Pharming « Terug naar discussie overzicht

Weekdraadje 17 tm 23 januari

76 Posts, Pagina: « 1 2 3 4 | Laatste
[verwijderd]
0
[verwijderd]
1
www.theglobeandmail.com/life/facts-an...

Dairy rabbits

In the Netherlands, genetically modified herds of rabbits are being reared to help treat heart patients with their milk, India’s Merinews.com reports. Scientists at the biotech company Pharming Group have genetically modified the rabbits, called dairy rabbits, to include a human gene and C1 inhibitor protein in their milk. Initial tests have shown a range of possible uses. If approved, the milk could become available in the market through the commercial milking of dairy rabbits.

[verwijderd]
1
quote:

Zakcentje schreef:

www.theglobeandmail.com/life/facts-an...

Dairy rabbits

In the Netherlands, genetically modified herds of rabbits are being reared to help treat heart patients with their milk, India’s Merinews.com reports. Scientists at the biotech company Pharming Group have genetically modified the rabbits, called dairy rabbits, to include a human gene and C1 inhibitor protein in their milk. Initial tests have shown a range of possible uses. If approved, the milk could become available in the market through the commercial milking of dairy rabbits.

En met het ''Merinews-stuk'' bedoelt hij dit:

www.merinews.com/article/commercial-m...

Commercial milking of rabbits, relief to heart patients

Scientists at Pharming - a biotech company have genetically modified the rabbits, called dairy rabbits, to include a human gene and C1 inhibitor protein. These genetically modified rabbits are being reared to treat heart patients with their milk.

CJ: Dr. Lalit kishore Mon, Jan 18, 2010 12:25:20 IST
World News :

IN HOLLAND, genetically modified herds of rabbits are being reared to help treat heart patients with their milk.

Scientists at Pharming - a biotech company have genetically modified the rabbits, called dairy rabbits, to include a human gene and C1 inhibitor protein.

Initial trials have shown that the milk of such rabbits has the following possibilities:
Helpful in tissue damage in survivours of heart strokes;
Helpful in preventing the rejection of transplant organs;
Potential to treat the hereditary immune disorder angioedema.
The European drug regulators have been approached for the approval of the product. Once approved, it could become available in the market through commercial milking of dairy rabbits.
[verwijderd]
0
''Pharming's Pompe debacle verfilmd..''

Nee hor... maar toch ;-)) wel een filmpie!

Pompe disease hits screens in "Extraordinary Measures"

Toni Clarke
BOSTON
Wed Jan 20, 2010 11:46am EST

Thu, Dec 3 2009BOSTON (Reuters) - "Extraordinary Measures", starring Harrison Ford and Brendan Fraser, opens on Friday and 101 employees from Genzyme Corp will gather in a Boston movie theater to see themselves portrayed in what some fear may be an unflattering light.

www.reuters.com/article/idUSTRE60J4Z9...
[verwijderd]
0
"Zakcentje schreef:

6EUR? ik kan me niet herinneren die koers gezien te hebben... 5EUR wel..."

Dat is nog van vóór de tijd dat je zakgeld kreeg.In juni 1999 beursintroductie in Amsterdam tegen een koers van rond € 8. Niet lang daarna zelfs (even) boven de € 30 genoteerd.
Nu meldt CEO trots dat hij een prachtig financieringsinstrument heeft geregeld, waarbij hij nog ruim € 23mln op kan halen door aandelen tegen € 0,50 per stuk op de markt te plempen. Oude, trouwe aandeelhouders kunnen hun geluk niet op.
[verwijderd]
0
zoals ik zeg... die 6EUR komt mij niet bekend voor... zal wel komen omdat ik toen nog met guldens betaalde ;-)) en er van EURO nog geen sprake was en ECU zelfs nog ''de munt'' zou worden.
[verwijderd]
0
Ze zijn wakker bij EMEA. De eerste nieuwsberichten zijn op de site geplaatst. Maar nog geen Pharming nieuws. Zie link (kopie uit weekdraad Zakcentje)

www.ema.europa.eu/whatsnewp.htm

[verwijderd]
0
"Zakcentje schreef:

zoals ik zeg... die 6EUR komt mij niet bekend voor... zal wel komen omdat ik toen nog met guldens betaalde ;-)) en er van EURO nog geen sprake was en ECU zelfs nog ''de munt'' zou worden."

Ín de beurs: euro m.i.v. 2002
Óp de beurs: euro m.i.v. 1999
[verwijderd]
0
Pharming Gives Update On Rhucin EU Marketing Authorization Application
CHMP raises no �major concerns’ on D120 List of Questions

Leiden, The Netherlands, January 22, 2010. Biotech company Pharming Group NV (“Pharming” or “the Company”) (NYSE Euronext: PHARM) today provided an update on the regulatory review by the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) of its Marketing Authorization Application (MAA) for Rhucin for the treatment of acute attacks of Hereditary Angioedema (HAE). The Company reports that it has received the Day 120 List of Questions (LoQ) from the CHMP. At this stage of the procedure, no �major concerns’ have been raised by the CHMP on the application. Pharming is confident on a positive outcome of the European MAA filing.

Pharming submitted the MAA for Rhucin to the European Medicines Agency in September 2009 and th e CHMP has issued the Day 120 List of Questions on 21 January 2010. The LoQ did not contain any �major concerns’. The CHMP review of the MAA will continue as soon as the clock starts after the response to the CHMP’s questions is submitted (Day 121). Pharming plans to submit its response within the regular three month clock stop period. Another one month clock stop may occur at Day 180 of the procedure to permit Pharming to respond to further questions from the CHMP and, in line with the regulatory timetable, the CHMP will reach its final opinion no later than Day 210. More information on this procedure can be found on www.ema.europa.eu.

Dr. Bruno Giannetti, Chief Operations Officer of Pharming, said: “We are very pleased with the EMA feed back on our dossier and therefore we continue to remain confident that our new MAA dossier has addressed all issues from the previous CHMP opinion in 2008. We believe that our current clinical database strongly supports the efficacy and safety of Rhucin for single and repeated use in the treatment of all types of acute angioedema attacks. We are confident that we will be able to satisfactorily address all outstanding CHMP questions in the coming months.”

Efficacy of Rhucin has been demonstrated in two randomized controlled studies and is supported by four open label studies, including the successful treatment of potentially life-threatening laryngeal attacks. In the RCT studies patients received Rhucin (100 U/kg or 50 U/kg body weight) or saline (placebo) control treatment. Patients receiving Rhucin responded rapidly to treatment, with statistically significant and clinically relevant shorter time to onset of relief and time to minimal symptoms compared to placebo. Following treatment with Rhucin, no relapse of attacks was recorded. Superiority over placebo was also consistently supported by exploratory endpoints, sensitivity analyses and subgroup statistical anal yses.

The updated safety dataset, submitted to the European Medicines Agency in September, comprises a total of 405 administrations in 139 subjects. Fourteen patients received at least five repeat administrations of Rhucin and one patient received 20 administrations. Rhucin was well tolerated with the adverse event profile observed in the controlled studies was similar to that of placebo. There were no significant infusion site reactions such as pain. Immunogenicity testing revealed a reassuring immuno-safety profile, without evidence for induction of neutralizing antibodies against Rhucin or for the induction of allergic responses.
[verwijderd]
0
Waarschijnlijk wacht men op een mogelijke toelichting (de Analisten er zal druk info verkeer zijn) In principe is dit gewoon net zo goed als goedkeuring alleen de procedure moet worden gevolgd.
Pharming zal zich hoeden te snel en dus misschien ondoordacht te antwoorden.
Alles zal uiters secuur wordn bekeken.

Maar de conclusie is we gaan de goede kant op.
Nu de koers nog.

Ruud.. Ik ga succes verder vandaag !!!
[verwijderd]
0
www.masshightech.com/stories/2010/01/...

Genzyme Corp. has announced that the U.S. Food and Drug Administration will issue a new decision on its drug for Pompe disease in June
[verwijderd]
0
Hey Grijpstuiver!
Gaat wat worden die week draad komende week iedereen wil Pharming aanbevelen.
Oei zie al die hot rapports al komen.

Thx voor een mooie weekdraad en Sorry voor de eigelijk onnodige dag openingen maar soms he !!!

Ruud..
jip banaan!
0
quote:

Declan. schreef:

Hey Grijpstuiver!
Gaat wat worden die week draad komende week iedereen wil Pharming aanbevelen.
Oei zie al die hot rapports al komen.

Thx voor een mooie weekdraad en Sorry voor de eigelijk onnodige dag openingen maar soms he !!!

Ruud..
Nounou... Declo, onnodige dag openingen??? Niet zo bescheiden hé!!!

groetjip
76 Posts, Pagina: « 1 2 3 4 | Laatste
Aantal posts per pagina:  20 50 100 | Omhoog ↑

Meedoen aan de discussie?

Word nu gratis lid of log in met uw e-mailadres en wachtwoord.

Direct naar Forum

Detail

Vertraagd 25 apr 2024 17:35
Koers 0,881
Verschil -0,024 (-2,60%)
Hoog 0,910
Laag 0,875
Volume 4.203.859
Volume gemiddeld 6.869.450
Volume gisteren 6.519.524

EU stocks, real time, by Cboe Europe Ltd.; Other, Euronext & US stocks by NYSE & Cboe BZX Exchange, 15 min. delayed
#/^ Index indications calculated real time, zie disclaimer, streaming powered by: Infront