Altimmune To Participate At Two Upcoming Investor Conferences

On June 3, 2022 Altimmune, Inc. (Nasdaq: ALT), a clinical-stage biopharmaceutical company, reported that members of the Company’s management team will participate at the following investor conferences in June 2022 (Press release, Altimmune, JUN 3, 2022, View Source [SID1234615525]):

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Jefferies 2022 Global Healthcare Conference in New York, NY
Friday, June 10, 2022
Fireside chat at 10:00 am Eastern Time
JMP Securities Life Sciences Conference in New York, NY
Thursday, June 16, 2022
Fireside chat at 9:00 am Eastern Time
The sessions will be webcast and can be accessed by visiting the Events section of the Altimmune website.

CYTOKINETICS TO PARTICIPATE IN UPCOMING INVESTOR CONFERENCES

On June 3, 2022 Cytokinetics, Incorporated (Nasdaq: CYTK) reported that Robert I. Blum, President and Chief Executive Officer, is scheduled to participate in the following investor conferences (Press release, Cytokinetics, JUN 3, 2022, View Source [SID1234615522]):

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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

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Jefferies Healthcare Conference on Thursday, June 9, 2022 at 10:00 AM ET in a presentation at the Marriott Marquis Hotel in New York City
Goldman Sachs 43rd Annual Healthcare Conference on Monday, June 13, 2022 at 2:40 PM PT in a fireside chat at the Terranea Resort in Rancho Palos Verdes
JMP Securities Life Sciences Conference on Wednesday, June 15, 2022 at 3:00 PM ET in a fireside chat at the Lotte New York Palace in New York City
Interested parties may access the live webcast of these presentations by visiting the Investors & Media section of the Cytokinetics website at www.cytokinetics.com. The webcast replay will be archived on the Presentations page within the Investors & Media section of Cytokinetics’ website for 90 days following the conclusion of the event.

Investigators from US Oncology Research, The US Oncology Network and Ontada Present Data Highlighting Key Advances and Insights at the 2022 American Society of Clinical Oncology Annual Meeting

On June 3, 2022 During the scientific program of the 2022 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting, principal investigators from US Oncology Research, The US Oncology Network (The Network) and Ontada reported that it will present detailed results from more than 80 studies (Press release, US Oncology, JUN 3, 2022, View Source [SID1234615521]). Presentations include 10 oral sessions on topics including lung and ovarian cancers, as well as research involving value-based care and the use of health technologies. The ASCO (Free ASCO Whitepaper) Annual Meeting, a leading conference delivering the latest in cancer science to the global community, will be held June 3-7, 2022 in Chicago.

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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

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"The oncology community is constantly transforming, and past discoveries provide rationale for the community structures we have today, but new challenges, like changes in the healthcare landscape, will always present themselves," said Robert L. Coleman, MD, chief scientific officer, US Oncology Research. "The strengths of community-based research and dedication to improving patients’ outcomes and cancer care experience provide the tenacity needed to turn these challenges into opportunities. Our team of community-based researchers are committed to advancing research, offering ways for patients to receive care from virtual locations, and making access to leading treatments possible for a myriad of patients more than ever before."

MYLUNG Consortium Data to be Highlighted in Two Presentations

Included in the research presentations during this year’s meeting will be findings from Protocol 2 of the Molecularly Informed Lung Cancer Treatment in a Community Cancer Network: A Pragmatic Consortium (MYLUNG Consortium) clinical trial platform in non-small cell lung cancer (Abstract #1503), which will be presented during an oral session by Elizabeth Koselke, PharmD, BCOP, senior clinical pharmacist with The Network. Protocol 2 of the study platform included an examination of an oncology clinical pharmacist on the research team and the impact on clinical trial enrollment. The abstract "Impact of oncology clinical pharmacist intervention on clinical trial enrollment in The US Oncology Network’s MYLUNG Consortium," will be featured in the "Care Delivery and Regulatory Policy" session on Monday, June 6 at 4 p.m.

"This is one of the first studies that looked at the effectiveness of pharmacists in this role," said Koselke. "Pharmacists are uniquely positioned to make an impact on all aspects of care, including potentially identifying a patient who may qualify for a clinical study. Enrolling clinical studies has become more challenging, and community research teams need to be more efficient when identifying potential candidates in order to generate meaningful advances at a faster rate. Our hope is that the impact seen within the MYLUNG Consortium will advance how we think and assemble clinical research teams."

In addition to the oral presentation, Nicholas Robert, MD, chief medical officer of Ontada, will lead a poster presentation (Abstract #9004) from a retrospective study of MYLUNG Consortium Protocol 1. The abstract, "Predictors of biomarker testing among patients (pts) with metastatic non-small cell lung cancer (mNSCLC)," analyzes the impact of clinical and/or social factors (such as race, histology and clinical practice size) on undertested populations. These data will be presented during the "Lung Cancer—Non-Small Cell Metastatic" session, which will be held Monday, June 6 at 8 a.m.

Additional Featured Research Selected for Presentation

An oral presentation (Abstract #LBA5500) on a phase 3 study evaluating rucaparib monotherapy titled, "ATHENA–MONO (GOG-3020/ENGOT-ov45): A randomized, double-blind, phase 3 trial evaluating rucaparib monotherapy versus placebo as maintenance treatment following response to first-line platinum-based chemotherapy in ovarian cancer," was co-authored by Dr. Coleman. These data will be presented during the "Gynecologic Cancer" session on Monday, June 6 at 8 a.m.

"Survivorship of women with advanced ovarian cancer has improved, primarily the result of two key agents, bevacizumab and the Poly (ADP-ribose) polymerase (PARP) inhibitors. In the ATHENA trial, we demonstrate the substantial efficacy and safety of a third agent (rucaparib) for primary maintenance treatment," said Dr. Coleman. "Our team looks forward to presenting our findings involving PARP inhibitors and immune checkpoint inhibitors and their potential as therapeutic options for patients in this population."

Alexander I. Spira, MD, PhD, FACP, director of the thoracic and Phase I program for Virginia Cancer Specialists, a practice in The Network, will have an oral presentation (Abstract #9002) on the effect of adagrasib (MRTX849) in patients with NSCLC titled, "KRYSTAL-1: Activity and safety of adagrasib (MRTX849) in patients with advanced/metastatic non-small cell lung cancer (NSCLC) harboring a KRASG12C mutation." These data will be presented during the "Lung Cancer—Non-Small Cell Metastatic" session on Friday, June 3 at 1:24 p.m.

Additional key NSCLC data presentations involving Dr. Spira’s research include a late breaking abstract (#LBA9009) titled "Activity of adagrasib (MRTX849) in patients with KRASG12C-mutated NSCLC and active, untreated CNS metastases in the KRYSTAL-1 trial," which is being held during the "Including the Excluded: Advancing Care for All Patients With Lung Cancer" clinical symposium on Monday, June 6 at 4:30 p.m. Dr. Spira was also involved in the research featured in (Abstract #9008), "Amivantamab in patients with NSCLC with MET exon 14 skipping mutation: Updated results from the CHRYSALIS study," selected for oral presentation during the "Lung Cancer—Non-Small Cell Metastatic" session, which will be held on Friday, June 3 at 3:24 p.m.

"Immunotherapy research will ultimately lead to greater knowledge and more precise treatments for patients," said Dr. Spira. "There is still so much to learn in the area of precision oncology and targeted therapies in NSCLC, and we are constantly working towards ways to develop new and effective therapies that can create better outcomes for patients. The vital research showcased in this clinical symposium and oral presentations on the effect of adagrasib (MRTX849) and amivantamab in patients with NSCLC will help inform the clinical development of these targeted therapies and explain their potential clinical utility and promise."

Featured Health Technology-Related Research

An oral presentation (Abstract #1507) evaluating health technologies and their impact on quality of care and health disparities was co-authored by Debra Patt, MD, PhD, MBA, executive vice president of public policy, payer relations and strategic initiatives at Texas Oncology, a practice in The Network. The presentation titled, "Evaluating mass implementation of digital health solutions to improve quality and reduce disparities in a large multisite community oncology practice," will be presented during the "Care Delivery and Regulatory Policy" session on Monday, June 6 at 5:12 p.m.

"Digital health solutions engage patients with our clinical teams and improve patient care," said Dr. Patt. "These solutions reduce response time for symptomatic patients and improve transparency and health literacy improving the partnership between our clinical teams and the patients we serve. Digital health solutions are of great value for all patients, especially those classified as ‘at risk’. I am grateful to be part of a practice leading some of these important efforts."

An abstract (#1521) evaluating the usage of a machine learning (ML) model titled "The initial outcome of deploying a mortality prediction tool at community oncology practices," will be presented during the "Care Delivery and Regulatory Policy" poster session. The ML model predicted 90-day mortality risk for patients with metastatic cancer and was designed to facilitate earlier end-of-life discussions, including hospice care, with the patients. These results, researched by members of The US Oncology Network, will be delivered on Saturday, June 4 at 1:15 p.m.

"Aligning care at the end of life with patients’ goals and values helps reduce the likelihood of undesirable hospitalization, ICU stays and side effects of therapy," said Ping Ye, PhD, a senior data scientist for The Network. "We deployed a predictive mortality tool to The Network practices to help physicians proactively initiate care discussions earlier with identified patients, allowing them access to care aligned with their wishes as they near life’s final stages."

Invitation to Scandion Oncology webcast and conference call June 10, 2022

On June 3, 2022 Scandion Oncology (Scandion), a biotech company developing first-in-class medicines aimed at treating cancer which is resistant to current treatment options, reported that it will on June 10, 2022, at 11:00 CET host a webcast and conference call (Press release, Scandion Oncology, JUN 3, 2022, View Source;2022,c3580063 [SID1234615520]). Here, the company’s Executive Management will present the Rights Issue announced on June 1, 2022.

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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

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REPLAY access:

Webcast replay will be available at View Source in the Investors section and at View Source

The information was provided by the contact person above for publication on June 3, 2022 at 14.30 CET.

Data Published in Annals of Oncology Reinforce Clinical Utility of Veracyte’s Decipher Prostate Genomic Classifier for Informing Treatment of Men Experiencing Prostate Cancer Progression

On June 3, 2022 Veracyte, Inc. (Nasdaq: VCYT) reported the publication of data reinforcing the clinical utility of the Decipher Prostate genomic classifier for helping to guide the timing and intensity of therapy in men experiencing prostate cancer recurrence following radical prostatectomy (RP) (Press release, Veracyte, JUN 3, 2022, View Source [SID1234615519]). The findings, from an ancillary study of the prospective open-label, multicenter, randomized phase 3 SAKK 09/10 trial conducted at 28 centers in Belgium, Germany, and Switzerland, appear in Annals of Oncology.

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It is estimated that more than 40 percent of men with intermediate- or high-risk prostate cancer may experience a biochemical disease recurrence after RP, which is characterized by rising levels of serum prostate-specific antigen (PSA). For men who experience a rising PSA, determining the optimal timing to initiate salvage radiotherapy (SRT) and whether to add androgen deprivation therapy (ADT) to SRT is challenging. This decision is important in part because the side effects of ADT when given concurrently with SRT are often difficult for patients to manage and are associated with long-term cardiovascular impact of hormone therapy.

"Each year in the United States, tens of thousands of men are diagnosed with biochemically recurrent prostate cancer, yet conventional clinical measures such as PSA and Gleason score are often insufficient to predict which of them will do well with SRT alone and who will need more intensive therapy to improve their oncologic outcomes," said Elai Davicioni, Ph.D., Veracyte’s medical director for urology. "The data from this study suggest that the Decipher Prostate genomic classifier can help fill this gap by providing objective information to guide customized treatment planning in the postoperative setting."

Researchers in the Swiss Group for Clinical Cancer Research (SAKK) and collaborating cancer centers assessed the clinical outcomes and Decipher Prostate genomic risk for 226 prostate cancer patients from the SAKK 09/10 trial, which randomized patients to standard vs. dose-escalated SRT. This study involved men experiencing a rise in PSA following RP, all of whom received SRT without the addition of ADT. Patients in the Decipher Prostate analysis were followed for a median of 6.3 years.

Findings suggest that Decipher Prostate can identify the patients who are at highest risk of cancer progression following RP and would benefit from earlier, more intensive treatment. Patients with a high Decipher score were more than twice as likely than those with a lower Decipher score to experience biochemical and clinical progression, and to receive long-term salvage hormone therapy. Additionally, patients with high Decipher scores had markedly improved outcomes when treated with SRT when the PSA burden was still low as compared to late SRT, when PSA levels have already risen.

"These findings add meaningfully to the existing literature supporting the use of the Decipher Prostate RP test in postoperative decision-making. Decipher Prostate RP is the only genomic test backed by evidence from randomized Phase 3 trials and we look forward to our continued collaboration with the SAKK team, with studies aimed at further elucidating the subset of men that benefit most from dose-escalation," said Dr. Davicioni.

About Decipher Prostate

Decipher Prostate is a 22-gene, microarray-based genomic test intended to help inform treatment decisions for men with localized prostate cancer at initial diagnosis (Decipher Prostate Biopsy) and after surgical removal of the prostate (Decipher Prostate RP). The test reports the Decipher Score, which prognosticates a patient’s risk of metastasis within five years and provides risk estimates of prostate cancer-specific outcomes. Decipher Prostate can help guide physicians to better select the appropriate therapy for a specific patient, which in turn can result in improved patient outcomes. Decipher Prostate is available as part of Veracyte’s CLIA-validated laboratory developed test (LDT) service. This test has not been cleared or approved by the FDA.