Mirati Therapeutics to Participate in Two Upcoming Healthcare Conferences

On September 22, 2022 Mirati Therapeutics, Inc. (NASDAQ: MRTX), a clinical-stage targeted oncology company, reported that it will participate in two upcoming healthcare conferences (Press release, Mirati, SEP 22, 2022, View Source [SID1234621391]).

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Thursday, September 29 at 10:00 a.m. ET / 7:00 a.m. PT at the Guggenheim Nantucket Therapeutics Conference. David Meek, chief executive officer, will represent the company in a fireside chat.
Monday, October 3 at 1:10 p.m. ET / 10:10 a.m. PT at the Bank of America Precision Oncology Conference. David Meek, chief executive officer, will represent the company in a fireside chat.
Investors and the general public are invited to listen to a live webcast of the sessions through the "Investors and Media" section on Mirati.com. A replay of the webcast will be made available following the event.

NeuBase to Participate at Chardan’s 6th Annual Genetic Medicines Conference

On September 22, 2022 NeuBase Therapeutics, Inc. (Nasdaq: NBSE) ("NeuBase" or the "Company"), a biotechnology platform company Drugging the Genome to address disease at the base level using a new class of precision genetic medicines, reported that company management will participate in-person for a fireside chat at Chardan’s 6th Annual Genetic Medicines Conference being held in New York City on October 3-4, 2022 (Press release, NeuBase Therapeutics, SEP 22, 2022, View Source [SID1234621375]).

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An audio replay of the webcast will be available following the presentation for 90 days. To access the replay, please click here. Please contact your representative at Chardan to schedule a one-on-one meeting with NeuBase management during the conference.

Aprea Therapeutics Announces Poster Presentation at the 2022 Rivkin Center and American Association for Cancer (AACR) Virtual Ovarian Cancer Research Seminar Series

On September 22, 2022 Aprea Therapeutics, Inc. (Nasdaq: APRE), a biopharmaceutical company focused on developing novel synthetic lethality-based cancer therapeutics targeting DNA damage response (DDR) pathways, reported that the abstract titled "ATRN-W1051, a novel and potent WEE1 inhibitor for the treatment of CCNE1-overexpressing ovarian cancer" will be presented at the 14th Biennial Virtual Ovarian Cancer Research Seminar Series presented by the Rivkin Center and the American Association for Cancer Research (AACR) (Free AACR Whitepaper) (Press release, Aprea, SEP 22, 2022, View Source [SID1234621374]). The series will take place on September 21, 22, 28, and 29, 2022, with each day scheduled to run from 12:00-2:00pm U.S. Pacific Time.

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"A growing body of scientific evidence provides exciting development opportunities for our WEE1 inhibitor, ATRN-W1051," said Oren Gilad, Ph.D., President and Chief Executive Officer of Aprea. "ATRN-W1051 is designed to be a potent and selective WEE1 inhibitor with a differentiated structure and potentially preferable pharmacokinetic properties. The presented data demonstrate anti-proliferative activity against a variety of cancer cell lines and tumor growth inhibition in a genetically-defined ovarian cancer xenograft model. We look forward to completing the IND-enabling studies and plan to initiate the clinical program shortly thereafter."

A copy of the poster will be accessible from the "Events Calendar" in the News and Events section of the Aprea website.

China CDE Grants CMG901 Breakthrough Therapy Designation for Claudin 18.2-Positive Advanced Gastric & Gastroesophageal Junction Cancer

On September 22, 2022 Keymed Biosciences (HKEX:02162) reported that the Center for Drug Evaluation (CDE) of the China National Medical Products Administration (NMPA) has granted CMG901 the Breakthrough Therapy Designation for the treatment of advanced gastric and gastroesophageal junction(GEJ) cancer which have relapsed and/or are intolerant to prior therapies (Press release, Keymed Biosciences, SEP 22, 2022, View Source;gastroesophageal-junction-cancer-301630843.html [SID1234621373]).

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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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About CMG901

CMG901 is a Claudin 18.2-targeted antibody-drug conjugate (ADC) developed for the treatment of Claudin 18.2-expressing solid tumors. In April 2022, the U.S. Food and Drug Administration (FDA) granted CMG901 Fast Track Designation[i] and Orphan Drug Designation[ii] as monotherapy for the treatment of unresectable or metastatic gastric and gastroesophageal junction (GEJ) cancer which are resistant/refractory to prior therapies.

About CDE’s Breakthrough Therapy Designation

CDE’s Breakthrough Therapy Designation is designed to expedite the clinical development of innovative drugs presenting significant clinical advantages. A breakthrough therapy must provide effective treatment for a seriously debilitating or life-threatening condition that has no effective therapy or demonstrate substantial improvement over available therapies. According to the CDE, BTD provides opportunities for more intensive CDE guidance and discussion with respect to clinical trials and development strategy, and for priority review later.

Memorial Sloan Kettering researchers present predictive findings from first use of Mission Bio’s scMRD assay for AML

On September 22, 2022 Mission Bio, Inc., the pioneer in high-throughput single-cell DNA and multi-omics analysis, reported the first findings by researchers using its new Tapestri Single-cell Multi-omics Measurable Residual Disease (scMRD) assay, as researchers from Memorial Sloan Kettering Cancer Center (MSK) discovered subclonal co-mutations and immunophenotypic profiles that can distinguish individual cells indicative of future acute myeloid leukemia (AML) relapse from others present after treatment (Press release, Memorial Sloan-Kettering Cancer Center, SEP 22, 2022, View Source [SID1234621372]). Because it is uniquely capable of both high sensitivity and specificity, the scMRD assay can distinguish between leukemic, preleukemic, and hematopoietic clones, and between donor and host cells following bone marrow transplantation. The findings have the potential to be applied to improve treatment prognostics, guiding doctors on patient need for a hematopoietic stem cell transplant, with future implications for both patient stratification in clinical trials and patient care — impacting disease surveillance, therapeutic selection, and patient outcomes.

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About half of all patients with AML relapse within a few years of their first treatments1. Currently, flow cytometry and single gene testing and/or bulk next-generation sequencing are used to detect the presence of measurable residual disease (MRD). However, even if both tests come back negative, many patients will still relapse. Mission Bio’s scMRD technology is designed to improve upon these assays by integrating DNA mutation and immunophenotypic signatures for each cell individually, enabling quantitative analysis of leukemia cells that may have gained new mutations causing treatment resistance or changed their immunophenotype from the start of the disease.

Researchers from the lab of Ross Levine, MD, Deputy Physician in Chief for Translational Research at MSK, used the assay to study the clonal architecture of cells that survived initial AML therapy. In data presented at Mission Bio’s Tapestri scMRD for AML Summit, the researchers illustrated several findings that could impact the predictive power of scMRD. For example, in patient samples drawn following chemotherapy, Levine’s team found the scMRD assay detected clinically relevant variants missed by bulk next-generation sequencing. Additionally, the researchers tapped the multi-omic capabilities of the assay to characterize both the mutational profile and immunophenotype of single cells and to illustrate the clonal architecture distinguishing leukemic clones from preleukemic clones and hematopoietic clones. Full publication of the data is forthcoming.

"We believe these findings are key to improving how patients are treated for leukemias and other cancers where MRD is relevant," said Todd Druley, MD, PhD, Chief Medical Officer of Mission Bio. "Partnering with both top academics like Ross’s team at MSK and industry partners for studies like this will be critical in establishing MRD as a surrogate endpoint, to one day incorporate into clinical trials and practice. It paves the way for not just predicting relapse but preventing it, by identifying high-risk clones for early eradication."

This summer, Mission Bio announced a program to give pioneering cancer researchers and biopharma partners early access to its research-use-only scMRD assay for AML, which uses the Tapestri Platform to identify single point mutations, copy number variants and structural lesions in DNA and immunophenotype data from the same cells. Through Mission Bio’s early access program, researchers, contract research organizations, and biopharma companies can utilize the scMRD assay for AML for proof-of-concept study research programs ahead of full-scale commercialization. For more information, visit View Source