Blue Earth Therapeutics Announces Participation in Upcoming B. Riley Securities Radiopharma Investor Conference

On February 28, 2024 Blue Earth Therapeutics, a Bracco company and emerging leader in the development of innovative next generation therapeutic radiopharmaceuticals, reported that it will be presenting at the upcoming B. Riley Securities’ Radiopharma Investor Conference (Press release, Blue Earth Therapeutics, FEB 28, 2024, View Source [SID1234640628]). The event will be held in New York, N.Y., on March 1, 2024. David Gauden, D. Phil., Chief Executive Officer of Blue Earth Diagnostics and Blue Earth Therapeutics, will present an overview of Blue Earth Therapeutics from 8:00 – 8:30 a.m. ET and participate in an expert panel discussion, "Opportunities and Challenges in 2024, Perspectives from Leaders in Radiopharma," from 9:15 – 9:50 a.m. ET. Dr. Dan Stevens, Vice President Clinical Development and Medical, Blue Earth Therapeutics, will participate in an expert panel, "Good But Not the Best Yet: Drug Designs to Beat Standard of Care," from 1:45 – 2:20 p.m. ET. The Company will also host 1:1 investor meetings at the conference.

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"Blue Earth Therapeutics continues to expand our leadership position in the rapidly growing area of radiopharmaceuticals," said David Gauden., D.Phil., Chief Executive Officer of the Company. "We are strongly positioned for continued progress across this exciting sector, and we look forward to sharing information about our innovative approach and next generation targeted radioligand therapy (RLT) technology at this important B. Riley Securities conference."

Naveris Announces New Data at ASTRO Multidisciplinary Head and Neck Cancers Symposium 2024

On February 28, 2024 Naveris, Inc., the leader in precision oncology diagnostics for viral-induced cancers, reported new data to be presented at The American Society for Radiation Oncology (ASTRO) Multidisciplinary Head and Neck Cancers Symposium (MHNCS) in Phoenix, AZ from February 29 – March 2, 2024 (Press release, Naveris, FEB 28, 2024, View Source [SID1234640627]).

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NavDx is the first and only clinically validated circulating Tumor Tissue Modified Viral (TTMV)-HPV DNA blood test that aids in the detection of HPV-driven cancer. The test provides a non-invasive and precise method for identifying HPV-driven cancers before there is clinical or radiographical evidence of disease. Data supporting the clinical validity and utility of NavDx have been published in nearly 20 peer-reviewed publications.

"We are thankful for the opportunity provided by ASTRO to share the latest findings, which emphasize the pivotal role of NavDx in influencing clinical management," commented Barry M. Berger, M.D., Chief Medical Officer at Naveris. "The data being showcased highlight the critical role circulating tumor HPV DNA assessment can play in shaping patient care strategies. We are enthusiastic about the progress made through our extensive collaborations with a diverse array of partners in the oncology community," he concluded.

These presentations showcase the utility of NavDx in the management of HPV-driven head and neck cancer at every stage of disease, from treatment response and guidance to surveillance and detection of recurrence:

127: Implications of rapid molecular responses to induction chemotherapy (IC) in Human Papilloma Virus (HPV) head and neck squamous cell carcinoma (HNSCC).
Presenting Author: Misiukiewicz, K.
Session, Date/Time: Poster Session I | February 29, 2024 | 3:00 PM – 3:30 PM MT
112: Comparison of TTMV-HPV DNA to Gold Standard PET for Evaluation of Treatment Response in HPV-Associated Oropharyngeal Cancer after Definitive Treatment
Presenting Author: Song, R.
Session, Date/Time: Poster Session I | February 29, 2024 | 3:00 PM – 3:30 PM MT
152: Tumor Tissue Modified Viral HPV DNA Monitoring in Patients with Recurrent, Metastatic HPV-driven Oropharyngeal Cancer
Presenting Author: Hanna, G. J.
Session, Date/Time: Poster Session II | February 29, 2024 | 4:45 PM – 5:45 PM MT
177: Prospective Study of Plasma Biomarker-Guided Surveillance of HPV-positive Oropharynx Cancer Using TTMV-HPV DNA: The SPHERE Study
Presenting Author: Rettig, E. M.
Session, Date/Time: Poster Session II | February 29, 2024 | 4:45 PM – 5:45 PM MT
132: Detectable Circulating Tumor Tissue Modified Viral (TTMV)-HPV DNA in Non-Oropharyngeal Head and Neck Cancers
Presenting Author: Duffy, E. W.
Session, Date/Time: Poster Session I | February 29, 2024 | 3:00 PM – 3:30 PM MT
Naveris will also be hosting an Industry Expert Theater at the meeting, focusing on the role of NavDx in optimizing post-treatment surveillance and monitoring for molecular residual disease:

Action to Insights: A Case-Based Discussion of the Role of NavDx in Post-treatment Surveillance of HPV-Driven OPSCC
Moderator: Marshall Posner, MD
Presenters: Meghan T. Turner, MD, and Adam Raben, MD
Session, Date/Time: Thursday, February 29, 2024 | 5:30pm MT
Naveris and NavDx will be on exhibit at ASTRO MHNCS 2024 at Booth #4.

Arcus Biosciences to Participate in Two Upcoming Investor Conferences

On February 28, 2024 Arcus Biosciences (NYSE:RCUS), a clinical-stage, global biopharmaceutical company focused on developing differentiated molecules and combination therapies for people with cancer, reported that its management team will participate in the following upcoming investor conferences in March (Press release, Arcus Biosciences, FEB 28, 2024, View Source [SID1234640626]):

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Leerink Global Biopharma Conference 2024
Date: Monday, March 11th, 2024 at 4:00 p.m. ET
Location: Miami Beach, FL
Format: Fireside Chat

Barclays 26th Annual Global Healthcare Conference
Date: Tuesday, March 12th, 2024 at 2:35 p.m. ET
Location: Miami Beach, FL
Format: Fireside Chat

Live webcasts of the fireside chats and panel will be available by visiting the "Investors & Media" section of the Arcus Biosciences website at www.arcusbio.com. Replays will be available following each live event.

Atara Biotherapeutics to Participate in Cell Therapy Panel Discussion at the Cowen 44th Annual Health Care Conference

On February 28, 2024 Atara Biotherapeutics, Inc. (Nasdaq: ATRA), a leader in T-cell immunotherapy, leveraging its novel allogeneic Epstein-Barr virus (EBV) T-cell platform to develop transformative therapies for patients with cancer and autoimmune diseases, reported that Pascal Touchon, President and Chief Executive Officer, will participate in a cell therapy panel discussion at the Cowen 44th Annual Health Care Conference on Wednesday, March 6, 2024 at 6:10 a.m. PST / 9:10 a.m. EST (Press release, Atara Biotherapeutics, FEB 28, 2024, View Source [SID1234640625]).

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A live webcast of the presentation will be available by visiting the Investors and Media section of atarabio.com. An archived replay of the webcast will be available on the Company’s website for 30 days following the live presentation.

Arcellx Provides Fourth Quarter and Year-End 2023 Financial Results and Business Highlights

On February 28, 2024 Arcellx, Inc. (NASDAQ: ACLX), a biotechnology company reimagining cell therapy through the development of innovative immunotherapies for patients with cancer and other incurable diseases, reported business highlights and financial results for the fourth quarter and year ended December 31, 2023 (Press release, Arcellx, FEB 28, 2024, View Source [SID1234640624]).

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"In 2023, our team built upon the momentum that has propelled Arcellx forward over the past two years," said Rami Elghandour, Arcellx’s Chairman and Chief Executive Officer. "We expanded our partnership with Kite, through a $200M investment, extending our cash runway into 2027 and deepened our collaboration by expanding into lymphomas. Additionally, we presented robust long-term data from our Phase 1 expansion study of anito-cel at the 65th ASH (Free ASH Whitepaper) Annual Meeting. These data support the potential for anito-cel to be a best-in-class treatment option for patients with relapsed or refractory multiple myeloma. In parallel to these milestones, we continued to scale our organization to deliver both operationally and strategically, strengthening our foundation with key progress in manufacturing, development, research, and commercial readiness. This year is poised to be another year of meaningful progress for our organization. We are focused on completing enrollment in the iMMagine-1 trial, initiating our clinical trial in earlier lines of multiple myeloma, and completing the technical transfer to Kite. Patients with relapsed or refractory multiple myeloma still have limited therapeutic options, and with our partners at Kite, we are committed to delivering anito-cel to help as many patients as possible. We believe that with our technology coupled with Kite’s recognized global leadership and established manufacturing expertise, we are well positioned to achieve this goal. Additionally, we continue to invest in research and believe the differentiation of the D-Domain technology provides an opportunity for us to expand our development pipeline in other therapeutic areas."

Recent Business Progress

Expanded strategic partnership with Kite Pharma, Inc., a Gilead Company, to include co-development of anito-cel for lymphomas and Kite exercising its option to license ACLX-001. On November 15, 2023, Arcellx and Kite, a Gilead Company, announced an expansion in their existing partnership, which was originally announced in December 2022. Kite has exercised its option to negotiate a license for Arcellx’s ARC-SparX program, ACLX-001. The companies have also expanded the scope of the collaboration to include lymphomas. Upon closing in December 2023, Arcellx received a $200 million equity investment at $61.68 per share and an $85 million upfront cash payment.

Presented continued robust long-term responses from lead product candidate anito-cel evaluated in a Phase 1 expansion trial in patients with relapsed or refractory multiple myeloma, at 65th ASH (Free ASH Whitepaper) Annual Meeting and Exposition. On December 11, 2023, Arcellx presented new clinical data from its ongoing Phase 1 expansion study of autologous anitocabtagene autoleucel (anito-cel), formerly known as CART-ddBCMA, at the 65th ASH (Free ASH Whitepaper) Annual Meeting and Exposition. The data continued to demonstrate deep and durable responses in patients with poor prognostic factors. Of the 38 evaluable patients with a median follow-up of 26.5 months, 100% overall response rate (ORR) was achieved in all patients and 29 of 38 (76%) evaluable patients achieved a complete response (CR) or a stringent complete response (sCR). Additionally, anito-cel continued to be well tolerated with no delayed neurotoxicity or parkinsonian symptoms observed. Median duration of response, progression free survival (PFS), and overall survival were not reached at the time of the October 15, 2023 data cut. Anito-cel continued to be well-tolerated at the time of the October 15, 2023 data cut.

Fourth Quarter and Full Year 2023 Financial Highlights

Cash, cash equivalents, and marketable securities:
As of December 31, 2023, Arcellx had cash, cash equivalents, and marketable securities of $729.2 million. Arcellx anticipates that its cash, cash equivalents, and marketable securities will fund its operations into 2027.

Collaboration revenue:
Collaboration revenue was $63.1 million and zero for the quarters ended December 31, 2023 and 2022, respectively. Collaboration revenue was $110.3 million and zero for the twelve months ended December 31, 2023 and 2022, respectively. The revenue results from the recognition of research and development performed under the arrangement described in the recent license and collaboration agreement with Kite Pharma, Inc. (Kite).

R&D expenses:
Research and development expenses were $28.8 million and $25.9 million for the quarters ended December 31, 2023 and 2022, respectively, an increase of $2.9 million. This increase was driven primarily by an increase in personnel and facility costs. Research and development expenses were $133.8 million and $149.6 million for the twelve months ended December 31, 2023 and 2022, respectively, a decrease of $15.8 million. This decrease was primarily driven by the accounting treatment for our Lonza manufacturing services agreement, which resulted in a non-cash expense in both years ended December 31, 2023 and 2022. This decrease was partially offset by an increase in personnel costs, which includes non-cash stock-based compensation expense.

G&A expenses:
General and administrative expenses were $19.4 million and $14.1 million for the quarters ended December 31, 2023 and 2022, respectively, an increase of $5.3 million. General and administrative expenses were $66.4 million and $41.7 million for the twelve months ended December 31, 2023 and 2022, respectively, an increase of $24.7 million. The increases were driven primarily by non-cash stock-based compensation expense.

Net income or loss:
Net income was $20.5 million for the quarters ended December 31, 2023 and net loss was $39.0 million for the quarter ended December 31, 2022. Net loss for the twelve months ended December 31, 2023 and 2022 were $70.7 million and $188.7 million, respectively.