Medpace Holdings, Inc. to Present at Two Upcoming Investor Conferences

On May 26, 2020 Medpace Holdings, Inc. (Nasdaq: MEDP) ("Medpace") reported that it will present at the following two investor conferences in June (Press release, Medpace, MAY 26, 2020, View Source [SID1234558496]):

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Jefferies Virtual Global Healthcare Conference
Date: Wednesday, June 3, 2020
Presentation: 8:30 a.m. ET
Speakers: August Troendle, President & Chief Executive Officer, Jesse Geiger, Chief Financial Officer & Chief Operating Officer, Laboratory Operations, and Kevin Brady, Executive Director of Finance

William Blair Virtual Annual Growth Stock Conference
Date: Tuesday, June 9, 2020
Presentation: 4:40 p.m. CT (5:40 p.m. ET)
Speakers: August Troendle, President & Chief Executive Officer, Jesse Geiger, Chief Financial Officer & Chief Operating Officer, Laboratory Operations, and Kevin Brady, Executive Director of Finance

A live webcast of the presentation will be accessible through the "Investors" section of the Company’s website at www.medpace.com and will be available for replay following the event.

Alpine Immune Sciences to Participate in Fireside Chat at the Jefferies Virtual Global Healthcare Conference

On May 26, 2020 Alpine Immune Sciences, Inc. (NASDAQ: ALPN), a leading clinical-stage immunotherapy company focused on developing innovative treatments for cancer and autoimmune/inflammatory diseases, reported its participation in an analyst-led fireside chat at the Jefferies Virtual Global Healthcare Conference on Tuesday, June 2, at 10:00 a.m. ET (Press release, Alpine Immune Sciences, MAY 26, 2020, View Source [SID1234558495]).

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A live webcast of the presentation will be available online in the investor relations section of the company’s website at View Source A replay of the presentation will be available on the company website for 90 days following the webcast.

Xencor to Present at Upcoming Investor Conferences

On May 26, 2020 Xencor, Inc. (NASDAQ: XNCR), a clinical-stage biopharmaceutical company developing engineered monoclonal antibodies for the treatment of cancer and autoimmune diseases, reported that Bassil Dahiyat, Ph.D., president and chief executive officer, will participate in two upcoming investor conferences (Press release, Xencor, MAY 26, 2020, View Source [SID1234558494]):

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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 Virtual Healthcare Conference
Date: Tuesday, June 2, 2020
Presentation Time: 2:30 p.m. ET / 11:30 a.m. PT
Raymond James Human Health Innovation Conference
Date: Monday, June 15, 2020
Immuno-Oncology Panel Time: 11:00 a.m. ET / 8:00 a.m. PT
A live webcast of the presentation at the Jefferies conference will be available under "Events & Presentations" in the Investors section of the Company’s website located at www.xencor.com. A replay will be posted on the Xencor website approximately one hour after the live event and will be available for 30 days.

Mauna Kea Technologies: Cellvizio® Endorsed By the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) as a Safe and Effective Diagnostic Tool

On May 26, 2020 Mauna Kea Technologies (Paris:MKEA) (OTCQX:MKEAY) (Euronext: MKEA) inventor of Cellvizio, the multidisciplinary probe- and needle-based confocal laser endomicroscopy (pCLE/nCLE) platform, reported that the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) Technology and Value Assessment Committee (TAVAC) published a review on the safety and efficacy of confocal laser endomicroscopy as a diagnostic tool for the evaluation of gastrointestinal pathologies (Press release, Mauna Kea Technologies, MAY 26, 2020, View Source [SID1234558493]). This article, entitled "SAGES TAVAC safety and efficacy analysis confocal laser endomicroscopy," was published in a peer reviewed international journal, Surgical Endoscopy (doi.org/10.1007/s00464-020-07607-3).

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SAGES TAVAC publishes Technology Alerts on a monthly basis and longer safety and efficacy reviews on a periodic basis. The publication in Surgical Endoscopy was based on TAVAC’s systematic review of clinical studies on PubMed/Medline involving CLE in May 2018 as well as bibliographies of key references for relevant studies not available on PubMed. TAVAC’s objective was to evaluate the safety, value, and efficacy of CLE in the gastrointestinal tract. The results of TAVAC’s analysis concluded that CLE offers an excellent safety profile with rare adverse events related to the use of fluorescent agents. It has been shown to increase the detection of dysplastic Barrett’s esophagus, gastric intraepithelial neoplasia/early gastric cancer, and dysplasia associated with inflammatory bowel disease when compared to standard screening protocols. It also aids in the differentiation and classification of colorectal polyps, indeterminate biliary strictures, and pancreatic cystic lesions.

"The process of the TAVAC review and experience of the Committee members show that Cellvizio has an excellent safety profile and clear clinical utility and efficacy as an adjunct to the standard of care across a range of gastrointestinal diseases and conditions," said Shawn Tsuda, MD, FACS, board-certified surgeon and Chair of the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) Technology and Value Assessment Committee (TAVAC). "Early diagnosis and effective surveillance can have significant positive impacts on therapeutic management, and Cellvizio is an essential tool to improve diagnostic accuracy and reduce inappropriate interventions."

"We are extremely pleased by SAGES’s endorsement of Confocal Laser Endomicroscopy in the diagnosis and surveillance of gastrointestinal diseases including GERD, Barrett’s Esophagus, and pancreatic cysts," said Robert L. Gershon, Chief Executive Officer of Mauna Kea Technologies. "This peer reviewed analysis reinforces the position of Cellvizio as an adjunct to the standard of care to effectively target biopsies and increase diagnostic yield, thereby improving patient outcomes and optimizing clinical costs through increased diagnostic accuracy."

In their analysis, the Committee outlined the high diagnostic accuracy of CLE as an advanced imaging adjunct across all gastrointestinal endoscopic indications compared to current standard of care. They also highlighted the improvement of diagnostic yield for specific indications such as chronic GERD, Barrett’s Esophagus, early gastric cancer, gastric intestinal neoplasia, and pancreatic cystic lesions, as well as the effectiveness for evaluation and ongoing surveillance of inflammatory bowel disease (IBD).

One important consideration for endorsement of a new technology for gastrointestinal disease diagnosis is its potential for reducing inappropriate or unnecessary therapy for non-neoplastic conditions, therefore improving overall procedure-related complications, optimizing surveillance intervals, reducing unnecessary interventions, and limiting histological analysis of insignificant lesions while detecting early dysplasia to improve patient outcomes.

About SAGES
SAGES (The Society of American Gastrointestinal and Endoscopic Surgeons) was founded in 1981 to foster, promote, support and encourage academic, clinical and research achievement in gastrointestinal endoscopic surgery. SAGES currently boast more than 6,500 general surgeon members from countries all around the world. SAGES annual meeting is oriented toward minimally invasive surgery and in 2018 had an attendance of over 2,700 surgeons.

Lucence Shares Data at ASCO20 Demonstrating High Sensitivity of AmpliMARK™ Sequencing Technology in Detecting Clinically Relevant Biomarkers in Lung Cancer

On May 26, 2020 precision oncology company Lucence reported that it will be presenting data this week demonstrating high sensitivity of its liquid biopsy technology in detecting clinically relevant biomarkers in lung cancer, alongside promising data in breast and blood cancers (Press release, Lucence, MAY 26, 2020, View Source [SID1234558492]). The data, presented as part of ASCO (Free ASCO Whitepaper)’s Virtual Scientific Program, show the Company’s AmpliMARK technology detection capability for recommended biomarkers with 97.4% concordance between two orthogonal liquid biopsy platforms in lung cancer. The Company is planning to make its LiquidHALLMARK test, powered by AmpliMARK, commercially available in the United States later this year for biomarker detection in lung cancer patients.

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Clinical utility of a liquid biopsy diagnostic approach in lung cancer using amplicon-based next-generation sequencing in parallel with allele-specific PCR presents data from a multinational study examining real-world diagnostic outcomes of Lucence’s liquid biopsy technology in 374 lung cancer patients. Patients who were tested with an innovative combination of two blood-based liquid biopsy platforms achieved a one-day result for a key treatment decision, together with a subsequent comprehensive analysis of recommended markers, with a 97.4% concordance between the two platforms. This study highlights that ultrasensitive blood-based liquid biopsy is a key platform to support lung cancer diagnosis and appropriate treatment selection.

Ultrasensitive multiplex detection of structural rearrangements in ALK, RET, ROS1 and PD-L1 using a comprehensive next-generation sequencing assay, #302, will be presented on Friday, May 29th from 8:00-11:00 am Eastern Time in a virtual session. This poster reports AmpliMARK’s high sensitivity in detecting cancer-related structural variants in cfDNA samples from lung cancer patients, cfDNA samples from lymphoma patients, and tumor tissue DNA samples from natural killer(NK)/T-cell lymphoma patients. A second poster, Detection of actionable gene mutations in breast cancer by amplicon-based next-generation sequencing liquid biopsy, #120, reports AmpliMARK’s high sensitivity in detecting key PIK3CA, ESR1 and other driver gene mutations non-invasively in plasma cfDNA of breast cancer patients in a multinational study.

These new studies suggest that the LiquidHALLMARK liquid biopsy test, powered by amplicon-based sequencing technology AmpliMARK, has the potential to shift the paradigm in precision oncology. LiquidHALLMARK offers highly sensitive, target-rich insights into established biomarkers spanning 80 gene mutations and 10 gene fusions in 15 cancer types (available in the United States starting Q3 2020 for investigational use only). The data showcase AmpliMARK’s excellent performance in rapidly detecting multiple somatic variants, highlighting the technology’s potential to deliver fast insights for clinicians to develop the most effective treatment plans for patients.

To adapt to the virtual format of ASCO (Free ASCO Whitepaper)20, Lucence has created an online hub at lucence.com/asco2020. Attendees can book a meeting with the Lucence team, see a complete list of posters and abstracts, and register for a webinar on COVID-19 and lung cancer presented by the Singapore Society of Oncology, taking place on June 4th, 2020 at 5 PM Pacific Time/8 PM Eastern Time and June 5th at 8 AM GMT+8.