New Survey Offers Perspective on Mental and Emotional Journey for Patients Diagnosed with Slow-Growing Blood Cancer

On June 24, 2022 AbbVie reported findings from the newly launched Emotional Impact Report, a survey of more than 300 chronic lymphocytic leukemia (CLL) patients, caregivers and healthcare providers (HCPs), which uncovered insights about the emotional journey associated with a CLL diagnosis (Press release, AbbVie, JUN 24, 2022, View Source [SID1234616232]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

CLL is a slow-growing form of blood cancer in which the bone marrow makes too many lymphocytes, a type of white blood cell.1 CLL progresses much slower than other forms of leukemia and many do not experience symptoms for several years. This leads to disease management with an approach called "watch and wait" in which the disease progression is monitored until treatment is deemed necessary.2

A CLL diagnosis can take a mental and emotional toll on patients, caregivers and HCPs and the Emotional Impact Report seeks to better understand that impact, raise awareness of the need for additional support and the importance of considering overall Quality of Life when making treatment decisions.3

Among a sample of 111 CLL patients, emotions ranged from angry and bitter to optimistic and grateful. For those CLL patients who were newly diagnosed and/or told by their HCP to watch and wait, many may feel hopeful (41%) and optimistic (36%), expressing they are looking forward to the future success of their treatment and their long-term prognosis. And once patients first receive treatment, many (42%) feel positive, including mentions of feeling confident, satisfied, or relieved as they see the medication working. Others mention feeling anxious, never knowing when they will need treatment again and not knowing what is next, further reinforcing the variation and complexity of emotions experienced by CLL patients.

"These findings highlight the ups and downs CLL patients can go through from potentially waiting to start treatment to the prospect of being on continuous therapy," said Ahmed Kotb, vice president, US medical affairs, oncology, AbbVie. "But patients don’t have to navigate a disease like CLL on their own. Based on insights from the Emotional Impact Report, there is an opportunity for increased dialogue between patients and their physicians to set treatment goals and understand available treatment options."

Furthermore, HCPs understand the importance of talking to their patients about the emotional impact of CLL. In fact, 71% said they are likely to discuss the emotional impact of CLL with their patients. Specifically, 90% recognize that a patient’s emotional well-being has an impact on their treatment plan. Physicians cited specific impacts, including adherence to treatment, ability to cope with treatment and how they respond to treatment. HCPs recognize that treating a CLL patient differs from treating other cancer patients, in that CLL is treated similarly to the way a chronic disease is treated, which increases the need to consider Quality of Life when making treatment decisions.

Among a sample of 100 caregivers, most (81%) feel positively about caring for someone with CLL and feel it is their duty to help their loved one. Yet, nearly three in four state that being a caregiver is more difficult than expected. As one caregiver noted, the biggest reason why they are nervous in their role is because they don’t know what’s going to happen from one minute to the next.

This U.S.-based survey was conducted between March 11 – April 7, 2022, and responses were obtained from 313 participants, which included 111 CLL patients, 100 caregivers and 102 HCPs. The online survey was sponsored by AbbVie and developed in consultation with C Space.

To learn more about CLL, navigating a diagnosis and understanding treatment goals, visit CLLCancer.com.

About Chronic Lymphocytic Leukemia
CLL is one of the two most common forms of leukemia in adults and is a type of cancer that can develop from cells in the bone marrow that later mature into certain white blood cells (called lymphocytes).1 While these cancer cells start in the bone marrow, they later spread into the blood. In 2019, there were approximately 200,766 people with CLL living in the United States with more than 20,000 new cases expected in 2022.4 CLL is predominately a disease of the elderly, with a median age at diagnosis of 65 to 70 years and is more common among men than women.5

About the Survey
Participants in the 31-35-question self-administered online survey included three groups, each with its own set and number of survey questions: patients, caregivers, and physicians who specialize in treating cancer. The patient group (n = 111) and the caregiver group (n = 100) included adults ages 18 and older from the U.S., and the physician group (n = 102) included board-certified hematologic oncologists, hematologists or medical oncologists who had treated at least five patients with CLL in the previous 12 months in the U.S. All surveys were completed between March 11, 2022, and April 7, 2022. Using the field services of C Space, the surveys asked both qualitative and quantitative questions. This online survey is not based on a probability sample and therefore no estimate of theoretical sampling error can be calculated.

About C Space
C Space is a global customer agency, that builds customers into the ways companies work.

Working with some of the world’s best-known brands – including Walmart, McDonald’s, IKEA and more – C Space builds the world’s most relevant brands by unlocking the power of human relationships. By building ongoing relationships with customers, brands can stay relevant, deliver superior experiences, and build loyalty. C Space’s customized customer programs are tailored based on specific business needs and include private online communities, in-person live events, visual storytelling, co-creation workshops, and business consulting.

Headquartered in Boston, C Space also has offices in London, New York, Tokyo, San Francisco, and Mexico City. C Space is a part of the Interbrand Group.

First Ever Phase 1B Trial of NK Cells with IL-2 and VACTOSERTIB

On June 24, 2022 Chimeric Therapeutics Ltd (ASX:CHM) reported the first ever trial studying NK cells in combination with IL-2 and Vactosertib, using Chimeric’s CORE NK platform cells (Press release, Chimeric Therapeutics, JUN 24, 2022, View Source [SID1234616225]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

The Phase 1B investigator-initiated trial has been approved by the US Food and Drug Administration (FDA) and will enrol 12 patients at UH Seidman Cancer Center in Ohio, with either locally advanced or metastatic colorectal cancer or relapsed/refractory blood cancers.

Chimeric’s CORE NK platform is a novel NK cell therapy platform of ex-vivo expanded non-HLA*-matched universal donor NK cells.

Safety and early efficacy demonstrated
The CORE NK platform was studied in a Phase 1A clinical trial demonstrating safety and an early efficacy signal in patients with metastatic colorectal cancer and refractory haematological malignancies.

The new study seeks to build upon responses observed during the initial CORE NK clinical trial, by co-administering the CORE NK cells with subcutaneous IL-2 and oral Vactosertib.

Study looks at combination
IL-2 is known to activate NK cells by stimulating proliferation and enhancing function.

Vactosertib is an oral TGF-β receptor inhibitor that can potentially disrupt the TGF-β signalling pathway, which has been shown to limit the effectiveness of immune therapies like NK cells.

"Vactosertib has never been used in combination with NK cells in the clinic, but it has been used in humans in other clinical trials," said UH Seidman oncologist Dr J Eva Selfridge, assistant professor at Case Western Reserve University School of Medicine in Ohio, who will lead the upcoming trial.

NK cells can "actually make it into the tumours"
"The goal of using it in this trial is to disrupt the TGF-β signaling pathway that is so strong in colorectal cancer and cells. We want to shut down that TGF-β signaling pathway so that the NK cells can actually make it into the tumours. Once they’re there, they have a chance of being active instead of just being silenced right away."

Dr. Selfridge says she is hopeful this new clinical trial at UH Seidman Cancer Center will present patients with more and better options for treatment and care: "T cell-directed immunotherapy is only available for 5% or less of cancer patients, but immunotherapy is really the only way we have to cure people with metastatic disease," she said.

"We’re just beginning our study, but ultimately the goal is to find immune therapies that work long-term."

Busy clinical pipeline
The study adds to CHM’s busy clinical pipeline, with now four clinical trials in progress or planned within 9 months.

"With the initial positive results seen in the Phase 1A clinical trial with our CORE NK Platform cells, we have been eager to accelerate the development opportunities for it," said Chimeric CEO Jennifer Chow.

"This study looks to combine novel therapeutics to overcome the challenges that are commonly thought to limit disease responses to NK cells.

"We hope that this combination will allow us to see more complete responses in patients with difficult to treat diseases, like the one seen in the Phase 1A study that has resulted in complete tumour eradication for more than 15 months now."

Immunicum AB: Immunicum Announces Corporate Rebranding and Name Change to Mendus AB

On June 23, 2022 Immunicum, a biopharmaceutical company focused on improving survival outcomes for cancer patients with tumor recurrence through cell-based immunotherapies, reported that it has changed its corporate name from Immunicum AB to Mendus AB (Press release, Immunicum, JUN 23, 2022, View Source [SID1234623752]). The name change is effective as of today and is approved by the Swedish Companies Registration Office. The rebranding to "Mendus" reflects the Company’s maturing clinical pipeline and its broader positioning in cancer recurrence immunotherapy. In addition, this marks an important operational transition as the Company continues to mature with a longer-term focus on a global reach. The Company will continue trading under the ticker symbol "IMMU.ST" and the new website for Mendus AB is www.mendus.com.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

"Today’s news marks an exciting step in a transformative period for the Company. Initiated with the merger and integration of Immunicum and DCprime and accelerated by subsequent directional pipeline decisions and promising novel R&D initiatives, these developments have resulted in a multi-faceted and broader long-term vision for the Company. The name Mendus captures our continued commitment to develop therapies that delay or reduce cases of cancer recurrence, while preserving the quality of life of people living with cancer," commented Erik Manting, PhD, Chief Executive Officer of Mendus. "As we move forward in this new phase of important growth, we look forward to continuing our dedicated work in the development of safe and effective cell-based therapies that we believe can significantly decrease the chance of cancer relapse and improve overall survival."

The Company received approval from its shareholders for the name change at the Annual General Meeting on May 10, 2022 and has since implemented the required legal and organizational changes. Mendus will continue to operate from its headquarters in Stockholm, Sweden, with an office in Gothenburg, Sweden and its main R&D center in Leiden, The Netherlands, which will be operating as a fully owned subsidiary Mendus BV. The Company’s stock ticker symbol will stay unchanged and Mendus AB will continue trading under the ticker symbol IMMU.ST at the Nasdaq Stockholm Main Market section.

In May 2022, the Company presented positive interim results from its ongoing ADVANCE II clinical study evaluating its most advanced proprietary development program, the cancer relapse vaccine DCP-001, as a maintenance therapy option in acute myeloid leukemia (AML). The trial is continuing follow-up of patients and Mendus expects to report on the status of key survival endpoints and immunomonitoring data in the fourth quarter of 2022. Mendus is preparing to advance the development of DCP-001 into a subsequent clinical study in AML maintenance and working to establish a scalable manufacturing infrastructure for the continued development of the program. The company also explores cancer relapse vaccination in ovarian cancer in an ongoing Phase I trial and is preparing for a signal-confirmatory trial in gastro-intestinal stromal tumors with its intratumoral immune primer ilixadencel. Mendus has established a broad collaboration network to further leverage its expertise in allogeneic dendritic cell biology to design novel immunotherapeutic approaches.

MDS, RUNX1 and GTC webinar

On June 23, 2022 GTC reported that it is honored to participate in a webinar hosted by RUNX1 and the MDS Foundation: Get Free Access to Genetic Testing for Underserved MDS and Hematologic Malignancy Patients (Press release, Genomic Testing Cooperative, JUN 23, 2022, View Source [SID1234618944])

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

The event will take place on June 23rd at 12:00 PM PST or 3 PM EST.

Register link: https://bit.ly/WebinarJune23

Agenda:

Intro:

Tracey Iraca, Executive Director – MDS Foundation

Katrin Erickson, Executive Director – RUNX1

Making Diagnosis of Hematologic Neoplasms in the Era of Genomics Available to All by Dr. Maher Albitar, CEO/CMO of Genomic Testing Cooperative

Value of Molecular Profiling for MDS by Dr. Rafael Bejar, UCSD Moores Cancer Center

Q&A

Please register by Tuesday, June 22nd. Upon registering, you will receive an email with a webinar link and a PASSWORD to connect through Zoom.

CAR T cells headline HER2 cell therapy pipeline

On June 23, 2022 Triumvira Immunologics reported At least 17 cell therapy programs are targeting solid tumor-selective HER2, 10 of which are CAR T cells. Companies are also expressing HER2 CARs on other cell types such as NK cells, myeloid cells, and macrophages (Press release, Triumvira Immunologics, JUN 23, 2022, View Source [SID1234616492]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

CAR T cell therapies have been highly effective against hematological malignancies, but solid tumors have been more challenging. Overcoming the major obstacles, including a lack of highly tumor-selective solid tumor targets, was a major theme at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) annual meeting in April.