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Aandeel VIVORYON THERAPEUTICS N.V. AEX:VVY.NL, NL00150002Q7

  • 0,470 18 apr 2024 17:35
  • +0,049 (+11,51%) Dagrange 0,422 - 0,488
  • 283.780 Gem. (3M) 590,3K

Vivoryon is de naam. Daarom nieuw draadje

6.265 Posts
Pagina: «« 1 ... 284 285 286 287 288 ... 314 »» | Laatste | Omlaag ↓
  1. forum rang 4 Kuiken 24 maart 2023 13:49
    quote:

    K. Wiebes schreef op 24 maart 2023 10:59:

    Twee nieuwe locaties:
    clinicaltrials.gov/ct2/history/NCT039...

    Nog niet bekeken:
    event.webcasts.com/starthere.jsp?ei=1...
    laatste gehoord en gezien: veel positieve elementen in deze presentatie met woorden als "strong evidence en significant results"
  2. forum rang 10 voda 28 maart 2023 07:34
    Vivoryon boekt vooruitgang met studies

    Naar behandeling Alzheimer.

    (ABM FN-Dow Jones) Vivoryon heeft vooruitgang geboekt in zijn lopende studies naar een middel voor de behandeling van Alzheimer. Dit maakte het biotechbedrijf dinsdagochtend bekend.

    De VIVIAD Fase 2b-studie in Europa ligt volgens Vivoryon op schema om in het eerste kwartaal van 2024 de laatste data te presenteren. Tot dusver wisten alle 259 geteste patiënten het kandidaatmiddel varoglutamstat goed te verdragen.

    Verder liet Vivoryon weten dat met de VIVA-MIND Fase 2 studie in de VS ook goede vooruitgang wordt geboekt en momenteel wordt uitgerold op 18 locaties. In de tweede helft van dit jaar verwacht het bedrijf hierover een statusupdate te geven.

    Door: ABM Financial News.

    info@abmfn.nl

    Redactie: +31(0)20 26 28 999
  3. forum rang 4 K. Wiebes 28 maart 2023 08:57
    www.vivoryon.com/investors-news/news/

    Niet echt veel nieuws; en met name qua update uit VIVA-MIND had ik toch op wat meer gehoopt.

    ..."Dr. Howard Feldman, Professor of Neurosciences...and the VIVA-MIND study director. “...It is encouraging to see the VIVA-MIND trial receive its most recent DSMB recommendation for the trial to continue forward based on their most recent safety review of March 13, 2023.”

    Dat was 't dan wel zo'n beetje.
  4. forum rang 10 DeZwarteRidder 28 maart 2023 08:59
    quote:

    voda schreef op 28 maart 2023 07:34:

    Vivoryon boekt vooruitgang met studies

    Naar behandeling Alzheimer.

    (ABM FN-Dow Jones) Vivoryon heeft vooruitgang geboekt in zijn lopende studies naar een middel voor de behandeling van Alzheimer. Dit maakte het biotechbedrijf dinsdagochtend bekend.

    De VIVIAD Fase 2b-studie in Europa ligt volgens Vivoryon op schema om in het eerste kwartaal van 2024 de laatste data te presenteren. Tot dusver wisten alle 259 geteste patiënten het kandidaatmiddel varoglutamstat goed te verdragen.

    Verder liet Vivoryon weten dat met de VIVA-MIND Fase 2 studie in de VS ook goede vooruitgang wordt geboekt en momenteel wordt uitgerold op 18 locaties. In de tweede helft van dit jaar verwacht het bedrijf hierover een statusupdate te geven.

    Door: ABM Financial News.

    info@abmfn.nl

    Redactie: +31(0)20 26 28 999
    Een mooi voorbeeld van non-nieuws.
  5. forum rang 4 Kuiken 28 maart 2023 09:18
    Halle (Saale) / Munich, Germany, March 28, 2023 – Vivoryon Therapeutics N.V. (Euronext Amsterdam: VVY; NL00150002Q7) (Vivoryon), a clinical stage company focused on the discovery and development of small molecule medicines to modulate the activity and stability of pathologically altered proteins, today provided an update on both clinical studies of its lead candidate, varoglutamstat, a small molecule medicine in development for the treatment of Alzheimer's disease (AD), VIVA-MIND (NCT03919162) and VIVIAD (NCT04498650). Furthermore, the Company presents updated safety data from its European Phase 2b study, VIVIAD, at the 2023 International Conference on Alzheimer’s and Parkinson’s Diseases and related neurological disorders (AD/PD) in Gothenburg, Sweden.

    “We are pleased to report that both of our ongoing studies are progressing steadily, and we continue to broaden the overall data package for varoglutamstat with consistently positive incremental results,” commented Dr. Ulrich Dauer, CEO of Vivoryon. “Varoglutamstat is strongly positioned as a differentiated oral, outpatient small molecule that has the potential to significantly impact the AD treatment landscape and address ongoing unmet need. Designed to modulate all major hallmarks of AD including Abeta aggregation, neuroinflammation and tau pathology, and also enabling improvement of synaptic function, varoglutamstat captures the key features of a novel drug that has already exhibited a favorable safety profile with no signs of ARIA side effects. We are incredibly encouraged by what we have been able to report to date, and we see a unique opportunity for ultimately realizing the promise of a widely accessible treatment option in AD with the realistic potential to reach the millions of patients in need.”

    Vivoryon is pursuing a unique and highly differentiated approach to AD treatment, with a meticulously designed clinical development strategy. Grounded in the discovery that the enzyme glutaminyl cyclase (QPCT) catalyzes formation of the neurotoxic Abeta variant N3pE- Abeta, a key driver of AD pathology, Vivoryon is pioneering small molecule-based therapies to block this disease pathway. Varoglutamstat is designed to prevent N3pE- Abeta formation, rather than aiming to clear existing plaques, making it an intervention upstream of other approaches such as monoclonal antibodies (mAbs). Through a second mode of action, varoglutamstat also modulates neuroinflammation via the CCL2 pathway, which, in turn, has an impact on tau pathology.

    “We are extremely encouraged by the exceptionally low discontinuation rates in both of our studies,” added Dr. Michael Schaeffer, CBO of Vivoryon. “Vivoryon is acutely focused on lessening the burden of AD for both patients and their families. As we are addressing an elderly patient population, we know how important it is to design a drug that is convenient. These patients typically have to live with and manage many different health conditions at the same time, which heavily impacts their everyday lives. Many feel overwhelmed by the sheer number of medicines they have to take every day and it is therefore our goal to make taking varoglutamstat as easy and convenient as possible. By investigating options to further optimize the formulation of our tablets, we feel that we have the unique chance to facilitate adherence to the correct dosing in our clinical studies and beyond.”



    deel twee volgt
  6. forum rang 4 Kuiken 28 maart 2023 09:19
    Clinical development of varoglutamstat

    Following a meticulously designed clinical development strategy, varoglutamstat was shown to be well-tolerated in both a completed first-in-human Phase 1 study in over 200 participants and the subsequent first-in-patient Phase 2a study, SAPHIR (NCT02389413), which enrolled 120 patients suffering from early AD. Importantly, after only 12 weeks of treatment, this study showed evidence of improving not only pathological hallmarks, but also synaptic function and connectivity, cognition, memory and attention in AD patients, including statistically significant changes from baseline in working memory.

    Building on these encouraging results, Vivoryon based the selection of endpoints for both VIVIAD and VIVA-MIND on the outcome of SAPHIR, as well as on the regulatory draft guidelines for AD drug development introduced by FDA and EMA in 2018. With these two complementary studies, the Company intends to assess if potential cognitive improvements in patients in the European VIVIAD study will translate into an established clinical endpoint in patients in the U.S. VIVA-MIND study.



    VIVIAD: European Phase 2b study in patients with mild cognitive impairment and mild AD

    VIVIAD is a state-of-the-art Phase 2b study being conducted in Europe and designed to evaluate the safety, tolerability and efficacy of varoglutamstat in 250 subjects with mild cognitive impairment (MCI) and mild AD compared to placebo over the course of 48 to 96 weeks of treatment. The highest dose investigated in the study (600 mg twice daily) was selected by an independent Data Safety Monitoring Board (DSMB) as final dose after the dose-escalation portion of the study. Enrollment was completed and the study was adapted to enable longer average treatment duration of participants (anticipated average treatment duration ~82 weeks) in the third quarter of 2022. The primary endpoint is a composite of the Neuropsychological Test Battery (NTB) focusing on changes in working memory and attention with secondary endpoints including multiple cognitive, safety and biomarker assessments.



    Highlights from AD/PD poster titled, VIVIAD, a Phase 2b study investigating varoglutamstat in patients with MCI and mild AD: Update on interim blinded safety results (Poster P0315/#2631)

    As of the data cut-off date of January 5, 2023, over 100 of the 259 participants randomized into the study had been treated for 48 weeks or more
    Varoglutamstat showed no on-target toxicity and no clinical signs of brain swelling or hemorrhages (ARIA), a clearly limiting class side effect of Abeta antibodies
    Overall, varoglutamstat was well tolerated in the study to date, with all of the adverse events (AEs) (except for COVID-19 infections) being gastrointestinal, general, or related to the nervous system or skin. Only 14 serious AEs (SAEs) have been reported
    A low number of treatment emergent adverse events (TEAEs) was observed, only 18% of which were considered to be potentially related to study treatment
    The occurrence of AEs normalized per 100 visits is stable at 31 and as few as 19 participants (6.5%) discontinued the study, with only six (2.3%) discontinuing due to AEs
    Both the total number of SAEs and the discontinuation rate were considerably lower than the respective numbers at the 800 mg BID varoglutamstat dose in Vivoryon’s completed Phase 2a SAPHIR study (15% SAEs, 33% discontinuation), while retaining a similar level of target inhibition at the dosing in both studies
    Data from these participants corroborate the beneficial safety data reported previously for varoglutamstat, with no on-study deaths, no on-target toxicity and no clinical signs of ARIA observed
    A new coding enrichment strategy was applied to ensure that the majority of participants exhibited rescuable deficits in attention and working memory at baseline, enabling reliable assessment of potential cognitive improvement after treatment
    Only five of the 259 participants exhibited normal performance on cognitive tests of the CogState NTB at baseline, demonstrating that the strategy of recruiting individuals with evidence of baseline deficits can be an effective method of enriching a study cohort
    Vivoryon remains on track to report the final data readout from the VIVIAD study in the first quarter of 2024.



    VIVA-MIND: U.S. Phase 2a/b in patients with early AD

    VIVA-MIND is a complementary Phase 2 study being conducted in the U.S., coordinated by the Alzheimer's Disease Cooperative Study (ADCS) at the University of California San Diego (UCSD) School of Medicine and supported by the National Institute on Aging (NIA), part of the National Institutes of Health (NIH) with a $15 million grant (NIA award number R01AG061146). The study seeks to enroll 180 patients into the Phase 2a adaptive dose-finding portion with the Phase 2b portion, enrolling an additional 234 patients treated at the selected dose for at least 72 weeks, with a total of 414 patients being treated on stable doses of varoglutamstat for 18 months. The VIVA-MIND design was adapted in the third quarter of 2022 to enable all 180 patients to be treated for at least 72 weeks, allowing for the opportunity to progress seamlessly to a potential Phase 3 study. The flexible study design is aimed at increasing the probability of success by broadening option space for adjustments in clinical development based on learnings from VIVIAD and other developments in the field. The primary endpoint for this study is clinical dementia rating scale - sum of boxes (CDR-SB), an established approvable endpoint measuring a combination of cognitive abilities and activities of daily living. Secondary efficacy endpoints include quantitative EEG theta power, ADAS-Cog 13 and others. Exploratory endpoints include mini-mental state examination (MMSE), Montreal cognitive assessment (MoCA), quantitative EEG alpha power, relative QPCT activity in CSF and others.

    deel drie volgt
  7. forum rang 4 Kuiken 28 maart 2023 09:20
    Highlighted study updates:

    Study is ongoing and continuing to recruit patients at 18 sites across the U.S. Vivoryon expects the first cohort to be fully randomized into the study within the second quarter of this year
    Focus on overcoming the challenges historically impacting AD drug development with a uniquely designed study, serving as a complementary to VIVIAD and following a specific dosing scheme implemented to investigate the feasibility of an accelerated uptitration regimen
    Objective to reach the 600 mg BID dose, the final dose selected in the VIVIAD study, without requiring slow uptitration to reduce the overall burden on patients and study sites
    The study’s independent Data Safety Monitoring Board (DSMB) has recently provided the unanimous recommendation to continue the study without modification
    Study design allows to potentially transform VIVA-MIND into a Phase 3 study and include further patients beyond the currently planned 414; the decision on actual size will be taken after the readout of the VIVIAD study
    Vivoryon expects to provide the next update on the VIVA-MIND study in the second half of 2023.



    “As a neurologist confronted with the severe impact this devastating disease has on peoples’ lives on a daily basis, I am very pleased to see the progress being made in Vivoryon’s varoglutamstat studies and the hope that this new treatment might offer to patients,” commented Dr. Howard Feldman, Professor of Neurosciences and Director of the ADCS at UC San Diego, and the VIVA-MIND study director. “While there remains much to be done in terms of research and development for safe and effective disease-modifying therapies that are widely available to patients, I believe that varoglutamstat represents a new approach to reducing the pathological events in AD. The complementary studies, VIVIAD and VIVA-MIND, present a strong clinical path forward for varoglutamstat. It is encouraging to see the VIVA-MIND trial receive its most recent DSMB recommendation for the trial to continue forward based on their most recent safety review of March 13, 2023.”
  8. forum rang 10 DeZwarteRidder 28 maart 2023 09:27
    quote:

    Kuiken schreef op 28 maart 2023 09:18:

    Halle (Saale) / Munich, Germany, March 28, 2023 – Vivoryon Therapeutics N.V. (Euronext Amsterdam: VVY; NL00150002Q7) (Vivoryon), a clinical stage company focused on the discovery and development of small molecule medicines to modulate the activity and stability of pathologically altered proteins, today provided an update on both clinical studies of its lead candidate, varoglutamstat, a small molecule medicine in development for the treatment of Alzheimer's disease (AD), VIVA-MIND (NCT03919162) and VIVIAD (NCT04498650). Furthermore, the Company presents updated safety data from its European Phase 2b study, VIVIAD, at the 2023 International Conference on Alzheimer’s and Parkinson’s Diseases and related neurological disorders (AD/PD) in Gothenburg, Sweden.

    “We are pleased to report that both of our ongoing studies are progressing steadily, and we continue to broaden the overall data package for varoglutamstat with consistently positive incremental results,” commented Dr. Ulrich Dauer, CEO of Vivoryon. “Varoglutamstat is strongly positioned as a differentiated oral, outpatient small molecule that has the potential to significantly impact the AD treatment landscape and address ongoing unmet need. Designed to modulate all major hallmarks of AD including Abeta aggregation, neuroinflammation and tau pathology, and also enabling improvement of synaptic function, varoglutamstat captures the key features of a novel drug that has already exhibited a favorable safety profile with no signs of ARIA side effects. We are incredibly encouraged by what we have been able to report to date, and we see a unique opportunity for ultimately realizing the promise of a widely accessible treatment option in AD with the realistic potential to reach the millions of patients in need.”

    Vivoryon is pursuing a unique and highly differentiated approach to AD treatment, with a meticulously designed clinical development strategy. Grounded in the discovery that the enzyme glutaminyl cyclase (QPCT) catalyzes formation of the neurotoxic Abeta variant N3pE- Abeta, a key driver of AD pathology, Vivoryon is pioneering small molecule-based therapies to block this disease pathway. Varoglutamstat is designed to prevent N3pE- Abeta formation, rather than aiming to clear existing plaques, making it an intervention upstream of other approaches such as monoclonal antibodies (mAbs). Through a second mode of action, varoglutamstat also modulates neuroinflammation via the CCL2 pathway, which, in turn, has an impact on tau pathology.

    “We are extremely encouraged by the exceptionally low discontinuation rates in both of our studies,” added Dr. Michael Schaeffer, CBO of Vivoryon. “Vivoryon is acutely focused on lessening the burden of AD for both patients and their families. As we are addressing an elderly patient population, we know how important it is to design a drug that is convenient. These patients typically have to live with and manage many different health conditions at the same time, which heavily impacts their everyday lives. Many feel overwhelmed by the sheer number of medicines they have to take every day and it is therefore our goal to make taking varoglutamstat as easy and convenient as possible. By investigating options to further optimize the formulation of our tablets, we feel that we have the unique chance to facilitate adherence to the correct dosing in our clinical studies and beyond.”
    deel twee volgt
    Veel geschreeuw en weinig wol.
  9. forum rang 4 Kuiken 29 maart 2023 10:15
    quote:

    K. Wiebes schreef op 29 maart 2023 09:04:

    www.biotechnologietage.de/de/programm...
    Een van de drie inleiders daar:

    Dr. Michael Schaeffer
    Vivoryon Therapeutics N. V.
    Michael Schaeffer has been Vivoryon’s Chief Business Officer since October 2018. He has around 20 years of experience across pharma and biotech in strategic business development, scientific project and alliance management.

    Michael Schaeffer is a highly experienced serial entrepreneur and was founder, CEO and Managing Director of the biotech companies CRELUX GmbH and SiREEN AG prior to joining Vivoryon. CRELUX is a world leader in biophysical and structure-based drug discovery services.He was responsible for integrating CRELUX into WuXiAppTec, a leading Shanghai based CRO with over 20,000 employees globally, following the acquisition of CRELUX by WuXiAppTec in 2016.

    Michael Schaeffer received his PhD in Molecular Biology from the Ludwig Maximilians University in Munich, Germany.
  10. forum rang 10 DeZwarteRidder 29 maart 2023 10:17
    quote:

    Kuiken schreef op 29 maart 2023 10:15:

    [...]Een van de drie inleiders daar:

    Dr. Michael Schaeffer
    Vivoryon Therapeutics N. V.
    Michael Schaeffer has been Vivoryon’s Chief Business Officer since October 2018. He has around 20 years of experience across pharma and biotech in strategic business development, scientific project and alliance management.

    Michael Schaeffer is a highly experienced serial entrepreneur and was founder, CEO and Managing Director of the biotech companies CRELUX GmbH and SiREEN AG prior to joining Vivoryon. CRELUX is a world leader in biophysical and structure-based drug discovery services.He was responsible for integrating CRELUX into WuXiAppTec, a leading Shanghai based CRO with over 20,000 employees globally, following the acquisition of CRELUX by WuXiAppTec in 2016.

    Michael Schaeffer received his PhD in Molecular Biology from the Ludwig Maximilians University in Munich, Germany.
    Allemaal gebakken lucht........!!!
6.265 Posts
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