Search This Blog

Monday, October 17, 2022

Tivic Health to Acquire Assets of Reliefband

 Company Intends to Dramatically Expand Product Offerings into Bioelectronic Treatment of Nausea

CEO to Host Investor Call/Webcast on Wednesday, October 19th at 1:30 PM PT / 4:30 PM ET

Tivic Health® Systems, Inc. (Nasdaq: TIVC) ("Tivic Health"), a commercial-phase health technology company focused on bioelectronic medicine, today announced it has entered into a definitive agreement to acquire the Reliefband product line for nausea treatment and all related assets from Reliefband Technologies, LLC.

Reliefband has been an innovator in wearable, FDA-cleared electronic therapeutics for treatment of nausea and vomiting. Reliefband has multiple products available both over-the-counter and by prescription.

Jennifer Ernst, CEO of Tivic Health, will host an investor conference call/webcast on Wednesday, October 19, 2022, at 1:30 PM PT / 4:30 PM ET.

Teleconference Details:
Toll-Free: 888-506-0062
International: 973-528-0011
Participant Access Code: 533904

Webcast Link:

https://www.webcaster4.com/Webcast/Page/2865/46849

https://finance.yahoo.com/news/tivic-health-acquire-assets-reliefband-123000021.html

Gilead, MacroGenics to Collaborate to Develop Bispecific Antibodies

 Gilead Granted Exclusive Option to License MGD024, a Phase 1 CD123×CD3 DART® Molecule with Potential to Treat Various Hematologic Malignancies 

 Potential for Companies to Collaborate on Two Additional Future Research Programs –

Gilead Sciences, Inc. (NASDAQ: GILD) and MacroGenics (NASDAQ: MGNX) today announced an exclusive option and collaboration agreement to develop MGD024, an investigational, bispecific antibody that binds CD123 and CD3 using MacroGenics’ DART® platform, and two additional bispecific research programs. The collaboration agreement grants Gilead the option to license MGD024, a potential treatment for certain blood cancers, including acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS).

https://finance.yahoo.com/news/gilead-macrogenics-announce-oncology-collaboration-113000496.html

NGM Misses Topline in Phase 2 Trial in Age-Related Macular Degeneration

 

  • Trial did not meet primary endpoint of statistically significant rate of change in GA lesion area using slope analysis over 52 weeks for NGM621 versus sham

  • NGM621 showed favorable safety and tolerability, with no evidence of increased CNV conversion and no treatment-related SAEs

  • Additional analyses to be presented in early November at The Retina Society Annual Scientific Meeting

  • NGM Bio to host conference call and webcast today at 8:00 a.m. ET

NGM Bio will host a conference call and webcast with slide presentation at 8:00 a.m. ET (5:00 a.m. PT) today. To access the live webcast and slides, please visit the “Investors & Media” section of NGM Bio’s website at https://ir.ngmbio.com/. The webcast will be archived for 30 days.

Athira Advances Phase 2/3 Study in Mild-to-Moderate Alzheimer’s

 Results support potential clinically meaningful activity of fosgonimeton without background therapy and mitigate program risk

Updated study well powered for primary endpoint with addition of fewer than 150 patients

Company targets completion of enrollment in mid-2023 and topline results in early 2024

Company to host live webcast today at 8:30 a.m. Eastern

Athira will host a live webcast to discuss the LIFT-AD interim analysis in greater detail at 8:30 a.m. Eastern Time today, Monday, Oct. 17, 2022. To access the live webcast, please visit https://us02web.zoom.us/webinar/register/WN_AtJ3jgG1RtmRRlcU_cYb-Q or the "Events and Presentations" page within the Investors section of the Athira website: https://investors.athira.com/news-and-events/events-and-presentations-investor. An archived replay will also be available on the website for at least 90 days following the event.

https://finance.yahoo.com/news/athira-pharma-advances-phase-2-110000499.html

Bayer extends elinzanetant trials to include breast cancer

 Bayer has added another clinical trial to its extensive phase 3 programme for oral neurokinin antagonist elinzanetant, hoping to show that it can treat vasomotor symptoms (VMS) in breast cancer patients.

Elinzanetant is already being tested in the OASIS trials for VMS associated with menopause – an indication in which Bayer is in a head-to-head race with Astellas and its fezolinetant drug candidate – and breast cancer could represent a sizeable additional patient population for the drug.

Bayer’s new study is OASIS 4, which will be carried out in breast cancer patients and women with high risk of breast cancer with vasomotor symptoms caused by endocrine therapy.

It will enrol around 400 patients at about 95 centres in 15 countries and will look at a 120 mg once daily dose of elinzanetant, the same as is being tested in Bayer’s menopausal VMS studies, which are due to read out later this year or in early 2023.

While a smaller patient group than menopausal women, carving out a niche in breast cancer could give Bayer an advantage over Astellas, which is currently in the lead with fezolinetant as it is due to hear from the FDA on a filing for the drug in menopausal VMS next February.

There are around 2.3 million new cases of breast cancer diagnosed globally every year, and 70% of them are so-called hormone receptor-positive – meaning they can be treated with endocrine therapies that put them at risk of VMS.

There is an acute medical need for an effective non-hormonal treatment for VMS caused by endocrine therapy in breast cancer patients and women at high risk for developing breast cancer as at the moment no treatment options are available, according to Bayer.

“For women treated with endocrine therapy for breast cancer – potentially for numerous years – vasomotor symptoms can intensively affect their quality of life and treatment continuation, which in turn might impact the effectiveness of their cancer therapy and hence their survival,” said Dr Christian Rommel, Bayer’s R&D chief.

“By adding OASIS 4 to our phase 3 programme with elinzanetant, we aim to help patients experiencing vasomotor symptoms caused by their endocrine therapy, to increase their quality of life,” he added.

There is an acute medical need for an effective non-hormonal treatment for VMS caused by endocrine therapy in breast cancer patients and women at high risk for developing breast cancer as, at the moment, no treatment options are available.

Bayer acquired elinzanetant as part of its takeover of UK biotech KaNDy Therapeutics in 2020, while Astellas acquired fezolinetant as part of its 2017 takeover of Ogeda.

https://pharmaphorum.com/news/bayer-extends-elinzanetant-trials-to-include-breast-cancer/

Clovis: Phase 1 Data of Targeted Radiotherapy Candidate

 

  • Updated LuMIERE Phase 1 data demonstrated a manageable safety profile with some preliminary evidence of anti-tumor activity

    • Eleven patients treated to date with 177Lu-FAP-2286 up to 7.4 GBq/dose

    • No serious adverse events, treatment discontinuations, or deaths related to 177Lu-FAP-2286 observed

    • Confirmed partial response (PR) in one patient who completed the maximum six administrations of 177Lu-FAP-2286 in the 3.7 GBq dose cohort

      • Patient continues without disease progression or subsequent anti-cancer therapy more than twelve months after first dose

    • Stable disease (SD) in one heavily pretreated patient who completed four administrations of 177Lu-FAP-2286 in the 5.55 GBq dose cohort

    • Recruitment of the 7.4 GBq dose cohort is ongoing

  • FAP-2286 has shown high tumor uptake and good prolonged retention across a range of solid tumors

GSK : FDA Oks Menveo In Single-vial Presentation for Meningococcal Disease

 GSK plc (GSK, GSK.L) said that the U.S. Food and Drug Administrationhas approved Menveo in a new single-vial presentation to help prevent disease caused by meningococcal bacteria serogroups A, C, Y, and W. The Single-vial presentation option removes the need for reconstitution of Menveo before use in individuals 10 through 55 years of age.

The Menveo one-vial presentation will initially be available to US federal customers, with broader availability anticipated in mid-2023.

The original two-vial presentation of Menveo requiring reconstitution, was approved by the FDA in 2010 and remains available for use in individuals from two months to 55 years of age.

The Menveo vaccine (supplied in a two-vial presentation) for meningococcal groups A, C, Y, and W has been approved in over 60 countries, with more than 72 million doses distributed worldwide since 2010. Menveo does not prevent Neisseria meningitidis serogroup B infections.

https://www.nasdaq.com/articles/gsk-:-fda-oks-menveo-in-single-vial-presentation-to-prevent-disease-caused-by