Spectrum Pharmaceuticals Announces Poster Presentation at Upcoming Miami Breast Cancer Conference

On February 26, 2021 Spectrum Pharmaceuticals (NasdaqGS: SPPI), a biopharmaceutical company focused on novel and targeted oncology therapies, reported a poster presentation on interim safety evaluation of same-day dosing of ROLONTIS (eflapegrastim) in patients with early-stage breast cancer receiving docetaxel and cyclophosphamide (Press release, Spectrum Pharmaceuticals, FEB 26, 2021, View Source [SID1234575772]). This presentation will take place as part of the 38th Annual Miami Breast Cancer Conference taking place virtually March 4-7, 2021. Details of the presentation are as follows:

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Title: Interim safety evaluation of same-day dosing of eflapegrastim in patients with early-stage breast cancer (ESBC) receiving docetaxel and cyclophosphamide (TC)
Speaker: Lee S. Schwartzberg. M.D., FACP
Session: Poster Presentation
Date and Time: March 4, 2021, 6:00pm EST

NICE recommends routine funding for Novartis’ Kisqali

On February 26, 2021 Novartis reported The UK’s National Institute for Health and Care Excellence (NICE) has recommended routine access to Kisqali in certain advanced breast cancer patients (Press release, Novartis, FEB 26, 2021, View Source [SID1234575790]).

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NICE’s draft guidance recommends Kisqali (ribociclib) in combination with fulvestrant for the treatment of locally advanced or metastatic breast cancer that is hormone receptor-positive and human epidermal growth factor receptor 2 (HER2)-negative.

It will be routinely available on the NHS for adults who have had previous endocrine therapy and where exemestane plus everolimus is the most appropriate alternative treatment.

Kisqali is taken as a once-daily pill and belongs to a class of drugs known as cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors.

The drug has been available to patients via the Cancer Drugs Fund (CDF) since 2019, while more evidence was collected to address uncertainties around how much it extends overall survival and its cost-effectiveness.

In a statement, NICE said that the new evidence demonstrates that people receiving Kisqali treatment live longer and experience longer periods before disease progression compared to fulvestrant alone.

"We are pleased therefore that our original decision to make Kisqali available through the CDF not only gave people access to it earlier than would otherwise have been possible, but has now, through the data collected during that time, allowed us to recommend it for routine use on the NHS," said Meindert Boysen, deputy chief executive and director of the NICE Centre for Health Technology Evaluation.

Following the recommendation for routine NHS funding, Kisqali treatment could now be an option for up to 3,300 women.

"It’s fantastic news that NICE has approved [Kisqali] ribociclib with fulvestrant for routine use on the NHS – this life-changing treatment will now bring thousands more women living with incurable secondary breast cancer hope of precious extra time to live well" said Baroness Delyth Morgan, chief executive at Breast Cancer Now.

"As well as offering certain patients with incurable breast cancer extra time with loved ones, this innovative drug combination can help delay the need for chemotherapy and its debilitating side effects," she added.

XNK partners with KI on Phase II study in MM with support from Sanofi

On February 26, 2021 XNK Therapeutics AB ("XNK") reported that it is entering into a joint Phase II clinical study to treat patients with multiple myeloma using XNK’s leading drug candidate in combination with Sanofi’s anti-CD38 antibody Sarclisa (isatuximab) (Press release, CellProtect Nordic Pharmaceuticals, FEB 26, 2021, View Source [SID1234575731]). XNK and Sanofi are both collaborative partners within NextGenNK Competence Center coordinated by Karolinska Institutet.

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The investigator-initiated Phase II study is made possible by the three parties’ contributions to the trial. XNK will provide its novel autologous NK cell-based product to the study set to take place at the Karolinska University Hospital in Stockholm, Sweden.

"Performing this Phase II study together with Karolinska Institutet is an important step for XNK in its ambition to combat multiple myeloma," said Johan Liwing, CEO of XNK Therapeutics. "Combining our efforts together with the present partners highlights just how far XNK has progressed with its patented technology platform."

"We really look forward towards conducting this exciting clinical trial including partnering with XNK Therapeutics," said Hareth Nahi, Associate Professor at KI.

The study ISA-HC-NK (EudraCT: 2020-000994-26) compares XNK’s leading drug candidate combined with isatuximab vs isatuximab as a consolidation treatment following autologous stem cell transplantation in patients with newly diagnosed multiple myeloma.

XNK is a collaborative partner within NextGenNK, a recently established Competence Center for the development of next-generation NK cell-based cancer immunotherapies coordinated by Karolinska Institutet and supported by Sweden’s Innovation Agency (Vinnova).

Change in number of shares and votes in Alligator Bioscience AB

On February 26, 2021 Alligator Bioscience AB ("Alligator") reported the number of shares and votes in has increased as a result of the completion of the rights issue of shares resolved upon by the Board of Directors of Alligator on December 15, 2020. Per February 26, 2021, the number of registered shares and votes in Alligator amounts to 85,666,338.

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This information is such information as Alligator Bioscience AB is obliged to make public pursuant to the Swedish Financial Instruments Trading Act. The information was submitted for publication, through the agency of the contact person set out above, at 11.00 CET on February 26, 2021.

Oncolytics Biotech® to Host Conference Call to Discuss Fourth Quarter and Full Year Financial Results and Operational Highlights

On February 26, 2021 Oncolytics Biotech Inc. (NASDAQ: ONCY) (TSX: ONC) reported that it will host a conference call and webcast on Friday, March 5, 2021, at 8:30 am ET to discuss a corporate update and financial results for the fourth quarter and full year 2020 (Press release, Oncolytics Biotech, FEB 26, 2021, https://ir.oncolyticsbiotech.com/news/detail/528/oncolytics-biotech-to-host-conference-call-to-discuss-fourth-quarter-and-full-year-financial-results-and-operational-highlights [SID1234575773]).

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Conference Call & Webcast

A live webcast of the call will also be available on the Investor Relations page of Oncolytics’ website, available by clicking here and will be archived for three months. A dial in replay will be available for one week and can be accessed by dialing (855) 859-2056 (North America) or (416) 849-0833 (International) and using reference code: 569-6653.