Nouscom Announces Janssen Receives US FDA IND Clearance for VAC85135, an ‘Off-The-Shelf’ Cancer Immunotherapy Developed using Nouscom’s Proprietary Viral Vector Platform

On May 17, 2022 Nouscom, a clinical stage immuno-oncology company developing both off-the-shelf and personalized cancer neoantigen immunotherapies, reported that Janssen Research & Development, LLC (Janssen) received U.S. Food and Drug Administration (FDA) clearance for its Investigational New Drug (IND) candidate VAC85135, an off-the-shelf, viral vector-based cancer vaccine for an oncologic indication. VAC85135 has been exclusively licensed to Janssen (Press release, NousCom, MAY 17, 2022, View Source [SID1234614775]).

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VAC85135 is based on Nouscom’s proprietary viral vector platform and is the first vaccine candidate to advance to this stage under a multi-project agreement with Janssen. Nouscom and Janssen have collaborated on the design and specific product research, with Nouscom accountable for process development activities and GMP manufacturing for VAC85135.

Under the terms of the agreement, Janssen has sole responsibility for clinical development of VAC85135. Financial terms, including individual product-specific upfront payments, potential development and commercial milestones, and future tiered royalties remain confidential.

Dr. Marina Udier, Chief Executive Officer of Nouscom, said, "We are very excited about Janssen’s IND clearance of VAC85135, the result of a long-standing and productive collaboration. This is another important milestone for Nouscom, the first licensed program, and the third clinical candidate after NOUS-209 and NOUS-PEV, to emerge from our immunologically potent viral vector platform."

Obsidian Therapeutics to Present Significant Advancements to its Proprietary cytoDRiVE® Technology at the American Society of Gene and Cell Therapy (ASGCT) Annual Meeting 2022

On May 17, 2022 Obsidian Therapeutics, Inc., a biotechnology company pioneering engineered cell and gene therapies, reported it will present enhancements to its proprietary cytoDRIVE technology during a poster presentation at the 25th ASGCT (Free ASGCT Whitepaper) Annual Meeting (Press release, Obsidian Therapeutics, MAY 17, 2022, View Source [SID1234614774]). The conference is being hosted in Washington, D.C., and virtually, May 16-19, 2022.

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The data to be presented outline next-generation advancements to Obsidian’s proprietary cytoDRiVE platform technology, which provides a way to precisely control the timing and level of protein function using FDA approved small molecules. Armoring cell therapies with potent cytokines such as IL12 is a promising approach to treating solid tumors, but uncontrolled constitutive expression of these payloads has limited their clinical use due to toxicity. The data to be presented demonstrate that Obsidian’s cytoDRiVE platform enables robust and reversible regulation of multiple cytokines such as IL12, IL23, IL2, and IFNα, potentially enabling their safe use in adoptive cell therapy applications.

"These advances in our regulation platform expand the versatility and breadth of potential applications for the cytoDRiVE technology," commented Jan ter Meulen, M.D., Ph.D., Chief Scientific Officer of Obsidian. "We look forward to continuing to leverage our technology to advance our pipeline of potential therapies designed to expand available treatment options and improve outcomes of patients using enhanced cell therapies, such as engineered tumor infiltrating lymphocytes."

Details of the poster presentation are as follows:

Poster Board Number: W-215
Session Title: Cancer – Immunotherapy, Cancer Vaccines III
Location: Hall D, Walter E. Washington Convention Center 801 Mt Vernon Pl NW Washington, D.C.
Date and Time: May 18, 2022, 5:30 p.m. to 6:30 p.m. ET
Title: Armoring T-cells with regulatable, membrane tethered cytokines using improved drug-responsive domain technology (cytoDRiVE)
Presenter: Dr. Dhruv K. Sethi, Director, Lead, Discovery & DRD Technologies, at Obsidian Therapeutics

Abstract Summary: Cytokines such as IL12 and IFNα have shown great promise in pre-clinical studies when expressed from genetically modified T-cells, however broad use is limited by toxicity from systemic exposure of constitutive expression. If concentration and localization of cytokines and other immunomodulators could be effectively regulated, they would strong candidates for armoring cellular therapies, such as chimeric antigen receptor T cells (CAR-T cells) or tumor infiltrating lymphocytes (TILs). Advancements to the cytoDRiVE platform, based on multimerization of DRDs with homologous or heterologous oligomerization domains to increase their degron effect, enable tight regulation with extremely low cell surface abundance in the absence of drug, and robust induction (10-20 fold) in the presence of drug. Design elements such as membrane-tethering to reduce risk of systemic toxicity and engineering of protease sites for controlled shedding enable fit-for-purpose engineering and potential to regulate multiple cytokines. cytoDRiVE provides full control of the abundance of IL12, IL23, IL2, and IFNα in genetically modified T-cells using a small molecule drug as the on/off switch for precise control of cytokine activity.

Medivir to present at the ABGSC Life Science Summit

On May 17, 2022 Medivir AB (Nasdaq Stockholm: MVIR) reported that the company will present at the ABGSC Life Science Summit on May 18, 2022. The company will be represented by CEO Jens Lindberg (Press release, Medivir, MAY 17, 2022, View Source [SID1234614773]).

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The presentation will be available after the meeting on Medivirs website; www.medivir.com.

Idera Pharmaceuticals Shares Positive Results from Investigator-Sponsored Trial in Melanoma Patients at Amsterdam UMC

On May 17, 2022 Idera Pharmaceuticals, Inc. ("Idera," "we," and "our") (Nasdaq: IDRA) reported that positive interim results from Amsterdam UMC, Vrije Universiteit Amsterdam, the Netherlands, regarding its investigator-sponsored trial, INTRIM 1, involving tilsotolimod, Idera’s synthetic Toll-like receptor 9 agonist. Based on these results, the trial has been stopped early (Press release, Idera Pharmaceuticals, MAY 17, 2022, View Source [SID1234614737]).

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INTRIM 1 is a randomized, double-blind, placebo-controlled Phase 2 trial among patients with localized, excised melanoma (pathological tumor stage 3-4) with no regional metastases detected and no evidence of distant metastasis. The trial involved a single, intradermal injection of 8 mg tilsotolimod or saline placebo given at the primary tumor excision site, followed by re-excision and sentinel lymph node (SLN) biopsy 7-10 days later. Noting that there were more patients with ulcerated lesions in the placebo arm compared to the tilsotolimod arm, topline interim results of the respective SLN-positivity rates showed a 70% lower SLN+ rate among patients injected with tilsotolimod as compared to those injected with placebo; the placebo SLN+ rate was in the mid-40%s. Statistical significance exceeded the pre-specified p-value of 0.008. Adverse reactions included injection site reactions, malaise, fever and flu-like symptoms.

"This is an exciting result from tilsotolimod, and we are pleased for the patients and their families to whom it offers hope for the future," said Vincent Milano, Idera’s Chief Executive Officer. "These results, together with data supporting tilsotolimod’s mechanism of action and encouraging safety profile from across the array of earlier pre-clinical and clinical work, reinforce the potential of tilsotolimod to offer benefit to patients with certain cancers. As a result, we plan to actively pursue a strategic partnership for tilsotolimod so that its full potential for patients may continue to be explored."

This interim result validates previously reported results from INTRIM 1 that showed immune activation, including elevated frequencies of key dendritic cells, in early analysis by flow cytometry of the SLN biopsies. The trial will continue to relapse-free survival (RFS) and overall survival (OS) at 5 and 10 years after SLN biopsy.

"Currently, there are limited adjuvant treatments available to improve survival after surgical excision of a primary melanoma," said Prof. Tanja de Gruijl of Amsterdam UMC. "We are delighted with the results we have seen in this study, which suggest that tilsotolimod administered at the excision site lowers the extent of tumor-positive lymph nodes and, if it improves overall survival, offers early melanoma patients a potential new treatment option." Amsterdam UMC investigators plan to present the full data set at an upcoming medical meeting.

About Melanoma

Melanoma is a cancer that begins in a type of skin cell called melanocytes. While melanoma is the least common type of skin cancer, it has a poor prognosis when not detected and treated early. Early stages of melanoma are treated by removing, or excising, the tumor surgically. However, even after surgery, nearly one-third of all melanoma patients will experience disease recurrence and most relapses eventually will progress to metastatic disease. When regional lymphatic metastases are present, the 10-year survival rate is 68% – 24%. SLN biopsy is a useful prognostic tool for the assessment of melanoma relapse and mortality risk. Ulceration is associated with more SLN positivity.

In many cases, additional cancer treatment, referred to as adjuvant therapy, is given after the primary excision of the melanoma. The goal of adjuvant therapy is to reduce the risk of melanoma returning and potentially metastasizing. The adjuvant market size for melanoma excision cases is over 1 million cases globally and about 300,000 in the US annually. As is the case in many forms of cancer, melanoma becomes more difficult to treat once the disease has spread, or metastasized, beyond the skin to other parts of the body.

About INTRIM 1

INTRIM 1 is a multi-center investigator-sponsored trial conducted by UMC Amsterdam among patients with pT3-4 cN0M0 melanoma. The study is a randomized, double-blind, placebo-controlled Phase 2 trial of a single, intradermal injection of 8 mg tilsotolimod or of saline placebo given at the primary tumor excision site 7-10 days prior to SLN biopsy.

INTRIM 1 is intended to examine the ability of tilsotolimod to induce loco-regional and systemic immune stimulation, and therefore, improve survival among the targeted patient population. Outcome measures of the trial include the following:

· Primary endpoint: rate of tumor positive SLN at the time of biopsy.
·Secondary endpoints:
·Immune response in the SLN and peripheral blood 7-10 days post-biopsy, as measured by frequency and activation state of lymph node resident (LNR) conventional dendritic cells (DC) and melanoma antigen-specific T cell responses in the SLN and peripheral blood.
·RFS, determined by the length of time from intradermal injection of tilsotolimod to first documentation of recurrence (RFS), measured at 5 and 10 years after SLN biopsy.
·OS at 5 and 10 years after SLN biopsy, determined by the length of time from intradermal injection of tilsotolimod to death from any cause.

While enrollment for the primary endpoint has been halted early as a result of the primary endpoint being met, the study will continue to its secondary endpoints. For more information on the INTRIM 1 trial, please visit www.ClinicalTrials.gov (NCT04126876).

About Tilsotolimod (IMO-2125)

Tilsotolimod is an investigational, synthetic Toll-like receptor 9 agonist. Tilsotolimod has been shown to promote both innate (Type-I IFN, antigen presentation) and adaptive (T cells) immune activation and may, in turn, contribute to tumor suppression and regression. For more information on tilsotolimod trials, please visit www.ClinicalTrials.gov.

Precigen to Participate in the 2022 H.C. Wainwright Global Investment Conference

On May 17, 2022 Precigen, Inc. (Nasdaq: PGEN), a biopharmaceutical company specializing in the development of innovative gene and cell therapies to improve the lives of patients, reported that Helen Sabzevari, PhD, President and CEO of Precigen, will participate in a virtual fireside chat at the 2022 H.C. Wainwright Global Investment Conference (Press release, Precigen, MAY 17, 2022, https://www.prnewswire.com/news-releases/precigen-to-participate-in-the-2022-hc-wainwright-global-investment-conference-301549528.html [SID1234614772]). A webcast of the event will be available beginning at 7:00 AM ET on Tuesday, May 24, 2022.

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Participants may register and access the webcast through Precigen’s website in the Events & Presentations section at investors.precigen.com/events-presentations.