Delcath Systems to Participate in Upcoming Investor Conferences

On March 8, 2024 Delcath Systems, Inc. (Nasdaq: DCTH), an interventional oncology company focused on the treatment of primary and metastatic cancers of the liver, reported that Company management will be attending the following upcoming investor conferences (Press release, Delcath Systems, MAR 8, 2024, View Source [SID1234640965]):

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Leerink Partners Global Biopharma Conference
Date: March 13, 2024
Location: Miami Beach, FL

36th Annual ROTH Conference
Date: March 18 – 19, 2024
Location: Dana Point, CA

Management is scheduled to host one-on-one meetings throughout the event. Investors interested in arranging one-on-one meetings should contact your conference representative. You may also call or email Ben Shamsian of Lytham Partners at 646-829-9701, or [email protected].

BIO-PATH HOLDINGS REPORTS FULL YEAR 2023 FINANCIAL RESULTS

On March 8, 2024 Bio-Path Holdings, Inc., (NASDAQ:BPTH), a biotechnology company leveraging its proprietary DNAbilize liposomal delivery and antisense technology to develop a portfolio of targeted nucleic acid cancer drugs, reported its financial results for the year ended December 31, 2023 and provided an update on recent corporate developments (Press release, Bio-Path Holdings, MAR 8, 2024, View Source [SID1234640963]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

"2023 was a year of focused execution, as evidenced by the continued progress across our pipeline of DNAbilize programs," said Peter Nielsen, President and Chief Executive Officer of Bio-Path Holdings. "In the fourth quarter, we were delighted to announce important enrollment updates in our Phase 1/1b clinical trial of BP1002 in refractory/relapsed Acute Myeloid Leukemia (AML) and our Phase 1 clinical trial of BP1002 in refractory/relapsed lymphoma and refractory/relapsed Chronic Lymphocytic Leukemia (CLL). As we look to the months and year ahead, we expect to build on the clinical progress achieved to date to bring potentially life-saving new medicines to patients battling cancers."

Recent Corporate Highlights

● Hosted Key Opinion Leader (KOL) Event to Discuss Prexigebersen and Advances in the AML Treatment Landscape. In October, Bio-Path hosted a virtual KOL event to discuss the current AML treatment landscape and the growing body of clinical evidence in support of prexigebersen as a treatment for AML. The event featured presentations from Jorge Cortes, M.D., Director, Georgia Cancer Center, Augusta University and Maro Ohanian, D.O., Department of Leukemia, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center.

● Successfully Completed First Dose Cohort of Phase 1/1b Clinical Trial of BP1002 in Refractory/Relapsed Acute Myeloid Leukemia. In December, the Company announced the completion of the first dose cohort of the dose escalation portion of its Phase 1/1b clinical trial of BP1002 evaluating the ability of BP1002, a liposomal Bcl-2 nanoparticle antisense, to treat refractory/relapsed AML patients including venetoclax-resistant patients.

● Completed First Dose Cohort in Phase 1 Clinical Trial Evaluating BP1002 to Treat Refractory/Relapsed Lymphoma and Refractory/Relapsed Chronic Lymphocytic Leukemia Patients. In December, Bio-Path announced completion of the first dose cohort of the dose escalation portion of its Phase 1 clinical trial of BP1002 evaluating the ability of BP1002 for the treatment of refractory/relapsed lymphoma and refractory/relapsed CLL patients.

Financial Results for the Year Ended December 31, 2023

● The Company reported a net loss of $16.1 million, or $33.63 per share, for the year ended December 31, 2023, compared to a net loss of $13.9 million, or $38.12 per share, for the year ended December 31, 2022.

● Research and development expense for the year ended December 31, 2023 increased to $11.6 million, compared to $9.2 million for the year ended December 31, 2022 primarily due to manufacturing expenses related to drug product releases in 2023 as well as an increase in expense related to our clinical trial for prexigebersen in AML due to increased patient enrollment in 2023.

● General and administrative expense for the year ended December 31, 2023 decreased to $4.2 million, compared to $4.7 million for the year ended December 31, 2022 primarily due to decreased salaries and benefits expense as well as franchise tax expenses.

● Change in fair value of the Company’s warrant liability for the year ended December 31, 2023 resulted in a non-cash loss of $0.3 million. The company did not have the warrant liability in 2022.

● As of December 31, 2023, the Company had cash of $1.1 million, compared to $10.4 million as of December 31, 2022. Net cash used in operating activities for the year ended December 31, 2023 was $11.5 million compared to $15.1 million for the comparable period in 2022. Net cash provided by financing activities for the year ended December 31, 2023 was $2.2 million.

Conference Call and Webcast Information

Bio-Path Holdings will host a conference call and webcast today at 8:30 a.m. ET to review these full-year 2023 financial results and to provide a general update on the Company. To access the conference call please dial (833) 630-1956 (domestic) or (412) 317-1837 (international). A live audio webcast of the call and the archived webcast will be available in the Media section of the Company’s website at www.biopathholdings.com.

Arbutus to Participate in Two Upcoming Investor Conferences

On March 8, 2024 Arbutus Biopharma Corporation (Nasdaq: ABUS), a clinical-stage biopharmaceutical company leveraging its extensive virology expertise to develop a functional cure for people with chronic hepatitis B virus (cHBV) infection, reported that the Arbutus management team will participate in and host one-on-one meetings at the following two upcoming investor conferences which are being held in Miami, FL (Press release, Arbutus Biopharma, MAR 8, 2024, View Source [SID1234640962]):

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Barclays 26th Annual Global Healthcare Conference: Formal Presentation on March 12, 2024 at 2:05 pm ET
Jefferies Biotech on the Bay Summit: March 13, 2024

To access the live webcast of the presentation at the Barclays 26th Annual Global Healthcare Conference please visit: View Source An archived replay of the webcast will be available on the Arbutus website for a limited time after the event.

First-line treatment for NSCLC! I-Mab initiates Phase II/III clinical trial of CD73 monoclonal antibody combined with toripalimab

On March 7, 2024 Tianjin Jiancheng Biopharma reported the company registered a Phase II/III, randomized, multicenter, open study on the Drug Clinical Trial Registration and Publicity Platform for the treatment of patients with previously untreated locally advanced, unresectable or metastatic PD-L1 and CD73 selective non-small cell lung cancer (NSCLC) with ulelimumab (CD73 monoclonal antibody) combined with toripalimab (PD-1), toripalimab alone, and pembrolizumab alone (Press release, TJ Bio, MAR 7, 2024, View Source [SID1234654000]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

The study plans to recruit 450 subjects in China, aiming to confirm the superiority of ulelimumab combined with toripalimab in prolonging PFS compared with pembrolizumab treatment. The main researchers include Professor Wu Yilong of Guangdong Provincial People’s Hospital. Ulelimab is an innovative humanized antibody targeting the CD73 target, independently developed by I-Mab. By binding to a new antigen epitope of the CD73 dimer molecule, Ulelimab can effectively inhibit the enzymatic activity of CD73 in a non-substrate competitive manner, reduce the production of adenosine, promote T cell activity and tumor suppression effect. At the 2023 ASCO (Free ASCO Whitepaper) conference, I-Mab announced the positive research results of the Phase Ib/II clinical trial (NCTO4322006) of the combination therapy of ulelimumab and toripalimab for the first-line treatment of advanced NSCLC. Among newly diagnosed NSCLC patients, 31% responded to the combination therapy; among patients with high CD73 expression and PD-L1 positive, 63% responded to the combination therapy.

BridGene Biosciences Announces FDA Acceptance of IND Application of Novel TEAD Inhibitor BGC515

On March 7, 2024 BridGene Biosciences, Inc., a pioneer in the development of covalent small molecule drugs for traditional "hard-to-drug" targets, reported that the U.S. Food and Drug Administration (FDA) has accepted its Investigational New Drug (IND) application for the clinical study of its TEAD inhibitor BGC515 for the treatment of cancers harboring genetic mutations in the hippo signaling pathway (Press release, Bridgene Biosciences, MAR 7, 2024, View Source [SID1234644278]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

"We are pleased to announce the FDA acceptance of our IND application for BGC515 and look forward to initiating this Phase I clinical study to evaluate the safety and efficacy profile of BGC515 in patients with advanced solid tumors," stated Ping Cao, Ph.D., Co-Founder and CEO of BridGene Biosciences. "Discovered through our unique chemoproteomic platform, IMTAC, the TEAD inhibitor BGC515 represents a significant breakthrough. The FDA’s endorsement of this IND not only validates our innovative platform but also highlights a critical step forward in our mission to develop pioneering treatments for cancer patients."