Anavex Ny tråd feb. 2023 - Nyt Parkinsonforsøg i Australien!
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Anavex Udskrift Q3 rapport.
Anavex Life Sciences Corp. (AVXL) Q3 2023 Earnings Call Transcript
Aug. 08, 2023 9:40 AM ETAnavex Life Sciences Corp. (AVXL)
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Anavex Life Sciences Corp. (NASDAQ:AVXL) Q3 2023 Earnings Conference Call August 8, 2023 8:30 AM ETCompany Participants
Clint Tomlinson - IR
Christopher Missling - President and CEO
Sandra Boenisch - Principal Financial Officer
Conference Call Participants
Soumit Roy - Jones Trading
Operator
Good morning and welcome to the Anavex Life Sciences' Fiscal 2023 Third Quarter Conference Call. My name is Clint Tomlinson, and I will be your host for today's call. At this time, all participants are in a listen-only mode. Later, we will conduct a question-and-answer session. [Operator Instructions] Please note that this conference is being recorded. The call will also be available for replay on Anavex's website at www.anavex.com.
With us today is Dr. Christopher Missling, President and Chief Executive Officer; and Sandra Boenisch, Principal Financial Officer.
Before we begin, please note that during this conference call, the company will make some projections and forward-looking statements. These statements are only predictions based on current information and expectations and involve a number of risks and uncertainties. We encourage you to review the company's filings with the SEC. This includes, without limitation, the company's Forms 10-K and 10-Q which identify the specific factors that may cause actual results or events to differ materially from those described in these forward-looking statements.
These factors may include, without limitation, risks inherent in the development and/or commercialization of potential products, uncertainty in the results of clinical trials or regulatory approvals, need and ability to obtain future capital, and maintenance of intellectual property rights.
And with that, I'd like to turn the call over to Dr. Missling.
Christopher Missling
Thank you Clint and good morning everyone. Thank you for being with us today to review our most recently reported financial results and to provide our quarterly business update. We are very excited to be entering an important phase of the company with several key data readouts within the remainder of 2023 for blarcamesine. First on Rett syndrome, in June we announced the completion of the placebo-controlled excellent Phase 2/3 clinical trial RS03 in pediatric patients with Rett syndrome and we're looking forward to the top-line data of this potentially pivotal clinical trial in the second half of 2023.
On June 12, we announced the publication of a new peer-reviewed study in the American Journal on Intellectual and Developmental Disabilities with relevance to this clinical trial entitled, "Rett syndrome" behavioral questionnaire in children and adults with 'Rett syndrome Psychometric Characterization and Revised Factor Structure.' In the EXCELLENCE clinical trial, the Characterized Rett syndrome Behaviour Questionnaire RSBQ together with a clinical global impression improvement scale CGI-I represents the co-primary efficacy endpoints of the trial. This psychosomatic study is timely and significant as it provides additional support for the use of the RSBQ in children and adults as well as reference values and revised subscales for its improved use. We have also been further encouraged for the results of this upcoming data readout based on recent long-term clinical trial results from the U.S. ANAVEX2-73-RS-001 clinical trial which we announced end of June.
The long-term data demonstrated disease-modifying effect of blarcamesine for adult patients with Rett syndrome. Results from pharmacometric modeling of the full clinical data from baseline of the double blind study to the end of the open label extension study indicated that the data are best characterized by a combined symptomatic and disease-modifying drug effect model meaning that blarcamesine exhibited both symptomatic and disease-modifying effects in the treatment of Rett syndrome in a clinical setting. Continued improvement from the drug as measured with the RSBQ total score was observed from the start of the double blind study to the end of the open label extension for patients continuing on blarcamesine.
Additionally, disease progression which is defined as the change in Rett syndrome disease severity with time was also reduced with long-term treatment with blarcamesine. In Alzheimer's disease, we look forward to presenting, including in a scientific journal once available, the complete data set of the recently completed phase 2/3 Alzheimer's disease trial of blarcamesine. With newly available preliminary efficacy results of surrogate biomarkers, we intend to initiate discussions with regulatory agencies in the context of the on-going clinical development of blarcamesine in this indication. With a goal of providing a much needed treatment for the millions of patients living with Alzheimer's disease in a convenient once-daily oral treatment, we expect to be able to announce this data also within the second half of 2033.
Following on the encouraging results of our Parkinson's and dementia clinical trial, including the results of the 48-week open-label extension of this trial, which we announced at the end of March, we intend to use the same endpoints in a forthcoming pivotal study of blarcamesine in Parkinson's disease, which is currently in the planning stages and we look forward to announcing the significant milestones of this clinical trial initiation as they are executed. Further, the pipeline expansions of the ANAVEX platform using gene biomarkers of response applying precision medicine for neurological disorders is expected, including a planned initiation of blarcamesine imaging-focused Parkinson's disease clinical trial sponsored by the Michael Fox Foundation, a planned initiation of a potentially pivotal blarcamesine phase 2/3 clinical trial in Fragile X syndrome, and a planned initiation of a phase 2 clinical trial in ANAVEX3-73in Schizophrenia.
We also are planning an initiation of a potentially pivotal blarcamesine trial phase 2/3 for the treatment of a new rare disease indication, which we announced accordingly. And we continue to expect clinical publications involving ANAVEX2-73, blarcamesine, and ANAVEX3-73.
In conjunction with these planned clinical developments, we continue to strive to remain at the forefront of innovation. In June, we announced we entered into a strategic partnership with Partex Group to leverage artificial intelligence for drug development and healthcare sales marketing, potentially involving a digital healthcare sales marketing pharma platform with the overall ambition to reshape the future of the biopharma business model.
By combining ANAVEX's innovative small molecule precision medicine drug development platform and Partex's disruptive approach of AI-enabled drug development and healthcare sales marketing, this collaboration is intended to drive efficiency, effectiveness, and innovation across the value chain with patients centric focused at every step.
Additionally, we continue to expand and strengthen our patent portfolio for blarcamesine with a new U.S. patent awarded expanding ANAVEX patent coverage of certain crystal forms of blarcamesine compositions, process of preparation, and uses thereof.
And now I would like to direct the call to Sandra Boenisch, Principal Financial Officer of ANAVEX, for a brief financial summary of the recently reported quarter.
Sandra Boenisch
Thank you, Christopher, and good morning to everyone. I am pleased to share with you today our third quarter financial results. During our most recent quarter, our general and administrative expenses remained consistent year-over-year at $3.2 million. Our research and development expenses for the quarter were $10.3 million as compared to $9.3 million in the comparable quarter of fiscal 2022. The increase in research and development costs year-over-year was primarily a result of our expanded team as well as a sustained increase in drug manufacturing activities and development for future clinical and potential market supply.
Overall, we reported a net loss of $11.3 million, which is $0.14 per share, inclusive of $3.9 million in non-cash items. Our cash position at June 30th was $154.8 million. During the quarter, we utilized cash and cash equivalents of $7.7 million to fund operations. At our current cash utilization rate, we believe we have continued to have sufficient cash runway to fund our operations and clinical programs beyond the next four years.
Thank you, and now I will turn it back over to you, Christopher.
Christopher Missling
Thank you, Sandra, and this is a really exciting time for the company, and we remain on track for readouts of completed clinical trials and initiation of additional biomarker-driven precision medicine clinical trials as planned.
I would now like to turn the call back to Clint for Q&A.
Question-and-Answer Session
Operator
Thank you. We will now begin the Q&A session. [Operator Instructions] So our first question is coming from Soumit Roy at Jones Research. You can go ahead and speak, Soumit.
Soumit Roy
Hi. Good morning, everyone, and congratulations on the solid quarter and all the progress. A question on the Alzheimer program. Are the patients continuing on a long-term study and any progress on the confirmatory study to initiate on?
Christopher Missling
Yes. Excellent question. So the patient on the extension study actually was given a name. It's called the ATTENTION-AD Study, and it's going over 96 weeks. We have been heard from KOLs that actually this extension study could be the confirmatory study of the ANAVEX2-73 Phase II, Phase III study itself. So we want to basically put this in context and see how this will progress. Accordingly, so we might already have started this confirmatory study with that open-label study, but it will be determined in discussion with regulatory agencies. But we would, of course, be able to, without a problem, initiate a study, if so required, at any time.
Soumit Roy
I see. Do you have any date in mind when the FDA conversation could happen if this study can translate into a confirmation study?
Christopher Missling
Yes. We are planning to do this once the data is available, which is expected this year. And thereafter, agency is able to address things with data as well. And that's what will happen with data, in presence of data.
Soumit Roy
Okay. And the biomarker study data, could you give us some color on how many patient results are going to present an expectation? Because this is not a targeted agent towards [Indiscernible]. So what should be Street's expectations? And could you refine the timeline? Is it going to be later, like in November timeline, or could be earlier in third quarter?
Christopher Missling
I would say we keep the, we want to surprise the market. So we, it's the second half of this year, and we be able to then provide the data once it's available. And regarding the color, so it will be the entire participants of the trial. And the majority of them have received blood biomarker assessment before and after, as well as MRI assessment. And a smaller sample size has also received CSF samples. So this is right now, the entire population of the trial.
Soumit Roy
Wow. That is really helpful. And one last question on the Rett program. Clearly you are heading towards getting the top-line data from the EXCELLENCE study. How are you thinking path forward? Are you thinking about commercializing yourself, or is it going to be a partnership program? If it's going to be by ANAVEX, the commercialization part, when should we start thinking about hiring the commercial team?
Christopher Missling
Yes. Excellent question. So with the collaboration with Partex, we already initiated the strategizing on the sales for numbers, the expansion of marketing strategies, but also we received unsolicited interest from across the globe, in all regions of the world, from all regions of the world, to either co-market or to license blarcamesine for Rett syndrome already. So we have multiple options open, and we try to make a decision based on shareholder value. So what will create more shareholder value accordingly? And we will base that decision based on that information once we are able to get terms on the table, which will likely happen after the data is out.
Soumit Roy
Thanks. Well, thank you again for taking all the questions and congratulations on all the progress.
Christopher Missling
Thank you.
Operator
I don't see any other analyst questions, Dr. Missling, if there's anything that you want to add here, you're more than welcome to.
Thank you very much. I think the question from Soumit was very comprehensive. Again, we like to very much point out that we're looking forward to a very excited second half of this year. We are very excited about the potential, what we build. We're expecting further publications and of our biomarker-driven precision medicine studies, which have all significant unmet need and economic burden. And we remain focused on execution as we prepare for a pivotal year ahead of us, potentially involving meaningful advances in our neuro developmental in neurodegenerative precision medicine portfolio. Thank you very much and stay tuned looking forward.
Operator
Thank you, Dr. Missling. Ladies and gentlemen, that will conclude our call for today. We appreciate your participation and you may now disconnect.
Til Akku:
Fase 4 eller kontrolforsøg kan køre efter og samtidig med en evt. acc. godkendelse, hvor stoffet kan markedsføres. Kontrolforsøget kan så understøtte en forsat godkendelse eller rejse spørgsmål eller stoppe markedsføring ved. evt. opståede bivirkninger mm. -
Hvis fase 3 (2b/3) har været mindre i størrelse eller resultater ikke har været helt overbevisende kræver fda ofte et fase 4 forsøg efter godkendelse af et stof.
I tilfældet Blarcamesine vil nogle nok mene, at der burde være to større forsøg før en godkendelse.
Men da AD er unmet need kan godkendelse ske på et mindre forsøg og efterfølgende vil et et fase 4 kunne cementere resultaterne. Ved negativt udfald af fase 4 kan godkendelse evt. tilbagekaldes.
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Mayomobiles referat og syn på kvartalsregnskabet og zoom mødet https://www.sotcanalytics.com/update-compendium-2023#h.xhufh3u0z28j
Han bekymrer sig om et fjendtligt bud.
Missling har efter min vurdering haft det i tankerne i årevis. Med indsættelse af poison pill i vedtægterne for et år eller to siden, mener jeg, at han har sikret sig imod det.
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Næææ, den er bare af flere gange trykket ned i 7,7 nu kom der så en modreaktion, som nok forstærkes af at støtten har holdt af flere omgang, så muligt der købes ind her, med forventning om at 7,7 er bunden... ?
Så må vi se om der sættes nye short oven på dagens stigning ?
1 god stigning efterfølges som regel af 2 efterfølgende børsdage med yderligere stigninger ! så skal vi jo håbe på noget nyhedsstof, som kan holde hånden under stigningerne, måske der er noget i vente, nogle ved altid noget før os andre....
Men nok mest det første + lykkeridder trader og andet godtfolk.
Det ville virkelig være Nice med breaking news, så kursen får et Los i røven, og bliver oppe uden den sædvanlige siven baglæns.
Men det jo ren gæt herfra, men dejligt med en god stigning, som forhåbentlig holder hele vejen hjem, og luk i dagens højste..
Mvh
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Anavex Ufatteligt at den mand ikke sidder i spjældet!
Det er igen igen det samme han henviser til vedr. det ene RETT forsøg, hvor Anavex efter aftale med FDA valgte et sværere opnåeligt endpoint, hvor de udover det normale spørgeskema fra familie/plejer inddragede lægernes evaluering af virkningen på de voksne RETT patienter.
Anavex meddelte dog først denne ændring få uger før afslutning af forsøget.
Den gang formåede AF at skabe så meget usikkerhed omkring ellers virkelige gode resultater, at shorterne havde nemt ved at banke kursen ned!Det er helt grotesk, hvordan denne manipulation forsat kan pågå så åbentlyst?
Håber Missling netop med Peer Reviwede data kan lukke munden på AF en gang for alle - og fange AF
s shortkumpaner med bukserne nede! Sjovt nok skriver han f.eks. ikke noget kritisk om, at patienterne dør i BPernes Alzheimer forsøg! -
Man kan kun ønske at den bliver den nye GameStop, så alle de parasitter fra Blackrock og Vanguard brænder fingrene til ukendelighed. Den aktie styres jo i den grad med hård hånd. Den skal med vold og magt holdes nede. Håbet er vel at de store pengetanke får gjort de fleste småsktionærer modløse og så i sidste ende købe for at afnotere skidtet. Og den gode Mistling hjælper jo i den grad til at Anavex er blevet til en krabbeaktie. Det er sku ved at være op ad bakke.
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Der er et par gode skribenter, der de seneste dage er kommet med en forklaring på hvorfor Missling gerne vil have rett som første godkendte indikation. Voucheren er en grundl men også noget med godkendelsesproceduren for stoffet i efterfølgende indikationer.
Covid har så været årsagen til at det hele trækker ud.
Jeg har ikke helt gennemskuet fordelen ved ovennævte endnu. Men vil prøve at få tid til at kigge på det.
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Missiling bør denne gang blive inspireret af SAVA.
AUSTIN, Texas, Nov. 03, 2022 (GLOBE NEWSWIRE) -- Cassava Sciences, Inc. (Nasdaq: SAVA), a clinical-stage biotechnology company, today announced that it has filed a lawsuit in federal court against certain individuals who executed a "short and distort" campaign against the Company. The 150+ page complaint alleges that the Defendants' disinformation campaign caused a precipitous decline in Cassava Sciences' stock price, a multi-billion dollar decline in its market capitalization, and delayed the Company's work in developing a treatment for Alzheimer's disease.
The lawsuit alleges: "Defendants placed personal enrichment over science, over the health of patients, and over the truth. Defendants saw an opportunity to manipulate a stock price and financially benefit from their 'short positions' by defaming a company developing a drug for people with Alzheimer's disease, a condition that afflicts millions of people. Defendants seized that opportunity and, while enriching themselves, caused irreparable harm to the company, its attempts to find a treatment for the disease, and patients waiting for that treatment. Defendants' conduct is beyond shameful. It is unlawful."
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Hvorfor bruge tid og penge på at jagte shortere - det er langt dyrere for dem at blive overrasket af Missling. Men irriterende er det !
Her er et af de indlæg jeg tidligere har henvist til:
Anavex Life Sciences Corp (AVXL): Yes. I think they'll present the OLE...
abew4me: Yes. I think they'll present the OLE as an alternative to a full-blown confirmatory trial because their NDA (New Drug Application) will be focused...
InvestorsHub (investorshub.advfn.com)
Med lidt yderligere forklaring:
Teorien er så, at Missling har følt sig mest sikker på rett indikationen og godkendelse i denne. Herefter skulle godkendelse af Blacamesine være lettere i efterfølgende indikationen.
Dette skulle forklare, at man træder vande mht partnerskaber og søge på data i alzheimers ?
Muligt det er rigtigt, men ikke noget der er nævnt af Anavex. Men selvfølgelig en katastrofe, at få afvist en NDA i alzheimers pga, at forsøget er for lille.
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Lidt ærgeligt den abe (Adam) kom på banen, det startet ellers som jeg tegnede op igår...
Han skulle have lov at krydse motorvejen, med 2 fyldte bæreposer med glas
det gas Fedt hvis der lander en god PR, som lige kunne sende os i den rigtige retning igen ...
Mvh
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Anavex. Kommunikation med FDA pågår løbende!
Med alle mulige forbehold, så har troværdige Trainguy1 fra Stocktwits igen haft kontakt med IR fra Anavex.
Iflg. ham, så er der en løbende kommunikation med FDA i processen.
Trainguy1 har gennem årene flere gange påstået at have kontaktet Anavex og fået mere eller mindre brugbare svar. IR/Anavex kan kun i begrænset og i et generelt omfang fortælle noget til enkeltpersoner - men positivt, at der åbenbart er en løbende dialog med myndighederne. (forventeligt med bl.a. Fast Track i flere indikationer i min optik)Question to IR fromTrainguy1 on ST-
If the FDA agrees to evaluate
Blarcamesine for accelerated
approval for Alzhiemers, has the FDA
indicated what parts of the standard
NDA need to be submitted to obtain
accelerated approval? Also, is
Anavex's response to 21 CFR 312.120
[Foreign Clinical Studies Not
Conducted Under An IND] required to
obtain accelerated approval?>IR-We communicate with the FDA if
and when needed, as such, final
decisions are made based on
management, board of directors and
scientific advisors input, as well as
potentially lawyers and others that
are well-versed in the dealings with
the FDA. Communications with the
FDA are ongoing and it would be
impossible to constantly disclose
each and every correspondence. If
and when something is material, we
will issue a press release and/or file
an 8K. -
Piotr har begået et nyt indlæg:
Interessant læsning. Han opfordre til, at man ser rett som første indikation der kan give medvind, idet han ser risiko for, at man afventer måske hele OLE forsøget i AD før man offentliggør noget.
Godt at han stadig er "sikker" på casen i AD. Modsat alle endre stoffer så ser det ud til, at Blarcamesine holder effekten over tid. Hvorfor OLE forsøget vil skyde enhver tvivl væk om hvorvidt Blarcamesine har effekt.
OLE forsøget er som forkortelsen siger, et open label extension forsøg. Derfor kan Anavex eller hvem de har til det hele tiden følge med i resultaterne. Mange pts er færdige og monitorering på de der stadig er i forsøg er tilgængelig. FDA kunne jo også kigge i dem og måske derfor, at Missling antyder, at det kunne udgøre et fase 4 forsøg.
Det at de taler fase 4 indikerer at approval eller NDA godt kan effektueres inden OLE er færdig, hvorfor tidslinien ikke nødvendigvis går helt medio 2024, som Piotr antyder (OLE slutter juli 2024).
Mange spændende måneder forude.
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