Ontvang nu dagelijks onze kooptips!

word abonnee
IEX 25 jaar desktop iconMarkt Monitor

Aandeel Arrowhead Pharmaceuticals OTC:ARWR.Q, US04280A1007

Vertraagde koers (usd) Verschil Volume
23,920   +0,650   (+2,79%) Dagrange 22,930 - 23,940 1.293.715   Gem. (3M) 1,4M

Forum Arrowhead Research geopend

8.634 Posts
Pagina: «« 1 ... 231 232 233 234 235 ... 432 »» | Laatste | Omlaag ↓
  1. nelis h 31 augustus 2021 22:59
    nu nog graag een hervatting van de ENAC trial dan is die donkere wolk ook verdwenen
    en heel benieuwd naar HIF2a in de hogere dosering
    en update HBV graag, dit jaar nog hopelijk
    het blijft enerverend allemaal (als je hier voor 90% in belegd bent)
    de andere 10% is Anavex, het mocht eens slagen in AD, Parkinson, RET etc
  2. wijzerplaat 1 september 2021 14:11
    Arrowhead Pharmaceuticals to Participate in Upcoming September 2021 Conferences
    September 1, 2021

    PASADENA, Calif.--(BUSINESS WIRE)--Sep. 1, 2021-- Arrowhead Pharmaceuticals Inc. (NASDAQ: ARWR) today announced that it is scheduled to participate in the following upcoming events:

    Citi’s 16th Annual BioPharma Virtual Conference – September 8-10, 2021
    September 9, 2021 – Arrowhead management will host a day of virtual investor meetings

    HC Wainwright 23rd Annual Global Investment Conference – September 13-15, 2021
    September 13, 2021 – Chris Anzalone, Ph.D., Arrowhead’s president and CEO, will participate in a fireside chat presentation

    Baird's 2021 Global Healthcare Conference – September 14-15, 2021
    September 14, 2021, 4:55 p.m. ET – Vince Anzalone, CFA, Arrowhead’s vice president of investor relations, will participate in a fireside chat presentation

    2021 Cantor Virtual Global Healthcare Conference – September 27-30, 2021
    September 29, 2021, 9:20 a.m. ET – Chris Anzalone, Ph.D., Arrowhead’s president and CEO, will participate in a fireside chat presentation
  3. Wil Helmus 6 september 2021 16:10
    quote:

    Tom3 schreef op 3 september 2021 18:49:

    Weer een gen therapie mislukking:

    www.fiercebiotech.com/biotech/after-c...

    Rnai blijft helaas een onder geschoven kindje (kijkend naar de koers van Intellia).
    En nog 1:

    BMRN FDA Placed a Clinical Hold on BMN 307 Phearless Phase 1/2 Gene Therapy Study due to safety issues. Gene therapy safety issues are spreading like wildfire

    investors.biomarin.com/2021-09-06-U-S...
  4. forum rang 6 de tuinman 13 september 2021 13:55
    quote:

    nelis h schreef op 13 september 2021 13:25:

    ENAC, "we continu to see a big (franchise) opportunity there"

    het woord franchise tussen haakjes, ik weet niet zeker of hij de term noemde
    Je kunt die haakjes weglaten. Ik begreep dat de problemen die ze vonden, zich niet voordeden bij primaten en de 1e studie bij mensen.
    Dus een goede hoop dat ze deze studie weer kunnen voortzetten.

    Geen woord over JNJ-3989?????
  5. G.dezwaluw 13 september 2021 14:35
    YMB:

    Aat
    Easl highlights
    Low levels of circulation
    Liver disease
    Designed to turn off aat
    Prevent accumulation of z protein in liver
    It works
    Lowering circulating levels substantially
    2 studies
    Open label exciting…small…nine patients
    All patients decreased in hepatic z protein
    Critical
    72 two 97 percent reduction
    On the right track
    A decrease in globules in all nine patients
    Rnai works
    We did not know how fast the liver would heal
    Shocked
    Six months of therapy two of four reduced fibrosis
    Four of five after one year
    Liver healing itself more rapidly than we expected
    Looking forward to phase 2 reading out sometime next year
    Btd with the fad
    Safety and tolerability
    Well tolerated
    Silencing gene in part intended to shield the lungs
    We give the investigators wide birth to administer as necessary

    Pivotal?
    Arwr is leading discussions for pivotal study
    We work closely with Takeda
    Our expectation is we will have a meeting with fda this year
    For pivotal study
    Endpoint should be lowering z protein
    We have a good relationship with the fad

    When is the potential for market?
    Too early to tell
    My hope is that we will be aligned with fad
    Sometime next year the blinded sequoia study will read out
    Fifty patients
    Fascinating
    Then approach fda again to get to patients quickly
    Given the data we are not too far from market
    At least close to pivotal

    Comp?
    There’s really no competition right now.
    Some sm corrector approaches that have not panned out
    We view comp as not competitive
    We will always be more durable than aso’s
    We’ll beat aso’s on depth of ko
    No close second, clear leader

    Apoc3
    Well validated target
    Also seen decrease of ldl, and increase of hdl
    Once a quarter to once every six months
    90% ko
    We can normalize those patients
    Compare to other modalities
    We move the needle
    Trigs above 500 and elevated ldl
    Exciting
    Big play
    Initial market are severe patients
    Fairly large market
    4 million in us
    No therapy now
    Approval endpoint is lowering trigs
    The regulatory pathway is clear

    Cadence of 2001 trial expectation for data?

    Other p2 studies

    Three primary buckets
    One: patients with fcs
    Trigs in 1000’s
    Phase three shortly
    Quick study…ultra orphan
    Fast path to market

    2: broader market…above 500
    P2 year long
    Pursuing now
    2-500 year long study
    Pushing quickly on all three

    We can hit market relatively quickly with fds patients
    Then other two buckets

    Ang3?

    Ang3 lowers trigs and ldl
    Important tool
    Against mixed dyslipidemia
    Year long study going on now
    Very large pop
    We believe that the pivotal study will be an outcome study
    Long expensive
    Hold onto ourselves
    The drug appears to work
    Substantial lowering

    Learn anything from inclisiran?
    Small companies can do outcome studies
    Faster/cheaper than historically done
    We now believe we can do it
    The data is compelling

    Enac?
    Background
    Halt?

    Enac is our first inhaled program
  6. G.dezwaluw 13 september 2021 14:39
    Enac?
    Background
    Halt?

    Enac is our first inhaled program
    Cf
    Excited about this franchise
    Continue to see this franchise app
    At least two additional cta’s in this space
    Did pause the study
    Good data in humans
    Well tolerated
    Acute studies in primates and rodents good
    Rodent studies
    Saw signs of lung inflammation
    Abundance of caution
    No signs in humans
    What the inflammation in rats is overloading that system
    Rats are more sensitive to overloading
    Monkey data will further validate
    Our greatest concern is safety

    End of year?

    Nhp data by end of the year
    Will answer some of th questions
    Q1 22 we should know
    Restart this program hopefully

    Hif2?

    Ko hif2 alpha
    Validated
    Rcc
    First foray into Onco
    See target engagement
    We see that
    Exciting
    Use rnai in onco
    In seven of nine biopsies
    We saw reduction of hif2 alpha
    Average 48%
    We saw one patient with decrease in tumor size
    Several patients stable
    Now lets see where it goes
    It’s a great first step

    Hsd?

    Exciting
    Nash target
    Good genetic data
    We are the first to go after this target
    Still p1/2
    Encouraging engagement/biopsies
    All Five decrease in had
    97 % reduction
    95% reduction
    Some below level of quantification
    Excited for p2b to see if we can decrease inflammation/fibrosis
  7. mvdln 13 september 2021 21:01
    quote:

    de tuinman schreef op 13 september 2021 13:55:

    [...]

    Je kunt die haakjes weglaten. Ik begreep dat de problemen die ze vonden, zich niet voordeden bij primaten en de 1e studie bij mensen.
    Dus een goede hoop dat ze deze studie weer kunnen voortzetten.

    Geen woord over JNJ-3989?????
    ARWR heeft niet (meer) het recht om over JNJ3989 te communiceren. Dat ligt bij JNJ. Ik verwacht dat JNJ in 2022 toch het doek van de motorkap gaat trekken van zodra ze intern de hoogst mogelijke FC-rate hebben vastgesteld in alle combo-studies.

    1st coming: FCS phase III aankondiging, ik verwacht okt/21 (een gokje)

    ENaC weten we dus Q1/22 welk vlees we in de kuip hebben. Mijn hoop op een doorstart groeit ondertussen.
8.634 Posts
Pagina: «« 1 ... 231 232 233 234 235 ... 432 »» | Laatste |Omhoog ↑

Meedoen aan de discussie?

Word nu gratis lid of log in met je emailadres en wachtwoord.