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Koers Genfit 2017

259 Posts, Pagina: « 1 2 3 4 5 6 7 8 9 10 11 12 13 » | Laatste
DeZwarteRidder
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quote:

me_n schreef op 27 maart 2017 10:53:

[...]Niet op reageren werkt het beste.
Genfit kan nog steeds zomaar ontploffen op een gerucht of een daadwerkelijk echte overname/partnerschap.
Genfit kan ook zomaar als een slappe pudding in elkaar zakken.....
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DeZwarteRidder schreef op 27 maart 2017 10:54:

[...]
Genfit kan ook zomaar als een slappe pudding in elkaar zakken.....
Vandaag schijnt de zon buiten, het zou morgen wel weer eens kunnen gaan regenen...
DeZwarteRidder
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me_n schreef op 27 maart 2017 17:32:

Oei oei gaat wel hard nu zeg...
Dus een 'bodem' van toiletpapier......

Of zouden de criminelen die voorkennis misbruiken nu andere 'voorkennis' hebben....???
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Overstappers naar Erytech (+76%) verklaart de daling bij Genfit vandaag.
Verwacht herstel komende dagen.
DeZwarteRidder
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Solietje schreef op 27 maart 2017 22:29:

Overstappers naar Erytech (+76%) verklaart de daling bij Genfit vandaag. Verwacht herstel komende dagen.
Slaat natuurlijk nergens op: waarom zou iemand die een overname van Genfit verwacht z'n aandelen omruilen voor een ander aandeel??
me_n
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quote:

Solietje schreef op 27 maart 2017 22:29:

Overstappers naar Erytech (+76%) verklaart de daling bij Genfit vandaag.
Verwacht herstel komende dagen.
Dat denk/hoop ik ook ja.
Blijf nog even zitten, ookal is dat nog best moeilijk.

Misschien komt hier nog wat moois uit:

March 28, 2017 02:31 ET | Source: Genfit
multilang-release
2017.03.28 PR GENFIT KOLs events.pdf
GENFIT to host a series of KOL Meetings in NASH

Planned events will feature presentations from renowned Key Opinion Leaders specialized in the clinical management of NASH
Meetings to kick off with a KOL lunch in Boston on March 30th followed by different cities in the US and EU, including events in New York, Amsterdam (EASL), and London
Lille (France), Cambridge (Massachusetts, United States), March 28, 2016 - GENFIT (Euronext: GNFT - ISIN: FR0004163111), a biopharmaceutical company at the forefront of developing therapeutic and diagnostic solutions in metabolic and inflammatory diseases, that notably affect the liver or the gastrointestinal system, announced today that it will host a series of Key Opinion Leader (KOL) meetings focused on the NASH space for institutional investors and research analysts in Europe and the United States over the course of the coming months.

The meetings will feature presentations by renowned Key Opinion Leaders in the NASH space and intend to provide a global overview on this disease, and an opportunity to the financial community for in-depth interactions with NASH experts. The topics of the meetings will include clinical management of NASH patients, diagnostics for NASH and potential combination therapy approaches. Additionally, GENFIT management will provide an overview of the Company's pipeline, including biomarker development program in NASH.

Details of the first upcoming KOL meetings are as follows:
Boston on March 30, 2017: NASH KOL Lunch with Dr. Manal F. Abdelmalek
Manal F Abdelmalek, MD, MPH is Associate Professor of Medicine in the Division of Gastroenterology and Hepatology at Duke University, with expertise in epidemiology, public health, clinical trial design, and clinical-translational research in NAFLD/NASH. She directs the Duke NAFLD Clinical Research Program. As one in the founding investigators in the field of NASH, she has 20 years experience in the successful implementation and conduct of clinical trials in NAFLD/NASH.

· New-York on April 4, 2017: NASH KOL Breakfast with Dr. Rohit Loomba
Dr. Rohit Loomba is Professor of Medicine (with tenure) in the Division of Gastroenterology, and Adjunct Professor in the Division of Epidemiology at University of California, San Diego. He is a leading expert in translational research and innovative clinical trial design in NAFLD (nonalcoholic fatty liver disease) and NASH. Dr. Loomba is the founding director of the UCSD NAFLD Translational Research Unit where his team is conducting cutting edge research in all aspects of NAFLD.

Attendance at the KOL events is intended for institutional investors and analysts.

About elafibranor:

Elafibranor is GENFIT's lead pipeline product. Elafibranor is an oral once-daily treatment, and a first-in-class drug acting via dual peroxisome proliferator-activated alpha/delta pathways developed to treat, in particular, nonalcoholic steatohepatitis (NASH). Elafibranor is believed to address multiple facets of NASH, including inflammation, insulin sensitivity, lipid/metabolic profile, and liver markers.

About NASH:

"NASH", or nonalcoholic steatohepatitis, is a liver disease characterized by an accumulation of fat (lipid droplets), along with inflammation and degeneration of hepatocytes. The disease is associated with long term risk of progression to cirrhosis, a state where liver function is diminished, leading to liver insufficiency, and also progression to liver cancer.

About GENFIT:

GENFIT is a biopharmaceutical company focused on the discovery and development of drug candidates in areas of high unmet medical needs corresponding to a lack of suitable treatment and an increasing number of patients worldwide. GENFIT's R&D efforts are focused on bringing new medicines to market for patients with metabolic, inflammatory, autoimmune and fibrotic diseases, that affect the liver (such as NASH - Nonalcoholic steatohepatitis) and more generally the gastro-intestinal arena. GENFIT's approach combines novel treatments and biomarkers. Its lead proprietary compound, elafibranor, is currently in a Phase 3 study. With facilities in Lille and Paris, France, and Cambridge, MA (USA), the Company has approximately 120 employees. GENFIT is a public company listed in compartment B of Euronext's regulated market in Paris (Euronext: GNFT - ISIN: FR0004163111). www.genfit.com

Forward Looking Statement / Disclaimer:

This press release contains certain forward-looking statements. Although the Company believes its expectations are based on reasonable assumptions, these forward-looking statements are subject to numerous risks and uncertainties, which could cause actual results to differ materially from those expressed in, or implied or projected by, the forward-looking statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, including related to biomarkers, progression of, and results of clinical data from, the RESOLVE-IT trial, review and approvals by regulatory authorities, such as the FDA or the EMA, regarding in particular, elafibranor in NASH and PBC, as well as other indications, and biomarkers, the success of any inlicensing strategies, the Company's continued ability to raise capital to fund its development, as well as those discussed or identified in the Company's public filings with the AMF, including those listed under Section 7 "Main Risks and Uncertainties" of the Company's Half Year 2016 Business and Financial Report, which is available on GENFIT's website (www.genfit.com) and on the website of the AMF (www.amf-france.org). Other than as required by applicable law, the Company does not undertake any obligation to update or revise any forward-looking information or statements.

This press release and the information contained herein do not constitute an offer to sell or a solicitation of an offer to buy or subscribe to shares in GENFIT in any country. This press release has been prepared in both French and English. In the event of any differences between the two texts, the French language version shall supersede.

CONTACT

GENFIT | Jean-François Mouney - Chairman & CEO | Ph. +333 2016 4000
MILESTONES - Press Relations | Bruno Arabian | Ph. +331 8362 3484 / +336 8788 4726 - barabian@milestones.fr
------------------------------------

globenewswire.com/news-release/2017/0...
DeZwarteRidder
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quote:

Beurspleintje schreef op 28 maart 2017 18:36:

Ik heb er een goed gevoel over.
Mooie uitvinding toch: KOL-meetings, KOL-events, KOL-breakfasts, KOL-lunches, etc. etc.
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Mbt persbericht over de KOL meetings; Genfit gaat zichzelf onder de aandacht brengen in de USA komende tijd.

Meetings zijn gericht op analisten en institutionele beleggers, we zullen in de koers en volumes terugzien hoe zij erover denken.

Verwacht zelf dat dit een aanloop is naar de NASDAQ notering op korte termijn.
DeZwarteRidder
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quote:

Solietje schreef op 28 maart 2017 22:13:

Mbt persbericht over de KOL meetings; Genfit gaat zichzelf onder de aandacht brengen in de USA komende tijd.
Meetings zijn gericht op analisten en institutionele beleggers, we zullen in de koers en volumes terugzien hoe zij erover denken.
Verwacht zelf dat dit een aanloop is naar de NASDAQ notering op korte termijn.
Als ze binnenkort worden overgenomen, waarom organiseren ze dan peperdure KOL-meetings en waarom willen ze dan naar de NASDAQ...???
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Als dit en als dat en als blablablabla, en waarom zo en waarom blablabla, en stel je voor en stel je blablabla. De Zwarte Droogbelegger GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAP
DeZwarteRidder
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Dit verhaal lijkt sprekend op Genfit:
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Corbus Pharmaceuticals (CRBP) waves a sea of hands in front of investors' eyes Thursday to obscure dismal results from another mid-stage study of its experimental anti-inflammatory drug anabasum.

In this four-month study of cystic fibrosis patients, the Corbus drug failed to improve lung function compared to a placebo. Overall respiratory symptoms, measured by a cystic fibrosis patient questionnaire, also showed no difference between anabasum and placebo.

These were the two most important, prospectively defined efficacy endpoints measured in the Corbus phase II study. Both came back zero. No benefit.

Instead of dealing with the clinical setback honestly, Corbus deflects with cherry-picked "positive" results from subsets of patients using endpoints not even written into the original design of the study.

Corbus claims a subset of patients treated with the highest dose of anabasum -- 20 mg taken twice daily -- reported a 75% reduction in "acute pulmonary exacerbations" compared to a placebo.

A 75% reduction sounds impressive but it wasn't. There was a one acute pulmonary exacerbation in patients treated with the 20 mg twice daily dose of anabasum compared to three of these events in placebo patients. In other words, Corbus got lucky with a tiny number of events.

Worse, this tiny numerical difference is probably due to imbalance in the baseline characteristics of patients in the study. Notably, significantly more patients in the 20 mg twice-daily arm were being treated with Vertex Pharma's (VRTX) cystic fibrosis drugs Orkambi or Kalydeco compared to the placebo patients. The Vertex drugs are proven to reduce pulmonary exacerbations.
DeZwarteRidder
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quote:

Pl4 schreef op 30 maart 2017 16:56:

Plas lijkt op gewoon water, maar dan sochtends met een gele kleur
Plas is toch een minister...???
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DeZwarteRidder schreef op 30 maart 2017 18:16:

[...]
Plas is toch een minister...???
Plas een minister? Dat lijkt me sterk..
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De verwachte nieuwsvoorziening rondom Genfit in 2017
Met dank aan Beursorama forum

- 4 April 2017: NASH KOL met Professor Rohit Loomba, New York
- 4-6 April 2017: Deelname aan NASH Summit 2017, Cambridge USA
- 18-19 April 2017: Deelname aan de 12e European Smallcap Event Parijs
- 19 April 2017: Deelname aan de 10e Kempen & Co Life Science Conference, Amsterdam

April 2017: publicatie van het referentiedocument en financieel jaarverslag

- 19-23 April 2017: deelname aan de International Liver Congress ™ 2017, Amsterdam
- 27 April 2017: Publicatie van omzet en kaspositie 31 maart 2017

- 5-6 Mei 2017: Deelname aan de 2e Internationale workshop NASH Biomarkers, USA
- 6-9 Mei 2017: Deelname aan de Digestive Disease Week, Chicago, USA

- 8 juni 2017: Deelname aan de 3e editie van Labiotech Refresh met presentatie tijdens een mondelinge sessie "Fireside Chat - NASH, de verborgen parel" van Dean Um, Chief Scientific Officer, Berlijn – Duitsland

- 1e halfjaar 2017: Afronding van het algoritme de ontdekking van biomarkers elementen voor het diagnosticeren van NASH patiënten

- 1e halfjaar 2017: Klaar voor Fase II studie van cirrose
- 1e halfjaar 2017: Aanwerving van 1 patiënt in de PBC
- 1e halfjaar 2017: Klaar voor pre-klinische studie samengesteld TGFTX4
- 16 juni 2017: Jaarlijkse Algemene Vergadering van Aandeelhouders.

Zomer 2017: Voltooiing van inschrijving voor subdeel H fase 3 RESOLVE-IT

- 2e halfjaar 2017: toetreding aanvraag NASH biomarkers

- 25 September 2017: Publicatie van de halfjaarresultaten 2017

16 oktober 2017: Publicatie van omzet en kaspositie op 30 September 2017

2017: De lancering van een fase III pediatrische NASH (indien eerdere fase ok)

Eind 2017: Validatie van NASH biomarker algoritme
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