Van beleggers
voor beleggers
desktop iconMarkt Monitor
  • Word abonnee
  • Inloggen

    Inloggen

    • Geen account? Registreren

    Wachtwoord vergeten?

Ontvang nu dagelijks onze kooptips!

word abonnee

Heeft CytoDyn het ultieme anti-HIV-middel??

1.071 Posts
Pagina: «« 1 ... 41 42 43 44 45 ... 54 »» | Laatste | Omlaag ↓
  1. Dappie 11 november 2020 16:59

    CytoDyn Completes Second Non-dilutive $28.5 Million Convertible Note Financing with Conversion Rate at $10.00 Per Share Without Warrants to Help Expedite License Applications Here and Abroad and Successful COVID-19 Trials

    November 11, 2020 6:00am EST

    VANCOUVER, Washington, Nov. 11, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing leronlimab (PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it completed an additional non-dilutive convertible debt offering with an institutional investor, which provides $25 million of immediately available capital. The note has a two-year maturity, bears interest at the rate of 10% per annum and is secured by all assets of the Company, excluding its intellectual property. The note may be converted at the option of the investor into shares of the Company’s common stock at a conversion price of $10.00 per share.

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, stated, “We are very pleased with the institution’s demonstration of confidence and their understanding of leronlimab’s positioning on its regulatory trajectory. This infusion of capital will enable us to accelerate efforts to file BLAs in Canada and the U.K. for leronlimab as a combination therapy for HIV patients with one dose (one 350 mg subcutaneous injection) per week. We continue to expedite enrollment in CD12 (currently at 260 patients), in addition to now accelerating a COVID-19 trial for long-hauler patients, who have no alternative therapy and are rapidly emerging as a widespread health concern. We are well-positioned to supply $2 billion worth of leronlimab to treat COVID-19, if emergency use authorization is approved in the next 2-4 months based on anticipated successful CD12 results.”
  2. forum rang 5 MisterBlues 11 november 2020 17:04
    quote:

    Dappie schreef op 11 november 2020 16:59:

    CytoDyn Completes Second Non-dilutive $28.5 Million Convertible Note Financing with Conversion Rate at $10.00 Per Share Without Warrants to Help Expedite License Applications Here and Abroad and Successful COVID-19 Trials

    November 11, 2020 6:00am EST

    VANCOUVER, Washington, Nov. 11, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing leronlimab (PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it completed an additional non-dilutive convertible debt offering with an institutional investor, which provides $25 million of immediately available capital. The note has a two-year maturity, bears interest at the rate of 10% per annum and is secured by all assets of the Company, excluding its intellectual property. The note may be converted at the option of the investor into shares of the Company’s common stock at a conversion price of $10.00 per share.

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, stated, “We are very pleased with the institution’s demonstration of confidence and their understanding of leronlimab’s positioning on its regulatory trajectory. This infusion of capital will enable us to accelerate efforts to file BLAs in Canada and the U.K. for leronlimab as a combination therapy for HIV patients with one dose (one 350 mg subcutaneous injection) per week. We continue to expedite enrollment in CD12 (currently at 260 patients), in addition to now accelerating a COVID-19 trial for long-hauler patients, who have no alternative therapy and are rapidly emerging as a widespread health concern. We are well-positioned to supply $2 billion worth of leronlimab to treat COVID-19, if emergency use authorization is approved in the next 2-4 months based on anticipated successful CD12 results.”
    Waarmee nog maar eens bewezen is dat Cydy niet op sterven na dood ligt als het om de financiën gaat.

    Close call, dat wel, maar met de HIV BLA succesjes en de verdere inspanningen hieromtrent en CD12 dat nog steeds kan slagen en relevant is zou het allemaal nog wel eens mee kunnen vallen.
  3. forum rang 5 MisterBlues 16 november 2020 13:46
    quote:

    Sub!et schreef op 15 november 2020 12:18:

    Stand van zaken mbt Cydy :

    Is There A Light At The End Of The Tunnel For A COVID-19 Therapeutic?

    talkmarkets.com/content/stocks--equit...
    Hartelijk dank. Goed artikel. Vandaag weer PB's die de titel onderschrijven.

    Health Canada Clears CytoDyn to File its BLA for Leronlimab as One Injection per Week for Combination HIV Therapy

    November 16, 2020 6:00am EST

    VANCOUVER, Washington, Nov. 16, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing leronlimab (PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today Health Canada has cleared CytoDyn to file its Biologics License Application (BLA) for leronlimab as a combination therapy for multi-drug resistance HIV patients in Canada.

    Health Canada’s clearance for the BLA filing includes a treatment regimen of one injection per week of 350 mg of the Company’s product leronlimab, as contrasted to the dosage used in the Phase 3 clinical trial conducted in the U.S. for this indication of two consecutive injections of 175 mg per week. Health Canada, a department of the Government of Canada, is responsible for Canada’s federal health policy and oversees the Public Health Agency of Canada. Health Canada’s team conducted a two-hour meeting with CytoDyn's team and were also updated on the progress of the Company’s COVID-19 trials and BLA application for the U.K. CytoDyn’s presentation team to Health Canada included Drs. Thomas Boyd, Nitya Ray and Kush Dhody for pre-clinical, manufacturing and clinical sections, respectively, of the application.

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, commented, “We are very pleased with Health Canada’s decision to clear our BLA for filing and our team is motivated to submit this filing in the very near future. Health Canada’s decision continues to validate the opportunity for leronlimab as a treatment for HIV patients around the world. Our lengthy meeting included an update on the progress of our COVID-19 trials and plans to simultaneously file our BLA for leronlimab as a combination therapy for HIV with the MHRA in the U.K. and Health Canada.”
  4. forum rang 5 MisterBlues 16 november 2020 13:51
    CytoDyn Announces Registration of Trademark for VYROLOGIX in Several Countries

    November 16, 2020 6:05am EST

    Vyrologix is the proprietary name for leronlimab

    VANCOUVER, Washington, Nov. 16, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing leronlimab (PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, today announced that nine of the Company’s trademark applications to register the VYROLOGIX mark have now successfully passed through formal examination.

    In summary, the U.S. and E.U. applications have been allowed, applications in Hong Kong, China and Russia have registered, and the Company’s applications in Australia, Israel, New Zealand and Singapore will each proceed to registration once they have passed through the opposition period unopposed.

    Vyrologix (pronounced - vie-ro-loj-iks) is the proprietary name for leronlimab and the trademark is now VYROLOGIX. Final approval of Vyrologix as the proprietary name for leronlimab is conditional on FDA approval of the Company’s Biologics License Application and new drug application. Our recently developed stylized trademark and logo are as follows:

    A Media Snippet accompanying this announcement is available by clicking on the image or link below:

    CytoDyn Inc.: Media Snippet

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, stated, “These multi-national acceptances of our trademark applications further demonstrate our commercial readiness to deliver leronlimab to patients of the world upon regulatory approval. Our team of legal advisors have been working on this important milestone for several months and we have now achieved one of many objectives in several major markets.”

    About Coronavirus Disease 2019


    CytoDyn completed its Phase 2 clinical trial (CD10) for COVID-19, a double-blinded, randomized clinical trial for mild-to-moderate patients in the U.S. which produced statistically significant results for NEWS2. Enrollment continues in its Phase 2b/3 randomized clinical trial for the severe-to-critically ill COVID-19 population in several hospitals and clinics throughout the U.S., which are identified on the Company’s website under the “Clinical Trial Enrollment” section of the homepage; an interim analysis on the first 195 patients was conducted mid-October and is expected to occur again after enrollment reaches 293 patients.

    About Leronlimab (PRO 140)
    The FDA has granted a Fast Track designation to CytoDyn for two potential indications of leronlimab for critical illnesses. The first indication is a combination therapy with HAART for HIV-infected patients and the second is for metastatic triple-negative breast cancer. Leronlimab is an investigational humanized IgG4 mAb that blocks CCR5, a cellular receptor that is important in HIV infection, tumor metastases, and other diseases, including NASH. Leronlimab has completed nine clinical trials in over 800 people and met its primary endpoints in a pivotal Phase 3 trial (leronlimab in combination with standard antiretroviral therapies in HIV-infected treatment-experienced patients).

    In the setting of HIV/AIDS, leronlimab is a viral-entry inhibitor; it masks CCR5, thus protecting healthy T cells from viral infection by blocking the predominant HIV (R5) subtype from entering those cells. Leronlimab has been the subject of nine clinical trials, each of which demonstrated that leronlimab could significantly reduce or control HIV viral load in humans. The leronlimab antibody appears to be a powerful antiviral agent leading to potentially fewer side effects and less frequent dosing requirements compared with daily drug therapies currently in use.

    In the setting of cancer, research has shown that CCR5 may play a role in tumor invasion, metastases, and tumor microenvironment control. Increased CCR5 expression is an indicator of disease status in several cancers. Published studies have shown that blocking CCR5 can reduce tumor metastases in laboratory and animal models of aggressive breast and prostate cancer. Leronlimab reduced human breast cancer metastasis by more than 98% in a murine xenograft model. CytoDyn is, therefore, conducting a Phase 1b/2 human clinical trial in metastatic triple-negative breast cancer and was granted Fast Track designation in May 2019.

    The CCR5 receptor appears to play a central role in modulating immune cell trafficking to sites of inflammation. It may be crucial in the development of acute graft-versus-host disease (GvHD) and other inflammatory conditions. Clinical studies by others further support the concept that blocking CCR5 using a chemical inhibitor can reduce the clinical impact of acute GvHD without significantly affecting the engraftment of transplanted bone marrow stem cells. CytoDyn is currently conducting a Phase 2 clinical study with leronlimab to support further the concept that the CCR5 receptor on engrafted cells is critical for the development of acute GvHD, blocking the CCR5 receptor from recognizing specific immune signaling molecules is a viable approach to mitigating acute GvHD. The FDA has granted orphan drug designation to leronlimab for the prevention of GvHD.
  5. forum rang 5 MisterBlues 17 november 2020 15:07
    CytoDyn Files Protocol with U.S. FDA for Phase 2 Clinical Trial for COVID-19 Patients with Long-Hauler Symptoms

    November 17, 2020 9:00am EST

    Rapid Enrollment Expected, As Many People Have Already Volunteered

    VANCOUVER, Washington, Nov. 17, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing leronlimab (PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it has filed a protocol with the U.S. Food and Drug Administration (FDA) for a Phase 2 clinical trial for leronlimab as a treatment for COVID-19 patients suffering from long-hauler symptoms.

    According to a recent article from The Journal of the American Medical Association and a study done by British scientists, researchers estimate about 10% of COVID-19 patients become long-haulers. Published studies and surveys conducted by patient groups indicate 50% to 80% of patients continue to have troublesome symptoms three months after the onset of COVID-19 — even after tests no longer detect virus in their body. The list of long-hauler symptoms is extensive and inconsistent. For some people, the lingering symptoms are nothing like the original symptoms when they were first infected with COVID-19. The most common long-hauler symptoms include:

    Coughing
    Ongoing, sometimes debilitating, fatigue
    Body aches
    Joint pain
    Heart issues
    Shortness of breath
    Loss of taste and smell
    Difficulty sleeping
    Headaches
    Brain fog

    CytoDyn’s protocol for its Phase 2 COVID-19 long-haulers trial is entitled: ”A Randomized, Double Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of Leronlimab in Patients Experiencing Prolonged Coronavirus Disease 2019 (COVID-19) Symptoms [Long-Haulers].” The planned number of patients is 102 to be enrolled in up to 10 sites. The study will have an interim analysis after half of the patients are enrolled and will allow CytoDyn to report the results.
  6. forum rang 5 MisterBlues 18 november 2020 13:01
    quote:

    Sub!et schreef op 17 november 2020 20:20:

    17 nov 20
    Korte Proactive video met op het einde wat over de $ (kas) van CYDY

    www.youtube.com/watch?v=a7FdFnCpAc0
    Dank.\

    Als de CCR5 receptor / LL wordt goedgekeurd voor HIV - monotherapie is het allemaal futiel: de geldproblemen, CD12.

    Ik hoop dat het BLA team's werk snel vordert: Receptor > Tropism > Mono
  7. forum rang 5 MisterBlues 23 november 2020 15:03
    CytoDyn Reaches Enrollment Target of 293 Patients for 2nd DSMC Interim Analysis of Phase 3 COVID-19 Trial
    and Expects to Enroll the Remaining 97 Patients in the Next Few Weeks to Complete the Trial This Year

    November 23, 2020 6:00am EST

    Concurrently, CytoDyn is working diligently with the FDA to initiate its Phase 2 COVID-19 Long Hauler Trial, with more than 100 volunteers wanting to enroll

    VANCOUVER, Washington, Nov. 23, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing Vyrologix™ (leronlimab-PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it has reached enrollment of 293 patients in its Phase 3 trial for COVID-19 patients with severe-to-critical symptoms, thereby meeting the requested criteria for a second interim efficacy analysis by the Data Safety Monitoring Committee (DSMC).

    After the first interim analysis, the DSMC requested a second interim analysis of all data after enrollment had reached 293 patients or 75% of the total patients for the trial. Approximately five weeks ago, the DSMC completed the first interim analysis on 195 patients (or 50% of the 390 planned patients) and recommended the trial continue without modification to achieve the primary endpoint and requested another interim analysis when enrollment reached 75% level (or 293 patients) to review patient mortality and other clinical outcome data.

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, commented, “In addition to filing our biologics license applications in Canada and the U.K. for HIV, the Company is in full swing to obtain full enrollment in the Phase 3 COVID-19 trial before year end and initiate our Phase 2 trial for COVID-19 patients with multiple long-hauler symptoms and perhaps complete enrollment in 4-6 weeks. On another front, CytoDyn is also about to enroll its first patient in the NASH trial this month. We are very appreciative of the all-out effort by our clinical operations team (especially Mr. Brian Brothen, the Company’s SVP of Global Oncology, and Dr. Kush Dhody from Amarex) and the clinical sites to expedite enrollment in this important trial and are hopeful the DSMC can complete their second interim analysis as quickly as possible. We continue to advance enrollment, without any pause to achieve the trial’s planned 390 patients and we are currently evaluating the ability to conduct an interim analysis as soon as possible. In the meantime, if the pace of enrollment we have experienced in the last two weeks continues, we will have the CD12 enrollment completed before the end of the year. These are exciting times for the Company and I am honored to be working alongside such dedicated co-workers.”
  8. forum rang 5 MisterBlues 23 november 2020 15:30
    Dit is precies wat er speelt met CD12 /S&C:

    clinicaltrials.gov/ct2/history/NCT043...

    Primary Outcome Measures: All-cause mortality at Day 28

    Secondary Outcome Measures: All-cause mortality at Day 14

    Ideally FDA and DMSC would get already unblinded data from Day 14. Anyaway - if day 28 shows what we hope, the FDA has no time to lose. The pressure on FDA would be enourmous. But FDA is aware of such situation and I am sure, FDA has staff allocated to leronlimab and managers are alerted about these timelines. So far NO drug has shown a reduced mortality in their phase II or Phase III randomised trials.

    A reduction of mortality would be a huge breakthrough in fighting most severe consequences of this pandemic. Any size of reduction of mortality (as long as statistically significant) could be directly translated to a number of death every day. 20 % of 1000 is 200 people, 40.... you know...

    FDA would have approve it within 1 max 2 days. And they would, because first they have followed (neither the trials, data or mechanism would new new for FDA) and secondly they could not stand the pressure from media and public to grant EUA and to give access to hospitals, doctors and patients.
    Based on average of 2 patients per day, I was expecting the enrollment to conclude at the end of November. But as of news today we completed it a week early. That gives us a great opportunity to accelerate the interim analysis and recieve it around the first week of January,2021. If we are are able to complete the 14 days analysis that NP pushing for, then we will be done with it by December 7, 2020. Exciting times.

    Just like the S/C, CytoDyn said 340. The FDA only increased it by 53, to 393.
    Now we see Leron proving as last resort effort @ minimum and 80-85% success in the pre-trial data.
    Safe, & "trending", is what the OWS & FDA will now see @ 293.
    We will get EUA and monitored out to 28/42 days.
    Just as i had/have, blabbled here since the Nov. 5th CC, 29 minute mark ---- " 14 day opportunity ", comment from Nader.
  9. Dappie 24 november 2020 00:15
    Vyrologix™ (leronlimab) has successfully replicated the CCR5 deficient phenotype in a pre-clinical animal study, and will now initiate HIV cure-focused clinical studies in collaboration with amfAR

    VANCOUVER, Washington, Nov. 23, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing Vyrologix (leronlimab-PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it signed an agreement with amfAR, The Foundation for AIDS Research (www.amfar.org), to test the ability of Vyrologix (leronlimab) to mediate a functional HIV cure. The international organization, amfAR, plays a vital role in AIDS research by identifying critical gaps in the knowledge of HIV and AIDS and supporting groundbreaking studies.

    In 2007, Timothy Brown, also known as the “Berlin patient,” became the first documented person cured of HIV following a stem cell transplant from a CCR5-deficient donor. Subsequent attempts to cure HIV via stem cell transplant from donors expressing CCR5 failed, indicating the critical role of CCR5 deficiency in HIV cure. Last year, Adam Castillejo, formerly the “London patient,” became the second documented case of HIV cure after a stem cell transplant from a CCR5-deficient donor. While it is now recognized that CCR5 is central to these two documented cases of HIV cure, natural CCR5-deficient individuals are rare and finding such donors is extremely difficult. Recently, Vyrologix (leronlimab) successfully protected macaques from retroviral infection, mirroring the protection from HIV seen in CCR5 deficient individuals. CytoDyn’s partnership with amfAR will advance clinical studies to incorporate Vyrologix to mimic a CCR5-deficient stem cell donor and attempt to functionally cure an HIV+ person receiving a stem cell transplant from a donor expressing CCR5.

    “Using leronlimab to pharmacologically copy a CCR5-deficient donor for HIV cure is an exciting next step in our journey towards a cure for the 38 million people living with HIV,” stated Kevin Robert Frost, Chief Executive Officer at amfAR. “While a stem cell transplant is unlikely to be rolled out as an HIV cure, demonstrating that leronlimab can functionally phenocopy CCR5 deficiency and replicate the London and Berlin patients would be a major advancement.” As part of the agreement, CytoDyn will provide leronlimab and study support, while amfAR will support groundbreaking study sites to incorporate leronlimab in their cure studies.

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, commented, “We are honored to be in partnership with amfAR and the opportunities to accelerate a search for an HIV cure using this scientific premise. Timothy Brown’s cure ignited hope that a cure can happen through bone marrow transplant from the rare individuals with a delta-32 mutation. The success in our animal studies for HIV with Vyrologix (leronlimab) has provided this opportunity. We are very excited to be supporting this project, and to be a part of this groundbreaking endeavor with amfAR.”
  10. Dappie 24 november 2020 00:29
    Ook nieuwe proactieve video.
    Lijkt er op dat Dsmc de 42 dagen na 75% afwacht om interim analyse te doen, en Men voor die tijd tot full enrollment wil komen, waarbij data direct aan UK en Canada voorgelegd zullen worden.
    FDA neemt nog steeds zijn tijd met CYDY, veel meer dan bij BP
    www.youtube.com/watch?v=i98QF1HNXCE
  11. forum rang 5 MisterBlues 24 november 2020 12:15
    quote:

    Dappie schreef op 24 november 2020 00:15:

    Vyrologix™ (leronlimab) has successfully replicated the CCR5 deficient phenotype in a pre-clinical animal study, and will now initiate HIV cure-focused clinical studies in collaboration with amfAR

    VANCOUVER, Washington, Nov. 23, 2020 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTC.QB: CYDY), (“CytoDyn” or the “Company"), a late-stage biotechnology company developing Vyrologix (leronlimab-PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications, announced today it signed an agreement with amfAR, The Foundation for AIDS Research (www.amfar.org), to test the ability of Vyrologix (leronlimab) to mediate a functional HIV cure. The international organization, amfAR, plays a vital role in AIDS research by identifying critical gaps in the knowledge of HIV and AIDS and supporting groundbreaking studies.

    In 2007, Timothy Brown, also known as the “Berlin patient,” became the first documented person cured of HIV following a stem cell transplant from a CCR5-deficient donor. Subsequent attempts to cure HIV via stem cell transplant from donors expressing CCR5 failed, indicating the critical role of CCR5 deficiency in HIV cure. Last year, Adam Castillejo, formerly the “London patient,” became the second documented case of HIV cure after a stem cell transplant from a CCR5-deficient donor. While it is now recognized that CCR5 is central to these two documented cases of HIV cure, natural CCR5-deficient individuals are rare and finding such donors is extremely difficult. Recently, Vyrologix (leronlimab) successfully protected macaques from retroviral infection, mirroring the protection from HIV seen in CCR5 deficient individuals. CytoDyn’s partnership with amfAR will advance clinical studies to incorporate Vyrologix to mimic a CCR5-deficient stem cell donor and attempt to functionally cure an HIV+ person receiving a stem cell transplant from a donor expressing CCR5.

    “Using leronlimab to pharmacologically copy a CCR5-deficient donor for HIV cure is an exciting next step in our journey towards a cure for the 38 million people living with HIV,” stated Kevin Robert Frost, Chief Executive Officer at amfAR. “While a stem cell transplant is unlikely to be rolled out as an HIV cure, demonstrating that leronlimab can functionally phenocopy CCR5 deficiency and replicate the London and Berlin patients would be a major advancement.” As part of the agreement, CytoDyn will provide leronlimab and study support, while amfAR will support groundbreaking study sites to incorporate leronlimab in their cure studies.

    Nader Pourhassan, Ph.D., President and Chief Executive Officer of CytoDyn, commented, “We are honored to be in partnership with amfAR and the opportunities to accelerate a search for an HIV cure using this scientific premise. Timothy Brown’s cure ignited hope that a cure can happen through bone marrow transplant from the rare individuals with a delta-32 mutation. The success in our animal studies for HIV with Vyrologix (leronlimab) has provided this opportunity. We are very excited to be supporting this project, and to be a part of this groundbreaking endeavor with amfAR.”
    Erg blij dat ze goed op HIV zitten nu. Hoop dat het partnerschap met amfAR idd die versnelling oplevert richting de HIV therapie. Daar zit de meeste potentie en zijn ze het verst.

    Nu nog de BLA en de FDA...

    Hier een goede beschrijving van wat er speelt rond HIV en Cydy en de partner:

    Aug. 17th, 2020: CytoDyn Will Attempt to Duplicate Berlin and London Patients’ HIV Cure by Using Leronlimab During Bone Marrow Transplant for 5 HIV Patients Who also have Cancer

    " CytoDyn believes its CCR5 blocking antibody, leronlimab, could be used in the setting of allogeneic stem cell transplantation to functionally convert a stem cell graft from a wildtype CCR5 stem cell donor into one from a CCR5 deficient donor, and thereby functionally cure the recipient of HIV".

    " CytoDyn believes leronlimab could be a once-a-month self-injectable, subcutaneous treatment for HIV PrEP and is in discussions with potential organizations to fund its next trial in HIV PrEP".

    " Our fourth path is an HIV-Cure, where 5 patients will be put to test to duplicate the Berlin and London patients’ HIV functional cure.”

    Nov. 23, 2020:
    " CytoDyn’s partnership with amfAR will advance clinical studies to incorporate Vyrologix to mimic a CCR5-deficient stem cell donor and attempt to functionally cure an HIV+ person receiving a stem cell transplant from a donor expressing CCR5".

    “Using leronlimab to pharmacologically copy a CCR5-deficient donor for HIV cure is an exciting next step in our journey towards a cure for the 38 million people living with HIV,” stated Kevin Robert Frost, Chief Executive Officer at amfAR".

    wow --- *** and thereby functionally cure the recipient of HIV ***

    This took alot of impressive data to get this organization to place Leronlimab into it's HIV sites and
    praise it like they did today.

    There you have it -- Leron is taking center stage see if she can also Cure through world-known amfAR.
  12. Sub!et 24 november 2020 13:03
    Vertaald uit het Engels-

    amfAR,

    de Stichting voor AIDS-onderzoek, tot 2005 bekend als de Amerikaanse Stichting voor AIDS-onderzoek, is een internationale non-profitorganisatie die zich inzet voor de ondersteuning van AIDS-onderzoek, HIV-preventie, behandelingseducatie en de pleitbezorging van AIDS-gerelateerd openbaar beleid.
  13. forum rang 5 MisterBlues 24 november 2020 13:24
    quote:

    Sub!et schreef op 24 november 2020 13:03:

    Vertaald uit het Engels-

    amfAR,

    de Stichting voor AIDS-onderzoek, tot 2005 bekend als de Amerikaanse Stichting voor AIDS-onderzoek, is een internationale non-profitorganisatie die zich inzet voor de ondersteuning van AIDS-onderzoek, HIV-preventie, behandelingseducatie en de pleitbezorging van AIDS-gerelateerd openbaar beleid.
    Is this the connection... NEW YORK, Nov. 16, 2020 --- amfAR, The Foundation for AIDS Research, has awarded funding to researchers exploring an HIV cure approach that has previously shown promise in cancer therapy.

    The only known cases of HIV cure to date occurred in people living with HIV—the Berlin and London patients—whose blood cancer was treated with a stem cell transplant. Both received stem cells from donors with a genetic mutation that left them with no functional CCR5 protein—the main gateway that enables most types of HIV to enter and infect cells...... www.amfar.org/Next-Generation-HIV-Cur...
  14. forum rang 5 MisterBlues 24 november 2020 21:01
    Oct. company Presentation, page 8: HIV - Cure

    5 patients/Timothy Brown model – Phase 2 – This trial is currently searching for
    potential HIV patient who is in need of bone marrow transplant similar to
    Timothy Brown. If leronlimab can mimic the delta-32 during a bone marrow
    transplant by covering all the CCR5 receptor, then the result could be a cure.
    First patient injection could be 2020 or early 2021.

    2 things;
    1) CytoDyn's Science Advisor was Mr. Browns doctor & now amfAR is on the scene.
    2) CytoDyn said Leron binds 100%

    Also, yesterday he reminded they are dosing the 1st NASH, this month.

    Page 14: First patient enrollment expected November 2020

    “CCR5 plays a central role in all the events related to liver matrix remodeling and it has been observed that patients with chronic liver disease present high levels of CCR5 and CCL5.”

    “Our result suggests that in early NASH, HSCs secrete Ccl5 which contributes to a broad array of mechanisms by which hepatic steatosis and inflammation are achieved.”

    “Our data indicate that chemokine (C-C motif) ligand 5 (Ccl5, a.k.a. Rantes) is one of the HSC-secreted mediators in NASH that directly induce steatosis and pro-inflammatory factors in initially healthy hepatocytes.”

    From Dr. Ken Sherman: "It is possible that someday all patients with HIV may be treated with a blocking agent as part of their HIV drug cocktail designed to protect the liver and regain and maintain liver health," Dr. Ken Sherman suggests.
  15. forum rang 5 MisterBlues 25 november 2020 11:17
    From Mel’s wiki page link to amfAR: “Under the Countdown to a Cure for AIDS, amfAR hosts an annual HIV Cure Summit, which aims to hear from voices in the research community on breakthroughs, as well as discuss discoveries that have motivated AIDS research, such as the breakthrough with the Berlin patient, who spurred the countdown in the first place.[56][60] In November 2020, amfAR signed an agreement with CytoDyn Inc. to explore the potential of its CCR-5 antagonist Vyrologix (Leronlimab) to mediate a functional HIV cure. According to Kevin Robert Frost, Chief Executive Officer at amfAR, ‘demonstrating that Leronlimab can functionally phenocopy CCR5 deficiency and replicate the London and Berlin patients would be a major advancement.’”

    Next HIV Summit will be awesome!
1.071 Posts
Pagina: «« 1 ... 41 42 43 44 45 ... 54 »» | Laatste |Omhoog ↑

Meedoen aan de discussie?

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

Direct naar Forum

Indices

AEX 874,20 +0,89%
EUR/USD 1,0662 +0,09%
FTSE 100 8.048,27 +0,30%
Germany40^ 18.022,20 +0,90%
Gold spot 2.299,27 -1,20%
NY-Nasdaq Composite 15.451,31 +1,11%

Stijgers

VIVORY...
+25,26%
ALLFUN...
+4,20%
PROSUS
+3,74%
JUST E...
+3,32%
Philip...
+2,22%

Dalers

RANDST...
-5,90%
Akzo N...
-5,14%
NSI
-3,34%
AMG Cr...
-1,79%
Alfen ...
-1,65%

Lees verder op het IEX netwerk Let op: Artikelen linken naar andere sites

Gesponsorde links