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Pharming November 2021

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0
quote:

Marijke schreef op 7 november 2021 20:07:

[...]

Ga jij nou maar pannekoeken eten, 't is zondag!! :-)))
Verzin eens wat nieuws.....

Dat over pannenkoeken is inmiddels al zo afgezaagd.
[verwijderd]
5
quote:

Eric de Rus schreef op 7 november 2021 21:01:

[...]

Verzin eens wat nieuws.....

Dat over pannenkoeken is inmiddels al zo afgezaagd.
Ik imiteer jou, jij komt zelden met iets nieuws. Nu stop ik met de ongein, veel te weinig Pharming gerelateerd.
Wilbar
0
quote:

B33rtj3 schreef op 7 november 2021 20:18:

[...]

Over Max gesproken wat een start! Hij laat weer even z'n skills zien.
Piece of cake :).

Gelukkig hebben Perez <> Hamilton het tot de laatste meters spannend gehuden.
St13rtj3
0
quote:

Wilbar schreef op 7 november 2021 21:45:

[...]
Piece of cake :).

Gelukkig hebben Perez <> Hamilton het tot de laatste meters spannend gehuden.
Haha , denk dat er anders maar weinig aan was..
[verwijderd]
3
Een ouder Chinees onderzoek(je) uit 2020, (misschien al is eerder gepost hier maar ik kon dat niet vinden) gedaan met muizen die geinfecteerd waren met covid. De onderzoekers hebben hier ook gebruik gemaakt van C1INH en zagen dat;

Met name een anti-MASP-2 monoklonaal antilichaam of C1INH, een remmer van MASP-2 ( 25), blokkeerde SARS-CoV-gepotentieerde C4-hydrolyse, wat suggereert dat N-eiwit-gepotentieerde C4-splitsing afhankelijk was van MASP-2-activering ( Fig. 2E en Fig. S2B). Bovendien bleek MERS-CoV N ook de C4-splitsing te versterken (Fig. S2C). Deze resultaten gaven aan dat N-eiwit C4-splitsing veroorzaakt en daarom complementactivering door MASP-2-associatie en -activering.

In overeenstemming met eerdere bevindingen had de pre-infectie van Ad-229E N en Ad-SARS N met respectievelijk de ?116-124- of ?321-323-deletie in het N-eiwit, significant verminderde effecten op de mortaliteit bij muizen. Belangrijk is dat wanneer anti-N, anti-MASP-2-antilichaam of C1INH gelijktijdig werd toegediend met LPS-toediening in de met Ad-SARS N vooraf geïnfecteerde muizen, zowel het sterftecijfer als de longweefselontsteking veroorzaakt door LPS significant werden verminderd

www.medrxiv.org/content/10.1101/2020....

boven in het artikel staat
Dit artikel is een voordruk en is niet door vakgenoten beoordeeld, heb de herdruk officiële uitgave er van helaas niet kunnen vinden
ffwachten nog
2
quote:

Marijke schreef op 7 november 2021 19:31:

[...]

Ik snap jou niet. Je hebt geen aandelen Pharming en je zult ze zeker ook niet aanschaffen. Als ik me niet vergis beleg je helemaal niet meer omdat je "de boel" wereldwijd niet vertrouwt.
Je berichten getuigen van spotten met Pharming en indirect met de Pharming aandeelhouders. Dit het liefst met een-tweetjes via Eric de Rus.
Nu met je pure bedreiging........je zit de boel op te naaien. Overdrijven is ook een vak. Gefeliciteerd met je 7 AB'tjes.

Pharming UP!! :-)
Beetje jammer Mar! Geen aandelen pharming klopt! Maar ik hou de ontwikkeling scherp in de gaten! Ik heb wel degelijk nog een aardig(!) bedrag in beleggingen maar voor mijn ogen zijn deze defensief of te hoopvol om er afstand van te doen dus een tijdje aan de zijkant geparkeerd. Een keer stroomt het bloed weer door de straten en op het moment dat iedereen de uitgang heeft verlaten stap ik weer volledig in. En wat die bedreiging betreft, lees het nog even na, ik schat je intelligentie hoog genoeg in om het te zien.
(EDIT)
De AB'tjes die ik krijg interesseren mij geen zier en Eric de Rus klopt een beetje, we zitten kennelijk op dezelfde golflengte, ik ken de man niet maar ben het vaak met hem eens!
LL
3

Phase 2 study results of Ionis' novel antisense treatment for hereditary angioedema to be presented at ACAAI annual meeting
November 7, 2021 at 7:05 AM EST
- Positive Phase 2 study results demonstrate significant efficacy of donidalorsen (formerly IONIS-PKK-LRx) in the reduction of hereditary angioedema attacks
- Based on the results of the Phase 2 study, Ionis plans to initiate a Phase 3 program of donidalorsen in people with HAE

CARLSBAD, Calif., Nov. 7, 2021 /PRNewswire/ -- Ionis Pharmaceuticals, Inc. (NASDAQ: IONS), the leader in RNA-targeted therapies, announced today that positive results from the Phase 2 study of its investigational antisense medicine, donidalorsen (formerly IONIS-PKK-LRx), will be presented at the American College of Asthma, Allergy & Immunology (ACAAI) Annual Scientific Meeting in New Orleans and via livestream, November 4-8. The Phase 2 study results support the clinical profile of donidalorsen as a potential, best-in-class prophylactic treatment for patients with hereditary angioedema (HAE), and underscore Ionis' commitment to advancing antisense technology to target the root cause of diseases.

(PRNewsfoto/Ionis Pharmaceuticals, Inc.)

HAE is a rare and potentially fatal autosomal dominant disease that results in recurrent, painful attacks of swelling affecting the hands, feet, limbs, face, abdomen, larynx and trachea. Donidalorsen is an investigational antisense medicine designed to reduce the production of prekallikrein, which plays a key role in the activation of inflammatory mediators associated with acute attacks of HAE. Donidalorsen was developed using Ionis' advanced LIgand-Conjugated Antisense (LICA) technology.

Topline results of the Phase 2 study, reported earlier this year, showed that donidalorsen met its primary and all secondary endpoints, achieving significant reductions in the number of attacks suffered by patients with hereditary angioedema (HAE) compared to placebo. These data support advancing donidalorsen into Phase 3 development, which Ionis plans to initiate this year.

bron:
ir.ionispharma.com/news-releases/news...
LL
2

BioCryst Presents New Data Showing Sustained Reduction of HAE Attack Rates and Improved Patient Satisfaction After Patients Switch to ORLADEYO® (berotralstat)


Data from APeX-S showed patients had more than 80 percent attack free months after switching to ORLADEYO from injectable prophylactic therapies

RESEARCH TRIANGLE PARK, N.C., Nov. 05, 2021 (GLOBE NEWSWIRE) -- BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today announced new long-term efficacy and safety data from studies evaluating oral, once-daily ORLADEYO® (berotralstat) for the prophylactic treatment of hereditary angioedema (HAE), including results showing sustained reduction of HAE attack rates and improved patient satisfaction after patients switched to ORLADEYO monotherapy from injectable prophylactic therapies (lanadelumab and C1 inhibitors).

The data are being presented at the 2021 Annual Scientific Meeting of the American College of Allergy, Asthma & Immunology (ACAAI), which is being conducted in New Orleans, Louisiana, and online, from November 4-8, 2021.

“We continue to see improvement in key indicators that demonstrate the value of oral, once-daily ORLADEYO as an excellent option for patients who want alternatives to injectable prophylactic therapies, which carry a high treatment burden,” said Dr. William Sheridan, chief medical officer of BioCryst. “The data we are presenting at ACAAI further support ORLADEYO as a transformative therapy for HAE patients, including those who are already well-controlled on other therapies.”

“The data from APeX-S showed that HAE patients who switched to ORLADEYO from an injectable prophylactic therapy had more than 80 percent attack free months,” said Marc Riedl, M.D., clinical director of the US HAEA Angioedema Center at the University of California San Diego. “These data show that, regardless of which therapy patients switched from, or when they switched, ORLADEYO provided consistently low attack rates when used as a monotherapy. These important findings add to real-world evidence that this oral, once-daily therapy is a beneficial treatment option for many HAE patients.”

“Increased satisfaction and improvement in quality of life continue to be major driving factors for patients who decide to switch to an oral prophylactic option, as shown in our analysis of patients who switched from injectable prophylaxis to ORLADEYO in APeX-2,” said Jonathan Bernstein, M.D., professor of medicine, department of internal medicine, division of allergy & immunology at the University of Cincinnati and partner of the Bernstein Allergy Group and Bernstein Clinical Research Center. “These results underscore what I see every day in clinical practice, that HAE patients want a more convenient treatment option to control their HAE attacks and reduce their overall burden of therapy.”

BioCryst ACAAI 2021 Presentation Highlights

Consistently Low Hereditary Angioedema (HAE) Attack Rates Observed in US Patients Treated with Berotralstat (Distinguished Industry Oral Presentation)

Highlights safety, effectiveness and patient-reported outcomes of ORLADEYO 150 mg in U.S. patients from APeX-S who completed 12 months of treatment (n=71).

Following initiation of ORLADEYO, patients experienced low HAE attack rates that were sustained throughout the treatment period (median attack rate of 0.0 attacks per month through month 12), consistent with previously reported data.

ORLADEYO was associated with prompt, sustained, statistically significant and clinically meaningful improvements in quality of life (-10.8 change from baseline at month 1 and -13.6 change from baseline at months 6 and 12; p<0.001) as measured by the AE-QoL (angioedema quality of life questionnaire) total score. These improvements exceeded the minimal clinically important difference (-6 change).

ORLADEYO was generally well tolerated, with no drug-related serious adverse events reported.

Berotralstat Demonstrates Low Hereditary Angioedema (HAE) Attack Rates in Patients Switching from Injectable Prophylaxis (poster #P045)

Patients at U.S. sites in APeX-S who switched to ORLADEYO (n=34) had more than 80 percent attack free months for up to 12 months after switching from long-term prophylactic treatment (LTP) (lanadelumab and C1 inhibitors).

After switching from prior injectable prophylaxis, mean monthly attack rates were consistently low (< 0.5 attacks per month) and median attack rates remained at 0.0 attacks per month throughout 12 months of treatment with ORLADEYO monotherapy.

The transition from injectable LTP to ORLADEYO was generally well tolerated with no additional safety signals.

Improved Patient Satisfaction with Berotralstat in Patients Switching from Injectable Hereditary Angioedema (HAE) Prophylactic Treatments (poster #P048)

Treatment satisfaction in patients who switched to ORLADEYO monotherapy from prior injectable LTP at U.S. sites in APeX-S was reported as assessed by the Treatment Satisfaction Questionnaire for Medication (TSQM).

Statistically significant improvements were observed in convenience and global satisfaction scores in patients who switched from lanadelumab or a subcutaneous C1 inhibitor to ORLADEYO (n=34), consistent with a positive experience using an oral HAE prophylactic therapy.

For all patients who switched to ORLADEYO, the most significant improvement was observed in convenience, with scores of more than 90 points at month 12 (33.4 point improvement; p<0.001).

From baseline to month 12, effectiveness scores remained consistently high, supporting patients’ perception that ORLADEYO is as effective as their prior prophylactic therapy.

Sustained Reduction in Hereditary Angioedema (HAE) Attack Rates Following Switch to Berotralstat: Subgroup Analysis from APeX-2 (poster #P053)

Long-term efficacy and safety data were analyzed in patients who switched to ORLADEYO 150 mg for parts 2 and 3 of the APeX-2 pivotal clinical trial after receiving placebo in part 1 of the trial (n=17).

A rapid reduction in attack rates was observed following the switch to ORLADEYO, with median attack rates of 0.0 attacks per month at more than 75 percent of all timepoints.

Sustained reductions in mean and median HAE attack rates were observed after patients switched to ORLADEYO.

ORLADEYO was generally well tolerated in patients who switched from placebo; safety data in this switch subset were consistent with those previously reported for the overall study patient population.

All e-posters are available online at epostersonline.com/acaai2021 and will be on display in the exhibit hall during the meeting.

bron:
ir.biocryst.com/news-releases/news-re...
St13rtj3
0
quote:

LL schreef op 8 november 2021 07:33:


BioCryst Presents New Data Showing Sustained Reduction of HAE Attack Rates and Improved Patient Satisfaction After Patients Switch to ORLADEYO® (berotralstat)


Data from APeX-S showed patients had more than 80 percent attack free months after switching to ORLADEYO from injectable prophylactic therapies

RESEARCH TRIANGLE PARK, N.C., Nov. 05, 2021 (GLOBE NEWSWIRE) -- BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today announced new long-term efficacy and safety data from studies evaluating oral, once-daily ORLADEYO® (berotralstat) for the prophylactic treatment of hereditary angioedema (HAE), including results showing sustained reduction of HAE attack rates and improved patient satisfaction after patients switched to ORLADEYO monotherapy from injectable prophylactic therapies (lanadelumab and C1 inhibitors).

The data are being presented at the 2021 Annual Scientific Meeting of the American College of Allergy, Asthma & Immunology (ACAAI), which is being conducted in New Orleans, Louisiana, and online, from November 4-8, 2021.

“We continue to see improvement in key indicators that demonstrate the value of oral, once-daily ORLADEYO as an excellent option for patients who want alternatives to injectable prophylactic therapies, which carry a high treatment burden,” said Dr. William Sheridan, chief medical officer of BioCryst. “The data we are presenting at ACAAI further support ORLADEYO as a transformative therapy for HAE patients, including those who are already well-controlled on other therapies.”

“The data from APeX-S showed that HAE patients who switched to ORLADEYO from an injectable prophylactic therapy had more than 80 percent attack free months,” said Marc Riedl, M.D., clinical director of the US HAEA Angioedema Center at the University of California San Diego. “These data show that, regardless of which therapy patients switched from, or when they switched, ORLADEYO provided consistently low attack rates when used as a monotherapy. These important findings add to real-world evidence that this oral, once-daily therapy is a beneficial treatment option for many HAE patients.”

“Increased satisfaction and improvement in quality of life continue to be major driving factors for patients who decide to switch to an oral prophylactic option, as shown in our analysis of patients who switched from injectable prophylaxis to ORLADEYO in APeX-2,” said Jonathan Bernstein, M.D., professor of medicine, department of internal medicine, division of allergy & immunology at the University of Cincinnati and partner of the Bernstein Allergy Group and Bernstein Clinical Research Center. “These results underscore what I see every day in clinical practice, that HAE patients want a more convenient treatment option to control their HAE attacks and reduce their overall burden of therapy.”

BioCryst ACAAI 2021 Presentation Highlights

Consistently Low Hereditary Angioedema (HAE) Attack Rates Observed in US Patients Treated with Berotralstat (Distinguished Industry Oral Presentation)

Highlights safety, effectiveness and patient-reported outcomes of ORLADEYO 150 mg in U.S. patients from APeX-S who completed 12 months of treatment (n=71).

Following initiation of ORLADEYO, patients experienced low HAE attack rates that were sustained throughout the treatment period (median attack rate of 0.0 attacks per month through month 12), consistent with previously reported data.

ORLADEYO was associated with prompt, sustained, statistically significant and clinically meaningful improvements in quality of life (-10.8 change from baseline at month 1 and -13.6 change from baseline at months 6 and 12; p<0.001) as measured by the AE-QoL (angioedema quality of life questionnaire) total score. These improvements exceeded the minimal clinically important difference (-6 change).

ORLADEYO was generally well tolerated, with no drug-related serious adverse events reported.

Berotralstat Demonstrates Low Hereditary Angioedema (HAE) Attack Rates in Patients Switching from Injectable Prophylaxis (poster #P045)

Patients at U.S. sites in APeX-S who switched to ORLADEYO (n=34) had more than 80 percent attack free months for up to 12 months after switching from long-term prophylactic treatment (LTP) (lanadelumab and C1 inhibitors).

After switching from prior injectable prophylaxis, mean monthly attack rates were consistently low (< 0.5 attacks per month) and median attack rates remained at 0.0 attacks per month throughout 12 months of treatment with ORLADEYO monotherapy.

The transition from injectable LTP to ORLADEYO was generally well tolerated with no additional safety signals.

Improved Patient Satisfaction with Berotralstat in Patients Switching from Injectable Hereditary Angioedema (HAE) Prophylactic Treatments (poster #P048)

Treatment satisfaction in patients who switched to ORLADEYO monotherapy from prior injectable LTP at U.S. sites in APeX-S was reported as assessed by the Treatment Satisfaction Questionnaire for Medication (TSQM).

Statistically significant improvements were observed in convenience and global satisfaction scores in patients who switched from lanadelumab or a subcutaneous C1 inhibitor to ORLADEYO (n=34), consistent with a positive experience using an oral HAE prophylactic therapy.

For all patients who switched to ORLADEYO, the most significant improvement was observed in convenience, with scores of more than 90 points at month 12 (33.4 point improvement; p<0.001).

From baseline to month 12, effectiveness scores remained consistently high, supporting patients’ perception that ORLADEYO is as effective as their prior prophylactic therapy.

Sustained Reduction in Hereditary Angioedema (HAE) Attack Rates Following Switch to Berotralstat: Subgroup Analysis from APeX-2 (poster #P053)

Long-term efficacy and safety data were analyzed in patients who switched to ORLADEYO 150 mg for parts 2 and 3 of the APeX-2 pivotal clinical trial after receiving placebo in part 1 of the trial (n=17).

A rapid reduction in attack rates was observed following the switch to ORLADEYO, with median attack rates of 0.0 attacks per month at more than 75 percent of all timepoints.

Sustained reductions in mean and median HAE attack rates were observed after patients switched to ORLADEYO.

ORLADEYO was generally well tolerated in patients who switched from placebo; safety data in this switch subset were consistent with those previously reported for the overall study patient population.

All e-posters are available online at epostersonline.com/acaai2021 and will be on display in the exhibit hall during the meeting.

bron:
ir.biocryst.com/news-releases/news-re...
Dit is bad news voor pharming!
Winst gevend
7
quote:

B33rtj3 schreef op 8 november 2021 08:18:

[...]

Dit is bad news voor pharming!
The safety and effectiveness of ORLADEYO for the treatment of acute HAE attacks have not been established. ORLADEYO should not be used for the treatment of acute HAE attacks. Additional doses or dosages of ORLADEYO higher than 150 mg once daily are not recommended due to the potential for QT prolongation.

Wel het hele verhaal vertellen voortaan.

TonR
0
quote:

Winst gevend schreef op 8 november 2021 08:32:

[...]

The safety and effectiveness of ORLADEYO for the treatment of acute HAE attacks have not been established. ORLADEYO should not be used for the treatment of acute HAE attacks. Additional doses or dosages of ORLADEYO higher than 150 mg once daily are not recommended due to the potential for QT prolongation.

Wel het hele verhaal vertellen voortaan.

Precies!
[verwijderd]
0
quote:

ffwachten nog schreef op 8 november 2021 00:02:

[...]Beetje jammer Mar! Geen aandelen pharming klopt! Maar ik hou de ontwikkeling scherp in de gaten! Ik heb wel degelijk nog een aardig(!) bedrag in beleggingen maar voor mijn ogen zijn deze defensief of te hoopvol om er afstand van te doen dus een tijdje aan de zijkant geparkeerd. Een keer stroomt het bloed weer door de straten en op het moment dat iedereen de uitgang heeft verlaten stap ik weer volledig in. En wat die bedreiging betreft, lees het nog even na, ik schat je intelligentie hoog genoeg in om het te zien.
(EDIT)
De AB'tjes die ik krijg interesseren mij geen zier en Eric de Rus klopt een beetje, we zitten kennelijk op dezelfde golflengte, ik ken de man niet maar ben het vaak met hem eens!
Beetje jammer.....kan ik mee leven. Je hebt een groot deel van je beleggingen afgestoten, niettemin heb je wel degelijk nog een aardig (met uitroepteken) bedrag in beleggingen. Conclusie : je bent een rijke stinkerd. ;-)

Ik kan die bedreiging niet teruglezen, maar ik herinner me niets van "ik kom je opzoeken"o.i.d. Daarbij is niets over Wilbar bekend. Angst heeft niets met intelligentie te maken. Men maakt elkaar een beetje gek.
déjà vu
3
quote:

B33rtj3 schreef op 8 november 2021 08:18:

[...]

Dit is bad news voor pharming!
Waarom ? Zij zitten pas in de Fase 2-onderzoeksresultaten.
Jij was toch ook laatst degene die €0,64 had gezien ?
Ga maar lekker short jij.
St13rtj3
2
quote:

Goldman schreef op 8 november 2021 08:36:

[...]

Waarom ? Zij zitten pas in de Fase 2-onderzoeksresultaten.
Jij was toch ook laatst degene die €0,64 had gezien ?
Ga maar lekker short jij.
Nou nou nou... wat een antwoord.

Ten eerste ik zit niet short.
Ten tweede bezit ik een behoorlijke positie in pharming dus ik heb net zo veel recht als spreken als dat jij dat heb.
Ten derde €0,64 is indd gezien 2018.

Dus doe maar gewoon weer normaal.
Bijlage:
St13rtj3
0
quote:

Winst gevend schreef op 8 november 2021 08:32:

[...]

The safety and effectiveness of ORLADEYO for the treatment of acute HAE attacks have not been established. ORLADEYO should not be used for the treatment of acute HAE attacks. Additional doses or dosages of ORLADEYO higher than 150 mg once daily are not recommended due to the potential for QT prolongation.

Wel het hele verhaal vertellen voortaan.

Long-term efficacy and safety data were analyzed in patients who switched to ORLADEYO 150 mg for parts 2 and 3 of the APeX-2 pivotal clinical trial after receiving placebo in part 1 of the trial (n=17).

A rapid reduction in attack rates was observed following the switch to ORLADEYO, with median attack rates of 0.0 attacks per month at more than 75 percent of all timepoints.
St13rtj3
0
quote:

TonR schreef op 8 november 2021 08:43:

[...]Ze zijn zo doorzichtig.
Wie? Vertel me dat maar eens?
Donquiche
0
Trouwens… eind van deze maand is het alweer 30 november!

Hmmm… wat was er ook alweer met die datum?

:-)
déjà vu
0
Zat de berichten nog eens terug te lezen van CriticalThinker, al zou ik hem dan bij voornaam mogen noemen dan zou ik zeggen Robert.

Wel zeer goede en inhoudelijke postings. Compliment !
Wel jammer dat hij meestal alleen op de achtergrond zit.

Keep the good work !
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