Galapagos « Terug naar discussie overzicht

Galapagos 2015: de inhoudelijke discussie

3.351 Posts, Pagina: « 1 2 3 4 5 6 ... 56 57 58 59 60 61 62 63 64 65 66 ... 164 165 166 167 168 » | Laatste
[verwijderd]
0
quote:

NielsjeB schreef op 16 oktober 2015 12:22:

De eerste biosimilar voor Humira staat al te popelen:

A RANDOMIZED, SINGLE-BLIND, SINGLE-DOSE, THREE-ARM, PARALLEL GROUP STUDY IN HEALTHY SUBJECTS DEMONSTRATING PHARMACOKINETIC EQUIVALENCE OF PROPOSED BIOSIMILAR ABP 501 WITH ADALIMUMAB

uegw.congress-online.com/guest/Abstra...
Viel me gister ook op dat naast Amgen (met ABP 501/710 biosimilairs) ook Pfizer werkt aan biosimilairs voor Humira (AbbVie) en Remicade (J&J).
zie pagina 11 van product pipeline van Pfizer.

Deze verkeren ook in Fase 3.

www.pfizer.com/sites/default/files/pr...

Amgen/Pfizer verkeren wel in positie dat patent van hun Anti-TNF middel Enbrel loopt t/m 2028! Dat hebben AbbVie en J&J duidelijk niet meer dat voordeel.
Patenten verlopen van hen tussen 2016-2018.

Daarom denk ik ook dat Amgen minder interessant is, omdat hun patent blijft staan. Al zullen zij ook wellicht mee moeten met lagere prijsvorming voor Anti-TNF middelen.

Kan niet inschatten wat bijwerkingsverschillen zijn tussen Humira, Remicade en Enbrel.

Interessant dat Amgen niets in de pipeline heeft aangaande specifiiek RA (Fase1-3). Wel nodige moleculen inzake Crohn en UC.

J&J heeft Sirumkab als IL-6 (Fase 3: spuitmiddel) en Stelara voor Crohn en UC.
[verwijderd]
2
Vertex Turns Up the Heat on Cystic Fibrosis Challengers

With two new correctors entering clinical development, Vertex is about to leave Galapagos and Concert in the dust.

Cory Renauer (crenauer) Oct 19, 2015 at 11:47AM
Kalydeco Packaging

SOURCE: VERTEX PHARMACEUTICALS.

Back in 2012, Vertex Pharmaceuticals (NASDAQ:VRTX) changed thousands of lives when it won approval to market Kalydeco to treat cystic fibrosis patients in the U.S. and EU. Cystic fibrosis, or CF, can be caused by one of many mutations along the CFTR gene. The trouble is, the therapy was initially approved for one specific mutation in the CFTR gene -- G551D -- leaving the vast majority of patients untreated.

Kalydeco's label now includes 10 specific mutations, but the big expansion came with the approval of combination therapy Orkambi. This combination of ivacaftor -- Kalydeco's active ingredient -- and lumacaftor is indicated for treatment of patients with two copies of the most common mutation, F508del, representing an estimated 8,500 of the 30,000 people in the U.S. living with the disease.

Orkambi is a huge improvement, but it still leaves the majority of CF patients untreated. The potential is not lost on two companies trying to unseat Vertex from its CF throne: Concert Pharmaceuticals (NASDAQ:CNCE) and Galapagos NV (NASDAQ:GLPG).

Deuterium, where's my hydrogen?
Concert is a clinical-stage pharmaceutical company founded on the premise that substituting a compound's hydrogen atoms for deuterium can improve safety and efficacy.

Deuterium
SOURCE: WIKIMEDIA COMMONS.

While deuterating existing compounds sounds like another flashy gimmick, the data so far is compelling. Earlier this month, Concert presented results from a 10-patient trial with CTP-656, a deuterated analog of Kalydeco. Patients receiving just 75mg of CTP-656 had higher plasma concentrations after 12 and 24 hours than patients receiving a 150mg dose of Kalydeco.

If these results can be repeated in larger trials, and the company doesn't get bogged down with a flurry of lawsuits, this improved profile could eventually pressure Kalydeco sales. Before you get too excited, it's important to remember that Kalydeco alone treats just a small subset of the overall CF population. Also, those results are from healthy volunteers, so we know nothing of CTP-656's efficacy in CF patients.

An improved pharmacokinetic profile should also improve the drug's efficacy, but we won't know for quite some time. Concert is going forward with another phase 1 trial in healthy volunteers, and we can expect those results in the first half of next year.

Class 3 contender
While Concert advances heavy hydrogen, Belgium's Galapagos also has a CF candidate in development. Analysts might be focused on the company's ill-fated rheumatoid arthritis partnership with AbbVie, but Vertex investors will want to keep an eye on its CF program.

Galapagos is developing GLPG1837 for treatment of patients with class 3 mutations -- a subset representing between 2% and 3% of the CF population. The company recently posted top-line results from a phase 1 trial that suggest the drug is safe and well-tolerated even at high doses. Like Concert's candidate, GLPG1837 was tested on healthy volunteers. Unlike Concert, however, Galapagos intends to begin a phase 2 study with actual CF patients before the end of the year.

Double entry
Both Concert and Galapagos are well behind Vertex, and it looks like the Cambridge company is about to widen the gap even further. Vertex just moved two next-generation correctors into clinical development that could more than double its CF franchise.

At a recent conference, Vertex announced it would advance VX-152 and VX-440 into clinical development. While Kalydeco is a potentiator that improves the ability of CFTR to function at the cell surface, it isn't much help if the protein never makes it there. This is where the new correctors come into play. Like lumacaftor -- the other active ingredient in Orkambi -- these two are designed to get CFTR to the cell surface where it can do its job.

What makes these compounds exciting is that they could speed Vertex toward its goal of treating the vast majority of CF patients. When applied to cell cultures in triple combinations -- VX-152/VX-661/Kalydeco and VX-440/VX-661/Kalydeco -- they have been shown to improve CFTR function in human cells with just one copy of the F508del mutation. Since an estimated 90% of CF patients have at least one copy of of the F508del mutation, eventual approval of just one of these combinations would create an enormous opportunity.

It's important to point out that Vertex's new correctors haven't been tested in CF patients yet. But with Galapagos and Concert at roughly the same stage with their first CF candidates, I'd say Vertex is in little danger of losing its market position soon.

In the first half of this year, Kalydeco brought in $285 million. When the company reports third-quarter earnings on Oct. 28, it will be able to include nearly two months of U.S. Orkambi sales as well. As exciting as those figures are, they would look weak in comparison to a combination therapy indicated for 90% of CF patients. Just one of the two triple therapies needs to win approval to make this happen. This is why I'll be watching their development very closely.

Cory Renauer has no position in any stocks mentioned. The Motley Fool recommends Vertex Pharmaceuticals. Try any of our Foolish newsletter services free for 30 days. We Fools may not all hold the same opinions, but we all believe that considering a diverse range of insights makes us better investors. The Motley Fool has a disclosure policy.

AUTHOR

Cory Renauer

Fool Contributor

Cory is a long-term minded analyst mainly focused on the biotechnology and pharmaceuticals. He genuinely enjoys cutting through the industry's complexities to help everyday investors make better decisions. You can contact Cory on Twitter @coryrenauer

ARTICLE INFO

Oct 19, 2015 at 11:47AM
Health Care

STOCKS

Vertex Pharmaceuticals
NASDAQ:VRTX
$116.94 $2.62 (2.29%)

Concert Pharmaceuticals
NASDAQ:CNCE
$23.72 $0.58 (2.51%)

GALAPAGOS NV SPON ADR REPR 1 ORD SHS
NASDAQ:GLPG
$51.30 $2.70 (5.56%)

www.fool.com/investing/general/2015/1...
Maycon
0
quote:

asti schreef op 19 oktober 2015 18:04:

Vertex Turns Up the Heat on Cystic Fibrosis Challengers

With two new correctors entering clinical development, Vertex is about to leave Galapagos and Concert in the dust.

Cory Renauer (crenauer) Oct 19, 2015 at 11:47AM
Kalydeco Packaging

SOURCE: VERTEX PHARMACEUTICALS.

Back in 2012, Vertex Pharmaceuticals (NASDAQ:VRTX) changed thousands of lives when it won approval to market Kalydeco to treat cystic fibrosis patients in the U.S. and EU. Cystic fibrosis, or CF, can be caused by one of many mutations along the CFTR gene. The trouble is, the therapy was initially approved for one specific mutation in the CFTR gene -- G551D -- leaving the vast majority of patients untreated.

Kalydeco's label now includes 10 specific mutations, but the big expansion came with the approval of combination therapy Orkambi. This combination of ivacaftor -- Kalydeco's active ingredient -- and lumacaftor is indicated for treatment of patients with two copies of the most common mutation, F508del, representing an estimated 8,500 of the 30,000 people in the U.S. living with the disease.

Orkambi is a huge improvement, but it still leaves the majority of CF patients untreated. The potential is not lost on two companies trying to unseat Vertex from its CF throne: Concert Pharmaceuticals (NASDAQ:CNCE) and Galapagos NV (NASDAQ:GLPG).

Deuterium, where's my hydrogen?
Concert is a clinical-stage pharmaceutical company founded on the premise that substituting a compound's hydrogen atoms for deuterium can improve safety and efficacy.

Deuterium
SOURCE: WIKIMEDIA COMMONS.

While deuterating existing compounds sounds like another flashy gimmick, the data so far is compelling. Earlier this month, Concert presented results from a 10-patient trial with CTP-656, a deuterated analog of Kalydeco. Patients receiving just 75mg of CTP-656 had higher plasma concentrations after 12 and 24 hours than patients receiving a 150mg dose of Kalydeco.

If these results can be repeated in larger trials, and the company doesn't get bogged down with a flurry of lawsuits, this improved profile could eventually pressure Kalydeco sales. Before you get too excited, it's important to remember that Kalydeco alone treats just a small subset of the overall CF population. Also, those results are from healthy volunteers, so we know nothing of CTP-656's efficacy in CF patients.

An improved pharmacokinetic profile should also improve the drug's efficacy, but we won't know for quite some time. Concert is going forward with another phase 1 trial in healthy volunteers, and we can expect those results in the first half of next year.

Class 3 contender
While Concert advances heavy hydrogen, Belgium's Galapagos also has a CF candidate in development. Analysts might be focused on the company's ill-fated rheumatoid arthritis partnership with AbbVie, but Vertex investors will want to keep an eye on its CF program.

Galapagos is developing GLPG1837 for treatment of patients with class 3 mutations -- a subset representing between 2% and 3% of the CF population. The company recently posted top-line results from a phase 1 trial that suggest the drug is safe and well-tolerated even at high doses. Like Concert's candidate, GLPG1837 was tested on healthy volunteers. Unlike Concert, however, Galapagos intends to begin a phase 2 study with actual CF patients before the end of the year.

Double entry
Both Concert and Galapagos are well behind Vertex, and it looks like the Cambridge company is about to widen the gap even further. Vertex just moved two next-generation correctors into clinical development that could more than double its CF franchise.

At a recent conference, Vertex announced it would advance VX-152 and VX-440 into clinical development. While Kalydeco is a potentiator that improves the ability of CFTR to function at the cell surface, it isn't much help if the protein never makes it there. This is where the new correctors come into play. Like lumacaftor -- the other active ingredient in Orkambi -- these two are designed to get CFTR to the cell surface where it can do its job.

What makes these compounds exciting is that they could speed Vertex toward its goal of treating the vast majority of CF patients. When applied to cell cultures in triple combinations -- VX-152/VX-661/Kalydeco and VX-440/VX-661/Kalydeco -- they have been shown to improve CFTR function in human cells with just one copy of the F508del mutation. Since an estimated 90% of CF patients have at least one copy of of the F508del mutation, eventual approval of just one of these combinations would create an enormous opportunity.

It's important to point out that Vertex's new correctors haven't been tested in CF patients yet. But with Galapagos and Concert at roughly the same stage with their first CF candidates, I'd say Vertex is in little danger of losing its market position soon.

In the first half of this year, Kalydeco brought in $285 million. When the company reports third-quarter earnings on Oct. 28, it will be able to include nearly two months of U.S. Orkambi sales as well. As exciting as those figures are, they would look weak in comparison to a combination therapy indicated for 90% of CF patients. Just one of the two triple therapies needs to win approval to make this happen. This is why I'll be watching their development very closely.

Cory Renauer has no position in any stocks mentioned. The Motley Fool recommends Vertex Pharmaceuticals. Try any of our Foolish newsletter services free for 30 days. We Fools may not all hold the same opinions, but we all believe that considering a diverse range of insights makes us better investors. The Motley Fool has a disclosure policy.

AUTHOR

Cory Renauer

Fool Contributor

Cory is a long-term minded analyst mainly focused on the biotechnology and pharmaceuticals. He genuinely enjoys cutting through the industry's complexities to help everyday investors make better decisions. You can contact Cory on Twitter @coryrenauer

ARTICLE INFO

Oct 19, 2015 at 11:47AM
Health Care

STOCKS

Vertex Pharmaceuticals
NASDAQ:VRTX
$116.94 $2.62 (2.29%)

Concert Pharmaceuticals
NASDAQ:CNCE
$23.72 $0.58 (2.51%)

GALAPAGOS NV SPON ADR REPR 1 ORD SHS
NASDAQ:GLPG
$51.30 $2.70 (5.56%)

www.fool.com/investing/general/2015/1...
Prima post Asti !!
NielsjeB
0
Mooi artikel Asti, AB. Zoals de auteur zelf al aangeeft wordt het leeuwendeel van de CF-patiënten op dit moment niet bediend. Voor zover ik weet heeft Vertex geen voorsprong op dat gebied. Natuurlijk heeft Vertex wel een bestaande positie op de CF-markt, dus de verkoopkanalen etc. zijn op orde. Het wordt spannend. Ik denk dat AbbVie zich nu wel 100% inzet om de CF-markt te betreden, of er moet nog een ABT-tje uit de hoge hoed komen ;)
aston.martin
0
quote:

asti schreef op 19 oktober 2015 18:04:

Vertex Turns Up the Heat on Cystic Fibrosis Challengers

With two new correctors entering clinical development, Vertex is about to leave Galapagos and Concert in the dust.

Cory Renauer (crenauer) Oct 19, 2015 at 11:47AM
Kalydeco Packaging

...

STOCKS

Vertex Pharmaceuticals
NASDAQ:VRTX
$116.94 $2.62 (2.29%)

Concert Pharmaceuticals
NASDAQ:CNCE
$23.72 $0.58 (2.51%)

GALAPAGOS NV SPON ADR REPR 1 ORD SHS
NASDAQ:GLPG
$51.30 $2.70 (5.56%)

www.fool.com/investing/general/2015/1...
Van een rose bril gesproken!!!

Ik zou het vel van de beer maar niet verkopen voor hij geschoten is.

NielsjeB
0
quote:

NielsjeB schreef op 19 oktober 2015 18:42:

Mooi artikel Asti, AB. Zoals de auteur zelf al aangeeft wordt het leeuwendeel van de CF-patiënten op dit moment niet bediend. Voor zover ik weet heeft Vertex geen voorsprong op dat gebied. Natuurlijk heeft Vertex wel een bestaande positie op de CF-markt, dus de verkoopkanalen etc. zijn op orde. Het wordt spannend. Ik denk dat AbbVie zich nu wel 100% inzet om de CF-markt te betreden, of er moet nog een ABT-tje uit de hoge hoed komen ;)
Ter aanvulling: het artikel rept alleen over GLPG1837, dus als contender in class III t.o.v. het bestaande medicijn van Vertex. Wat de Galapagos CF-pipeline nu zo aantrekkelijk maakt is de triple combo, waarmee bijna alle CF-patients behandeld kunnen worden, mits succesvol ontwikkeld uiteraard. Het is nu juist die combo waarmee Vertex wellicht ingehaald kan worden. Maar dat is natuurlijk ook het betere rozebrillen-werk. We gaan het zien.
[verwijderd]
0

''Cory Renauer has no position in any stocks mentioned. The Motley Fool recommends Vertex Pharmaceuticals. ''

Wiens brood men eet diens woord men spreekt...
[verwijderd]
0
Goed geplaatst asti. 'The new generation CF correctors haven't been tested on patients yet' (Vertex) en vervolgens zegt hij dat Galapagos en Concert ongeveer even ver zijn in hun stadium met die CF-correctoren maardat dit positie Vertex niet aantast.

Wat een auteur. Zeker persbericht van Galapagos onlangs gemist.

Dacht eerder gelezen te hebben dat Vertex in H2 2016 wil starten met triple combi therapie.
Galapagos/AbbVie start met toedienen triple combi in H1 2017.

Dat zit dicht bij elkaar en dan is vraag wie scoort beste en wie loopt nog vertraging op.
AbbVie heeft hier hoop bij te winnen, evenals Galapagos.
[verwijderd]
0
files.shareholder.com/downloads/JNJ/8...

Nieuws J&J omtrent hun Crohn onderzoek = human interleukin (IL)-12 and IL-23 antagonist

October 19, 2015

Phase 3 Data Show STELARA® Induced Clinical Response And Remission In The Treatment Of Patients With Moderate To Severe Crohn's Disease

Efficacy and Safety Results from First STELARA® Phase 3 Induction Study (UNITI-2) Presented at the American College of Gastroenterology Annual Meeting

Honolulu, HI, October 19, 2015 - Phase 3 data presented for the first time showed treatment with STELARA® (ustekinumab) induced clinical response and clinical remission in patients with moderate to severe Crohn's disease who had previously failed conventional therapy, the majority of whom were naïve to treatment with anti-tumor necrosis factor (TNF)-alpha therapy. The
Phase 3 Janssen Research & Development, LLC-sponsored UNITI-2 study achieved its primary endpoint with STELARA® treatment groups demonstrating significantly higher rates of clinical response at week 6 when compared with the placebo
group. Major secondary endpoints of clinical response and clinical remission at week 8 were also significantly higher among patients receiving STELARA® compared with patients receiving placebo. STELARA®, approved for the treatment of moderate to severe plaque psoriasis and active psoriatic arthritis in many countries, is a monoclonal antibody that targets interleukin (IL)-
12 and IL-23 cytokines believed to play a role in immune-mediated diseases, including Crohn's disease.

"The UNITI-2 study results show STELARA® induced clinical response and remission in patients with moderate to severe Crohn's disease who had failed steroids and/or immunosuppressive therapy, but had not failed TNF inhibitors," said Brian
Feagan, M.D., Professor of Medicine, Chief Executive Officer and Senior Medical Director, Robarts Research Institute, University of Western Ontario, and study investigator. "Findings from this Phase 3 program provide an important first look into the efficacy and safety of STELARA® induction therapy in the treatment of inflammatory bowel disease-a disease where new therapeutic options are needed as the incidence continues to rise globally."

Patients participating in the Phase 3 UNITI-2 study received a single intravenous (I.V.) infusion of placebo, STELARA® 130 mg or STELARA® ~6 mg/kg (weight-tiered dosing: patients weighing less than or equal to 55 kg received 260 mg; patients weighing more than 55 kg and less than or equal to 85 kg received 390 mg; and patients weighing more than 85 kg received 520 mg) at week 0. Enrolled patients had previously failed steroids and/or immunomodulators and were either naïve to or had been exposed to anti-TNF-alpha therapy, but had not failed such biologic therapy.

At week 6, 52 percent of patients receiving STELARA® 130 mg and 56 percent of patients receiving STELARA® ~6 mg/kg achieved clinical response, as defined by a reduction from baseline in the Crohn's Disease Activity Index (CDAI) score of at
least 100 points, compared with 29 percent of patients receiving placebo (P < 0.001). CDAI is a symptom-based disease
assessment tool commonly used in clinical trials to quantify Crohn's disease activity.

At week 8, 47 percent and 58 percent of patients receiving STELARA® 130 mg and STELARA® ~6 mg/kg, respectively, achieved clinical response, compared with 32 percent of patients receiving placebo (P < 0.001). In addition, 31 percent of
patients receiving STELARA® 130 mg and 40 percent of patients receiving STELARA® ~6 mg/kg achieved clinical remission at week 8, as defined by a CDAI score of less than 150 points, compared with 20 percent of patients receiving placebo (P = 0.009 for STELARA® 130 mg; P < 0.001 for STELARA® ~6 mg/kg).


In addition to significant improvements in signs and symptoms as measured by CDAI, both doses of STELARA® resulted in statistically significant improvements in the Inflammatory Bowel Disease Questionnaire (IBDQ), a health-related quality of life measure for patients with IBD, as well as markers of inflammation, including C-reactive protein (CRP), fecal lactoferrin and calprotectin.

Through week 8, adverse events (AEs), serious AEs and infections (including serious infections) were reported in similar proportions across STELARA® and placebo treatment groups. No malignancies, deaths, opportunistic infections, cases of tuberculosis or major adverse cardiovascular events (MACE) were observed in patients treated with STELARA®.
[verwijderd]
0

"The STELARA® Phase 3 UNITI-2 induction results are important findings, as induction of clinical response and clinical remission are important goals in the management of Crohn's disease," said Newman Yeilding, M.D., Head of Immunology
Development, Janssen Research & Development, LLC. "We look forward to filing applications this year seeking approval of STELARA® for the treatment of moderate to severe Crohn's disease and remain committed to the continued development of this innovative medicine for the treatment of immune-mediated diseases."

About the UNITI-2 Trial
UNITI-2, a Phase 3, multicenter, randomized, double-blind, placebo-controlled, parallel group study, evaluated the efficacy and safety of STELARA® induction therapy in patients with moderate to severe Crohn's disease. Patients (n=628) were randomized equally to receive a single I.V. infusion of placebo, STELARA® 130 mg or STELARA® ~6 mg/kg (weight-tiered dosing: patients
weighing less than or equal to 55 kg received 260 mg; patients weighing more than 55 kg and less than or equal to 85 kg received 390 mg; and patients weighing more than 85 kg received 520 mg) at week 0. All participating patients had previously failed steroids and/or immunomodulators and were either naïve to or had been exposed to anti-TNF-alpha therapy, but had not failed such biologic therapy. The primary endpoint was clinical response at week 6, measured by the proportion of patients who achieved at least a 100-point reduction from baseline CDAI scores. Major secondary endpoints at week 8 included clinical
response and clinical remission (defined by CDAI scores less than 150 points). At week 8, patients either transitioned to the IMUNITI maintenance study or participated in safety follow-up through week 20.

UNITI-2 is part of a comprehensive Phase 3 clinical development program investigating STELARA® for the treatment of moderate to severe Crohn's disease. Data from the UNITI-1 induction study in anti-TNF-alpha refractory patients and the IMUNITI maintenance study will be presented at future medical congresses.

About Crohn's Disease
More than five million people worldwide are living with Crohn's disease and ulcerative colitis-collectively known as inflammatory
bowel disease (IBD).1
Crohn's disease is a chronic inflammatory condition of the gastrointestinal tract that affects approximately
700,000 Americans2 and nearly 250,000 Europeans.3
The cause of Crohn's disease is not known, but the disease is
associated with abnormalities of the immune system that could be triggered by a genetic predisposition or diet and other
environmental factors. Symptoms of Crohn's disease can vary but often include abdominal pain and tenderness, frequent
diarrhea, rectal bleeding, weight loss and fever. There is currently no cure for Crohn's disease.
de tuinman
0
Interessant. JJ heeft dus een Crohn onderzoek lopen.
Gala zal dus beter moeten presteren dan deze.

Bovendien is er een kans dat JJ geen behoefte heeft om Filgotinib door te ontwikkelen tegen Crohn.
[verwijderd]
0
Stelara is spuitmiddel.
Galapagos is tablet-vorm.
Dat is sowieso al een voordeel voor Galapagos.

Zal moeten blijken hoe goed de JAK1 van Galapagos binnen Crohn is.
Vooral remissie is enorm belangrijk.

40% remissie is goed maar kan niet inschatten hoe goed.

RA-middel (is ander ziektegbied) van Galapagos heeft
bijvoorbeeld ook remissie van 40% en nog eens 24% bijna geen last meer.
Zie onderstaande link.

www.gva.be/cnt/dmf20150731_01798723/m...

[verwijderd]
0
Wel goed dat we nu vergelijkingsmateriaal hebben.
Ook de studie van Fitzroy Fase2 is kort van aard.

Scores 10-weeks in november 2015
Scores 20 weeks in februari 2016
[verwijderd]
0
Commentaar erbij van derden m.b.t. Stelara van (J&J).

www.reuters.com/article/2015/10/19/us...

Johnson & Johnson's Stelara succeeds in Phase III Crohn's disease trial

Johnson & Johnson's Stelara was significantly better than placebo at inducing clinical response and remissions in patients with moderate to severe Crohn's disease, according to data from a late stage trial, providing ammunition for a potential expanded approval of the medicine.

Stelara, a biotech medicine that blocks inflammation, is approved to treat the skin condition scaly plaque psoriasis and a type of arthritis associated with psoriasis

J&J reported $613 million in third-quarter Stelara sales. The company said it was on track for global approval filings for Crohn's this year.

Subjects in the 628-patient trial presented on Monday received either a single infusion of 130 milligrams of Stelara, a Stelara infusion of 6 mg per kilogram of weight or a placebo.

After six weeks, 52 percent of those in the 130 mg group and 56 percent in the 6mg/kg group experienced a clinical response, defined as a reduction from baseline of at least 100 points in the Crohn's Disease Activity Index score. That compared with 29 percent in the placebo group.

In addition, 31 percent of the Stelara 130 mg group and 40 percent in the other dosing arm achieved clinical remission by week 8 of the study, versus 20 percent for placebo.

The results were deemed to be statistically significant.

"I think this is an approvable drug," said Dr. Brian Feagan, co-lead investigator of the study presented at the American College of Gastroenterology meeting in Honolulu.

"We need drugs that are alternatives to TNF blockers," he said of widely used biologic medicines such as AbbVie's Humira. "This drug can be a first-line biologic therapy."

Patients in the study had previously failed to be helped by steroids or immunomodulator drugs, such as methotrexate. Another study is testing Stelara in those who failed anti-TNF therapy.

Crohn's disease is a chronic inflammatory condition of the gastrointestinal tract that affects about 700,000 Americans and 250,000 Europeans. Symptoms can include frequent diarrhea, abdominal pain and rectal bleeding.

In addition to reductions in signs and symptoms of disease, Stelara patients reported significant improvements in the Inflammatory Bowel Disease Questionnaire, a health-related quality of life measure, researchers said.

The rate of serious side effects, including infections, was similar for Stelara and placebo.

"Serious infection is really the thing that clinicians worry about and there was not a signal here, which is surprisingly great news," Feagan said.
NielsjeB
0
_Giulietta_
0
Wat zou dit kunnen betekenen?

www.selleckchem.com/products/filgotin...

Op deze site staat ook nog de volgende opmerking: Selleck becomes a licensed supplier of Pfizer's bioactive compounds.
NielsjeB
0
quote:

_Giulietta_ schreef op 22 oktober 2015 13:14:

Wat zou dit kunnen betekenen?

www.selleckchem.com/products/filgotin...

Op deze site staat ook nog de volgende opmerking: Selleck becomes a licensed supplier of Pfizer's bioactive compounds.
Niets voor zover ik weet. Van de website:
Selleck Chemicals supplies over 3,000 inhibitors used in the study of cell signaling pathways. We actively tracks the latest science so our customers can rely on us to be the leading supplier of the newest inhibitors.
3.351 Posts, Pagina: « 1 2 3 4 5 6 ... 56 57 58 59 60 61 62 63 64 65 66 ... 164 165 166 167 168 » | 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 14 feb 2025 17:35
Koers 23,920
Verschil +0,140 (+0,59%)
Hoog 24,880
Laag 23,780
Volume 267.751
Volume gemiddeld 119.005
Volume gisteren 290.694

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