Oramed Pharmaceuticals Inc
WKN: A1CTNU / ISIN: US68403P2039Oramed Pharmaceuticals Inc.
| eröffnet am: | 28.03.07 13:46 von: | OttomanRosendahl |
| neuester Beitrag: | 04.07.25 17:17 von: | woroda |
| Anzahl Beiträge: | 991 | |
| Leser gesamt: | 321634 | |
| davon Heute: | 5 | |
bewertet mit 5 Sternen |
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10.06.14 17:27
#403
ellogo2
@ixurt
Mal abwarten......scheint ein guter Zeitpunkt gewesen zu sein.
Dachte mir, so kurz vor dem Meeting der ADA (ab 14.06.) könnte gut passen.
Hoffe natürlich, dass es paar gute News gibt.
Nachdem die ja den gleichen Weg einschlagen wie wir und unsere Daten sehr gut aussehen.......bisher!!!!! Habe ich Hoffnung, dass ein Big Player Interesse daran findet.
Manche Pipeline ist ja, wie schon im anderen Thread besprochen, ziemlich leer.
http://seekingalpha.com/article/2251533-the-importance-of-being-oral
Dachte mir, so kurz vor dem Meeting der ADA (ab 14.06.) könnte gut passen.
Hoffe natürlich, dass es paar gute News gibt.
Nachdem die ja den gleichen Weg einschlagen wie wir und unsere Daten sehr gut aussehen.......bisher!!!!! Habe ich Hoffnung, dass ein Big Player Interesse daran findet.
Manche Pipeline ist ja, wie schon im anderen Thread besprochen, ziemlich leer.
http://seekingalpha.com/article/2251533-the-importance-of-being-oral
10.06.14 21:55
#404
deAlex
Regels stockt weiter auf
http://ir.oramed.com/phoenix.zhtml?c=180902&p=irol-sec
10.06.14 23:35
#405
ixurt
@ellogo2
hast recht mal abwarten...
zur Zeit recht positive Aussichten...
denn
nebst dem Meeting der ADA (ab 14.06.)
wurde in der letzten Woche lehrbuchmäßig
dass letzte noch offene Gap bei 7,19 USD geschlossen.
Desweiteren wurde am Freitag der Stichtag (6.6) für das Einlösen der Management-Optionen überwunden.
Und nun Schlag auf Schlag...
News:
zur Zeit recht positive Aussichten...
denn
nebst dem Meeting der ADA (ab 14.06.)
wurde in der letzten Woche lehrbuchmäßig
dass letzte noch offene Gap bei 7,19 USD geschlossen.
Desweiteren wurde am Freitag der Stichtag (6.6) für das Einlösen der Management-Optionen überwunden.
Und nun Schlag auf Schlag...
News:
10.06.14 23:54
#406
deAlex
Auf den Gap Close
Hätte ich verzichten können... Kurse unter 10usd hätte ich das mal früher gewusst ;-)
Naja abgerechnet wird am Schluss ne
Naja abgerechnet wird am Schluss ne
11.06.14 16:05
#407
deAlex
mit bisher
Volumen 44,611 das Ding 6% nach oben geschoben...sehr interessant.
11.06.14 20:48
#409
ellogo2
Tja
Tja Alex...das ist eben immer so eine Sache mit dem "früher wissen"....habe ich mir auch schon oft gedacht, bei manchen Aktien ;-)
Aber so ist´s eben........wie du schreibst, abgerechnet wird am Schluss!
Aber so ist´s eben........wie du schreibst, abgerechnet wird am Schluss!
11.06.14 22:03
#413
deAlex
Wenn die Shorts
anfangen zu brennen geht's hier steil.
Volumen war heute schonmal nicht schlecht, bin auf morgen gespannt.
Volumen war heute schonmal nicht schlecht, bin auf morgen gespannt.
11.06.14 22:40
#414
schultebrand
jetzt noch die ein oder andere gute news und
das covern wird eine teure angelegenheit.
12.06.14 09:02
#415
deAlex
@schulte
Und da nun bald die ADA beginnt können die auch schnell folgen :-)
http://oramed.com/ufiles/Oramed%20-%20ADA%20posters.pdf
http://oramed.com/ufiles/Oramed%20-%20ADA%20posters.pdf
12.06.14 16:29
#417
ellogo2
@ixurt
Scheint so, als hätten wir wirklich einen guten Einstiegszeitpunkt gefunden :-)
12.06.14 20:01
#418
ixurt
ellogo2, sieht erfreulicherweise sehr danach aus
Wollte Dir einen Grünen schenken... leider verhindern die Regeln es....
Wenn ich dir eine Bewertung schicken möchte
kommt folgende Anzeige:
"Von Ihnen kommen bereits 7 der letzten 20 (oder weniger) positiven Bewertungen für ellogo2. "
Gruß ixurt ;-)
12.06.14 21:02
#419
ellogo2
ixurt, dass ist nett
...aber allein der Wille zählt, wenn der Grüne nicht will, kann man nix machen ;-)
Gruß aus der sonnigen Pfalz ;-)
Gruß aus der sonnigen Pfalz ;-)
15.06.14 11:01
#421
ellogo2
Poster 1 ADA
Presentation Abstract
Session: Publish Only
Abstract Number: 2411-PO
Title: Comparative Assessment of the Glucose-Lowering Effect of Multiple Oral Insulin (ORMD-0801) Formulation Variants in Pigs
Presentation Start: 6/15/2014 5:00:00 AM
Presentation End: 6/15/2014 6:00:00 AM
Authors: MIRIAM KIDRON, EHUD ARBIT, YAEL SHUSHLAV, Jerusalem, Israel, Kfar HaOranim, Israel
Abstract: Oral drug delivery platforms are being actively pursued to provide an oral insulin solution to diabetes patients. ORMD-0801, designed using the PODTM technology, has established the indispensability of antiproteolytic support and absorption enhancing factors toward effective passage of orally delivered insulin through the gastrointestinal tract to its site of action. ORMD-0801 has elicited improved glycemic control in type 1 and type 2 diabetes patients and is currently being assessed in large-scale clinical trials. In efforts to further enhance formulation stability and bioperformance, a comparative analysis of the glucose-lowering effects of two surfactant combinations (herein, EC-TA and SW-G), added to the basic oral insulin (ORMD-0801) formulation, was performed following their administration to healthy, fasting pigs (n=3-4). At each session, a single dose of an ORMD-0801 formulation variant, was directly administered to the duodenum, under endoscopic guidance, and blood glucose levels were monitored for the ensuing 150 minutes. All tested formulations, including the surfactant-free variant, induced a significant glucose-lowering effect within 30 min of administration, with Cmin obtained within 30-90 min of dosing. All but the SW-G formulations led to glucose lows which plateaued for 45-60 min before beginning to return to baseline levels. The overall effect of EC-TA-supplemented formulations on mean blood glucose concentrations, was significantly greater than those supplemented with SW-G, for all tested doses (p<0.04). The glucose area under the curve of mean EC-TA-elicited responses was 34% lower than that obtained with the SW-G-supplemented formulation and the surfactant-free formulation. This study demonstrated the primacy of the EC-TA surfactant combination in the tested oral insulin formulation; further studies will be required to evaluate its translation in the clinic.
Session: Publish Only
Abstract Number: 2411-PO
Title: Comparative Assessment of the Glucose-Lowering Effect of Multiple Oral Insulin (ORMD-0801) Formulation Variants in Pigs
Presentation Start: 6/15/2014 5:00:00 AM
Presentation End: 6/15/2014 6:00:00 AM
Authors: MIRIAM KIDRON, EHUD ARBIT, YAEL SHUSHLAV, Jerusalem, Israel, Kfar HaOranim, Israel
Abstract: Oral drug delivery platforms are being actively pursued to provide an oral insulin solution to diabetes patients. ORMD-0801, designed using the PODTM technology, has established the indispensability of antiproteolytic support and absorption enhancing factors toward effective passage of orally delivered insulin through the gastrointestinal tract to its site of action. ORMD-0801 has elicited improved glycemic control in type 1 and type 2 diabetes patients and is currently being assessed in large-scale clinical trials. In efforts to further enhance formulation stability and bioperformance, a comparative analysis of the glucose-lowering effects of two surfactant combinations (herein, EC-TA and SW-G), added to the basic oral insulin (ORMD-0801) formulation, was performed following their administration to healthy, fasting pigs (n=3-4). At each session, a single dose of an ORMD-0801 formulation variant, was directly administered to the duodenum, under endoscopic guidance, and blood glucose levels were monitored for the ensuing 150 minutes. All tested formulations, including the surfactant-free variant, induced a significant glucose-lowering effect within 30 min of administration, with Cmin obtained within 30-90 min of dosing. All but the SW-G formulations led to glucose lows which plateaued for 45-60 min before beginning to return to baseline levels. The overall effect of EC-TA-supplemented formulations on mean blood glucose concentrations, was significantly greater than those supplemented with SW-G, for all tested doses (p<0.04). The glucose area under the curve of mean EC-TA-elicited responses was 34% lower than that obtained with the SW-G-supplemented formulation and the surfactant-free formulation. This study demonstrated the primacy of the EC-TA surfactant combination in the tested oral insulin formulation; further studies will be required to evaluate its translation in the clinic.
15.06.14 11:02
#422
ellogo2
Poster 2 ADA
Presentation Abstract
Session: Late Breaking Poster Session
Abstract Number: 87-LB
Title: Bedtime Oral Insulin Lowers Fasting Blood Glucose Levels in T2DM Patients
Presentation Start: 6/15/2014 12:00:00 PM
Presentation End: 6/15/2014 2:00:00 PM
Authors: JOEL NEUTEL, MIRIAM KIDRON, EHUD ARBIT, KENNETH HOMER, Tustin, CA, Jerusalem, Israel, Cedar Knolls, NJ
Abstract: Bedtime insulin administration has been suggested to best counteract abnormal morning fasting blood glucose (FBG) levels, a harbinger of diabetes and a key obstacle to optimal glycemic management in T2DM patients. However, many early-stage patients resist introduction of insulin injections into their routine. The pursuit of an orally bioavailable insulin formulation has been driven by the notion that it can both increase patient compliance, and better mimic the physiological route of naturally secreted insulin, consequently lowering risk of hypoglycemia. In this randomized, double-blind, placebo-controlled study, the pharmacokinetics and pharmacodynamics of bedtime administration of the ORMD-0801 oral insulin were assessed in 30 adult T2DM patients inadequately controlled with diet and exercise and/or metformin. Following a 5-day placebo run-in period, a blinded continuous glucose monitor (CGM) was implanted and patients received a single placebo dose on day 1, followed by a 7-day, bedtime placebo or ORMD-0801 (460 IU or 690 IU) treatment in an inpatient setting. Plasma insulin and c-peptide levels were monitored for 5-hours postdosing. A manufacturing fault limited 690 IU dose efficacy; the data were excluded from the analysis. No hypoglycemic events were recorded throughout the entire study period. ORMD-0801-treated patients showed consistently higher mean plasma insulin levels throughout the 180 min Day 8 postdosing period, when compared to baseline. Moreover, in the first 60 min postdosing, plasma insulin exposure was 20.53 μIU*h/mL greater among ORMD-0801-treated patients when compared to the placebo arm and followed a concentration-time course similar to that of plasma c-peptide. Fasting CGM data demonstrated a mean -30.24 mg/dL difference between the last two days of active versus placebo treatment. Overall, ORMD-0801 led to a stable, consistent and short-acting rise in plasma insulin levels, which positively impacted FBG concentrations in the treated T2DM patients.
Session: Late Breaking Poster Session
Abstract Number: 87-LB
Title: Bedtime Oral Insulin Lowers Fasting Blood Glucose Levels in T2DM Patients
Presentation Start: 6/15/2014 12:00:00 PM
Presentation End: 6/15/2014 2:00:00 PM
Authors: JOEL NEUTEL, MIRIAM KIDRON, EHUD ARBIT, KENNETH HOMER, Tustin, CA, Jerusalem, Israel, Cedar Knolls, NJ
Abstract: Bedtime insulin administration has been suggested to best counteract abnormal morning fasting blood glucose (FBG) levels, a harbinger of diabetes and a key obstacle to optimal glycemic management in T2DM patients. However, many early-stage patients resist introduction of insulin injections into their routine. The pursuit of an orally bioavailable insulin formulation has been driven by the notion that it can both increase patient compliance, and better mimic the physiological route of naturally secreted insulin, consequently lowering risk of hypoglycemia. In this randomized, double-blind, placebo-controlled study, the pharmacokinetics and pharmacodynamics of bedtime administration of the ORMD-0801 oral insulin were assessed in 30 adult T2DM patients inadequately controlled with diet and exercise and/or metformin. Following a 5-day placebo run-in period, a blinded continuous glucose monitor (CGM) was implanted and patients received a single placebo dose on day 1, followed by a 7-day, bedtime placebo or ORMD-0801 (460 IU or 690 IU) treatment in an inpatient setting. Plasma insulin and c-peptide levels were monitored for 5-hours postdosing. A manufacturing fault limited 690 IU dose efficacy; the data were excluded from the analysis. No hypoglycemic events were recorded throughout the entire study period. ORMD-0801-treated patients showed consistently higher mean plasma insulin levels throughout the 180 min Day 8 postdosing period, when compared to baseline. Moreover, in the first 60 min postdosing, plasma insulin exposure was 20.53 μIU*h/mL greater among ORMD-0801-treated patients when compared to the placebo arm and followed a concentration-time course similar to that of plasma c-peptide. Fasting CGM data demonstrated a mean -30.24 mg/dL difference between the last two days of active versus placebo treatment. Overall, ORMD-0801 led to a stable, consistent and short-acting rise in plasma insulin levels, which positively impacted FBG concentrations in the treated T2DM patients.
16.06.14 16:18
#423
deAlex
Grün?!
Also ich hätte heute mit rot gerechnet, die Aktie hat echt ein Eigenleben...
16.06.14 17:14
#425
deAlex
hat jemand ne Idee oder News?
Ich bin echt völlig planlos
Volumen ist nicht gut aber auch nicht schlecht...
aber lieber mit kleinem Volumen Up als mit großem Down...
Auf eine weitere wohl spannende Woche!
Volumen ist nicht gut aber auch nicht schlecht...
aber lieber mit kleinem Volumen Up als mit großem Down...
Auf eine weitere wohl spannende Woche!

