iSpecimen® to Report Third Quarter 2021 Results on November 4, 2021

On October 21, 2021 iSpecimen Inc. (NASDAQ: ISPC) ("iSpecimen" or the "Company"), an online marketplace for human biospecimens, reported that it will report its financial results for the third quarter ended September 30, 2021, before the market open on Thursday, November 4, 2021 (Press release, iSpecimen, OCT 21, 2021, View Source [SID1234591741]).

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The Company will host a conference call and audio webcast that morning at 8:30 a.m. Eastern Time featuring remarks by Christopher Ianelli, MD, PhD, CEO and President, Tracy Curley, CFO, and Jill Mullan, COO.

Sumitomo Dainippon Pharma Oncology Announces First Patient Dosed in Phase 1 Study of DSP-0390 in Patients with Recurrent High-Grade Glioma

On October 21, 2021 Sumitomo Dainippon Pharma Oncology, Inc., a clinical-stage company focused on research and development for novel cancer therapeutics, reported the first patient has been dosed in a Phase 1 study evaluating its investigational agent DSP-0390, an emopamil-binding protein (EBP) inhibitor, for the treatment of patients with recurrent high-grade glioma (Press release, Sumitomo Dainippon Pharma, OCT 21, 2021, View Source [SID1234591740]).

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High grade gliomas are the most common type of malignant brain tumor and cause significant morbidity and mortality.1 Preclinical studies have shown DSP-0390 may have anti-tumor activity that may help address this persistent unmet medical need.

"Dosing the first patient in this study represents another important milestone for SDP Oncology and broadens our fight against brain tumors along with our investigational agent WT1 immunotherapeutic cancer vaccine," said Patricia S. Andrews, Chief Executive Officer and Global Head of Oncology, Sumitomo Dainippon Pharma Oncology (SDP Oncology). "We look forward to generating data to guide the development of DSP-0390 with the goal of developing meaningful treatments for patients with brain cancer."

The primary objective of the first-in-human, open-label, dose-escalation study is to assess the safety and tolerability of DSP-0390 in patients with recurrent high-grade glioma. The trial will also determine the maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE). The secondary objective is to characterize the pharmacokinetic (PK) profile of DSP-0390.

Following the completion of the dose-escalation portion of the trial, the study will move into a Part 2 expansion to evaluate whether there is preliminary antitumor activity of DSP-0390 and establish the recommended Phase 2 dose (RP2D) in recurrent World Health Organization (WHO) Grade III or IV malignant glioma.

The trial is being conducted in the United States and Japan. Additional information, including comprehensive inclusion and exclusion criteria, can be accessed at www.ClinicalTrials.gov (NCT05023551).

About DSP-0390

DSP-0390 is an emopamil-binding protein (EBP) inhibitor, that is currently being investigated in a Phase 1 study in patients with recurrent high-grade glioma (NCT05023551). EBP is an endoplasmic reticulum membrane protein involved in cholesterol biosynthesis.2 Since most cancer cells are characterized by an upregulation of the various pathways responsible for their biosynthesis and the demand for cholesterol to support cell proliferation is high,3,4,5 the inhibition of EBP by DSP-0390 therefore is expected to lead to disruption of cholesterol homeostasis and induce cell death in cancer cells.6,7 Moreover, as EBP is reported to be highly expressed in several types of cancer and correlates with an aggressive phenotype of certain types of cancers, DSP-0390 has the potential to have anti-tumor activity in these cancers.8,9

Kintor Pharma Announces PD-L1/TGF-β dual-targeting antibody (GT90008) Approved for Advanced Solid Tumour Clinical Trial in China

On October 21, 2021 Kintor Pharmaceutical Limited ("Kintor Pharma", HKEX: 9939), a clinical-stage biotechnology company developing innovative small molecule and biological therapeutics, reported that the clinical trial of PD-L1/TGF-β dual-targeting antibody (GT90008) for the treatment of advanced solid tumours was approved by the National Medical Products Administration (NMPA) of China on 21 October 2021 (Press release, Suzhou Kintor Pharmaceuticals, OCT 21, 2021, View Source;dual-targeting-antibody-gt90008-approved-for-advanced-solid-tumour-clinical-trial-in-china-301405880.html [SID1234591739]).

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GT90008 is a PD-L1/TGF-β dualtargeting antibody which has a high activity in inhibiting both PD-L1 and TGF-βR2. GT90008 has the potential to be a best-in-class drug globally. Kintor Pharma obtained an exclusive license in Greater China for GT90008 from US-based company Gensun in August 2020.

Dr. Youzhi Tong, founder, Chairman and CEO of Kintor Pharma, commented, "We are delighted to obtain the approval from NMPA to conduct the clinical trial of PD-L1/TGF-β dual-targeting antibody. GT90008 is the second novel antibody drug that has entered the clinical stage. The rapid progress from in-license to IND approval has demonstrated our team’s great execution capability. Though there has been headwind on dual-targets antibody of this category, we are confident with our antibody and actively exploring the combination therapies with our GT90001(ALK-1) antibody on advanced tumours. We wish the combo design of GT90008 and GT90001 would benefit patients with advanced tumours. "

Johnson & Johnson Announces Quarterly Dividend for Fourth Quarter 2021

On October 21, 2021 Johnson & Johnson (NYSE: JNJ) reported that its Board of Directors has declared a cash dividend for the fourth quarter of 2021 of $1.06 per share on the company’s common stock (Press release, Johnson & Johnson, OCT 21, 2021, View Source;johnson-announces-quarterly-dividend-for-fourth-quarter-2021-301406101.html [SID1234591738]). The dividend is payable on December 7, 2021 to shareholders of record at the close of business on November 23, 2021. The ex-dividend date is November 22, 2021.

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The dark matter of the genome: Flamingo Therapeutics taps potential of mysterious RNA for cancer therapies

On October 21, 2021 Flamingo Therapeutics reported that was born out of a collaboration between three partners in Flanders – VIB, UGent and KU Leuven – and the University of Michigan in the US (Press release, Flamingo Therapeutics, OCT 21, 2021, View Source;utm_medium=rss&utm_campaign=the-dark-matter-of-the-genome-flamingo-therapeutics-taps-potential-of-mysterious-rna-for-cancer-therapies [SID1234591687]). "The foundations of the company were laid in 2016, when the research groups of prof. Pieter Mestdagh at UGent and prof. Jean-Christophe Marine at VIB and KU Leuven published a paper revealing a connection between certain long non-coding RNAs and malignant melanoma, the most aggressive form of skin cancer," explains Floor Stam, COO at Flamingo. These insights were later linked to research carried out at the University of Michigan.

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Thanks to this unique expertise, the young biotech company is currently one of the only players in the world that is able to explore the potential of these long-coding RNAs (lncRNAs, pronounced as ‘link RNA’). According to Flamingo, lncRNAs account for 27% of the non-coding RNA genes, which make up around two-thirds of all genes. Non-coding RNA genes are not translated into proteins and the function of most of them is currently very unclear (hence the ‘dark matter’ moniker).

Cancer targets from out of the dark
"For a long time, the non-coding portion of the genome was considered to be useless ‘junk DNA’. But it actually has an enormous potential for new therapies against many different diseases," says Stam. Flamingo is specifically looking into the possibilities for cancer therapies, as lncRNAs play a role in the energy provision of cancer cells when they divide uncontrollably. If you can manipulate that process, you should be able to produce a very targeted treatment that attacks the cancer cells and leaves healthy cells alone.

Flamingo’s approach could possibly limit the side effects of innovative cancer therapies. Stam also believes this new solution could be produced more rapidly than more traditional therapies that target proteins. "Because we have access to the unparalleled screening and hit identification capabilities of our collaborators at Ionis, a clinical candidate molecule can be developed in 12 to 14 months," specifies Stam.

"For a long time, the non-coding portion of the genome was considered to be useless ‘junk DNA’. But it actually has an enormous potential for new therapies against many different diseases." – Floor Stam, Flamingo Therapeutics

To identify targets for cancer therapies in this predominantly uncharted region of the genome, the company has developed the unique discovery engine FLAME (Flamingo LncRNA Antisense Mining Engine). Based on the findings in the groundbreaking 2016 paper, the initial focus has predominantly been on finding targets for treating the aggressive skin cancer melanoma, where the Flamingo team has been focusing on a lncRNA molecule named SAMMSON.

High profile partnership
Thanks to a recently-signed collaboration agreement with the American company Ionis Pharmaceuticals – a global leader in RNA-targeted therapies – Flamingo is now expanding its activities dramatically. The company is taking over three clinical programs for RNA-targeted cancer therapeutics from Ionis, as well as one preclinical program concentrating on lncRNAs.

"Ionis has been at the forefront of RNA-targeted therapy for thirty years… We are also a very interesting partner for them, because we concentrate on RNA-targeting therapies in oncology and have unique expertise in the field of lncRNAs." – Mike Garrett, Flamingo Therapeutics

"From the start, Ionis has been a crucial shareholder of ours, helping us to go in the right direction," says Mike Garrett, CEO of Flamingo. "Ionis has been at the forefront of RNA-targeted therapy for thirty years and offers invaluable knowhow and experience in clinical programs. We are also a very interesting partner for them, because we concentrate on RNA-targeting therapies in oncology and have unique expertise in the field of lncRNAs." While Flamingo’s headquarters are located at the biotech incubator in Leuven, much of its activities also take place in facilities at San Diego close to Ionis’ home base.

Potential solutions for a range of cancer types
Flamingo’s most advanced drug candidate in development is called danvatirsen and targets the STAT-3 gene. "It is showing great potential in the battle against head and neck cancers and lymphoma," says Garrett. Other drug candidates, targeting the androgen receptor and IRF4 gene, are being developed to fight prostate cancer and multiple myeloma (a type of bone marrow cancer).

Read this BioVox article to learn about Precirix, another start-up tackling cancer with an innovative approach.

The Flemish company has also taken over a preclinical-stage program focusing on a well-characterized lncRNA target named MALAT1. "This pioneering research could lead to solutions for different cancers, but for the moment we especially foresee therapeutic benefits for patients with triple-negative breast cancer," says COO Floor Stam. The preclinical stage of this program should be finished by the end of 2022. In ideal circumstances, the clinical programs could lead to new therapies on the market already in 2026.

To support the company’s rapid expansion, Flamingo is now preparing a new investment round. For the moment, its main investors are the well-known biotechnology investors PMV and Kurma Partners, Belgian and French respectively.