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GLPG0634 (Filgotinib)

894 Posts, Pagina: « 1 2 3 4 5 6 ... 35 36 37 38 39 40 41 42 43 44 45 » | Laatste
MtBaker
0
quote:

C200 schreef op 14 januari 2021 09:34:

Waarom staat er eigenlijk nog Gilead op die potjes?
Die hebben toch niets te maken met de Europese markt?
koop een bril of kijk 2 tot 4 posts terug. juridisch dus.
harvester
3
quote:

de tuinman schreef op 28 december 2020 22:38:

[...]

Bedankt voor je antwoord.
Lokale vertegenwoordiger...... klinkt bijna als beledigend gezien het feit dat Galapagos Filgotinib volledig ontwikkeld heeft.
ach het is gewoon het gevolg van de oude deal.
Galapagos verkocht de wereldwijderechten voor een royalty.en mag vervolgens helpen bij de verkoop en is in enkele landen de locale alleenvertegenwoordiger.

Just part of the first great deal met Gilead, waar de 2e deal op volgde.
Persoonlijk denk ik dat Galapagos (door Michele Manto en meer flexibiliteit in sales bonussen direct gelinkt aan EU markt) succesvoller was met de opbouw van het verkoop team in Europa dan Gillend en dat daarom Gilead wel oren had naar heet benoemen van Galapagos als Europese distributeur.

Die verkopers van Galapagos steken het heus niet onder stoelen of banken dat het een In EU en door het Europees bedrijf Galapagos ontwikkeld product is.
winx09
3
quote:

winx09 schreef op 28 november 2020 12:32:

[...]

btw, iemand een idee waar Divergence1 (NCT03046056) blijft ?

Bijzonder. Gister verscheen 1 secondary endpoint op de sheet. We missen de primary endpoint, resultaten voor de 100mg en 32 patiënten.

Er zullen dus wel geen pb´s met resultaten van Divergence 1 &2 komen.

Wat is de boodschap van de disclaimer onder aan de sheet (10) ?
Wall Street Trader
1
quote:

winx09 schreef op 15 januari 2021 09:23:

[...]

Bijzonder. Gister verscheen 1 secondary endpoint op de sheet. We missen de primary endpoint, resultaten voor de 100mg en 32 patiënten.

Er zullen dus wel geen pb´s met resultaten van Divergence 1 &2 komen.

Wat is de boodschap van de disclaimer onder aan de sheet (10) ?
Lama Daila asked the same question to Bertrand Delsuc.

At the bottom of the slide “DIVERGENCE1 was stopped early”. I don’t remember if this was communicated yet. I see at the start of the study 100 patients anticipated and now 78 actual.

Bertrand Delsuc replied

It was, on clinicaltrials.gov. When COVID started, they closed the enrollment early in February and never re-opened it, not a big deal.
A lot of companies have been doing this for their early stages studies in the past months.
Bijlage:
winx09
1
@WST
Timeline does not fit with Covid.
Divergence 1 nummer of participants was altered 24 february 2020. Covid was just appearing on the radar of most. imho Covid could not have been the reason.
Divergence 2 number of participants was altered 26-august 2020 (could be covid related)

btw indeed it was already noticed on the board in February. point is, why put this extra comment on the sheet. What is the intention to communicate ?
Wall Street Trader
1
Lama Daila
0
quote:

Lama Daila schreef op 4 november 2020 07:34:

In Spanje al goedkeuring sinds 9 oktober, maar nog geen vermarkting momenteel:
cima.aemps.es/cima/publico/detalle.ht...

Marktgoedkeuring in Spanje ook nog bezig:
AUTHORISED( 09/10/2020 ) NOT MARKETED
de tuinman
0
quote:

Lama Daila schreef op 20 januari 2021 09:12:

[...]
Marktgoedkeuring in Spanje ook nog bezig:
AUTHORISED( 09/10/2020 ) NOT MARKETED

Ook nog bezig?? Ze hebben toch goedkeuring?
Lama Daila
1
quote:

de tuinman schreef op 20 januari 2021 09:17:

[...]

Ook nog bezig?? Ze hebben toch goedkeuring?
Ik bedoel “onderhandelingen terugbetaling”. Zolang die niet rond zijn zal Jyseleca niet op de markt komen in Spanje.
de tuinman
0
quote:

Lama Daila schreef op 20 januari 2021 09:20:

[...]
Ik bedoel “onderhandelingen terugbetaling”. Zolang die niet rond zijn zal Jyseleca niet op de markt komen in Spanje.
Ok, tx.
Lama Daila
2
quote:

Lama Daila schreef op 27 november 2020 07:48:

[...]
Het is niet zeker dat deze studie er gekomen is op vraag van de FDA en mocht dat toch zo zijn, dan zie ik niet de link met het al dan niet gegeven van feedback van de type A meeting.
Deze studie zou er ook kunnen gekomen zijn op vraag van de EMA:
www.ema.europa.eu/en/documents/produc...

Lipids
Treatment with filgotinib was associated with dose-dependent increases in lipid parameters, including total cholesterol, and high-density lipoprotein (HDL) levels, while low-density lipoprotein (LDL) levels were slightly increased (see section 4.8). LDL cholesterol returned to pre-treatment levels in the majority of patients who started statin therapy while taking filgotinib. The effect of these lipid parameter elevations on cardiovascular morbidity and mortality has not been determined (see section 4.2 for monitoring guidance).

No clinical studies have been performed to investigate interactions with OATP1B1 and OATP1B3 substrates. Therefore, it cannot be excluded that co-administration of filgotinib with OATP1B1 or OATP1B3 substrates may increase their exposure and the risk of adverse events. Co-administration with sensitive OATP1B1 or OATP1B3 substrates (e.g., valsartan, statins) is therefore not recommended.

Other medicines and Jyseleca
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, especially if you use medicines that affect your immune system (such as azathioprine, ciclosporin and tacrolimus).
It is also very important to talk to your doctor of pharmacist if you are taking any of the following:
• medicines to treat heart failure, coronary disease or high blood pressure (such as digoxin, diltiazem, carvedilol or valsartan)
• medicines to treat high cholesterol (such as fenofibrate or statins including atorvastatin, pravastatin or simvastatin)

Ondertussen is deze studie “Completed”:

clinicaltrials.gov/ct2/history/NCT046...

Study to Evaluate Organic Anion Transporting Polypeptide (OATP) Transporter-Mediated Drug-Drug Interactions Between Filgotinib and Statins as Probe Drugs in Healthy Participants

Lama Daila
0
quote:

Lama Daila schreef op 5 december 2020 10:55:

[...]

Binnenkort vermoedelijk het verslag van deze NICE-meeting.
ml-eu.globenewswire.com/Resource/Down...

www.nice.org.uk/guidance/indevelopmen...

Provisional Schedule

Final appraisal document 21 January 2021 - 04 February 2021
Expected publication 24 February 2021
Lama Daila
0
Geen vermelding van de dosis die NICE aanbeveelt. Ik vermoed beide dosissen? Of hoeft NICE daar geen uitspraak over te doen en ligt dit eerder bij NHS ?
Sir Piet
0
quote:

Lama Daila schreef op 21 januari 2021 09:09:

Geen vermelding van de dosis die NICE aanbeveelt. Ik vermoed beide dosissen? Of hoeft NICE daar geen uitspraak over te doen en ligt dit eerder bij NHS ?

Lijkt mij beide doseringen .
harvester
0
quote:

Sir Piet schreef op 21 januari 2021 10:12:

[...]

Lijkt mij beide doseringen .
Lijkt mij ook, want in lijn met CHMP aanbeveling. Daar zaten volgens mij ook destijds de UK experts mede achter.
Wall Street Trader
2
NATIONAL INSTITUTE FOR HEALTH AND CARE EXCELLENCE

Why the committee made these recommendations

Expected publication date: 24 February 2021

People with severe rheumatoid arthritis have a number of advanced treatment
options (biological and targeted synthetic DMARDs) available to them if their disease
has not responded well enough to 2 or more conventional DMARDs. These
advanced treatment options are currently not available for people with moderate
rheumatoid arthritis.

Clinical trials show that filgotinib with methotrexate or other conventional DMARDs is
more effective than adalimumab with methotrexate or methotrexate alone for treating
moderate to severe rheumatoid arthritis that has not responded well enough to 2 or
more conventional DMARDs. It is also more effective than conventional DMARDs
alone for treating moderate to severe active rheumatoid arthritis that has not
responded well enough to 1 or more biological DMARDs.

There are no trials comparing filgotinib with the full range of biological and targeted
synthetic DMARDs in severe disease. However, an indirect comparison shows that
filgotinib with conventional DMARDs (including methotrexate) works as well as the
biological and targeted synthetic DMARDs recommended by NICE.

The most likely cost-effectiveness estimates show that filgotinib with methotrexate is
an acceptable use of NHS resources for some people with moderate and severe
rheumatoid arthritis (see sections 1.1 to 1.3).

The cost effectiveness of filgotinib monotherapy is more uncertain but is still likely to
be within what NICE considers an acceptable use of NHS resources, therefore it is
recommended.

www.nice.org.uk/guidance/gid-ta10541/...
Lama Daila
0
www.nice.org.uk/Media/Default/About/w...

In appendix B een mooi stappenplan van de “ STA process timelines”.
Week 21:
Appraisal Committee meeting to develop appraisal consultation document (ACD) or final appraisal determination (FAD). Note: CHMP positive opinion required by this point for single technology appraisal to proceed

Wall Street Trader
0
quote:

Lama Daila schreef op 21 januari 2021 09:09:

Geen vermelding van de dosis die NICE aanbeveelt. Ik vermoed beide dosissen? Of hoeft NICE daar geen uitspraak over te doen en ligt dit eerder bij NHS ?

Healthcare professionals should choose the most appropriate treatment
after discussing the options with the person having treatment


3.26 The committee recalled that having a range of treatment options was
important in rheumatoid arthritis (see section 3.1). It also recalled that a
range of biological and targeted synthetic DMARDs are already available
for severe rheumatoid arthritis (see section 3.2). It noted that a number of
NICE technology appraisals are currently ongoing for moderate
rheumatoid arthritis (GID-TA10759 and GID-TA10586). The committee
concluded that healthcare professionals should choose the most
appropriate treatment after discussing the advantages and disadvantages
of the treatments available with the person having treatment. If more than
1 treatment is suitable, they should start treatment with the least
expensive drug (taking into account administration costs, dose needed
and product price per dose). This may vary from person to person
because of differences in how the drugs are taken and treatment
schedules.


Choose the most appropriate treatment after discussing the advantages
and disadvantages of the treatments available with the person having
treatment. If more than 1 treatment is suitable, start treatment with the
least expensive drug (taking into account administration costs, dose
needed and product price per dose). This may vary from person to person
because of differences in how the drugs are taken and treatment
schedules.


www.nice.org.uk/guidance/gid-ta10541/...

Treatment pathway for moderate-severe RA and proposed position of filgotinib

www.nice.org.uk/guidance/gid-ta10541/...

Lama Daila
4
www.pharmastar.it/news//italia/27-nuo...

Jyseleca op de markt in Italië vanaf 01/02:

JYSELECA 30 cpr rev 100 mg filgotinib
GILEAD SCIENCES AIC: 049054012 1572,14 € Cnn / RNRL on the market since: 01/02/2021

JYSELECA 30 cpr rev 200 mg filgotinib
GILEAD SCIENCES AIC: 049054036 1572.14 € Cnn / RNRL on the market from: 01/02/2021

Cnn:
pharmaboardroom.com/legal-articles/re...
Class C(nn): separate class for centrally approved medicinal products which pricing and reimbursement decision in Italy has not yet been taken. These are not reimbursed by the SSN.

RNRL:
www.micromedexsolutions.com/micromede...
RNRL: Recipe Repeated Limited with Restrictions: drugs which require a receipt done by a medical specialist or authorised medical unit. The receipt can be used just once.

galaking
1
Zojuist de publicatie van de agenda van CHMP van deze week
www.ema.europa.eu/en/documents/agenda...

Onder 5.1.6 Jyseleca - filgotinib - EMEA/H/C/005113/II/0001 staat action: for adoption
Betekent dit dat Jyseleca op de agenda staat voor positief advies van de CHMP voor UC?
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