'500 (1) 05:55:02
0.215 20'000 (1) 06:25:00
0.21 100 (1) 08:17:22
Bestens 50'100 (2) 08:29:36
08:18:37 32'000 (6) Bestens
05:55:02 4'000 (1) 0.22
08:30:25 53'920 (4) 0.215
08:30:04 21'629 (3) 0.214
08:31:49 87'420 (8) 0.21
05:55:02 13'958 (2) 0.204
05:55:02 59'889 (2) 0.202
07:40:02 85'000 (8) 0.20
08:23:13 20'000 (1) 0.199
08:14:53 23'000 (2) 0.195
Zeit Vol. Geld Geldkurs (bid)
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Kann mir jemand sagen warum NRX Pharma (ehem. Big Rock Partners & Neurox) von der Zulassung nicht auch wesentlich profitieren solten? Was meint Ihr, sollte man dort einsteigen? Verdient Relief an dem Verkauf von ZYESAMI in Amerika mit? Oder bleibt dort alles bei NRX. Wie sieht es mit dem Rest der Welt aus? Indien? Wer darf dann wo auf der Welt sein Medikament verkaufen?
GENEVA, Switzerland and RADNOR, Pa., Sept. 21, 2020 /PRNewswire/ -- RELIEF THERAPEUTICS Holding SA (SIX: RLF,OTCQB: RLFTF) ("Relief" or the "Company") and NeuroRx, Inc. today announced the completion of their partnership agreement for the commercialization of RLF-100(Aviptadil) worldwide. The two organizations have agreed to share all profits from sales of RLF-100 for all indications related to COVID-19 and potentially other respiratory indications on a global basis. They have agreed that NeuroRx will lead commercialization in the United States, Canada, and Israel, while Relief will lead commercialization in Europe and the rest of the world. Profits from sales will be allocated to Relief and NeuroRx on a 50/50 basis in the U.S., Canada and Israel, 85/15 (in favor of Relief) in Europe, and 80/20 (in favor of Relief) in all other territories.
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Von welcher Marktkapitalisierung träumst du denn? :-)
investiert sein grinsen wir zusammen .
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Echt zum k...
Muss ich denn jetzt meinen ganzen Text umformulieren, um dann die gleiche Nachricht zu erhalten?
Wenn Onvista nicht will , dass man gute und informative Beiträge verfasst verabschiede ich mich hier wieder. Ich sehe in meinem ganzen Text nicht eine einzige Passage, in der eventuell ein verwerfliches Wort stehen würde.
Ich wünsche euch dennoch alles Gute und vielleicht bis dann
https://www.investoren.team/threads/rlf-relief-therapeutics.2/
https://www.youtube.com/watch?v=MONezF-sIw0 Video Youtube
To open the online version please click here.
Dear Sir or Madam,
We would like to draw your attention to the following press release of RELIEF THERAPEUTICS Holding AG:
Relief Therapeutics Reports that Collaboration Partner, NRx Pharmaceuticals, has Announced Additional Results from the Aviptadil U.S. Expanded Access Protocol for Patients with Critical COVID-19
Geneva, Switzerland, June 16, 2021 RELIEF THERAPEUTICS Holding AG (SIX: RLF, OTCQB: RLFTF) (Relief), a biopharmaceutical company with its lead compound RLF-100 (aviptadil) in advanced clinical development to treat COVID-19-induced respiratory disorders, reported today that its collaboration partner, NRx Pharmaceuticals, Inc., (Nasdaq: NRXP) (NRx) has announced additional results from the aviptadil U.S. Expanded Access Protocol (EAP). The EAP included 240 patients in the intensive care unit (ICU) with critical COVID-19 respiratory failure requiring either invasive or non-invasive mechanical ventilation, or high flow rate oxygen by nasal cannula, and not eligible for the recently completed phase 2b/3 clinical trial with IV aviptadil. According to NRxs press release, these EAP data are being submitted by NRx to the U.S. Food and Drug Administration (FDA) as real world evidence in support of the findings from the phase 2b/3 trial. The related NRx press release can be accessed through the following link.
###
ABOUT RELIEF
Relief focuses primarily on clinical-stage programs based on molecules with a history of clinical testing and use in human patients or a strong scientific rationale. Reliefs lead drug candidate RLF-100TM (aviptadil), a synthetic form of Vasoactive Intestinal Peptide (VIP), is in late-stage clinical development in the U.S. for the treatment of respiratory deficiency due to COVID-19. As part of its pipeline diversification strategy, in March 2021, Relief entered into a Collaboration and License Agreement with Acer Therapeutics for the worldwide development and commercialization of ACER-001. ACER-001 is a taste-masked and immediate release proprietary powder formulation of sodium phenylbutyrate (NaPB) for the treatment of Urea Cycle Disorders and Maple Syrup Urine Disease.
RELIEF THERAPEUTICS Holding AG is listed on the SIX Swiss Exchange under the symbol RLF and quoted in the U.S. on OTCQB under the symbol RLFTF. For more information, visit www.relieftherapeutics.com.
Follow us on LinkedIn.
CONTACT:
RELIEF THERAPEUTICS Holding AG
Jack Weinstein
Chief Financial Officer and Treasurer
Mail: contact@relieftherapeutics.com
§
FOR MEDIA/INVESTOR INQUIRIES:
MC Services AG
Anne Hennecke
Tel.: +49 (0) 211-529-252-22
Mail: relief@mc-services.eu
Disclaimer: This communication expressly or implicitly contains certain forward-looking statements concerning RELIEF THERAPEUTICS Holding AG, and there can be no assurance that NRx's application for EUA will be approved by the FDA or that Relief will be successful in obtaining approval for the product in Europe or other territories. Such statements involve certain known and unknown risks, uncertainties and other factors, which could cause the actual results, financial condition, performance or achievements of RELIEF THERAPEUTICS Holding AG to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. RELIEF THERAPEUTICS Holding AG is providing this communication as of this date and do not undertake to update any forward-looking statements contained herein as a result of new information, future events or otherwise.
+++ End of press release +++
Should you have any questions or would like to receive further information, please do not hesitate to contact us.
Best regards,
Laurie Doyle
MC Services AG
phone: +1 347 804 6686
email: relief@mc-services.eu
www.mc-services.eu
MC Services AG
Handelsregister/Commercial Register: Amtsgericht Augsburg HRB 2117
Vorstand/Management Board: Raimund Gabriel, Anne Hennecke
Aufsichtsrat/Supervisory Board: Johannes Gabriel (Vorsitzender/Chairman)
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zur Gilde big Pharma . Nichts desto trotz wird weiter kräftig gewerkelt im
Hintergrund und auch in Europa . Hier mal was Interressantes von Advita !! :-)
https://advita-lifescience.com/newsroom/
Die COVID-19-Fallzahlen sinken weiter aber ein Ende der Pandemie ist nicht absehbar. Von verschiedenen Klinikern in Europa wurde der Wunsch geäußert, an der COVID-19-Studie mit inhalativem Aviptadil unter Leitung von Prof. Leuppi teilzunehmen. Die dafür notwendige EudraCT-Nr. wurde uns gestern mitgeteilt. Dadurch kann jedes Krankenhaus innerhalb der EU teilnehmen.
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