On September 10, 2021 Kazia Therapeutics Limited (NASDAQ: KZIA; ASX: KZA), an oncology-focused drug development company, reported that CEO, Dr James Garner, will be presenting at the HC Wainwright 23rd Annual Global Investment Conference, to be held virtually from 13-15 September 2021 (Press release, Kazia Therapeutics, SEP 10, 2021, https://www.prnewswire.com/news-releases/kazia-therapeutics-to-present-at-hc-wainwright-23rd-annual-global-investment-conference-301373181.html [SID1234587563]).

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The HC Wainwright Annual Global Investment Conference is one of the key events in the investor calendar and Kazia’s participation comes at an important time for the company. Kazia’s lead program, paxalisib, is currently in a pivotal study for glioblastoma, the most common and most aggressive form of brain cancer. If successful, paxalisib has the potential to become the first new drug treatment for newly diagnosed patients in almost twenty years, addressing a market worth US$ 1.5 billion per annum. More than 12,500 patients are diagnosed with glioblastoma each year, and the current standard of care treatment, temozolomide, is ineffective for approximately two-thirds of cases.

Dr Garner will provide an overview of Kazia’s key developments during FY2021, including:

Commencement of the GBM AGILE pivotal study for paxalisib in January 2021;
Out-licensing deal with Simcere Pharmaceutical for Greater China rights to paxalisib in March 2021, realizing an US$11 million upfront consideration;
Transformative in-licensing of EVT801 from Evotec, providing the company with a highly attractive second oncology asset.
Dr Garner will also share insights on Kazia’s objectives for FY2022 and outline the rich suite of catalysts that the company expects to announce during the remainder of CY2021.

This year’s HC Wainwright Annual Global Investment Conference will be conducted virtually from Monday 13th to Wednesday 15th and will feature more than 850 presenting companies, as well as a keynote presentation from Dr Scott Gottleib, former commissioner of the FDA.

Dr Garner commented, "Kazia’s presentation will be available to attendees on-demand, while the company will also meet individually with key investors and analysts over the duration of the conference to further advocate on behalf of the company’s compelling story."

On September 10, 2021 BioEclipse Therapeutics, a clinical-stage immuno-oncology company focused on developing innovative therapeutics based on its patented natural killer T-cell (NKT)/oncolytic virus technology platform, reported that Pamela Reilly Contag, Ph.D., Founder and CEO, will present at the H.C. Wainwright Annual Global Healthcare Conference taking place virtually September 13-15, 2021 (Press release, BioEclipse Therapeutics, SEP 10, 2021, View Source [SID1234587562]). The prerecorded presentation will be available online starting at 7 a.m. ET on September 13, 2021 and can be accessed via the conference’s virtual platform by registered conference attendees.

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Dr. Contag and members of the BioEclipse management team are also hosting one-on-one meetings with registered investors and biopharmaceutical industry executives.

During her presentation, Dr. Contag will provide an overview of BioEclipse’s business and highlight the company’s proprietary technology platform and the role it plays in the development of a new class of immune therapeutics. These therapies pair the tumor-locating ability of cytokine-induced killer (CIK) cells with the power of an oncolytic virus that selectively infects and kills malignant cells to create a multi-modal therapy that overcomes the limitations that have previously hobbled the efficacy of cellular and oncolytic viral therapies.

Details of the presentation are as follows:

Event:

H.C. Wainwright Annual Global Healthcare Conference

Date:

September 13-15, 2021

Time:

Presentation available online beginning at 7 a.m. ET, September 13, 2021

Registration:

View Source

On September 10, 2021 NexImmune, Inc. (Nasdaq: NEXI), a clinical-stage biotechnology company developing a novel approach to immunotherapy designed to orchestrate a targeted immune response by directing the function of antigen-specific T cells, reported that Scott Carmer, Chief Executive Officer, will participate in a fireside chat during the Morgan Stanley 19th Annual Global Healthcare Conference today, September 10, 2021 at 1:15p.m. Eastern time.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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The webcast will be accessible on the Investor Relations page of NexImmune’s website at Events and Presentations | NexImmune, Inc. A replay of the presentation will be available at the same location for 30 days following the conference.

On September 10, 2021 Y-mAbs Therapeutics, Inc. (the "Company" or "Y-mAbs") (Nasdaq: YMAB) a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, antibody-based therapeutic products for the treatment of cancer, reported that it will host a key opinion leader ("KOL") webinar on DANYELZA frontline and HITS data in high-risk neuroblastoma on Thursday, September 23, 2021 at 12 p.m. ET (Press release, Y-mAbs Therapeutics, SEP 10, 2021, View Source [SID1234587547]).

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This webinar will feature presentations from KOLs Jaume Mora, M.D., Ph.D., SJD Barcelona Children’s Hospital, and Shakeel Modak, M.D., MRCP, Memorial Sloan Kettering. Additionally, Thomas Gad, Chairman, Founder, and President at Y-mAbs, will provide a brief introduction followed by presentations from Steen Lisby, M.D., DMSc, SVP, Chief Scientific Officer at Y-mAbs, and Claus J. Moller San-Pedro, M.D., Ph.D., Chief Executive Officer at Y-mAbs.

Dr. Mora will present frontline data for DANYELZA in High-Risk Neuroblastoma
Dr. Modak will present HITS data for DANYELZA in High-Risk Neuroblastoma
Dr. Lisby will review Y-mAbs’ preclinical and research pipeline including its SADA technology
Dr. Moller will provide a corporate update
Thomas Gad as well as Drs. Modak, Mora, Lisby, and Moller will be available for questions following the presentations.

To register for the event, please click here.

Shakeel Modak, M.D., MRCP is a pediatric hematology-oncology doctor at Memorial Sloan Kettering Cancer Center, Department of Pediatrics in New York. He received his MBBS and M.D. degrees from TN Medical College, Bombay, as well as his MRCP degree from Royal College of Physicians, London. Dr. Modak specializes in the treatment of children and young adults with neuroblastoma and other solid tumors, such as DSRCT. He has been named to Best Doctors, New York City by Castle Connolly for the past six years in a row and in 2014. Dr. Modak has been the principal investigator on more than 12 studies in neuroblastoma and DSRCT. He has also been the co-investigator on over 50 trial protocols.

Jaume Mora, M.D., Ph.D. is the scientific director of the Oncology and Hematology area at SJD Barcelona Children’s Hospital, as well as the director of the Developmental Tumors Laboratory at SJD Barcelona Children’s Hospital. Dr. Mora is a member of several; national and international scientific societies, including the International Pediatric Oncology Society, which has awarded him the Schweisguth Prize, and the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) ("ASCO"), which honored him with the young investigator award ("YIA") in 2000, as well as the Career Development Award ("CDA"). In 2011, Dr. Mora was the recipient of the annual BBVA Foundation Award and, in 2006, of the First Prize of the Spanish Association Against Cancer ("AECC") award for the study of childhood cancer.

About DANYELZA (naxitamab-gqgk)

DANYELZA (naxitamab-gqgk) is indicated, in combination with granulocyte-macrophage colony-stimulating factor ("GM-CSF"), for the treatment of pediatric patients one year of age and older and adult patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow who have demonstrated a partial response, minor response, or stable disease to prior therapy. This indication was approved by the FDA under accelerated approval based on overall response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefits in a confirmatory trial. DANYELZA includes a Boxed Warning for serious infusion-related reactions, such as cardiac arrest and anaphylaxis, and neurotoxicity, such as severe neuropathic pain and transverse myelitis. See full Prescribing Information for complete Boxed Warning and other important safety information.

On September 10, 2021 VBL Therapeutics (NASDAQ: VBLT) reported the Company will present in the following upcoming industry conferences (Press release, VBL Therapeutics, SEP 10, 2021, View Source [SID1234587546]):

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H.C. Wainwright 23rd Annual Global Investment Conference
Mon., Sept. 13, 2021
Fireside chat available on-demand beginning at 7:00 a.m. ET

Cell & Gene Therapy World Asia 2021 conference
Wed., Sept. 15, 2021
Presentation Time: 4:45 PM (SGT)
Keynote Presentation Topic: VB-111: Transformative Gene therapy with the Potential to Change the Treatment Paradigm for Solid Tumors

Oppenheimer Fall Healthcare Life Sciences & MedTech Summit
Wed., Sept. 22, 2021
Fireside chat at 1:15 PM – 1:55 PM (ET).

Webcasts will be available via the Events and Presentations section of the Company’s Investor Relations page.