EORTC TOLERANCE trial in elderly patients with advanced soft tissue sarcoma receives support from Rising Tide Foundation

On November 17, 2021 EORTC reported that Rising Tide Foundation for Clinical Cancer Research awards a grant 1976 Soft Tissue Bone Sarcoma Group (STBSG) & Quality of Life Group (QLG) TOLERANCE academic clinical trial, a study on health-related quality of life of elderly patients with advanced soft tissue sarcoma (Press release, EORTC, NOV 17, 2021, View Source [SID1234595732]).

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The challenge of treating the fast-growing population of elderly patients with cancer urgently requires adequate treatment, for which guidelines and evidence-based data are lacking.

To date, there is no consensus on the best treatment for elderly patients with inoperable or metastatic soft tissue sarcoma (STS). The numerous side effects associated with the standard doxorubicin-based treatments make the treatment of elderly patients very challenging.

TOLERANCE is an academic clinical trial comparing different treatments for elderly patients with inoperable or metastatic STS, taking into account patients’ priorities in terms of quality of life and the impact of treatment on their ability to conduct daily activities, ultimately aiming to identify the best care for the elderly population.

Rising Tide Foundation awarded €500K to the EORTC 1976-STBSG-QLG study, marking the second collaboration between the two organisations. "Partnering with like-minded organisations is key to addressing unmet patient-centred needs in clinical cancer research, especially in rare cancers and underrepresented populations. The Rising Tide Foundation for Clinical Cancer Research is an invaluable ally. Their substantial support in the EORTC TOLERANCE trial will contribute to an important international randomised clinical trial that will set a new standard of care for the elderly", commented Dr Denis Lacombe, EORTC CEO.

"Rising Tide Foundation for Clinical Cancer Research was founded to help patients improve their quality of life and win the fight against cancer. Our partnership with EORTC will work to propel the research to the next level and bring ground-breaking treatment options to the bedside of patients", explains Wendelin Zellmayer, Director of the RTFCCR.

The study

EORTC 1976-STBSG-QLG TOLERANCE is a 3-arm randomised, open label, phase 3 trial coordinated by the EORTC HQ in Brussels. A total number of 185 patients aged from 65 years-old and diagnosed with advanced or metastatic STS will be enrolled over a period of 3.5 years. The trial will open in 34 reference cancer centres in 9 countries (CY, DK, DE, IT, JO, NL, ES, UK).

The primary objective of the study is to assess whether a higher health-related quality of life (HRQoL), in terms of impact of the disease and its treatment on physical and role functioning, is achieved with metronomic schedules of doxorubicin or cyclophosphamide plus prednisolone versus the standard doxorubicin treatment (3 treatment arms).

Secondary objectives include assessment of whether there is an improvement in quality of life, in terms of impact of the disease and its treatment on social, emotional and cognitive functioning as well as self-reported symptoms, among patients treated in each of the three arms. Furthermore, the study will assess whether there is a difference in the progression free survival, overall survival and tumor response while at the same time monitoring the toxicity profile and tolerability of the three treatment arms.

HRQoL assessment will be performed every 3 weeks during the first 12 weeks and every 12 weeks thereafter until month 12 after start of treatment. Disease evaluation will be performed every 12 weeks until progression.

Patient follow-up duration until primary objective, after LPI (last patient in), is estimated at 25 months to provide the targeted number of events for the study analysis. The overall duration of this study is 7 years and is coordinated by Professor Winette van der Graaf (Netherlands Cancer Institute Amsterdam).

EORTC recognizes patient involvement as a vital component of its clinical research activities, members of the EORTC Group of Patient Experts and Patient Panel were invited to review the patient information sheet and informed consent. Five sarcoma cancer survivors and caregivers have helped us to strike the balance between completeness of the information, document length and relevance of the research objectives for the patients.

"Patient engagement is a key principle of the Rising Tide Foundation for Clinical Cancer Research" explains Shawn Stephenson, Chairman of the Foundation. The TOLERANCE study is a leading example of patient involvement in clinical trial design. "We are excited to partner with EORTC on this multicenter phase 3 study, with the potential to provide better treatment options and improved quality of life for elderly patients."

On the study’s importance, Professor Winette van der Graaf commented: "With a general rise in age, we diagnose more soft issues sarcomas in elderly people than before, but we lack data to support an optimal treatment schedule in case of advanced or metastatic disease in this age group. We are delighted that we will run a study with a novel trial design with widely available drugs, which will increase our knowledge both in term of efficacy and quality of life in this patient population."

Lilly to Participate in Fourth Annual Evercore ISI HealthCONx Conference

On November 17, 2021 Eli Lilly and Company (NYSE: LLY) reported that it will participate in the fourth annual Evercore ISI HealthCONx Conference on Tuesday, Nov. 30, 2021. Daniel Skovronsky, M.D., Ph.D., Lilly’s chief scientific and medical officer, and president of Lilly Research Laboratories, will participate in a fireside chat at 12:10 p.m., Eastern time (Press release, Eli Lilly, NOV 17, 2021, https://investor.lilly.com/news-releases/news-release-details/lilly-participate-fourth-annual-evercore-isi-healthconx [SID1234595731]).

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A live audio webcast will be available on the "Webcasts & Presentations" section of Lilly’s Investor website at View Source A replay of the presentation will be available on this same website for approximately 90 days.

BioVaxys Co-Founder and Chief Medical Officer David Berd, MD, to Present at World Vaccine & Immunotherapy Congress West Coast 2021

On November 17, 2021 BioVaxys Technology Corp. (CSE: BIOV, FRA:5LB,OTCQB:BVAXF) ("BioVaxys" or "Company"), a clinical-stage immunotherapy company, reported that Company Co-Founder and Chief Medical Officer David Berd, MD, will present at the World Vaccine & Immunotherapy Congress West Coast 2021 taking place November 30-December 2, 2021 in San Diego (Press release, BioVaxys Technology, NOV 17, 2021, https://biovaxys.com/2021/11/17/biovaxys-co-founder-and-chief-medical-officer-david-berd-md-to-present-at-world-vaccine-immunotherapy-congress-west-coast-2021/ [SID1234595730]).

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Dr. Berd will discuss the role of immunotherapeutic vaccines in cancer, the potential of haptenized autologous tumor cell vaccines for treating a range of cancer types, and BioVaxys’ advancement of haptenized viral antigens as a platform for addressing SARS-CoV-2, SARS-CoV-1, and other sarbecoviruses.

Details of the presentation are as follows:

Title: Haptenized Vaccines for Viral Diseases & Cancer

When: December 1, 2021 @ 17:10
Where: Lowes Coronado Hotel, San Diego, CA

"BioVaxys is honored to be invited to speak at the World Vaccine & Immunotherapy Congress alongside a prestigious group of vaccine and immunology experts. We look forward to sharing how we are leveraging our haptenized protein platform to create autologous cancer immunotherapies synergistic with checkpoint inhibitors, as well as protein-based vaccines for infectious disease," said Dr. Berd.

A medical oncologist, Dr. Berd has a life-long record of clinical research in medical oncology and cancer immunotherapy. For more than 20 years, he was a professor of medicine at Thomas Jefferson University, where he conducted clinical research on melanoma vaccines. Over the course of his career, Dr. Berd has published more than 85 original papers in numerous medical journals in addition to myriad editorials, reviews, and abstracts. He has 10 issued cancer vaccines patents.

Greenwich LifeSciences to Participate in Jefferies’ 12th Annual London Healthcare Conference

On November 17, 2021 Greenwich LifeSciences, Inc. (Nasdaq: GLSI) (the "Company"), a clinical-stage biopharmaceutical company focused on the development of GP2, an immunotherapy to prevent breast cancer recurrences in patients who have previously undergone surgery, reported CEO Snehal Patel will participate in the virtual portion of Jefferies’ Annual London Healthcare Conference held from November 16-19, 2021 (Press release, Greenwich LifeSciences, NOV 17, 2021, View Source [SID1234595727]).

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Jefferies’ Annual London Healthcare Conference

Jefferies’ 12th Annual London Healthcare Conference is the largest healthcare-dedicated conference in Europe. Participation is by invitation only and will feature leading public and private companies from the pharmaceuticals, biotechnology, medical technology, and healthcare services sectors from the Americas, Europe, Middle East, Africa, Asia, and Australia. For more information please visit: Jefferies London Healthcare Conference

About FLAMINGO-01 and GLSI-100

The Phase III clinical trial will be called FLAMINGO-01 and the combination of GP2 + GM-CSF will be called GLSI-100. The Phase III trial is comprised of 2 blinded, randomized, placebo-controlled arms for approximately 500 HLA-A*02 patients and 1 open label arm of up to 100 patients for all other HLA types. An interim analysis has been designed to detect a hazard ratio of 0.3 in IDFS, where 28 events will be required. An interim analysis for superiority and futility will be conducted when at least half of those events, 14, have occurred. This sample size provides 80% power if the annual rate of events in placebo-treated subjects is 2.4% or greater. The trial is currently being registered on clinicaltrials.gov and the link and trial identifier will be published shortly. For future updates about FLAMINGO-01 please visit the Company’s clinical trial tab at View Source

About Breast Cancer and HER2/neu Positivity

One in eight U.S. women will develop invasive breast cancer over her lifetime, with approximately 282,000 new breast cancer patients and 3.8 million breast cancer survivors in 2021. HER2/neu (human epidermal growth factor receptor 2) protein is a cell surface receptor protein that is expressed in a variety of common cancers, including in 75% of breast cancers at low (1+), intermediate (2+), and high (3+ or over-expressor) levels.

Redx to Present at Jefferies London Healthcare Conference

On November 17, 2021 Redx Pharma (AIM: REDX), the clinical-stage biotechnology company focused on discovering and developing novel, small molecule, highly targeted therapeutics for the treatment of cancer and fibrotic disease, announces that Lisa Anson, Chief Executive Officer, reported that it will be presenting at the Jefferies London Healthcare Conference today, Wednesday 17 November at 08:40am GMT (Press release, Redx Pharma, NOV 17, 2021, View Source [SID1234595726]).

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The webcast can be accessed here: View Source