Compugen to Present at the Oppenheimer 31st Annual Healthcare Conference

On March 8, 2021 Compugen Ltd. (NASDAQ: CGEN), a leader in predictive discovery and development of first-in-class therapeutics for cancer immunotherapy, reported that management will present at the Oppenheimer 31st Annual Healthcare Conference (virtual), on Tuesday, March 16, 2021 at 10:40 AM ET (Press release, Compugen, MAR 8, 2021, View Source [SID1234576253]).

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A live webcast of the presentation will be available on Compugen’s website. A replay will be available after the presentation ends.

Clinton Health Access Initiative and American Cancer Society announce agreement to expand Cancer Access Partnership

On March 8, 2021 The Clinton Health Access Initiative (CHAI) and the American Cancer Society (ACS) reported the expansion of the Cancer Access Partnership (CAP) to further increase access to lifesaving cancer treatments in low- and middle-income countries in Africa and Asia (Press release, Clinton Health Access Initiative, MAR 8, 2021, View Source [SID1234576252]). The announcement was made alongside the launch of the World Health Organization’s (WHO) new Global Breast Cancer Initiative which aims to bring together partners to reduce global breast cancer mortality by 2.5 percent per year, thereby averting 2.5 million breast cancer deaths globally between 2020 and 2040.

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Biocon Biologics Limited will join the growing list of companies in the CAP which currently includes Novartis, Pfizer, and Viatris. This expanded partnership will make 26 medications in 39 formulations affordably available to low- and middle-income countries across Africa and Asia, including key chemotherapies, hormonal therapies, biologics, and supportive therapies essential for the treatment of 30 cancers, including breast cancer. The agreements will provide access to 25 regimens for the treatment of breast cancer— which is now the most commonly diagnosed cancer globally—and has the potential to generate an expected overall savings of 60 percent on purchased medications for governments.

"This expanded partnership takes us another step closer to ensuring that the same cancer treatments are available to patients no matter where they live," stated Dr. Iain Barton, CEO of CHAI.

"Every person with cancer deserves affordable treatment that meets the high quality standards set by a stringent regulatory authority and these new agreements will make that possible for many people in Africa and Asia" said Dr. Bill Cance, Chief Medical and Scientific Officer of the American Cancer Society.

The addition of Biocon Biologics to the partnership, along with an expanded portfolio of biosimilars from Pfizer, will enable access to best-in-class therapies that are currently out of reach for patients in low- and middle-income countries. The agreements will now enable access to high quality trastuzumab, rituximab, and pegfilgrastim biosimilars in addition to previously available biosimilar filgrastim from Novartis.

Kiran Mazumdar-Shaw, Executive Chairperson, Biocon Biologics said, "We are pleased to collaborate with CHAI and ACS for their Cancer Access Partnership (CAP) for patients in Sub- Saharan Africa & Asia. Biocon Biologics is committed to expand access to affordable biologics in LMICs through strategic partnerships with global health organizations. Through CAP, our products will support the global efforts directed at expanding therapy options available to healthcare systems in several Asian and African countries for advancing the fight against cancer. This partnership further strengthens our resolve to address the unmet patient needs for high quality, affordable biosimilars for cancer, like bTrastuzumab and bPegfilgrastim."

ACS and CHAI began partnering with governments and cancer treatment institutions across sub-Saharan Africa in 2015 to improve cancer treatment and care. Patients in sub-Saharan Africa are twice as likely to die from cancer as those in the United States, and the number of cases in the region continues to grow with an estimated 800,000 new cases and 500,000 deaths in 2020. Annual cancer deaths in sub-Saharan Africa are projected to almost double by 2030. Seventy percent of cancer deaths occur in low- and middle-income countries.

In June of 2020, CHAI and ACS announced the creation of the Cancer Access Partnership alongside Novartis, Viatris, and existing partner, Pfizer. Since that time, partners have made significant commitments to increase access to high-quality products, leading to direct sales of cancer medicines in eight countries with purchasers in additional countries engaged further. The expanding list of countries indicates continued willingness to serve ever greater populations. The partners are also committed to continually monitoring the impact of the partnership on patients.

"Novartis is proud to reconfirm our commitment to cancer patients in helping to enable broader access to cancer care in sub-Saharan Africa. We are happy to see the partnership expand and welcome the new cancer allies, as we know it takes a joint effort to tackle this life-threatening disease. Together we have the ability to help reduce mortality, broaden access opportunities and positively impact the patient journey. I would like to take the opportunity to invite colleagues from the medical device space to join and help contribute to strengthening diagnosis and screening in SSA," said Racey Muchilwa, Head of Novartis SSA.

"The battle against cancer can only be won when strong partnerships across and within countries address the challenges faced by people seeking care, their caregivers and the health systems that support them holistically," said Michelle Akande, Vice President of Pfizer Global Health Partnerships. "We have been a proud partner to this effort spanning several years, working towards one of our common goals, which is helping patients gain access to the medicines they need to live longer and healthier lives. We are very excited to see this partnership grow and to now bring Pfizer biosimilars to the collaboration in order to offer an even broader range of treatment options to patients in need."

The market access agreements are part of a broader effort to improve access to quality cancer care in Africa. In 2019, ACS, CHAI, the African Cancer Coalition, the National Comprehensive Cancer Network (NCCN), and IBM joined to form Allied Against Cancer. This coalition is leveraging the strengths of each organization to connect with and empower the African oncology community to deliver high-quality cancer care and is working to pursue additional market-based collaborations to increase access to cancer medicines in the region. A recently launched Treatment Access Fund invites the support of multiple companies and other funders to support Allied Against Cancer activities.

Countries covered by the new agreements include Botswana, Burkina Faso, Cameroon, Democratic Republic of Congo, Eswatini, Ethiopia, Ghana, India, Cote d’Ivoire, Kenya, Lesotho, Liberia, Malawi, Mali, Mozambique, Myanmar, Namibia, Nigeria, Lao PDR, Papua New Guinea, Rwanda, Senegal, Sierra Leone, South Africa, Sudan, Tanzania, Uganda, Vietnam, Zambia, and Zimbabwe. Not all products are offered in every country.

Nordic Nanovector to present at 11th Annual World ADC Europe 2021 Digital

On March 8, 2021 Nordic Nanovector ASA (OSE: NANOV) reported that its Chief Scientific Officer, Jostein Dahle, will give a presentation on 9 March at the 11th Annual World ADC Europe 2021 Digital event (8-11 March 2021) in the Discovery stream discussing the question: Should Payloads be Super-Potent? (Press release, Nordic Nanovector, MAR 8, 2021, View Source [SID1234576251])

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Presentation details are as follows:

Title: Targeting CD37 with Alpha- & Beta-Emitting Radioimmunoconjugates

Date/time: Tuesday, 9 March 2021 at 11:40am GMT

During his presentation, Dr Dahle with cover the following points:

Review CD37 as target for radioimmunotherapy
Analyse preclinical and clinical data for treatment of Non-Hodgkin’s Lymphoma (NHL) with the beta-emitting radioimmunoconjugate 177Lu-lilotomab satetraxetan (Betalutin)
Evaluate preclinical data for treatment of Chronic Lymphocytic Leukaemia and NHL with the alpha-emitting radioimmunoconjugate 212Pb-TCMC-NNV003 (Alpha37)
World ADC Europe is an industry-leading conference and Europe’s largest gathering of ADC stakeholders. It brings together 300 drug developers from 160 active ADC organisations to help forward-thinking researchers from the pharmaceutical, biotech and academic community advance the development of antibody-drug conjugates.

Stockholders of NantKwest Approve Merger With ImmunityBio

On March 8, 2021 NantKwest, Inc. (NASDAQ: NK), a clinical-stage, natural killer cell-based therapeutics company, reported that its stockholders approved by the required vote each of the proposals related to the pending merger of NantKwest and ImmunityBio, Inc (Press release, NantKwest, MAR 8, 2021, View Source [SID1234576249]). presented at the special meeting of stockholders held earlier in the day, including approval of the merger by a majority of unaffiliated stockholders of NantKwest. Final voting results for NantKwest’s special meeting of stockholders will be disclosed in a Form 8-K to be filed by NantKwest with the Securities and Exchange Commission.

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The merger is expected to close on March 9, 2021, subject to the satisfaction of customary closing conditions. Following the closing of the transaction, the combined company will assume the ImmunityBio name and its shares of common stock are expected to trade on NASDAQ under the symbol "IBRX" commencing on March 10, 2021.

Castle Biosciences Launches DecisionDx-Melanoma Integrated Test Result Utilizing Artificial Intelligence to Predict Individualized Risk

On March 8, 2021 Castle Biosciences, Inc. (Nasdaq: CSTL), a skin cancer diagnostics company providing personalized genomic information to improve cancer treatment decisions, reported that DecisionDx-Melanoma, Castle’s prognostic gene expression profile test for cutaneous melanoma, now utilizes an Integrated Test Result (ITR), designed to provide a more precise risk prediction in patients with stage I, II or III melanoma (Press release, Castle Biosciences, MAR 8, 2021, View Source [SID1234576248]). The Company plans to launch an app later in 2021 for dermatology clinicians, featuring an interactive algorithm using the 31-GEP test score and traditional clinicopathologic factors to predict risk.

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DecisionDx-Melanoma now outputs an ITR. The ITR is calculated by an independently validated algorithm (i31-GEP), designed to provide a more precise and personalized prediction of sentinel lymph node (SLN) positivity in order to guide discussions and recommendations, within current risk-based guidelines, for the SLN biopsy (SLNB) surgical procedure. i31-GEP is an artificial intelligence-based neural network algorithm (independently validated in a cohort of 1,674 prospective, consecutively tested patients with T1-T4 cutaneous melanoma) that integrates the DecisionDx-Melanoma test result with the patient’s traditional clinicopathologic features.

"We have demonstrated our ability to bring high value, clinically actionable genomic tests to market," said Derek Maetzold, president and chief executive officer of Castle Biosciences. "We start by identifying dermatologic diseases with high unmet clinical need. We then use the gene expression profile of the patient’s tumor biology to provide clinicians and their patients with precise, personalized risk prediction, better informing management decisions to optimize health outcomes and reduce healthcare costs.

"We recognize the complexity of cancer and the necessity of diagnostics to utilize advanced approaches to provide actionable results, as exemplified in the use of artificial intelligence for our i31-GEP and updated integrated patient test result. Castle continues to evolve, as we advance our expertise in dermatologic diagnostics, in alignment with our commitment to inform treatment decisions and improve health outcomes along the patient care continuum."

In addition to the likelihood of SLN positivity, the updated DecisionDx-Melanoma patient report includes predictions of 5-year outcomes of melanoma specific survival, distant metastasis free survival and recurrence free survival, updated with an expanded dataset, by DecisionDx-Melanoma class result: lowest risk (Class 1A), increased risk (Class 1B/2A) or highest risk (Class 2B). This personalized risk information supports clinicians and their patients in making cancer management decisions, such as intensity of surveillance and follow-up frequency.

The Company expects to launch an app based on i31-GEP and the ITR later in 2021. The app’s first phase is expected to provide dermatologic clinicians an interactive experience to determine the risk of SLN positivity for an individual patient, based on the clinicopathologic factors and i31-GEP score entered.

DecisionDx-Melanoma is Castle’s gene expression profile test that uses an individual patient’s tumor biology to predict individual risk of cutaneous melanoma metastasis or recurrence, independent of traditional staging factors. The personalized information provided on the ITR is designed to help clinicians and their patients make more informed decisions about the sentinel lymph node biopsy (SLNB) surgical procedure and follow-up management and care plans.

About DecisionDx-Melanoma

DecisionDx-Melanoma is a gene expression profile test that uses an individual patient’s tumor biology to predict individual risk of cutaneous melanoma metastasis or recurrence, as well as sentinel lymph node positivity, independent of traditional staging factors, and has been studied in more than 5,700 patient samples. Using tissue from the primary melanoma, the test measures the expression of 31 genes. The test has been validated in four archival risk of recurrence studies of 901 patients and six prospective risk of recurrence studies including more than 1,600 patients. To predict likelihood of sentinel lymph node positivity, the Company utilizes its proprietary algorithm, i31-GEP, to produce an integrated test result. i31-GEP is an artificial intelligence-based neural network algorithm (independently validated in a cohort of 1,674 prospective, consecutively tested patients with T1-T4 cutaneous melanoma) that integrates the DecisionDx-Melanoma test result with the patient’s traditional clinicopathologic features. Impact on patient management plans for one of every two patients tested has been demonstrated in four multicenter and single-center studies including more than 560 patients. The consistent performance and accuracy demonstrated in these studies provides confidence in disease management plans that incorporate DecisionDx-Melanoma test results. Through December 31, 2020, DecisionDx-Melanoma has been ordered more than 68,920 times for use in patients with cutaneous melanoma.