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de tuinman
0
All of this puts us on solid footing, but the elephant risk in the room is COVID-19. This has to be the lens through which you view our business, at least in the near- to mid-term. Therefore, I will use my portion of this call to provide a high-level overview of our programs and how they may be affected by the outbreak.

Let’s start with ARO-AAT, our investigation medicine against alpha-1 liver disease. In March, we voluntarily paused new patient screening and enrollment for at least a 4-week period in the Phase 2/3 SEQUOIA study and the AROAAT2002 open label study. We are now working with sites and investigators to begin the process of resuming screening and enrollment. Any patients already enrolled in these studies continue to be dosed per protocol and continue to come in for their follow up visits. Importantly, protocol deviations have not been out of the ordinary. Before the enrollment pause, we were already fully enrolled in the first cohort of the 2002 study, so we are still on schedule to collect 6-month biopsies in the summer. We intend to report those data in the fall at an appropriate venue

Dus als ik het goed lees is hier wel een pauze in de studie, maar krijgen we van het najaar wel een tussentijdse uitslag?

ir.arrowheadpharma.com/static-files/5...
Al Kipone
0
quote:

Marble Arch schreef op 8 mei 2020 14:32:

Cantor herhaalt koopadvies: 58 USD

Oppenheimer upgrade van market perform > outperform; 58 USD

www.marketbeat.com/stocks/NASDAQ/ARWR...
Cantor cuts ARWR price target to $58 from $60. Maintains overweight
Wil Helmus
0
quote:

G.dezwaluw schreef op 8 mei 2020 16:31:

Van +5% naar -1,5%, dus toch niet goed ontvangen
Deze had ik niet zien aankomen. Wat zal de reden zijn? De pauze in de studie ARO-AAT zoals de tuinman hierboven aangeeft, de gestegen cash burn of misschien wordt het covid avontuur toch niet zo goed ontvangen? Ik denk dat het wachten is op studie resultaten. Pas als die goed zijn kunnen we verder omhoog
Marble Arch
1
quote:

Al Kipone schreef op 8 mei 2020 17:17:

[...]

Cantor cuts ARWR price target to $58 from $60. Maintains overweight
Mijn glas is halfvol: Nogmaals Cantor herhaalt het koopadvies
RW1963
0
quote:

beleggala schreef op 8 mei 2020 12:49:

37,6 usd voorbeurs ! :)
Nou en? Ik zie weer een daling op de borden :-(
de tuinman
0
quote:

Wil Helmus schreef op 8 mei 2020 17:28:

[...]
Deze had ik niet zien aankomen. Wat zal de reden zijn? De pauze in de studie ARO-AAT zoals de tuinman hierboven aangeeft, de gestegen cash burn of misschien wordt het covid avontuur toch niet zo goed ontvangen? Ik denk dat het wachten is op studie resultaten. Pas als die goed zijn kunnen we verder omhoog
Bij biotech wordt er nooit zo positief gereageerd op financiële cijfers. Inderdaad kunnen alleen positieve studie resultaten voor aandeelhouders waarde zorgen.
Wil Helmus
0
quote:

Hulskof schreef op 8 mei 2020 20:17:

Ik heb nog wat bijgekocht. Geloof wel in een forse stijging op termijn.
Ik ook. Komt op termijn echt wel goed. Ik ken geen enkel ander aandeel met zo'n pijplijn die aan deze koers te koop is.
holenbeer
0
quote:

Missolapola schreef op 8 mei 2020 10:29:

[...]

Bedankt Holenbeer om hier af en toe de interessante zaken van het Yahoo-ARWR forum te plaatsen.
Het is vreemd maar sedert een paar maanden kan ik daar maar een heel beperkt aantal berichten lezen en ik weet echt niet waar dit aan zou kunnen liggen.
Misschien eens met een ander device proberen?
Ik zal hier af en toe leuke zaken plaatsen. Leuk om te zien dat het hier ook wat meer begint te leven.
Wil Helmus
0
Ik hoop dat we 14 of 20 mei data te zien krijgen tijdens één van onderstaande conferenties:

BofA Securities 2020 Health Care Conference– May 12-14, 2020

May 14, 11:00 a.m. EDT – Chris Anzalone, Ph.D., Arrowhead’s president and CEO, will deliver corporate presentation

RBC Global Healthcare Conference– May 19-20, 2020

May 20, 2:30 p.m. EDT – Dr. Anzalone will participate in a fireside chat presentation

Missolapola
0
Is Arrowhead Pharmaceuticals Close to a Cure for HBV?
The collaboration between a pharmaceutical giant and a mid-cap biotech company may have accomplished the impossible.

Zhiyuan Sun
(TMFZhiyuanSun)
Apr 30, 2020 at 7:52AM

Arrowhead Pharmaceuticals (NASDAQ:ARWR) saw its stock price rise from $20 to over $70 last year on the basis of no news. A similar decline occurred in reverse this year -- again on the basis of no material news whatsoever. Massive speculation on the stock may be related to its flagship candidate, ARO-HBV, which has demonstrated in clinical trials to best efficacy against current standards of care for combating the hepatitis B virus (HBV). Is this potentially a functional cure for the condition, or have investors become too hyped on its potential? Let's find out together.

What are Hepatitis B and ARO-HBV?
Hepatitis B is a serious infection of the liver caused by HBV; it's spread via body fluids. The disease affects an estimated 257 million people worldwide, including about 850,000 in the U.S. Its total addressable market is estimated to scale to $3 billion globally by 2024. Although there is a vaccine available, it has no therapeutic effect if it is not given in a timely manner after exposure.

Currently, patients living with chronic hepatitis B face risk of permanent scarring of liver tissues, or even death. As a result, they must be administered nucleotide analogues (NAs, compounds similar to naturally occurring DNA or RNA and combined with sugar) such as entecavir or tenofovir to maintain a low viral load. Unfortunately, after five years of receiving these analogues, fewer than 3% of patients will be cured of the condition. However, there may be light at the end of the tunnel.

ARO-HBV is a ribonucleic acid interference (RNAi) therapy. In this therapeutic class, small RNA molecules are injected into a particular area of the patient's body to inhibit the expression of viral genes. ARO-HBV was specifically designed to silence the levels of DNA to RNA transcription in the HBV virus.

How does clinical data look?
In phase 1 clinical trials, patients were given a combination of NAs and three doses of ARO-HBV over a period of two months, then evaluated in a follow-up period for a total of four months. The critical primary outcome was measuring declines in patients' HBV surface antigen levels (HBsAg), which indicates the severity of the current infection.

Before the trial began, patients' mean HBsAg levels ranged from 3,212 IU/ml to 9,381 IU/ml across six cohorts. Four months after treatment with ARO-HBV and NAs, five of seven patients in the 100mg ARO-HBV cohort, five of six patients in the 200mg ARO-HBV cohort, six of eight patients in the 300mg ARO-HBV cohort, and five of seven patients in the 400mg ARO-HBV cohorts saw their HBsAg levels decline to less than 100 IU/ml. In other words, a vast majority of patients were functionally cured of the condition!

Is the company a buy?
Outstanding efficacy in early trials is a good indicator of success in latter investigations. Currently, Arrowhead has licensed ARO-HBV to Johnson & Johnson's (NYSE:JNJ) Janssen Pharmaceuticals subsidiary. Under this deal, Arrowhead would be eligible to receive up to $3.5 billion in milestone payments in the likely event of clinical success. If the drug is approved by the U.S. Food and Drug Administration, the company would also be eligible for mid-teen percentages in royalties of product sales. Phase 2 data from ARO-HBV are set to be released by the end of this year and would act as a significant catalyst for the stock price.

Furthermore, investors are well guarded against stock dilution while they wait for results. The company possesses more than $400 million cash on hand to fund research and development expenses, compared with a near $4 billion market cap. Additionally, Arrowhead has plenty of other promising candidates in its pipeline that are worthy of a look. Biotech investors who are interested in innovations in RNAi should definitely add Arrowhead to their portfolios.
Missolapola
0
Dit bovenvermeld artikel was al eerder geplaatst via een link door Wil Helmus maar nu kan het gelezen worden zonder op de link te moeten klikken...
Missolapola
0
Ik heb gisteren niet bijgekocht zoals Hulskof en Wil Helmus maar wel extra puts geschreven.
Dit is mijn manier om de aandelen te verwerven : ik schrijf op korte, middellange en lange termijn. Het is de bedoeling om de meeste puts gewoon te laten aflopen en dan krijg ik de aandelen aan strike hoger dan de dan geldende koers bij expiratie toegewezen en heb ik de premie van de strike lager dan de koers bij expiratie ‘in the pocket’. Ik schrijf ook meer puts aan lagere strike dan aan hogere strike, waardoor ik de toegewezen aandelen netto voor een prikje krijg toegewezen. Is er nog iemand die op die manier werkt en zijn er optie-specialisten die mij hun eventuele opmerkingen omtrent deze werkwijze kunnen geven?
Ik voel mij het beste bij het schrijven van puts omdat dit mij meer bewegingsvrijheid geeft. Al een paar keer heb ik het kopen van calls bekeken maar dan toch gelaten voor wat het is.
Voor mij zijn Arrowhead en ook Galapagos de ideale aandelen om op deze manier te werk te gaan.
nb
1
Heb me er nooit in verdiept en weet daarom niet wat je precies bedoeld of hoe je het doet, M.
Welke nadelen heeft het tov gewoon de aandelen kopen?
de tuinman
0
Heeft er iemand een link naar een pagina waarop staat wanneer de uitslagen worden verwacht van de verschillende studies?
mvdln
0
De conference call was weer oerdegelijk! Het management blaakt van vertrouwen en er is zoveel gaande op de achtergrond. COPD target (ARO-Lung2) kan een markt van 22 miljard betreden. Enorm marktpotentieel!

COVID-19 nu ook toegevoegd aan het doel. Ik heb de indruk dat ze daar toch wat meer open aan werken dan deze versie specifiek. Het zou mooi zijn moesten ze alle varianten kunnen bestrijden.

@ de tuinman:

Het CC transcript bevat heel veel informatie:

ARO-AAT: We intend to report those data in the fall at an appropriate venue.

ARO-APOC3: our hope is that we can start a pivotal study in the first half of 2021. We believe that should be a relatively short study, so we continue to believe that ARO-APOC3 could be our first market product. We continue to generate data in the Phase I/II plan study. It was nearly fully enrolled prior to the COVID-19 outbreak and we have experienced a slight delay in accruing the remaining patients. We already have a substantial amount of data that we intend to present at various times this year and are hopeful that we may -- that we will be able to present a full data set later this year.

ARO-ANG3: We plan on engaging with FDA this year and hope to initiate the Phase 2b in the first half of 2021. The ARO-ANG3 Phase 1/2 study is making good progress, even in the COVID-19 environment. The study is fully enrolled, so we do not expect any real delays as we continue to follow patients and generate data. We believe we will have a full dataset to report later in the year and will also look for opportunities to share data subsets throughout the year.

ARO-HIF2: We expect to potentially have proof-of-concept data for the candidate and for the tumor targeted TRiMTM platform this year, but the timing may be too tight to report anything publicly until next year.

ARO-ENaC: we don't know if we will have enough data by key abstract deadlines to present data at scientific conferences this year. If the data are supportive of further development we hope to launch a Phase 3 study in 2021

ARO-Lung2: plan on filing a CTA in the first half of 2021 to begin first-in-human studies.

ARO-HSD: ARO-HSD began dosing in a Phase 1/2 study in March. We are through the first cohort and we previously received approval from the safety monitoring committee to escalate to the next higher dose.
mvdln
0
Wat ik vooral heb onthouden:

- ARO-APOC3 could be our first market product. (2022 gok ik dan)

- A number of factors give us confidence that we could play an important role in the current novel coronavirus in future coronaviruses and other pulmonary-borne packages. First we are clear RNAi leaders in addressing the lung and have a clinic-ready inhaling program; second history suggests that we are faster than any RNAi company and arguably any other biotech company going from concept to clinic; and third we are the leading RNAi company in antivirals and are known as HBV thought leaders.

- I believe we have unmatched reach into diverse indications, unmatched speed to the clinic and unmatched depth of pipeline for a company of our size. Our partner programs continue to look good as well. Amgen stated on its recent quarterly conference call that it expects to begin a Phase II study with AMG 890 in the second half of this year. Janssen continues to conduct its first two Phase IIb studies with JNJ-3989 against chronic HBV and we are actively working together on the three undisclosed additional targets.

Ik koop bij aan deze prijzen!
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