Hummingbird Bioscience Announces Trial in Progress Poster Presentation at the European Society for Medical Oncology Congress 2022

On September 8, 2022 Hummingbird Bioscience, a data-driven precision biotherapeutics company discovering and developing transformative biologic medicines for hard-to-treat diseases, reported that Johann de Bono, Regius Professor of Cancer Research and a Professor in Experimental Cancer Medicine at The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, will present a trial in progress poster outlining the Phase 1 clinical trial design for HMBD-001 at the European Society for Medical Oncology Congress (ESMO 2022) (Press release, Hummingbird Bioscience, SEP 8, 2022, View Source [SID1234619250]). Hummingbird Bioscience management will attend ESMO (Free ESMO Whitepaper) 2022, which takes place in Paris from 9-13 September 2022.

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The Phase 1 clinical trial in the United Kingdom is being sponsored and managed by Cancer Research UK’s Centre for Drug Development and led by Chief Investigator, Professor Johann De Bono.

The trial began enrolling in October 2021 and is ongoing in the UK. The trial in progress poster will summarize the Phase 1 clinical trial design for HMBD-001 (NCT05057013). The Phase 1, open-label, multi-center, first-in-human trial seeks to evaluate HMBD-001 as a monotherapy and in combination with other agents to determine the maximum tolerated dose and investigate the anti-cancer activity of HMBD-001.

"We are excited to discuss our Phase 1 clinical strategy for HMBD-001 and longer-term clinical development plans with the wider oncology community at ESMO (Free ESMO Whitepaper) 2022," said Jerome Boyd-Kirkup, Ph.D., Chief Scientific Officer. "The unique mechanism of action of HMBD-001 gives us hope that HMBD-001 will provide significant benefit to patients with HER3-driven cancers."

Nigel Blackburn, Ph.D., Director of Cancer Research UK’s Centre for Drug Development, said: "Our Centre for Drug Development has an outstanding track record in designing and managing clinical trials, so we are really proud to see that this work, in collaboration with Hummingbird Bioscience, will be showcased to an audience of our peers at the ESMO (Free ESMO Whitepaper) 2022 conference."

ESMO Poster Presentation Details
Poster Title: A CRUK phase I/IIA, first in human dose-escalation and expansion trial of HMBD-001 (an anti-HER-3 antibody) in patients with advanced HER3-positive solid tumours
Number: 493 TiP
Date: Monday, 12th September, 2022
Poster Hours: 09:00-17:00 CEST (discussion: 12:00-13:00 CEST)
Location: Poster Area, Hall 4, Paris Expo Porte de Versailles, Paris, France

About HMBD-001
HMBD-001 is a clinical-stage IgG1 antibody designed to target HER3. Discovered using Hummingbird Bioscience’s proprietary Rational Antibody Discovery (RAD) platform, HMBD-001 is now in development for the treatment of multiple solid tumors. We believe HMBD-001 is the only anti-HER3 antibody in development that has the potential to fully block both ligand-dependent and -independent HER3 activation and oncogenic signaling, by targeting a key epitope located at the interface where HER3 forms heterodimers with HER2 or EGFR. In preclinical models evaluating HMBD-001, the company has observed superior affinity and more potent tumor growth inhibition compared to existing anti-HER3 antibodies. Near-term development plans for HMBD-001 focus on a few priority, high-value indications with strong scientific rationale and supporting preclinical data, which includes HER3-driven cancers and NRG1 fusion-driven cancers.

GT Biopharma to Participate in the H.C. Wainwright 24th Annual Global Investment Conference in September

On September 8, 2022 GT Biopharma, Inc. (NASDAQ: GTBP), a clinical stage immuno-oncology company focused on developing innovative therapeutics based on the Company’s proprietary natural killer (NK) cell engager, TriKE platform, reported that management will present in-person at H.C. Wainwright’s 24th Annual Global Investment Conference taking place September 12-14, 2022 at the Lotte New York Palace (Press release, GT Biopharma, SEP 8, 2022, https://ir.gtbiopharma.com/news/detail/257/gt-biopharma-to-participate-in-the-h-c-wainwright-24th-annual-global-investment-conference-in-september [SID1234619249]). Company management will also be participating in 1×1 meetings during the event.

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H.C. Wainwright 24th Annual Global Investment Conference – September 12-14, 2022

Title: GT Biopharma (GTBP) Company Presentation
Date: Tuesday, September 13, 2022
Time: 10:30 – 11:00 am EDT
Location: Kennedy II, 4th Floor, Lotte New York Palace
Webcast Link: Register here
*a replay of the presentation will be available for 90 days
If you are interested in arranging a 1×1 meeting request with management, please contact your bank conference representative. To access the archived recording for replay, please see the Presentations section of GT Biopharma’s corporate website.

Genprex to Present at Upcoming September Investor Conference  

On September 8, 2022 Genprex, Inc. ("Genprex" or the "Company") (NASDAQ: GNPX), a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, reported that its Chief Financial Officer, Ryan Confer, will be providing a virtual overview of the Company’s gene therapies for cancer and diabetes at the following investor conference in September 2022 (Press release, Genprex, SEP 8, 2022, View Source [SID1234619248]).

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Event: H.C. Wainwright 24th Annual Global Investment Conference

Conference Dates: September 12-14, 2022

Virtual Presentation: On-demand within the virtual platform for all delegates starting September 12 at 7:00 a.m. ET

Presenter: Ryan Confer, Genprex’s Chief Financial Officer

Mr. Confer will deliver an overview of the Company’s pioneering gene therapies for cancer and diabetes and Company management will be available for in-person one-on-one meetings with investors through the H.C. Wainwright conference platform.

A recording of this presentation will be available for replay on Genprex’s website for a period of time.

Silence Therapeutics Announces FDA Fast Track Designation for SLN124, a Novel Investigational siRNA Therapy for the Treatment of Polycythemia Vera

On September 8, 2022 Silence Therapeutics plc, Nasdaq: SLN ("Silence" or "the Company"), a leader in the discovery, development and delivery of novel short interfering ribonucleic acid (siRNA) therapeutics for the treatment of diseases with significant unmet medical need, reported that the U.S. Food and Drug Administration ("FDA") has granted Fast Track Designation to SLN124, a novel siRNA targeting the TMPRSS6 gene, for the treatment of polycythemia vera ("PV") (Press release, Silence Therapeutics, SEP 8, 2022, View Source [SID1234619247]). The Company plans to start a phase 1/2 study in PV patients this year.

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SLN124 is designed to address a range of hematological diseases by targeting TMPRSS6 to increase endogenous hepcidin, the body’s master regulator of iron balance and distribution. SLN124 demonstrated proof of mechanism and was well tolerated in a healthy volunteer study completed last year.

"The granting of Fast Track Designation represents an important recognition by the FDA of SLN124’s potential to address a significant unmet need in the treatment of PV," said Craig Tooman, President and Chief Executive Officer of Silence. "We plan to leverage Fast Track to expedite our development path as we seek to provide an important new treatment option to those suffering from this very serious and chronic genetic disease."

Fast Track designation aims to facilitate the development and accelerate the review of new therapeutics that are intended to treat serious or life-threatening conditions and that potentially address an unmet medical need. Drugs that are granted this designation are given the opportunity for more frequent interactions with the FDA, as well as potential pathways for expedited approval.

In addition to PV, SLN124 is being evaluated in a phase 1 study in patients with thalassemia. SLN124 has orphan disease designations for PV, thalassemia, and myelodysplastic syndrome as well as a rare pediatric disease designation for thalassemia.

Dynavax to Present at the H.C. Wainwright 24th Annual Global Investment Conference

On September 8, 2022 Dynavax Technologies Corporation (Nasdaq: DVAX), a commercial-stage biopharmaceutical company developing and commercializing innovative vaccines, reported that Ryan Spencer, Chief Executive Officer, will participate in a virtual fireside chat at the H.C. Wainwright 24th Annual Global Investment Conference, being held September 12-14, 2022 (Press release, Dynavax Technologies, SEP 8, 2022, View Source [SID1234619245]).

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The on demand presentation will be available, beginning Monday, September 12, 2022 at 7:00 a.m. E.T. and may be accessed through the "Events & Presentations" page on the "Investors" section of the Company’s website at View Source