Ascentage Pharma Announces First Patient Dosed in Europe in the Phase Ib/II Study of the Bcl-2 inhibitor APG-2575 in Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

On November 24, 2020 Ascentage Pharma (6855.HK), a globally focused, clinical-stage biotechnology company engaged in developing novel therapies for cancers, chronic hepatitis B (CHB), and age-related diseases, reported that a Phase Ib/II clinical study of the company’s novel Bcl-2 inhibitor APG-2575, as a single agent or in combinations for the treatment of patients with relapsed/refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (r/r CLL/SLL) (APG2575CU101; EudraCT#2020-002736-73), has dosed its first patient in Ukraine (Press release, Ascentage Pharma, NOV 24, 2020, View Source [SID1234571682]). This is the first global clinical study conducted by Ascentage Pharma in Europe.

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This global multicenter Phase Ib/II study was designed to evaluate the safety and efficacy of APG-2575 as a single agent or in combinations for the treatment of patients with r/r CLL/SLL. The study has recently obtained Clinical Trial Application (CTA) approvals from the Ministry of Health of Ukraine and the Ministry of Health of the Russian Federation.

CLL is a hematologic malignancy caused by mature B-cell neoplasms and constitutes the most common form of adult leukemia in North America and Europe, accounting for about 30% of all new leukemia cases. The annual incidence rate of CLL is around 2-6 cases per 100,000, and 12.8 cases per 100,000 in the population aged 65 years or older. Despite significant initial responses to current first-line treatments, many patients with CLL need ongoing treatment to maintain these responses, and relapse often portends a poor prognosis. Recent studies in CLL showed that combining a BTK inhibitor with a Bcl-2 inhibitor can deepen responses and shorten treatment durations from long-term to cyclic treatments, making it possible for patients to achieve complete remission and therefore discontinue treatment[1],[2]. These findings have provided a compelling rationale for exploring APG-2575 in combination with BTK inhibitors.

APG-2575 is a novel, orally administered Bcl-2‒selective inhibitor being developed by Ascentage Pharma. APG-2575 is designed to treat several hematologic malignancies by selectively blocking Bcl-2 to restore the normal apoptosis process in cancer cells. APG-2575 is the first China-developed Bcl-2 inhibitor having entered clinical development in China. APG-2575 has received clearances and approvals for multiple Phase Ib/II clinical studies in China, Australia, and the US, and is currently being developed in a range of hematologic malignancies globally. This year, APG-2575 has been granted two Orphan Drug Designations from the US FDA for the treatment of Waldenström macroglobulinemia (WM) and CLL.

"Dosing the first patient in our first clinical study in Europe marks yet another major milestone for Ascentage Pharma. This is the first step for Ascentage to execute expansion of clinical studies to Europe," said Dr. Yifan Zhai, Chief Medical Officer of Ascentage Pharma. "APG-2575 is a key drug candidate in our pipeline targeting apoptosis, and it has demonstrated great therapeutic potential in the treatment of hematologic malignancies. We will expedite the clinical development of APG-2575 and make strides toward offering more treatment options to patients with CLL/SLL globally including in Europe."

Symvivo Corporation Announces Research Collaboration With Janssen

On November 24, 2020 Symvivo Corporation, a clinical-stage biotechnology company advancing a proprietary bacTRL gene delivery platform, reported that it has entered into a research collaboration with Janssen Biotech, Inc. (Janssen), one of the Pharmaceutical Companies of Johnson & Johnson. Under the terms of the agreement, Janssen will have the exclusive option to research, develop and commercialize novel biological therapeutic candidates based on Symvivo’s bacTRL platform technology (Press release, Symvivo, NOV 24, 2020, View Source [SID1234571681]). The agreement was facilitated by Johnson & Johnson Innovation.

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"We are gratified to be collaborating with Janssen on this important research," said Lloyd Mackenzie, President and Chief Operating Officer at Symvivo. "This agreement continues to expand novel applications for the bacTRL platform."

Legend Biotech to Host Virtual Investor KOL Event Reviewing Latest CARTITUDE-1 Data from the 62nd American Society of Hematology (ASH) Annual Meeting

On November 24, 2020 Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech) reported that it will host a virtual Key Opinion Leader (KOL) event on Monday, December 7 at 7 pm ET highlighting the latest data from the Phase 1b/2 CARTITUDE-1 study (NCT03548207) of ciltacabtagene autoleucel (cilta-cel), an investigational BCMA-directed CAR-T cell therapy being studied for the treatment of patients with relapsed or refractory multiple myeloma (Press release, Legend Biotech, NOV 24, 2020, View Source [SID1234571680]). This will follow the oral presentation of the study results (Abstract #177) at the 2020 ASH (Free ASH Whitepaper) Annual Meeting.

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Intended for investors and other interested audiences, the event includes presentations by Ying Huang, PhD, CEO and CFO of Legend Biotech, along with the following leading professionals in hematology and oncology:

Sundar Jagannath, MD, Professor of Medicine, Hematology and Medical Oncology, Mount Sinai School of Medicine; Director, Multiple Myeloma Program at Mount Sinai Hospital.
Thomas G. Martin, MD, Clinical Professor of Medicine, Adult Leukemia and Bone Marrow Transplantation Program, and Associate Director, Myeloma Program, UCSF; Co-Leader, Hematopoietic Malignancies Program, Helen Diller Family Comprehensive Cancer Center.
To register and to view the live webcast, please visit: LegendBiotechASH2020.Convene.com.

About CARTITUDE-1

Cilta-cel is currently being investigated in the Phase 1b/2 CARTITUDE-1 (MMY2001, NCT03548207) registration study conducted in the US and Japan for the treatment of patients with multiple myeloma who have received at least 3 prior lines of therapy or are double refractory to a PI and IMiD, received a PI, an IMiD, and anti-CD38 antibody and documented disease progression within 12 months of starting the most recent therapy.

About Cilta-cel

Cilta-cel is an investigational chimeric antigen receptor T (CAR-T) cell therapy, formerly identified as JNJ-4528 in the U.S. and Europe and LCAR-B38M in China, that is being studied in a comprehensive clinical development program for the treatment of patients with relapsed or refractory multiple myeloma and in earlier lines of treatment. The design consists of a structurally differentiated CAR-T with two BCMA-targeting single domain antibodies. In December 2017, Legend Biotech, Inc. entered into an exclusive worldwide license and collaboration agreement with Janssen Biotech, Inc. (Janssen) to develop and commercialize cilta-cel. In addition to a Breakthrough Therapy Designation (BTD) granted in the U.S. in December 2019, cilta-cel received a PRIority MEdicines (PRiME) designation from the European Commission in April 2019 and BTD in China in August 2020. In addition, Orphan Drug Designation was granted for cilta-cel by the U.S. FDA in February 2019, and by the European Commission in February 2020.

Rocket Pharmaceuticals Announces Participation at Upcoming Conferences

On November 24, 2020 Rocket Pharmaceuticals, Inc. (NASDAQ: RCKT) ("Rocket"), a clinical-stage company advancing an integrated and sustainable pipeline of genetic therapies for rare childhood disorders, reported participation at the following upcoming conferences (Press release, Rocket Pharmaceuticals, NOV 24, 2020, View Source [SID1234571678]):

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Piper Sandler 32nd Annual Virtual Healthcare Conference
Tuesday, December 1, 2020
Evercore ISI 3rd Annual HealthCONx Conference
Gaurav Shah, M.D., President and CEO, is scheduled to participate in a fireside chat on Wednesday, December 2, 2020, at 3:30 p.m. Eastern Time.
A live audio webcast of the presentation will be available on the Investors section of the company’s website, www.rocketpharma.com. A replay of the presentation will be archived on the Rocket website following the conferences.

Repertoire Immune Medicines to Present at the 32nd Annual Piper Sandler Virtual Healthcare Conference

On November 24, 2020 Repertoire Immune Medicines, a clinical-stage biotech company creating a new category of immune therapies for cancer, autoimmune and infectious disease, reported that it will present at the 32nd Annual Piper Sandler Virtual Healthcare Conference on Monday, November 30, 2020 (Press release, Repertoire, NOV 24, 2020, View Source [SID1234571677]).

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